ESENS group,
I just a found great website by Dr. Carley with more information on how vaccines cause auto-immune diseases (and demyelination, which I have) and much more. I am glad to see that Dr. Carley is a proponent of bovine colostrum in her protocol to recover from this condition (and autism). My hunch is that electrical sensitivity is a demyelinating auto-immune disorder caused by viruses (measles causes demyelination) in a vaccine weakened immune system and stressed by an environmental overload (radiation, toxins, chemicals, etc). I hope more people with ES will get tested for demyelination and the presence of auto-immune anti-bodies to confirm this relationship. I will let you know more on the healing protocol if it works for me. Andrew Excerpts from http://drcarley.com/ AUTISM IS SUBACUTE SCLEROSING PANENCEPHALITIS INOCULATIONS ARE CAUSING THE CORRUPTION OF THE IMMUNE SYSTEM LEADING TO ALL AUTOIMMUNE DISEASE AND CANCER IN PEOPLE AND PETS. ...by directly injecting organisms into the body leads to a corruption in the immune system...As a result, the pathogenic viruses or bacteria cannot be eliminated by the immune system and remain in the body, where they cause chronic disease and thus further grow and/or mutate as the individual is exposed to ever more antigens and toxins in the environment. In fact, the “prevention” of a disease via vaccination is, in reality, an inability to expel organisms due to the suppression of the cell-mediated response. Thus, rather than preventing disease, the disease is actually prevented from ever being resolved. The organisms continue circulating through the body, adapting to the hostile environment by transforming into other organisms depending on acidity, toxicity and other changes to the internal terrain of the body as demonstrated by the works of Professor Antoine Béchamp. He established this prior to the development of the “germ theory” of disease by Louis Pasteur. Pasteur’s “germ theory” was a plagiarist’s attempt to reshape the truth from Béchamp into his own “original” premise – the beLIEf that germs are out to “attack” us, thereby causing dis-ease. Thus, treatment of infection with antibiotics as well as “prevention” of disease with vaccines are both just corrupted attempts at cutting off the branches of dis-ease, when the root of the cause is a toxic internal environment combined with nutritional deficiency. However, since Pasteur’s germ theory was conducive to the profits of the burgeoning pharmaceutical cartels that only manage dis-ease, no mention of the work of Professor Béchamp is made in medical school curricula. If components of the myelin sheath (the insulating covering of nerve fibers which allows proper nerve conduction) or the actual neurofilaments themselves are attacked by auto-antibodies, the resultant condition is determined solely by the location of the damage done. Such neurological conditions include but are not limited to minimal brain dysfunction, ADD/ADHD, learning disabilities, mental retardation, criminal behavior, the spectrum of pervasive developmental disorders (including autism), multiple sclerosis, Parkinson’s disease, Lou Gehrig’s disease, Guillen Barre’, seizure disorders, etc., etc. etc. (Please note that other factors are also sometimes involved, such as: the spirochete which causes Lymes disease, aspartame and mercury in cases of MS; aspartame in seizures; or pesticides in cases of Parkinson’s). Thus, when detoxing to reverse these diseases, these other substances must also be removed to obtain a full recovery. However, the corruption of the immune system caused by the injection of vaccines is a key component in these disease states leading to immune malfunction, and is the reason why an autistic child may also have leaky gut or eczema, etc. Note that myelin production, for the most part, does not begin until after birth. Most myelin is apparently laid down by age 5 years and usually completed by age 10 years, judging by the level of success at various ages in reversing autistic and other neurological VIDS symptoms that this author has observed in hundreds of children by detoxing the viruses with homeopathic nosodes5, and repairing the immune corruption by simultaneous administration of bovine colostrum (i.e., after 10 years of age, the ability to stop and repair auto-antibody induced damage in the myelin sheath and neurofilaments themselves is dramatically decreased). # The antigens present in the culture media itself cannot be completely filtered and separated from the organisms cultured thereon. Thus, any antibodies formed against antigens from the culture cells themselves (for example myelin basic protein from chick embryos or the 13 vaccines which now contain aborted human fetal cells) can cross-react to form an autoimmune reaction against the myelin basic protein in your myelin sheath, etc. See the package insert from Pfizer’s Rabies vaccine from the “10th Edition of the Compendium of Veterinary Products” published in 2007 posted on www.drcarley.com, which states “tissue origin vaccines contain extraneous protein in addition to the [rabies] antigen that can lead to autoimmune disease”. THIS IS TRUE FOR ALL VACCINES, BUT THIS IS THE FIRST TIME I HAVE SEEN IT ADMITTED BY ANY VACCINE MANUFACTURER. Although the symptoms of mercury poisoning have been described as identical to the symptoms of autism, it should be noted that most children who descend into the hellish state known as autism do so after the MMR vaccine. The MMR vaccine is one of the few vaccines that do not contain mercury; in fact, it has NEVER contained mercury. Thus, it is self-evident that the removal of mercury will not make vaccines “safe”. (This is why the mercury is the only thing being addressed at all; because when the people reading this paper realize that the very mechanism by which vaccines corrupt the immune system means that NO vaccine is safe and effective; there will be an evolution of consciousness where the structure of lies telling us vaccines are safe and effective disintegrates.) The good news is that these VIDS can be reversed using natural remedies (especially homeopathy) contained in the Hippocrates Protocol (www.drcarley.com). the genocidal plan could drop anytime with activation of the Model State Health Emergency Powers Act whenever the next fabricated terrorist attack using biological agents occurs. The “bird flu” is apparently going to be used as an excuse to inoculate the masses soon, as predictions of a pandemic are being made by the media almost every day. Little do people know that the 1918 Flu pandemic was actually caused by inoculations given to soldiers in WW 1, as reported on p. 28 of the book Vaccination the Silent Killer by Ida Honorof & E. McBean. [as recent evidence see: Vaccines as Biological Weapons? Live Avian Flu Virus Placed in Baxter Vaccine Materials Sent to 18 Countries http://www.naturalnews.com/025760.html] As stated in Harrison's Principles of Internal Medicine , 6th edition, p. 943: "RARELY IS PREVENTION OF INFECTION PER SE CONSIDERED TO BE AN IMPORTANT GOAL OF VACCINATION. In fact, asymptomatic infection after vaccination can serve to enhance and prolong the immune response." Of course, if the immune response has been overwhelmed or corrupted, the "asymptomatic infection" will become a CHRONIC DISEASE. In fact, on the same page of Harrison's, in the following paragraph, it states the following: "PERSISTENCE AND LATENCY. Many viruses persist in host tissues for months or years without causing overt disease. A FLARE-UP OF THESE LATENT INFECTIONS MAY BE INDUCED BY TRAUMA, INTERCURRENT DISEASE, DECLINE IN ANTIBODY TITERS, OR UNKNOWN STIMULI. Experiments with tissue cultures and laboratory animals reveal that persistence of virus in tissue results from an interplay of various factors peculiar to each virus and its host. LATENCY IS PROMOTED BY THE PRESENCE OF ANTIBODY OR OTHER VIRAL INHIBITORS THAT PREVENT EXTENSIVE CELL-TO-CELL SPREAD OF VIRUS. IF ANTIBODY IS WITHDRAWN, VIRAL MULTIPLICATION OFTEN RESUMES, WITH CONCOMITANT CELLULAR NECROSIS." In the same (6th) Edition of Harrison's Principles of Internal Medicine , it is stated on page 975 in regards to the poliomyelitis vaccine: "Vaccine virus multiplies in the intestinal tract and remains at this site. LIVE VACCINE VIRUS SPREADS AND INFECTS CONTACTS OF VACCINATED INDIVIDUALS. This type of immunization in the presence of epidemic poliomyelitis may lead to REPLACEMENT OF THE "WILD" PARALYTOGENIC STRAIN BY THE ONE IN THE VACCINE....." In direct contradiction to this statement, the 1/1/2000 Vaccine Information statement put out by the U.S. Department of Health & Human Services, Centers for Disease Control and Prevention National Immunization Program states that the "OPV (Oral Polio Vaccine) is better at keeping the disease from spreading to other people. However, it does state in this document that "OPV actually causes polio". The inoculation of organisms causes disease both by direct introduction of organisms (including viruses that cause cancer) into the bloodstream, as well as corruption of the immune system leading to autoimmune disease (was posted on the CDC's own website and then removed) OCSO - OPHR - CDC's Research Agenda - Starter List Comments , where Dr. Carley's paper "Inoculation the True Weapons of Mass Destruction causing an Epidemic of Genocide" was posted, and describes the mechanism whereby corruption of the immune system occurs). In this paper (which Dr. William Atkinson of the CDC's immunization program has refused to respond to), it states that the hyperactivity of the humeral arm of the immune system in autoimmune disease is caused by adjuvants added just for that purpose. However, the damage caused by the autoimmunity (i.e., antibody against self) has several mechanisms, including the following: 1. The antigens present in the culture media itself cannot be completely filtered and separated from the organisms cultured thereon. Thus, any antibodies formed against antigens from the culture cells themselves (for example myelin basic protein from chick embryos or the 13 vaccines which now contain aborted human fetal cells) can cross-react to form an autoimmune reaction against the myelin basic protein in your myelin sheath, etc. causing DEMYELINATION. 2. Molecular mimicry is due to similarity of proteins contained in organisms and mammals. (For example, the measles virus is made up of proteins similar to myelin basic protein; thus, antibodies formed against the measles virus antigens subsequently also cause an auto-antibody attack against myelin basic protein in the myelin sheath due to cross reactivity of these antibodies) causing DEMYELINATION (leading to Autism, as proven below). In the aforementioned 6th edition of Harrison's Principles of Internal Medicine on p. 1791, under the heading "Multiple Sclerosis and other DEMYELINATING Diseases", it states the following: "A large and important group of neurologic disorders are termed the demyelinating diseases because they share the common pathologic feature of foci of degeneration, involving the myelin sheath of nerves. These foci vary in size, shape, distribution, and rate of development in the different illnesses. The axis cylinder often suffers damage, as does the myelin sheath, but the destruction of myelin is considered the primary change...syndromes can be clearly distinguished....(including) acute disseminated encephalomyelitis (including post infectious and POSTVACCINAL ENCEPHALOMYELITIS)...(P. 1798) - "the association of the neurologic disorder with vaccination or inoculation usually leaves the diagnosis in little doubt, and the characteristic combination of encephalitic and myelitic features will help to distinguish the condition from meningitis, viral encephalitis, and poliomyelitis". This self evident fact has been taken out of subsequent editions of Harrison's Principles of Internal Medicine , since as the vaccine schedule has dramatically increased over the years, the incidence of vaccine induced demyelination has correspondingly increased. This is most evident in the case of autism, which has now risen to epidemic proportions in this country. Yet, whereas there is almost no history of the disease in the families of these children in most cases, and the parents report the onset of symptoms after the child receives the MMR vaccine, the various arms of the medical establishment (including the CDC) conclude that this is just a "coincidence"; rather than that the association of the neurologic disorder (autism) with vaccination or inoculation usually leaves the diagnosis in little doubt. The way that the true etiology of autism is hidden from doctors is by changing the name of the vaccine induced disease. For example, SUB ACUTE SCLEROSING PAN ENCEPHALITIS (SSPE) has been changed to AUTISM, as is demonstrated in the 10th edition of Harrison's Principles of Internal Medicine where, on page 2096, the following information about SSPE is included: "...The disease affects boys 3 to 10 times as frequently as girls...Characteristically, they are entirely well until the disease begins. The onset of usually insidious mental deterioration, often expressed by a decline in the patient's schoolwork, is the presenting symptom . Incoordination, ataxia, and myoclonic jerks develop within a few months along with abnormalities of the pyramidal and extrapyramidal motor systems....Elevated levels of measles antibody are found in the serum and CSF....Measles virus is the etiologic agent....Staining of brain tissue from patients with the disease demonstrates measles virus antigen in the inclusions....A few reported cases have been related to measles vaccination." Of course, the vaccine etiology has been deleted from the 16th edition of Harrison's Principles of Internal Medicine , although the age of onset has been changed to 2 years in that edition. What becomes SELF EVIDENT from these various editions of Harrison's Principles of Internal Medicine (the "Bible" by which all medical students learn about internal medicine) is that the source of almost all of the viruses that cause demyelinating diseases is actually VACCINES; and that the names of the diseases are changed to hide the true etiology. Another example of this can be found on page 2104 of the 10th edition of Harrison's Principles of Internal Medicine, under the discussion of ACUTE NECROTIZING HEMORRHAGIC ENCEPHALOMYELITIS, which is described as a "tissue destructive disease of the central nervous system which occurs with explosive suddenness within a few days of an upper respiratory infection. The pathologic findings are distinctive. On sectioning the brain, much of the white matter of one or both hemispheres is seen to be destroyed almost to the point of liquefaction. The involved tissue is pink or yellowish-gray and flecked with multiple small hemorrhages. Sometimes similar changes are localized to the brainstem or spinal cord. As in acute disseminated encephalomyelitis in showing perivenular foci of demyelination, all of like age.....The cerebrospinal fluid examination discloses a more intense reaction than in other demyelinating diseases....The etiology of this disease is not established; however, the entire clinical-pathologic entity bears a close resemblance to a hyper acute form of EAE which can be induced in animals by administration of endotoxin, PERTUSSIS VACCINE, or its histamine sensitizing factor coincident with or shortly after injection of myelin in adjuvant. What is self evident from this description is that this disease is actually SIDS (Sudden Infant Death Syndrome) or many of the cases of Shaken Baby Syndrome (the differentiation being whether the child has any evidence of trauma that the prosecutor can use to make a case for shaken baby and subsequently charge a parent with murder, as happened in the well-known case of Alan Yurko in Florida). Thus, once again, the name of the disease has been changed to conceal the fact that the pertussis vaccine is the cause of SIDS and many cases of Shaken Baby Syndrome. |
Hi Andrew You might find a book by Dr Jean Elmiger, of France and Switzerland, called "Rediscovering Real Medicine" of interest. "Over years of practice, Dr Elmiger became convinced of the progressive destruction of the foundations of good health, such as the prolific inoculation of young children, the use of antibiotics and the effects of shock or trauma, including surgical operations. His search resulted in an entirely new vision of the origins of illness and how to eradicate it using homoeopathy in a completely different way (sequential homoeopathic therapy)". The book is out of print but you can find used copies on the internet. I found one for about $20.00. It is very interesting reading. It tells what causes the problems and the necessary sequence of treatments to fix the problems using homoeopathy. The web site is: http://www.jelmiger.com/ <http://www.jelmiger.com/> Bill --- In [hidden email], Andrew McAfee <amcafeerr@...> wrote: > > ESENS group, > I just a found great website by Dr. Carley with more information on how > vaccines cause auto-immune diseases (and demyelination, which I have) > and much more. > I am glad to see that Dr. Carley is a proponent of bovine colostrum in > her protocol to recover from this condition (and autism). > My hunch is that electrical sensitivity is a demyelinating auto-immune > disorder caused by viruses (measles causes demyelination) in a vaccine > weakened immune system and stressed by an environmental overload > (radiation, toxins, chemicals, etc). > I hope more people with ES will get tested for demyelination and the > presence of auto-immune anti-bodies to confirm this relationship. > I will let you know more on the healing protocol if it works for me. > Andrew > > Excerpts from http://drcarley.com/ > > AUTISM IS SUBACUTE SCLEROSING PANENCEPHALITIS > > INOCULATIONS ARE CAUSING THE CORRUPTION OF THE IMMUNE SYSTEM LEADING > ALL AUTOIMMUNE DISEASE AND CANCER IN PEOPLE AND PETS. > > ...by directly injecting organisms into the body leads to a corruption > in the immune system...As a result, the pathogenic viruses or bacteria > cannot be eliminated by the immune system and remain in the body, where > they cause chronic disease and thus further grow and/or mutate as the > individual is exposed to ever more antigens and toxins in the > environment. > > In fact, the "prevention" of a disease via vaccination is, in reality, > an inability to expel organisms due to the suppression of the > cell-mediated response. Thus, rather than preventing disease, the > disease is actually prevented from ever being resolved. The organisms > continue circulating through the body, adapting to the hostile > environment by transforming into other organisms depending on acidity, > toxicity and other changes to the internal terrain of the body as > demonstrated by the works of Professor Antoine Béchamp. He established > this prior to the development of the "germ theory" of disease by Louis > Pasteur. Pasteur's "germ theory" was a plagiarist's attempt to reshape > the truth from Béchamp into his own "original" premise the beLIEf > that germs are out to "attack" us, thereby causing dis-ease. Thus, > treatment of infection with antibiotics as well as "prevention" of > disease with vaccines are both just corrupted attempts at cutting off > the branches of dis-ease, when the root of the cause is a toxic > internal environment combined with nutritional deficiency. However, > since Pasteur's germ theory was conducive to the profits of the > burgeoning pharmaceutical cartels that only manage dis-ease, no mention > of the work of Professor Béchamp is made in medical school curricula. > > If components of the myelin sheath (the insulating covering of nerve > fibers which allows proper nerve conduction) or the actual > neurofilaments themselves are attacked by auto-antibodies, the > resultant condition is determined solely by the location of the damage > done. Such neurological conditions include but are not limited to > minimal brain dysfunction, ADD/ADHD, learning disabilities, mental > retardation, criminal behavior, the spectrum of pervasive developmental > disorders (including autism), multiple sclerosis, Parkinson's disease, > Lou Gehrig's disease, Guillen Barre', seizure disorders, etc., etc. > etc. (Please note that other factors are also sometimes involved, such > as: the spirochete which causes Lymes disease, aspartame and mercury in > cases of MS; aspartame in seizures; or pesticides in cases of > Parkinson's). Thus, when detoxing to reverse these diseases, these > other substances must also be removed to obtain a full recovery. > However, the corruption of the immune system caused by the injection of > vaccines is a key component in these disease states leading to immune > malfunction, and is the reason why an autistic child may also have > leaky gut or eczema, etc. Note that myelin production, for the most > part, does not begin until after birth. Most myelin is apparently laid > down by age 5 years and usually completed by age 10 years, judging by > the level of success at various ages in reversing autistic and other > neurological VIDS symptoms that this author has observed in hundreds of > children by detoxing the viruses with homeopathic nosodes5, and > repairing the immune corruption by simultaneous administration of > bovine colostrum (i.e., after 10 years of age, the ability to stop and > repair auto-antibody induced damage in the myelin sheath and > neurofilaments themselves is dramatically decreased). > > # The antigens present in the culture media itself cannot be completely > filtered and separated from the organisms cultured thereon. Thus, any > antibodies formed against antigens from the culture cells themselves > (for example myelin basic protein from chick embryos or the 13 vaccines > which now contain aborted human fetal cells) can cross-react to form an > autoimmune reaction against the myelin basic protein in your myelin > sheath, etc. See the package insert from Pfizer's Rabies vaccine from > the "10th Edition of the Compendium of Veterinary Products" published > in 2007 posted on www.drcarley.com, which states "tissue origin > vaccines contain extraneous protein in addition to the [rabies] antigen > that can lead to autoimmune disease". THIS IS TRUE FOR ALL VACCINES, > BUT THIS IS THE FIRST TIME I HAVE SEEN IT ADMITTED BY ANY VACCINE > MANUFACTURER. > > Although the symptoms of mercury poisoning have been described as > identical to the symptoms of autism, it should be noted that most > children who descend into the hellish state known as autism do so after > the MMR vaccine. The MMR vaccine is one of the few vaccines that do > not contain mercury; in fact, it has NEVER contained mercury. Thus, it > is self-evident that the removal of mercury will not make vaccines > "safe". (This is why the mercury is the only thing being addressed at > all; because when the people reading this paper realize that the very > mechanism by which vaccines corrupt the immune system means that NO > vaccine is safe and effective; there will be an evolution of > consciousness where the structure of lies telling us vaccines are safe > and effective disintegrates.) > > The good news is that these VIDS can be reversed using natural > remedies (especially homeopathy) contained in the Hippocrates Protocol > (www.drcarley.com). > > the genocidal plan could drop anytime with activation of the Model > State Health Emergency Powers Act whenever the next fabricated > terrorist attack using biological agents occurs. The "bird > apparently going to be used as an excuse to inoculate the masses soon, > as predictions of a pandemic are being made by the media almost every > day. Little do people know that the 1918 Flu pandemic was actually > caused by inoculations given to soldiers in WW 1, as reported on p. 28 > of the book Vaccination the Silent Killer by Ida Honorof & E. McBean. > > [as recent evidence see: Vaccines as Biological Weapons? Live Avian Flu > Virus Placed in Baxter Vaccine Materials Sent to 18 Countries > http://www.naturalnews.com/025760.html] > > As stated in Harrison's Principles of Internal Medicine , 6th edition, > p. 943: "RARELY IS PREVENTION OF INFECTION PER SE CONSIDERED TO BE AN > IMPORTANT GOAL OF VACCINATION. In fact, asymptomatic infection after > vaccination can serve to enhance and prolong the immune response." Of > course, if the immune response has been overwhelmed or corrupted, the > "asymptomatic infection" will become a CHRONIC DISEASE. In fact, on > the same page of Harrison's, in the following paragraph, it states the > following: > "PERSISTENCE AND LATENCY. Many viruses persist in host tissues for > months or years without causing overt disease. A FLARE-UP OF THESE > LATENT INFECTIONS MAY BE INDUCED BY TRAUMA, INTERCURRENT DISEASE, > DECLINE IN ANTIBODY TITERS, OR UNKNOWN STIMULI. Experiments with > tissue cultures and laboratory animals reveal that persistence of > in tissue results from an interplay of various factors peculiar to each > virus and its host. LATENCY IS PROMOTED BY THE PRESENCE OF ANTIBODY OR > OTHER VIRAL INHIBITORS THAT PREVENT EXTENSIVE CELL-TO-CELL SPREAD OF > VIRUS. IF ANTIBODY IS WITHDRAWN, VIRAL MULTIPLICATION OFTEN RESUMES, > WITH CONCOMITANT CELLULAR NECROSIS." > > In the same (6th) Edition of Harrison's Principles of Internal > Medicine , it is stated on page 975 in regards to the poliomyelitis > vaccine: "Vaccine virus multiplies in the intestinal tract and remains > at this site. LIVE VACCINE VIRUS SPREADS AND INFECTS CONTACTS OF > VACCINATED INDIVIDUALS. This type of immunization in the presence of > epidemic poliomyelitis may lead to REPLACEMENT OF THE "WILD" > PARALYTOGENIC STRAIN BY THE ONE IN THE VACCINE....." In direct > contradiction to this statement, the 1/1/2000 Vaccine Information > statement put out by the U.S. Department of Health & Human Services, > Centers for Disease Control and Prevention National Immunization > Program states that the "OPV (Oral Polio Vaccine) is better at keeping > the disease from spreading to other people. However, it does state in > this document that "OPV actually causes polio". > > The inoculation of organisms causes disease both by direct > of organisms (including viruses that cause cancer) into the > bloodstream, as well as corruption of the immune system leading to > autoimmune disease (was posted on the CDC's own website and then > removed) OCSO - OPHR - CDC's Research Agenda - Starter List Comments , > where Dr. Carley's paper "Inoculation the True Weapons of Mass > Destruction causing an Epidemic of Genocide" was posted, and describes > the mechanism whereby corruption of the immune system occurs). In > this paper (which Dr. William Atkinson of the CDC's immunization > program has refused to respond to), it states that the hyperactivity of > the humeral arm of the immune system in autoimmune disease is caused by > adjuvants added just for that purpose. However, the damage caused by > the autoimmunity (i.e., antibody against self) has several mechanisms, > including the following: > > 1. The antigens present in the culture media itself cannot be > completely filtered and separated from the organisms cultured thereon. > Thus, any antibodies formed against antigens from the culture cells > themselves (for example myelin basic protein from chick embryos or the > 13 vaccines which now contain aborted human fetal cells) can > cross-react to form an autoimmune reaction against the myelin basic > protein in your myelin sheath, etc. causing DEMYELINATION. > > 2. Molecular mimicry is due to similarity of proteins contained > in organisms and mammals. (For example, the measles virus is made up > of proteins similar to myelin basic protein; thus, antibodies formed > against the measles virus antigens subsequently also cause an > auto-antibody attack against myelin basic protein in the myelin sheath > due to cross reactivity of these antibodies) causing DEMYELINATION > (leading to Autism, as proven below). > > In the aforementioned 6th edition of Harrison's > Principles of Internal Medicine on p. 1791, under the heading > "Multiple Sclerosis and other DEMYELINATING Diseases", it states the > following: "A large and important group of neurologic disorders are > termed the demyelinating diseases because they share the common > pathologic feature of foci of degeneration, involving the myelin > of nerves. These foci vary in size, shape, distribution, and rate of > development in the different illnesses. The axis cylinder often > suffers damage, as does the myelin sheath, but the destruction of > myelin is considered the primary change...syndromes can be clearly > distinguished....(including) acute disseminated encephalomyelitis > (including post infectious and POSTVACCINAL ENCEPHALOMYELITIS)...(P. > 1798) - "the association of the neurologic disorder with vaccination or > inoculation usually leaves the diagnosis in little doubt, and the > characteristic combination of encephalitic and myelitic features will > help to distinguish the condition from meningitis, viral encephalitis, > and poliomyelitis". This self evident fact has been taken out of > subsequent editions of Harrison's Principles of Internal Medicine , > since as the vaccine schedule has dramatically increased over the > years, the incidence of vaccine induced demyelination has > correspondingly increased. This is most evident in the case of autism, > which has now risen to epidemic proportions in this country. Yet, > whereas there is almost no history of the disease in the families of > these children in most cases, and the parents report the onset of > symptoms after the child receives the MMR vaccine, the various arms of > the medical establishment (including the CDC) conclude that this is > just a "coincidence"; rather than that the association of the > neurologic disorder (autism) with vaccination or inoculation usually > leaves the diagnosis in little doubt. The way that the true etiology > of autism is hidden from doctors is by changing the name of the > induced disease. For example, SUB ACUTE SCLEROSING PAN ENCEPHALITIS > (SSPE) has been changed to AUTISM, as is demonstrated in the 10th > edition of Harrison's Principles of Internal Medicine where, on page > 2096, the following information about SSPE is included: > > "...The disease affects boys 3 to 10 times as frequently > as girls...Characteristically, they are entirely well until the disease > begins. The onset of usually insidious mental deterioration, often > expressed by a decline in the patient's schoolwork, is the presenting > symptom . Incoordination, ataxia, and myoclonic jerks develop within a > few months along with abnormalities of the pyramidal and extrapyramidal > motor systems....Elevated levels of measles antibody are found in the > serum and CSF....Measles virus is the etiologic agent....Staining of > brain tissue from patients with the disease demonstrates measles virus > antigen in the inclusions....A few reported cases have been related to > measles vaccination." Of course, the vaccine etiology has been deleted > from the 16th edition of Harrison's Principles of Internal Medicine , > although the age of onset has been changed to 2 years in that edition. > > What becomes SELF EVIDENT from these various editions of > Harrison's Principles of Internal Medicine (the "Bible" by which all > medical students learn about internal medicine) is that the source of > almost all of the viruses that cause demyelinating diseases is > VACCINES; and that the names of the diseases are changed to hide the > true etiology. Another example of this can be found on page 2104 of > the 10th edition of Harrison's Principles of Internal Medicine, under > the discussion of ACUTE NECROTIZING HEMORRHAGIC ENCEPHALOMYELITIS, > which is described as a "tissue destructive disease of the central > nervous system which occurs with explosive suddenness within a few days > of an upper respiratory infection. The pathologic findings are > distinctive. On sectioning the brain, much of the white matter of one > or both hemispheres is seen to be destroyed almost to the point of > liquefaction. The involved tissue is pink or yellowish-gray and > flecked with multiple small hemorrhages. Sometimes similar changes are > localized to the brainstem or spinal cord. As in acute disseminated > encephalomyelitis in showing perivenular foci of demyelination, all of > like age.....The cerebrospinal fluid examination discloses a more > intense reaction than in other demyelinating diseases....The etiology > of this disease is not established; however, the entire > clinical-pathologic entity bears a close resemblance to a hyper acute > form of EAE which can be induced in animals by administration of > endotoxin, PERTUSSIS VACCINE, or its histamine sensitizing factor > coincident with or shortly after injection of myelin in adjuvant. What > is self evident from this description is that this disease is actually > SIDS (Sudden Infant Death Syndrome) or many of the cases of Shaken > Syndrome (the differentiation being whether the child has any evidence > of trauma that the prosecutor can use to make a case for shaken baby > and subsequently charge a parent with murder, as happened in the > well-known case of Alan Yurko in Florida). Thus, once again, the name > of the disease has been changed to conceal the fact that the pertussis > vaccine is the cause of SIDS and many cases of Shaken Baby Syndrome. > [Non-text portions of this message have been removed] |
In reply to this post by Andrew McAfee
Is the MS test for myelin basic protein antibodies the test you hadfor
demyelination? I was negative for that. I'm not sure that ES is one condition. Note that experiments have shown altered EEGs for healthy people with microwave exposure. I think to some extent ES is just someone who can't recover from EMFs quickly enough to not have an obvious problem. And lots of things could cause that. Bill B On Thu, Mar 12, 2009 at 7:52 AM, Andrew McAfee <[hidden email]> wrote: > ESENS group, > I just a found great website by Dr. Carley with more information on how > vaccines cause auto-immune diseases (and demyelination, which I have) > and much more. > I am glad to see that Dr. Carley is a proponent of bovine colostrum in > her protocol to recover from this condition (and autism). > My hunch is that electrical sensitivity is a demyelinating auto-immune > disorder caused by viruses (measles causes demyelination) in a vaccine > weakened immune system and stressed by an environmental overload > (radiation, toxins, chemicals, etc). > I hope more people with ES will get tested for demyelination and the > presence of auto-immune anti-bodies to confirm this relationship. > I will let you know more on the healing protocol if it works for me. > Andrew > > Excerpts from http://drcarley.com/ > > AUTISM IS SUBACUTE SCLEROSING PANENCEPHALITIS > > INOCULATIONS ARE CAUSING THE CORRUPTION OF THE IMMUNE SYSTEM LEADING TO > ALL AUTOIMMUNE DISEASE AND CANCER IN PEOPLE AND PETS. > > ...by directly injecting organisms into the body leads to a corruption > in the immune system...As a result, the pathogenic viruses or bacteria > cannot be eliminated by the immune system and remain in the body, where > they cause chronic disease and thus further grow and/or mutate as the > individual is exposed to ever more antigens and toxins in the > environment. > > In fact, the prevention of a disease via vaccination is, in reality, > an inability to expel organisms due to the suppression of the > cell-mediated response. Thus, rather than preventing disease, the > disease is actually prevented from ever being resolved. The organisms > continue circulating through the body, adapting to the hostile > environment by transforming into other organisms depending on acidity, > toxicity and other changes to the internal terrain of the body as > demonstrated by the works of Professor Antoine Béchamp. He established > this prior to the development of the germ theory of disease by Louis > Pasteur. Pasteurs germ theory was a plagiarists attempt to reshape > the truth from Béchamp into his own original premise the beLIEf > that germs are out to attack us, thereby causing dis-ease. Thus, > treatment of infection with antibiotics as well as prevention of > disease with vaccines are both just corrupted attempts at cutting off > the branches of dis-ease, when the root of the cause is a toxic > internal environment combined with nutritional deficiency. However, > since Pasteurs germ theory was conducive to the profits of the > burgeoning pharmaceutical cartels that only manage dis-ease, no mention > of the work of Professor Béchamp is made in medical school curricula. > > If components of the myelin sheath (the insulating covering of nerve > fibers which allows proper nerve conduction) or the actual > neurofilaments themselves are attacked by auto-antibodies, the > resultant condition is determined solely by the location of the damage > done. Such neurological conditions include but are not limited to > minimal brain dysfunction, ADD/ADHD, learning disabilities, mental > retardation, criminal behavior, the spectrum of pervasive developmental > disorders (including autism), multiple sclerosis, Parkinsons disease, > Lou Gehrigs disease, Guillen Barre, seizure disorders, etc., etc. > etc. (Please note that other factors are also sometimes involved, such > as: the spirochete which causes Lymes disease, aspartame and mercury in > cases of MS; aspartame in seizures; or pesticides in cases of > Parkinsons). Thus, when detoxing to reverse these diseases, these > other substances must also be removed to obtain a full recovery. > However, the corruption of the immune system caused by the injection of > vaccines is a key component in these disease states leading to immune > malfunction, and is the reason why an autistic child may also have > leaky gut or eczema, etc. Note that myelin production, for the most > part, does not begin until after birth. Most myelin is apparently laid > down by age 5 years and usually completed by age 10 years, judging by > the level of success at various ages in reversing autistic and other > neurological VIDS symptoms that this author has observed in hundreds of > children by detoxing the viruses with homeopathic nosodes5, and > repairing the immune corruption by simultaneous administration of > bovine colostrum (i.e., after 10 years of age, the ability to stop and > repair auto-antibody induced damage in the myelin sheath and > neurofilaments themselves is dramatically decreased). > > # The antigens present in the culture media itself cannot be completely > filtered and separated from the organisms cultured thereon. Thus, any > antibodies formed against antigens from the culture cells themselves > (for example myelin basic protein from chick embryos or the 13 vaccines > which now contain aborted human fetal cells) can cross-react to form an > autoimmune reaction against the myelin basic protein in your myelin > sheath, etc. See the package insert from Pfizers Rabies vaccine from > the 10th Edition of the Compendium of Veterinary Products published > in 2007 posted on www.drcarley.com, which states tissue origin > vaccines contain extraneous protein in addition to the [rabies] antigen > that can lead to autoimmune disease. THIS IS TRUE FOR ALL VACCINES, > BUT THIS IS THE FIRST TIME I HAVE SEEN IT ADMITTED BY ANY VACCINE > MANUFACTURER. > > Although the symptoms of mercury poisoning have been described as > identical to the symptoms of autism, it should be noted that most > children who descend into the hellish state known as autism do so after > the MMR vaccine. The MMR vaccine is one of the few vaccines that do > not contain mercury; in fact, it has NEVER contained mercury. Thus, it > is self-evident that the removal of mercury will not make vaccines > safe. (This is why the mercury is the only thing being addressed at > all; because when the people reading this paper realize that the very > mechanism by which vaccines corrupt the immune system means that NO > vaccine is safe and effective; there will be an evolution of > consciousness where the structure of lies telling us vaccines are safe > and effective disintegrates.) > > The good news is that these VIDS can be reversed using natural > remedies (especially homeopathy) contained in the Hippocrates Protocol > (www.drcarley.com). > > the genocidal plan could drop anytime with activation of the Model > State Health Emergency Powers Act whenever the next fabricated > terrorist attack using biological agents occurs. The bird flu is > apparently going to be used as an excuse to inoculate the masses soon, > as predictions of a pandemic are being made by the media almost every > day. Little do people know that the 1918 Flu pandemic was actually > caused by inoculations given to soldiers in WW 1, as reported on p. 28 > of the book Vaccination the Silent Killer by Ida Honorof & E. McBean. > > [as recent evidence see: Vaccines as Biological Weapons? Live Avian Flu > Virus Placed in Baxter Vaccine Materials Sent to 18 Countries > http://www.naturalnews.com/025760.html] > > As stated in Harrison's Principles of Internal Medicine , 6th edition, > p. 943: "RARELY IS PREVENTION OF INFECTION PER SE CONSIDERED TO BE AN > IMPORTANT GOAL OF VACCINATION. In fact, asymptomatic infection after > vaccination can serve to enhance and prolong the immune response." Of > course, if the immune response has been overwhelmed or corrupted, the > "asymptomatic infection" will become a CHRONIC DISEASE. In fact, on > the same page of Harrison's, in the following paragraph, it states the > following: > "PERSISTENCE AND LATENCY. Many viruses persist in host tissues for > months or years without causing overt disease. A FLARE-UP OF THESE > LATENT INFECTIONS MAY BE INDUCED BY TRAUMA, INTERCURRENT DISEASE, > DECLINE IN ANTIBODY TITERS, OR UNKNOWN STIMULI. Experiments with > tissue cultures and laboratory animals reveal that persistence of virus > in tissue results from an interplay of various factors peculiar to each > virus and its host. LATENCY IS PROMOTED BY THE PRESENCE OF ANTIBODY OR > OTHER VIRAL INHIBITORS THAT PREVENT EXTENSIVE CELL-TO-CELL SPREAD OF > VIRUS. IF ANTIBODY IS WITHDRAWN, VIRAL MULTIPLICATION OFTEN RESUMES, > WITH CONCOMITANT CELLULAR NECROSIS." > > In the same (6th) Edition of Harrison's Principles of Internal > Medicine , it is stated on page 975 in regards to the poliomyelitis > vaccine: "Vaccine virus multiplies in the intestinal tract and remains > at this site. LIVE VACCINE VIRUS SPREADS AND INFECTS CONTACTS OF > VACCINATED INDIVIDUALS. This type of immunization in the presence of > epidemic poliomyelitis may lead to REPLACEMENT OF THE "WILD" > PARALYTOGENIC STRAIN BY THE ONE IN THE VACCINE....." In direct > contradiction to this statement, the 1/1/2000 Vaccine Information > statement put out by the U.S. Department of Health & Human Services, > Centers for Disease Control and Prevention National Immunization > Program states that the "OPV (Oral Polio Vaccine) is better at keeping > the disease from spreading to other people. However, it does state in > this document that "OPV actually causes polio". > > The inoculation of organisms causes disease both by direct introduction > of organisms (including viruses that cause cancer) into the > bloodstream, as well as corruption of the immune system leading to > autoimmune disease (was posted on the CDC's own website and then > removed) OCSO - OPHR - CDC's Research Agenda - Starter List Comments , > where Dr. Carley's paper "Inoculation the True Weapons of Mass > Destruction causing an Epidemic of Genocide" was posted, and describes > the mechanism whereby corruption of the immune system occurs). In > this paper (which Dr. William Atkinson of the CDC's immunization > program has refused to respond to), it states that the hyperactivity of > the humeral arm of the immune system in autoimmune disease is caused by > adjuvants added just for that purpose. However, the damage caused by > the autoimmunity (i.e., antibody against self) has several mechanisms, > including the following: > > 1. The antigens present in the culture media itself cannot be > completely filtered and separated from the organisms cultured thereon. > Thus, any antibodies formed against antigens from the culture cells > themselves (for example myelin basic protein from chick embryos or the > 13 vaccines which now contain aborted human fetal cells) can > cross-react to form an autoimmune reaction against the myelin basic > protein in your myelin sheath, etc. causing DEMYELINATION. > > 2. Molecular mimicry is due to similarity of proteins contained > in organisms and mammals. (For example, the measles virus is made up > of proteins similar to myelin basic protein; thus, antibodies formed > against the measles virus antigens subsequently also cause an > auto-antibody attack against myelin basic protein in the myelin sheath > due to cross reactivity of these antibodies) causing DEMYELINATION > (leading to Autism, as proven below). > > In the aforementioned 6th edition of Harrison's > Principles of Internal Medicine on p. 1791, under the heading > "Multiple Sclerosis and other DEMYELINATING Diseases", it states the > following: "A large and important group of neurologic disorders are > termed the demyelinating diseases because they share the common > pathologic feature of foci of degeneration, involving the myelin sheath > of nerves. These foci vary in size, shape, distribution, and rate of > development in the different illnesses. The axis cylinder often > suffers damage, as does the myelin sheath, but the destruction of > myelin is considered the primary change...syndromes can be clearly > distinguished....(including) acute disseminated encephalomyelitis > (including post infectious and POSTVACCINAL ENCEPHALOMYELITIS)...(P. > 1798) - "the association of the neurologic disorder with vaccination or > inoculation usually leaves the diagnosis in little doubt, and the > characteristic combination of encephalitic and myelitic features will > help to distinguish the condition from meningitis, viral encephalitis, > and poliomyelitis". This self evident fact has been taken out of > subsequent editions of Harrison's Principles of Internal Medicine , > since as the vaccine schedule has dramatically increased over the > years, the incidence of vaccine induced demyelination has > correspondingly increased. This is most evident in the case of autism, > which has now risen to epidemic proportions in this country. Yet, > whereas there is almost no history of the disease in the families of > these children in most cases, and the parents report the onset of > symptoms after the child receives the MMR vaccine, the various arms of > the medical establishment (including the CDC) conclude that this is > just a "coincidence"; rather than that the association of the > neurologic disorder (autism) with vaccination or inoculation usually > leaves the diagnosis in little doubt. The way that the true etiology > of autism is hidden from doctors is by changing the name of the vaccine > induced disease. For example, SUB ACUTE SCLEROSING PAN ENCEPHALITIS > (SSPE) has been changed to AUTISM, as is demonstrated in the 10th > edition of Harrison's Principles of Internal Medicine where, on page > 2096, the following information about SSPE is included: > > "...The disease affects boys 3 to 10 times as frequently > as girls...Characteristically, they are entirely well until the disease > begins. The onset of usually insidious mental deterioration, often > expressed by a decline in the patient's schoolwork, is the presenting > symptom . Incoordination, ataxia, and myoclonic jerks develop within a > few months along with abnormalities of the pyramidal and extrapyramidal > motor systems....Elevated levels of measles antibody are found in the > serum and CSF....Measles virus is the etiologic agent....Staining of > brain tissue from patients with the disease demonstrates measles virus > antigen in the inclusions....A few reported cases have been related to > measles vaccination." Of course, the vaccine etiology has been deleted > from the 16th edition of Harrison's Principles of Internal Medicine , > although the age of onset has been changed to 2 years in that edition. > > What becomes SELF EVIDENT from these various editions of > Harrison's Principles of Internal Medicine (the "Bible" by which all > medical students learn about internal medicine) is that the source of > almost all of the viruses that cause demyelinating diseases is actually > VACCINES; and that the names of the diseases are changed to hide the > true etiology. Another example of this can be found on page 2104 of > the 10th edition of Harrison's Principles of Internal Medicine, under > the discussion of ACUTE NECROTIZING HEMORRHAGIC ENCEPHALOMYELITIS, > which is described as a "tissue destructive disease of the central > nervous system which occurs with explosive suddenness within a few days > of an upper respiratory infection. The pathologic findings are > distinctive. On sectioning the brain, much of the white matter of one > or both hemispheres is seen to be destroyed almost to the point of > liquefaction. The involved tissue is pink or yellowish-gray and > flecked with multiple small hemorrhages. Sometimes similar changes are > localized to the brainstem or spinal cord. As in acute disseminated > encephalomyelitis in showing perivenular foci of demyelination, all of > like age.....The cerebrospinal fluid examination discloses a more > intense reaction than in other demyelinating diseases....The etiology > of this disease is not established; however, the entire > clinical-pathologic entity bears a close resemblance to a hyper acute > form of EAE which can be induced in animals by administration of > endotoxin, PERTUSSIS VACCINE, or its histamine sensitizing factor > coincident with or shortly after injection of myelin in adjuvant. What > is self evident from this description is that this disease is actually > SIDS (Sudden Infant Death Syndrome) or many of the cases of Shaken Baby > Syndrome (the differentiation being whether the child has any evidence > of trauma that the prosecutor can use to make a case for shaken baby > and subsequently charge a parent with murder, as happened in the > well-known case of Alan Yurko in Florida). Thus, once again, the name > of the disease has been changed to conceal the fact that the pertussis > vaccine is the cause of SIDS and many cases of Shaken Baby Syndrome. > > > > ------------------------------------ > > Yahoo! Groups Links > > > > [Non-text portions of this message have been removed] |
In reply to this post by Andrew McAfee
Hi, Andrew, Celiac disease causes demyelination, too. And I suspect the fish toxin--forget how to spell it--cigularia? does too. An interesting thing I discovered recently was that cigularia also causes tight junction malfunction. So it looks like cigularia is also a problem es people would want to get checked out. Thanks for the info, Andrew. I am anxious to hear how it goes foryou. Diane --- On Thu, 3/12/09, Andrew McAfee <[hidden email]> wrote: > From: Andrew McAfee <[hidden email]> > Subject: [eSens] demyelination/vaccines/autism/Lyme/colostrum > To: [hidden email] > Cc: [hidden email] > Date: Thursday, March 12, 2009, 9:52 AM > ESENS group, > I just a found great website by Dr. Carley with more > information on how > vaccines cause auto-immune diseases (and demyelination, > which I have) > and much more. > I am glad to see that Dr. Carley is a proponent of bovine > colostrum in > her protocol to recover from this condition (and autism). > My hunch is that electrical sensitivity is a demyelinating > auto-immune > disorder caused by viruses (measles causes demyelination) > in a vaccine > weakened immune system and stressed by an environmental > overload > (radiation, toxins, chemicals, etc). > I hope more people with ES will get tested for > demyelination and the > presence of auto-immune anti-bodies to confirm this > relationship. > I will let you know more on the healing protocol if it > works for me. > Andrew > > Excerpts from http://drcarley.com/ > > AUTISM IS SUBACUTE SCLEROSING PANENCEPHALITIS > > INOCULATIONS ARE CAUSING THE CORRUPTION OF THE IMMUNE > SYSTEM LEADING TO > ALL AUTOIMMUNE DISEASE AND CANCER IN PEOPLE AND PETS. > > ...by directly injecting organisms into the body leads to a > corruption > in the immune system...As a result, the pathogenic viruses > or bacteria > cannot be eliminated by the immune system and remain in the > body, where > they cause chronic disease and thus further grow and/or > mutate as the > individual is exposed to ever more antigens and toxins in > the > environment. > > In fact, the “prevention” of a disease via vaccination > is, in reality, > an inability to expel organisms due to the suppression of > the > cell-mediated response. Thus, rather than preventing > disease, the > disease is actually prevented from ever being resolved. The > organisms > continue circulating through the body, adapting to the > hostile > environment by transforming into other organisms depending > on acidity, > toxicity and other changes to the internal terrain of the > body as > demonstrated by the works of Professor Antoine Béchamp. > He established > this prior to the development of the “germ theory” of > disease by Louis > Pasteur. Pasteur’s “germ theory” was a > plagiarist’s attempt to reshape > the truth from Béchamp into his own “original” premise > – the beLIEf > that germs are out to “attack” us, thereby causing > dis-ease. Thus, > treatment of infection with antibiotics as well as > “prevention” of > disease with vaccines are both just corrupted attempts at > cutting off > the branches of dis-ease, when the root of the cause is a > toxic > internal environment combined with nutritional deficiency. > However, > since Pasteur’s germ theory was conducive to the profits > of the > burgeoning pharmaceutical cartels that only manage > dis-ease, no mention > of the work of Professor Béchamp is made in medical school > curricula. > > If components of the myelin sheath (the insulating > covering of nerve > fibers which allows proper nerve conduction) or the actual > neurofilaments themselves are attacked by auto-antibodies, > the > resultant condition is determined solely by the location of > the damage > done. Such neurological conditions include but are not > limited to > minimal brain dysfunction, ADD/ADHD, learning disabilities, > mental > retardation, criminal behavior, the spectrum of pervasive > developmental > disorders (including autism), multiple sclerosis, > Parkinson’s disease, > Lou Gehrig’s disease, Guillen Barre’, seizure > disorders, etc., etc. > etc. (Please note that other factors are also sometimes > involved, such > as: the spirochete which causes Lymes disease, aspartame > and mercury in > cases of MS; aspartame in seizures; or pesticides in cases > of > Parkinson’s). Thus, when detoxing to reverse these > diseases, these > other substances must also be removed to obtain a full > recovery. > However, the corruption of the immune system caused by the > injection of > vaccines is a key component in these disease states leading > to immune > malfunction, and is the reason why an autistic child may > also have > leaky gut or eczema, etc. Note that myelin production, for > the most > part, does not begin until after birth. Most myelin is > apparently laid > down by age 5 years and usually completed by age 10 years, > judging by > the level of success at various ages in reversing autistic > and other > neurological VIDS symptoms that this author has observed in > hundreds of > children by detoxing the viruses with homeopathic nosodes5, > and > repairing the immune corruption by simultaneous > administration of > bovine colostrum (i.e., after 10 years of age, the ability > to stop and > repair auto-antibody induced damage in the myelin sheath > and > neurofilaments themselves is dramatically decreased). > > # The antigens present in the culture media itself cannot > be completely > filtered and separated from the organisms cultured thereon. > Thus, any > antibodies formed against antigens from the culture cells > themselves > (for example myelin basic protein from chick embryos or the > 13 vaccines > which now contain aborted human fetal cells) can > cross-react to form an > autoimmune reaction against the myelin basic protein in > your myelin > sheath, etc. See the package insert from Pfizer’s Rabies > vaccine from > the “10th Edition of the Compendium of Veterinary > Products” published > in 2007 posted on www.drcarley.com, which states “tissue > origin > vaccines contain extraneous protein in addition to the > [rabies] antigen > that can lead to autoimmune disease”. THIS IS TRUE FOR > ALL VACCINES, > BUT THIS IS THE FIRST TIME I HAVE SEEN IT ADMITTED BY ANY > VACCINE > MANUFACTURER. > > Although the symptoms of mercury poisoning have been > described as > identical to the symptoms of autism, it should be noted > that most > children who descend into the hellish state known as autism > do so after > the MMR vaccine. The MMR vaccine is one of the few > vaccines that do > not contain mercury; in fact, it has NEVER contained > mercury. Thus, it > is self-evident that the removal of mercury will not make > vaccines > “safe”. (This is why the mercury is the only thing > being addressed at > all; because when the people reading this paper realize > that the very > mechanism by which vaccines corrupt the immune system means > that NO > vaccine is safe and effective; there will be an evolution > of > consciousness where the structure of lies telling us > vaccines are safe > and effective disintegrates.) > > The good news is that these VIDS can be reversed using > natural > remedies (especially homeopathy) contained in the > Hippocrates Protocol > (www.drcarley.com). > > the genocidal plan could drop anytime with activation of > the Model > State Health Emergency Powers Act whenever the next > fabricated > terrorist attack using biological agents occurs. The > “bird flu” is > apparently going to be used as an excuse to inoculate the > masses soon, > as predictions of a pandemic are being made by the media > almost every > day. Little do people know that the 1918 Flu pandemic was > actually > caused by inoculations given to soldiers in WW 1, as > reported on p. 28 > of the book Vaccination the Silent Killer by Ida Honorof > & E. McBean. > > [as recent evidence see: Vaccines as Biological Weapons? > Live Avian Flu > Virus Placed in Baxter Vaccine Materials Sent to 18 > Countries > http://www.naturalnews.com/025760.html] > > As stated in Harrison's Principles of Internal > Medicine , 6th edition, > p. 943: "RARELY IS PREVENTION OF INFECTION PER SE > CONSIDERED TO BE AN > IMPORTANT GOAL OF VACCINATION. In fact, asymptomatic > infection after > vaccination can serve to enhance and prolong the immune > response." Of > course, if the immune response has been overwhelmed or > corrupted, the > "asymptomatic infection" will become a CHRONIC > DISEASE. In fact, on > the same page of Harrison's, in the following > paragraph, it states the > following: > "PERSISTENCE AND LATENCY. Many viruses persist in > host tissues for > months or years without causing overt disease. A FLARE-UP > OF THESE > LATENT INFECTIONS MAY BE INDUCED BY TRAUMA, INTERCURRENT > DISEASE, > DECLINE IN ANTIBODY TITERS, OR UNKNOWN STIMULI. > Experiments with > tissue cultures and laboratory animals reveal that > persistence of virus > in tissue results from an interplay of various factors > peculiar to each > virus and its host. LATENCY IS PROMOTED BY THE PRESENCE OF > ANTIBODY OR > OTHER VIRAL INHIBITORS THAT PREVENT EXTENSIVE CELL-TO-CELL > SPREAD OF > VIRUS. IF ANTIBODY IS WITHDRAWN, VIRAL MULTIPLICATION > OFTEN RESUMES, > WITH CONCOMITANT CELLULAR NECROSIS." > > In the same (6th) Edition of Harrison's > Principles of Internal > Medicine , it is stated on page 975 in regards to the > poliomyelitis > vaccine: "Vaccine virus multiplies in the intestinal > tract and remains > at this site. LIVE VACCINE VIRUS SPREADS AND INFECTS > CONTACTS OF > VACCINATED INDIVIDUALS. This type of immunization in the > presence of > epidemic poliomyelitis may lead to REPLACEMENT OF THE > "WILD" > PARALYTOGENIC STRAIN BY THE ONE IN THE VACCINE....." > In direct > contradiction to this statement, the 1/1/2000 Vaccine > Information > statement put out by the U.S. Department of Health & > Human Services, > Centers for Disease Control and Prevention National > Immunization > Program states that the "OPV (Oral Polio Vaccine) is > better at keeping > the disease from spreading to other people. However, it > does state in > this document that "OPV actually causes polio". > > The inoculation of organisms causes disease both by direct > introduction > of organisms (including viruses that cause cancer) into the > > bloodstream, as well as corruption of the immune system > leading to > autoimmune disease (was posted on the CDC's own website > and then > removed) OCSO - OPHR - CDC's Research Agenda - Starter > List Comments , > where Dr. Carley's paper "Inoculation the True > Weapons of Mass > Destruction causing an Epidemic of Genocide" was > posted, and describes > the mechanism whereby corruption of the immune system > occurs). In > this paper (which Dr. William Atkinson of the CDC's > immunization > program has refused to respond to), it states that the > hyperactivity of > the humeral arm of the immune system in autoimmune disease > is caused by > adjuvants added just for that purpose. However, the damage > caused by > the autoimmunity (i.e., antibody against self) has several > mechanisms, > including the following: > > 1. The antigens present in the culture media itself > cannot be > completely filtered and separated from the organisms > cultured thereon. > Thus, any antibodies formed against antigens from the > culture cells > themselves (for example myelin basic protein from chick > embryos or the > 13 vaccines which now contain aborted human fetal cells) > can > cross-react to form an autoimmune reaction against the > myelin basic > protein in your myelin sheath, etc. causing DEMYELINATION. > > 2. Molecular mimicry is due to similarity of proteins > contained > in organisms and mammals. (For example, the measles virus > is made up > of proteins similar to myelin basic protein; thus, > antibodies formed > against the measles virus antigens subsequently also cause > an > auto-antibody attack against myelin basic protein in the > myelin sheath > due to cross reactivity of these antibodies) causing > DEMYELINATION > (leading to Autism, as proven below). > > In the aforementioned 6th edition of > Harrison's > Principles of Internal Medicine on p. 1791, under the > heading > "Multiple Sclerosis and other DEMYELINATING > Diseases", it states the > following: "A large and important group of neurologic > disorders are > termed the demyelinating diseases because they share the > common > pathologic feature of foci of degeneration, involving the > myelin sheath > of nerves. These foci vary in size, shape, distribution, > and rate of > development in the different illnesses. The axis cylinder > often > suffers damage, as does the myelin sheath, but the > destruction of > myelin is considered the primary change...syndromes can be > clearly > distinguished....(including) acute disseminated > encephalomyelitis > (including post infectious and POSTVACCINAL > ENCEPHALOMYELITIS)...(P. > 1798) - "the association of the neurologic disorder > with vaccination or > inoculation usually leaves the diagnosis in little doubt, > and the > characteristic combination of encephalitic and myelitic > features will > help to distinguish the condition from meningitis, viral > encephalitis, > and poliomyelitis". This self evident fact has been > taken out of > subsequent editions of Harrison's Principles of > Internal Medicine , > since as the vaccine schedule has dramatically increased > over the > years, the incidence of vaccine induced demyelination has > correspondingly increased. This is most evident in the > case of autism, > which has now risen to epidemic proportions in this > country. Yet, > whereas there is almost no history of the disease in the > families of > these children in most cases, and the parents report the > onset of > symptoms after the child receives the MMR vaccine, the > various arms of > the medical establishment (including the CDC) conclude that > this is > just a "coincidence"; rather than that the > association of the > neurologic disorder (autism) with vaccination or > inoculation usually > leaves the diagnosis in little doubt. The way that the > true etiology > of autism is hidden from doctors is by changing the name of > the vaccine > induced disease. For example, SUB ACUTE SCLEROSING PAN > ENCEPHALITIS > (SSPE) has been changed to AUTISM, as is demonstrated in > the 10th > edition of Harrison's Principles of Internal Medicine > where, on page > 2096, the following information about SSPE is included: > > "...The disease affects boys 3 to 10 > times as frequently > as girls...Characteristically, they are entirely well until > the disease > begins. The onset of usually insidious mental > deterioration, often > expressed by a decline in the patient's schoolwork, is > the presenting > symptom . Incoordination, ataxia, and myoclonic jerks > develop within a > few months along with abnormalities of the pyramidal and > extrapyramidal > motor systems....Elevated levels of measles antibody are > found in the > serum and CSF....Measles virus is the etiologic > agent....Staining of > brain tissue from patients with the disease demonstrates > measles virus > antigen in the inclusions....A few reported cases have been > related to > measles vaccination." Of course, the vaccine etiology > has been deleted > from the 16th edition of Harrison's Principles of > Internal Medicine , > although the age of onset has been changed to 2 years in > that edition. > > What becomes SELF EVIDENT from these various > editions of > Harrison's Principles of Internal Medicine (the > "Bible" by which all > medical students learn about internal medicine) is that the > source of > almost all of the viruses that cause demyelinating diseases > is actually > VACCINES; and that the names of the diseases are changed to > hide the > true etiology. Another example of this can be found on > page 2104 of > the 10th edition of Harrison's Principles of Internal > Medicine, under > the discussion of ACUTE NECROTIZING HEMORRHAGIC > ENCEPHALOMYELITIS, > which is described as a "tissue destructive disease of > the central > nervous system which occurs with explosive suddenness > within a few days > of an upper respiratory infection. The pathologic findings > are > distinctive. On sectioning the brain, much of the white > matter of one > or both hemispheres is seen to be destroyed almost to the > point of > liquefaction. The involved tissue is pink or > yellowish-gray and > flecked with multiple small hemorrhages. Sometimes similar > changes are > localized to the brainstem or spinal cord. As in acute > disseminated > encephalomyelitis in showing perivenular foci of > demyelination, all of > like age.....The cerebrospinal fluid examination discloses > a more > intense reaction than in other demyelinating > diseases....The etiology > of this disease is not established; however, the entire > clinical-pathologic entity bears a close resemblance to a > hyper acute > form of EAE which can be induced in animals by > administration of > endotoxin, PERTUSSIS VACCINE, or its histamine sensitizing > factor > coincident with or shortly after injection of myelin in > adjuvant. What > is self evident from this description is that this disease > is actually > SIDS (Sudden Infant Death Syndrome) or many of the cases of > Shaken Baby > Syndrome (the differentiation being whether the child has > any evidence > of trauma that the prosecutor can use to make a case for > shaken baby > and subsequently charge a parent with murder, as happened > in the > well-known case of Alan Yurko in Florida). Thus, once > again, the name > of the disease has been changed to conceal the fact that > the pertussis > vaccine is the cause of SIDS and many cases of Shaken Baby > Syndrome. > > > > ------------------------------------ > > Yahoo! Groups Links > > > |
In reply to this post by BiBrun
Hi, Bill, I agree with you that es is a condition caused by various and not just one cause (regardless, I still think celiac disease is ONE of those causes and many people who have cd don't know it; so if you are es from that and don'tknow it, you have zero chance of recovery.) But it does seem that the various causes also have various similarities--lymphatic congestion +/or adrenal influences; causing various nutritional deficiencies (or causing the need for various nutrients to be greater); affecting the nervous systems.... I agree that you don't necessarily have to have demyelination, but to recover from es would necessitate overcoming that if you had it. I personally still think maybe a link between all the various problems that cause es is tight-junction permeability. You have to have a gene for it and without the gene you would not react as we do to emfs no matter how much was in your atmosphere. (You might come down with cancer, or something else from emfs, but you would never be aware it was from emfs because you would not feel them.) But as to the precipitating factors, I agree that can be from different problems/ailments and we should not necessarily think everything that helps one will help all. My 2 cents, Diane --- On Fri, 3/13/09, Bill Bruno <[hidden email]> wrote: > From: Bill Bruno <[hidden email]> > Subject: Re: [eSens] demyelination/vaccines/autism/Lyme/colostrum > To: [hidden email] > Date: Friday, March 13, 2009, 12:29 PM > Is the MS test for myelin basic protein antibodies the test > you hadfor > demyelination? > > I was negative for that. I'm not sure that ES is one > condition. > Note that experiments have shown altered EEGs for healthy > people with microwave exposure. I think to some extent ES > is > just someone who can't recover from EMFs quickly enough > to > not have an obvious problem. And lots of things could > cause > that. > > Bill B > > On Thu, Mar 12, 2009 at 7:52 AM, Andrew McAfee > <[hidden email]> wrote: > > > ESENS group, > > I just a found great website by Dr. Carley with more > information on how > > vaccines cause auto-immune diseases (and > demyelination, which I have) > > and much more. > > I am glad to see that Dr. Carley is a proponent of > bovine colostrum in > > her protocol to recover from this condition (and > autism). > > My hunch is that electrical sensitivity is a > demyelinating auto-immune > > disorder caused by viruses (measles causes > demyelination) in a vaccine > > weakened immune system and stressed by an > environmental overload > > (radiation, toxins, chemicals, etc). > > I hope more people with ES will get tested for > demyelination and the > > presence of auto-immune anti-bodies to confirm this > relationship. > > I will let you know more on the healing protocol if it > works for me. > > Andrew > > > > Excerpts from http://drcarley.com/ > > > > AUTISM IS SUBACUTE SCLEROSING PANENCEPHALITIS > > > > INOCULATIONS ARE CAUSING THE CORRUPTION OF THE IMMUNE > SYSTEM LEADING TO > > ALL AUTOIMMUNE DISEASE AND CANCER IN PEOPLE AND PETS. > > > > ...by directly injecting organisms into the body leads > to a corruption > > in the immune system...As a result, the pathogenic > viruses or bacteria > > cannot be eliminated by the immune system and remain > in the body, where > > they cause chronic disease and thus further grow > and/or mutate as the > > individual is exposed to ever more antigens and toxins > in the > > environment. > > > > In fact, the “prevention” of a disease via > vaccination is, in reality, > > an inability to expel organisms due to the suppression > of the > > cell-mediated response. Thus, rather than preventing > disease, the > > disease is actually prevented from ever being > resolved. The organisms > > continue circulating through the body, adapting to the > hostile > > environment by transforming into other organisms > depending on acidity, > > toxicity and other changes to the internal terrain of > the body as > > demonstrated by the works of Professor Antoine > Béchamp. He established > > this prior to the development of the “germ theory” > of disease by Louis > > Pasteur. Pasteur’s “germ theory” was a > plagiarist’s attempt to reshape > > the truth from Béchamp into his own “original” > premise – the beLIEf > > that germs are out to “attack” us, thereby causing > dis-ease. Thus, > > treatment of infection with antibiotics as well as > “prevention” of > > disease with vaccines are both just corrupted attempts > at cutting off > > the branches of dis-ease, when the root of the cause > is a toxic > > internal environment combined with nutritional > deficiency. However, > > since Pasteur’s germ theory was conducive to the > profits of the > > burgeoning pharmaceutical cartels that only manage > dis-ease, no mention > > of the work of Professor Béchamp is made in medical > school curricula. > > > > If components of the myelin sheath (the insulating > covering of nerve > > fibers which allows proper nerve conduction) or the > actual > > neurofilaments themselves are attacked by > auto-antibodies, the > > resultant condition is determined solely by the > location of the damage > > done. Such neurological conditions include but are > not limited to > > minimal brain dysfunction, ADD/ADHD, learning > disabilities, mental > > retardation, criminal behavior, the spectrum of > pervasive developmental > > disorders (including autism), multiple sclerosis, > Parkinson’s disease, > > Lou Gehrig’s disease, Guillen Barre’, seizure > disorders, etc., etc. > > etc. (Please note that other factors are also > sometimes involved, such > > as: the spirochete which causes Lymes disease, > aspartame and mercury in > > cases of MS; aspartame in seizures; or pesticides in > cases of > > Parkinson’s). Thus, when detoxing to reverse these > diseases, these > > other substances must also be removed to obtain a full > recovery. > > However, the corruption of the immune system caused by > the injection of > > vaccines is a key component in these disease states > leading to immune > > malfunction, and is the reason why an autistic child > may also have > > leaky gut or eczema, etc. Note that myelin > production, for the most > > part, does not begin until after birth. Most myelin is > apparently laid > > down by age 5 years and usually completed by age 10 > years, judging by > > the level of success at various ages in reversing > autistic and other > > neurological VIDS symptoms that this author has > observed in hundreds of > > children by detoxing the viruses with homeopathic > nosodes5, and > > repairing the immune corruption by simultaneous > administration of > > bovine colostrum (i.e., after 10 years of age, the > ability to stop and > > repair auto-antibody induced damage in the myelin > sheath and > > neurofilaments themselves is dramatically decreased). > > > > # The antigens present in the culture media itself > cannot be completely > > filtered and separated from the organisms cultured > thereon. Thus, any > > antibodies formed against antigens from the culture > cells themselves > > (for example myelin basic protein from chick embryos > or the 13 vaccines > > which now contain aborted human fetal cells) can > cross-react to form an > > autoimmune reaction against the myelin basic protein > in your myelin > > sheath, etc. See the package insert from Pfizer’s > Rabies vaccine from > > the “10th Edition of the Compendium of Veterinary > Products” published > > in 2007 posted on www.drcarley.com, which states > “tissue origin > > vaccines contain extraneous protein in addition to the > [rabies] antigen > > that can lead to autoimmune disease”. THIS IS TRUE > FOR ALL VACCINES, > > BUT THIS IS THE FIRST TIME I HAVE SEEN IT ADMITTED BY > ANY VACCINE > > MANUFACTURER. > > > > Although the symptoms of mercury poisoning have been > described as > > identical to the symptoms of autism, it should be > noted that most > > children who descend into the hellish state known as > autism do so after > > the MMR vaccine. The MMR vaccine is one of the few > vaccines that do > > not contain mercury; in fact, it has NEVER contained > mercury. Thus, it > > is self-evident that the removal of mercury will not > make vaccines > > “safe”. (This is why the mercury is the only > thing being addressed at > > all; because when the people reading this paper > realize that the very > > mechanism by which vaccines corrupt the immune system > means that NO > > vaccine is safe and effective; there will be an > evolution of > > consciousness where the structure of lies telling us > vaccines are safe > > and effective disintegrates.) > > > > The good news is that these VIDS can be reversed > using natural > > remedies (especially homeopathy) contained in the > Hippocrates Protocol > > (www.drcarley.com). > > > > the genocidal plan could drop anytime with activation > of the Model > > State Health Emergency Powers Act whenever the next > fabricated > > terrorist attack using biological agents occurs. The > “bird flu” is > > apparently going to be used as an excuse to inoculate > the masses soon, > > as predictions of a pandemic are being made by the > media almost every > > day. Little do people know that the 1918 Flu pandemic > was actually > > caused by inoculations given to soldiers in WW 1, as > reported on p. 28 > > of the book Vaccination the Silent Killer by Ida > Honorof & E. McBean. > > > > [as recent evidence see: Vaccines as Biological > Weapons? Live Avian Flu > > Virus Placed in Baxter Vaccine Materials Sent to 18 > Countries > > http://www.naturalnews.com/025760.html] > > > > As stated in Harrison's Principles of Internal > Medicine , 6th edition, > > p. 943: "RARELY IS PREVENTION OF INFECTION PER > SE CONSIDERED TO BE AN > > IMPORTANT GOAL OF VACCINATION. In fact, asymptomatic > infection after > > vaccination can serve to enhance and prolong the > immune response." Of > > course, if the immune response has been overwhelmed or > corrupted, the > > "asymptomatic infection" will become a > CHRONIC DISEASE. In fact, on > > the same page of Harrison's, in the following > paragraph, it states the > > following: > > "PERSISTENCE AND LATENCY. Many viruses persist > in host tissues for > > months or years without causing overt disease. A > FLARE-UP OF THESE > > LATENT INFECTIONS MAY BE INDUCED BY TRAUMA, > INTERCURRENT DISEASE, > > DECLINE IN ANTIBODY TITERS, OR UNKNOWN STIMULI. > Experiments with > > tissue cultures and laboratory animals reveal that > persistence of virus > > in tissue results from an interplay of various factors > peculiar to each > > virus and its host. LATENCY IS PROMOTED BY THE > PRESENCE OF ANTIBODY OR > > OTHER VIRAL INHIBITORS THAT PREVENT EXTENSIVE > CELL-TO-CELL SPREAD OF > > VIRUS. IF ANTIBODY IS WITHDRAWN, VIRAL MULTIPLICATION > OFTEN RESUMES, > > WITH CONCOMITANT CELLULAR NECROSIS." > > > > In the same (6th) Edition of Harrison's > Principles of Internal > > Medicine , it is stated on page 975 in regards to the > poliomyelitis > > vaccine: "Vaccine virus multiplies in the > intestinal tract and remains > > at this site. LIVE VACCINE VIRUS SPREADS AND INFECTS > CONTACTS OF > > VACCINATED INDIVIDUALS. This type of immunization in > the presence of > > epidemic poliomyelitis may lead to REPLACEMENT OF THE > "WILD" > > PARALYTOGENIC STRAIN BY THE ONE IN THE > VACCINE....." In direct > > contradiction to this statement, the 1/1/2000 Vaccine > Information > > statement put out by the U.S. Department of Health > & Human Services, > > Centers for Disease Control and Prevention National > Immunization > > Program states that the "OPV (Oral Polio > Vaccine) is better at keeping > > the disease from spreading to other people. However, > it does state in > > this document that "OPV actually causes > polio". > > > > The inoculation of organisms causes disease both by > direct introduction > > of organisms (including viruses that cause cancer) > into the > > bloodstream, as well as corruption of the immune > system leading to > > autoimmune disease (was posted on the CDC's own > website and then > > removed) OCSO - OPHR - CDC's Research Agenda - > Starter List Comments , > > where Dr. Carley's paper "Inoculation the > True Weapons of Mass > > Destruction causing an Epidemic of Genocide" was > posted, and describes > > the mechanism whereby corruption of the immune system > occurs). In > > this paper (which Dr. William Atkinson of the > CDC's immunization > > program has refused to respond to), it states that the > hyperactivity of > > the humeral arm of the immune system in autoimmune > disease is caused by > > adjuvants added just for that purpose. However, the > damage caused by > > the autoimmunity (i.e., antibody against self) has > several mechanisms, > > including the following: > > > > 1. The antigens present in the culture media > itself cannot be > > completely filtered and separated from the organisms > cultured thereon. > > Thus, any antibodies formed against antigens from the > culture cells > > themselves (for example myelin basic protein from > chick embryos or the > > 13 vaccines which now contain aborted human fetal > cells) can > > cross-react to form an autoimmune reaction against the > myelin basic > > protein in your myelin sheath, etc. causing > DEMYELINATION. > > > > 2. Molecular mimicry is due to similarity of > proteins contained > > in organisms and mammals. (For example, the measles > virus is made up > > of proteins similar to myelin basic protein; thus, > antibodies formed > > against the measles virus antigens subsequently also > cause an > > auto-antibody attack against myelin basic protein in > the myelin sheath > > due to cross reactivity of these antibodies) causing > DEMYELINATION > > (leading to Autism, as proven below). > > > > In the aforementioned 6th edition of > Harrison's > > Principles of Internal Medicine on p. 1791, under > the heading > > "Multiple Sclerosis and other DEMYELINATING > Diseases", it states the > > following: "A large and important group of > neurologic disorders are > > termed the demyelinating diseases because they share > the common > > pathologic feature of foci of degeneration, involving > the myelin sheath > > of nerves. These foci vary in size, shape, > distribution, and rate of > > development in the different illnesses. The axis > cylinder often > > suffers damage, as does the myelin sheath, but the > destruction of > > myelin is considered the primary change...syndromes > can be clearly > > distinguished....(including) acute disseminated > encephalomyelitis > > (including post infectious and POSTVACCINAL > ENCEPHALOMYELITIS)...(P. > > 1798) - "the association of the neurologic > disorder with vaccination or > > inoculation usually leaves the diagnosis in little > doubt, and the > > characteristic combination of encephalitic and > myelitic features will > > help to distinguish the condition from meningitis, > viral encephalitis, > > and poliomyelitis". This self evident fact has > been taken out of > > subsequent editions of Harrison's Principles of > Internal Medicine , > > since as the vaccine schedule has dramatically > increased over the > > years, the incidence of vaccine induced demyelination > has > > correspondingly increased. This is most evident in > the case of autism, > > which has now risen to epidemic proportions in this > country. Yet, > > whereas there is almost no history of the disease in > the families of > > these children in most cases, and the parents report > the onset of > > symptoms after the child receives the MMR vaccine, the > various arms of > > the medical establishment (including the CDC) conclude > that this is > > just a "coincidence"; rather than that the > association of the > > neurologic disorder (autism) with vaccination or > inoculation usually > > leaves the diagnosis in little doubt. The way that > the true etiology > > of autism is hidden from doctors is by changing the > name of the vaccine > > induced disease. For example, SUB ACUTE SCLEROSING > PAN ENCEPHALITIS > > (SSPE) has been changed to AUTISM, as is demonstrated > in the 10th > > edition of Harrison's Principles of Internal > Medicine where, on page > > 2096, the following information about SSPE is > included: > > > > "...The disease affects boys 3 to > 10 times as frequently > > as girls...Characteristically, they are entirely well > until the disease > > begins. The onset of usually insidious mental > deterioration, often > > expressed by a decline in the patient's > schoolwork, is the presenting > > symptom . Incoordination, ataxia, and myoclonic jerks > develop within a > > few months along with abnormalities of the pyramidal > and extrapyramidal > > motor systems....Elevated levels of measles antibody > are found in the > > serum and CSF....Measles virus is the etiologic > agent....Staining of > > brain tissue from patients with the disease > demonstrates measles virus > > antigen in the inclusions....A few reported cases have > been related to > > measles vaccination." Of course, the vaccine > etiology has been deleted > > from the 16th edition of Harrison's Principles of > Internal Medicine , > > although the age of onset has been changed to 2 years > in that edition. > > > > What becomes SELF EVIDENT from these > various editions of > > Harrison's Principles of Internal Medicine (the > "Bible" by which all > > medical students learn about internal medicine) is > that the source of > > almost all of the viruses that cause demyelinating > diseases is actually > > VACCINES; and that the names of the diseases are > changed to hide the > > true etiology. Another example of this can be found > on page 2104 of > > the 10th edition of Harrison's Principles of > Internal Medicine, under > > the discussion of ACUTE NECROTIZING HEMORRHAGIC > ENCEPHALOMYELITIS, > > which is described as a "tissue destructive > disease of the central > > nervous system which occurs with explosive suddenness > within a few days > > of an upper respiratory infection. The pathologic > findings are > > distinctive. On sectioning the brain, much of the > white matter of one > > or both hemispheres is seen to be destroyed almost to > the point of > > liquefaction. The involved tissue is pink or > yellowish-gray and > > flecked with multiple small hemorrhages. Sometimes > similar changes are > > localized to the brainstem or spinal cord. As in > acute disseminated > > encephalomyelitis in showing perivenular foci of > demyelination, all of > > like age.....The cerebrospinal fluid examination > discloses a more > > intense reaction than in other demyelinating > diseases....The etiology > > of this disease is not established; however, the > entire > > clinical-pathologic entity bears a close resemblance > to a hyper acute > > form of EAE which can be induced in animals by > administration of > > endotoxin, PERTUSSIS VACCINE, or its histamine > sensitizing factor > > coincident with or shortly after injection of myelin > in adjuvant. What > > is self evident from this description is that this > disease is actually > > SIDS (Sudden Infant Death Syndrome) or many of the > cases of Shaken Baby > > Syndrome (the differentiation being whether the child > has any evidence > > of trauma that the prosecutor can use to make a case > for shaken baby > > and subsequently charge a parent with murder, as > happened in the > > well-known case of Alan Yurko in Florida). Thus, once > again, the name > > of the disease has been changed to conceal the fact > that the pertussis > > vaccine is the cause of SIDS and many cases of Shaken > Baby Syndrome. > > > > > > > > ------------------------------------ > > > > Yahoo! Groups Links > > > > > > > > > > > [Non-text portions of this message have been removed] > > > > ------------------------------------ > > Yahoo! Groups Links > > > |
In reply to this post by Andrew McAfee
Andrew how do you get tested for the demyelination? I don't mean to be asking a silly question - because I know that a doctor would order it - but howdo you know whether it is worth testing for it? I ask this because my doctor shows a marked reluctance to do tests - any tests - when i ask for them.What symptoms would have to be presenting before demyelination would be suspected? I'm interested in this because I have been wondering about this for some time but haven't been well enough to even research it on the computer.
Best wishes Steph --- On Thu, 12/3/09, Andrew McAfee <[hidden email]> wrote: From: Andrew McAfee <[hidden email]> Subject: [eSens] demyelination/vaccines/autism/Lyme/colostrum To: [hidden email] Cc: [hidden email] Date: Thursday, 12 March, 2009, 1:52 PM ESENS group, I just a found great website by Dr. Carley with more information on how vaccines cause auto-immune diseases (and demyelination, which I have) and much more. I am glad to see that Dr. Carley is a proponent of bovine colostrum in her protocol to recover from this condition (and autism). My hunch is that electrical sensitivity is a demyelinating auto-immune disorder caused by viruses (measles causes demyelination) in a vaccine weakened immune system and stressed by an environmental overload (radiation, toxins, chemicals, etc). I hope more people with ES will get tested for demyelination and the presence of auto-immune anti-bodies to confirm this relationship. I will let you know more on the healing protocol if it works for me. Andrew Excerpts from http://drcarley.com/ AUTISM IS SUBACUTE SCLEROSING PANENCEPHALITIS INOCULATIONS ARE CAUSING THE CORRUPTION OF THE IMMUNE SYSTEM LEADING TO ALL AUTOIMMUNE DISEASE AND CANCER IN PEOPLE AND PETS. ....by directly injecting organisms into the body leads to a corruption in the immune system...As a result, the pathogenic viruses or bacteria cannot be eliminated by the immune system and remain in the body, where they cause chronic disease and thus further grow and/or mutate as the individual is exposed to ever more antigens and toxins in the environment. In fact, the “prevention” of a disease via vaccination is, in reality, an inability to expel organisms due to the suppression of the cell-mediated response. Thus, rather than preventing disease, the disease is actually prevented from ever being resolved. The organisms continue circulating through the body, adapting to the hostile environment by transforming into other organisms depending on acidity, toxicity and other changes to the internal terrain of the body as demonstrated by the works of Professor Antoine Béchamp. He established this prior to the development of the “germ theory” of disease by Louis Pasteur. Pasteur’s “germ theory” was a plagiarist’s attempt to reshape the truth from Béchamp into his own “original” premise– the beLIEf that germs are out to “attack” us, thereby causing dis-ease.. Thus, treatment of infection with antibiotics as well as “prevention” of disease with vaccines are both just corrupted attempts at cutting off the branches of dis-ease, when the root of the cause is a toxic internal environment combined with nutritional deficiency. However, since Pasteur’s germ theory was conducive to the profits of the burgeoning pharmaceutical cartels that only manage dis-ease, no mention of the work of Professor Béchamp is made in medical school curricula. If components of the myelin sheath (the insulating covering of nerve fibers which allows proper nerve conduction) or the actual neurofilaments themselves are attacked by auto-antibodies, the resultant condition is determined solely by the location of the damage done. Such neurological conditions include but are not limited to minimal brain dysfunction, ADD/ADHD, learning disabilities, mental retardation, criminal behavior, the spectrum of pervasive developmental disorders (including autism), multiple sclerosis, Parkinson’s disease, Lou Gehrig’s disease, Guillen Barre’, seizure disorders, etc., etc. etc. (Please note that other factors are also sometimes involved, such as: the spirochete which causes Lymes disease, aspartame and mercury in cases of MS; aspartame in seizures; or pesticides in cases of Parkinson’s). Thus, when detoxing to reverse these diseases, these other substances must also be removed to obtain a full recovery. However, the corruption of the immune system caused by the injection of vaccines is a key component in these disease states leading to immune malfunction, and is the reason why an autistic child may also have leaky gut or eczema, etc. Note that myelin production, for the most part, does not begin until after birth. Most myelin is apparently laid down by age 5 years and usually completed by age 10 years, judging by the level of success at various ages in reversing autistic and other neurological VIDS symptoms that this author has observed in hundreds of children by detoxing the viruses with homeopathic nosodes5, and repairing the immune corruption by simultaneous administration of bovine colostrum (i.e., after 10 years of age, the ability to stop and repair auto-antibody induced damage in the myelin sheath and neurofilaments themselves is dramatically decreased). # The antigens present in the culture media itself cannot be completely filtered and separated from the organisms cultured thereon. Thus, any antibodies formed against antigens from the culture cells themselves (for example myelin basic protein from chick embryos or the 13 vaccines which now contain aborted human fetal cells) can cross-react to form an autoimmune reaction against the myelin basic protein in your myelin sheath, etc. See the package insert from Pfizer’s Rabies vaccine from the “10th Edition of the Compendium of Veterinary Products”published in 2007 posted on www.drcarley.com, which states “tissue origin vaccines contain extraneous protein in addition to the [rabies] antigen that can lead to autoimmune disease”. THIS IS TRUE FOR ALL VACCINES, BUT THIS IS THE FIRST TIME I HAVE SEEN IT ADMITTED BY ANY VACCINE MANUFACTURER. Although the symptoms of mercury poisoning have been described as identical to the symptoms of autism, it should be noted that most children who descend into the hellish state known as autism do so after the MMR vaccine. The MMR vaccine is one of the few vaccines that do not contain mercury; in fact, it has NEVER contained mercury. Thus, it is self-evident that the removal of mercury will not make vaccines “safe”. (This is why the mercury is the only thing being addressed at all; because when the people reading this paper realize that the very mechanism by which vaccines corrupt the immune system means that NO vaccine is safe and effective; there will be an evolution of consciousness where the structure of lies telling us vaccines are safe and effective disintegrates.) The good news is that these VIDS can be reversed using natural remedies (especially homeopathy) contained in the Hippocrates Protocol (www.drcarley.com). the genocidal plan could drop anytime with activation of the Model State Health Emergency Powers Act whenever the next fabricated terrorist attack using biological agents occurs. The “bird flu” is apparently going to be used as an excuse to inoculate the masses soon, as predictions of a pandemic are being made by the media almost every day. Little do people know that the 1918 Flu pandemic was actually caused by inoculations given to soldiers in WW 1, as reported on p. 28 of the book Vaccination the Silent Killer by Ida Honorof & E. McBean. [as recent evidence see: Vaccines as Biological Weapons? Live Avian Flu Virus Placed in Baxter Vaccine Materials Sent to 18 Countries http://www.naturalnews.com/025760.html] As stated in Harrison's Principles of Internal Medicine , 6th edition, p. 943: "RARELY IS PREVENTION OF INFECTION PER SE CONSIDERED TO BE AN IMPORTANT GOAL OF VACCINATION. In fact, asymptomatic infection after vaccination can serve to enhance and prolong the immune response." Of course, if the immune response has been overwhelmed or corrupted, the "asymptomatic infection" will become a CHRONIC DISEASE. In fact, on the same page of Harrison's, in the following paragraph, it states the following: "PERSISTENCE AND LATENCY. Many viruses persist in host tissues for months or years without causing overt disease. A FLARE-UP OF THESE LATENT INFECTIONS MAY BE INDUCED BY TRAUMA, INTERCURRENT DISEASE, DECLINE IN ANTIBODY TITERS, OR UNKNOWN STIMULI. Experiments with tissue cultures and laboratory animals reveal that persistence of virus in tissue results from an interplay of various factors peculiar to each virus and its host. LATENCY IS PROMOTED BY THE PRESENCE OF ANTIBODY OR OTHER VIRAL INHIBITORS THAT PREVENT EXTENSIVE CELL-TO-CELL SPREAD OF VIRUS. IF ANTIBODY IS WITHDRAWN, VIRAL MULTIPLICATION OFTEN RESUMES, WITH CONCOMITANT CELLULAR NECROSIS." In the same (6th) Edition of Harrison's Principles of Internal Medicine , it is stated on page 975 in regards to the poliomyelitis vaccine: "Vaccine virus multiplies in the intestinal tract and remains at this site. LIVE VACCINE VIRUS SPREADS AND INFECTS CONTACTS OF VACCINATED INDIVIDUALS. This type of immunization in the presence of epidemic poliomyelitis may lead to REPLACEMENT OF THE "WILD" PARALYTOGENIC STRAIN BY THE ONE IN THE VACCINE....." In direct contradiction to this statement, the 1/1/2000 Vaccine Information statement put out by the U.S. Department of Health & Human Services, Centers for Disease Control and Prevention National Immunization Program states that the "OPV (Oral Polio Vaccine) is better at keeping the disease from spreading to other people. However, it does state in this document that "OPV actually causes polio". The inoculation of organisms causes disease both by direct introduction of organisms (including viruses that cause cancer) into the bloodstream, as well as corruption of the immune system leading to autoimmune disease (was posted on the CDC's own website and then removed) OCSO - OPHR - CDC's Research Agenda - Starter List Comments , where Dr. Carley's paper "Inoculation the True Weapons of Mass Destruction causing an Epidemic of Genocide" was posted, and describes the mechanism whereby corruption of the immune system occurs). In this paper (which Dr. William Atkinson of the CDC's immunization program has refused to respond to), it states that the hyperactivity of the humeral arm of the immune system in autoimmune disease is caused by adjuvants added just for that purpose. However, the damage caused by the autoimmunity (i.e., antibody against self) has several mechanisms, including the following: 1. The antigens present in the culture media itself cannot be completely filtered and separated from the organisms cultured thereon. Thus, any antibodies formed against antigens from the culture cells themselves (for example myelin basic protein from chick embryos or the 13 vaccines which now contain aborted human fetal cells) can cross-react to form an autoimmune reaction against the myelin basic protein in your myelin sheath, etc. causing DEMYELINATION. 2. Molecular mimicry is due to similarity ofproteins contained in organisms and mammals. (For example, the measles virus is made up of proteins similar to myelin basic protein; thus, antibodies formed against the measles virus antigens subsequently also cause an auto-antibody attack against myelin basic protein in the myelin sheath due to cross reactivity of these antibodies) causing DEMYELINATION (leading to Autism, as proven below). In the aforementioned 6th edition of Harrison's Principles of Internal Medicine on p. 1791, under the heading "Multiple Sclerosis and other DEMYELINATING Diseases", it states the following: "A large and important group of neurologic disorders are termed the demyelinating diseases because they share the common pathologic feature of foci of degeneration, involving the myelin sheath of nerves. These foci vary in size, shape, distribution, and rate of development in the different illnesses. The axis cylinder often suffers damage, as does the myelin sheath, but the destruction of myelin is considered the primary change...syndromes can be clearly distinguished....(including) acute disseminated encephalomyelitis (including post infectious and POSTVACCINAL ENCEPHALOMYELITIS)...(P. 1798) - "the association of the neurologic disorder with vaccination or inoculation usually leaves the diagnosis in little doubt, and the characteristic combination of encephalitic and myelitic features will help to distinguish the condition from meningitis, viral encephalitis, and poliomyelitis". This self evident fact has been taken out of subsequent editions of Harrison's Principles of Internal Medicine , since as the vaccine schedule has dramatically increased over the years, the incidence of vaccine induced demyelination has correspondingly increased. This is most evident in the case of autism, which has now risen to epidemic proportions in this country. Yet, whereas there is almost no history of the disease in the families of these children in most cases, and the parents report the onset of symptoms after the child receives the MMR vaccine, the various arms of the medical establishment (including the CDC) conclude that this is just a "coincidence"; rather than that the association of the neurologic disorder (autism) with vaccination or inoculation usually leaves the diagnosis in little doubt. The way that the true etiology of autism is hidden from doctors is by changing the name of the vaccine induced disease. For example, SUB ACUTE SCLEROSING PAN ENCEPHALITIS (SSPE) has been changed to AUTISM, as is demonstrated in the 10th edition of Harrison's Principles of Internal Medicine where, on page 2096, the following information about SSPE is included: "...The diseaseaffects boys 3 to 10 times as frequently as girls...Characteristically, they are entirely well until the disease begins. The onset of usually insidious mental deterioration, often expressed by a decline in the patient's schoolwork, is the presenting symptom . Incoordination, ataxia, and myoclonic jerks develop within a few months along with abnormalities of the pyramidal and extrapyramidal motor systems....Elevated levels of measles antibody are found in the serum and CSF....Measles virus is the etiologic agent....Staining of brain tissue from patients with the disease demonstrates measles virus antigen in the inclusions....A few reported cases have been related to measles vaccination." Of course, the vaccine etiology has been deleted from the 16th edition of Harrison's Principles of Internal Medicine , although the age of onset has been changed to 2 years in that edition. What becomes SELF EVIDENT from these various editions of Harrison's Principles of Internal Medicine (the "Bible" by which all medical students learn about internal medicine) is that the source of almost all of the viruses that cause demyelinating diseases is actually VACCINES; and that the names of the diseases are changed to hide the true etiology. Another example of this can be found on page 2104 of the 10th edition of Harrison's Principles of Internal Medicine, under the discussion of ACUTE NECROTIZING HEMORRHAGIC ENCEPHALOMYELITIS, which is described as a "tissue destructive disease of the central nervous system which occurs with explosive suddenness within a few days of an upper respiratory infection. The pathologic findings are distinctive. On sectioning the brain, much of the white matter of one or both hemispheres is seen to be destroyed almost to the point of liquefaction. The involved tissue is pink or yellowish-gray and flecked with multiple small hemorrhages. Sometimes similar changes are localized to the brainstem or spinal cord. As in acute disseminated encephalomyelitis in showing perivenular foci of demyelination, all of like age.....The cerebrospinal fluid examination discloses a more intense reaction than in other demyelinating diseases....The etiology of this disease is not established; however, the entire clinical-pathologic entity bears a close resemblance to a hyper acute form of EAE which can be induced in animals by administration of endotoxin, PERTUSSIS VACCINE, or its histamine sensitizing factor coincident with or shortly after injection of myelin in adjuvant. What is self evident from this description is that this disease is actually SIDS (Sudden Infant Death Syndrome) or many of the cases of Shaken Baby Syndrome (the differentiation being whether the child has any evidence of trauma that the prosecutor can use to make a case for shaken baby and subsequently charge a parent with murder, as happened in the well-known case of Alan Yurko in Florida). Thus, once again, the name of the disease has been changed to conceal the fact that the pertussis vaccine is the cause of SIDS and many cases of Shaken Baby Syndrome. ------------------------------------ Yahoo! Groups Links [Non-text portions of this message have been removed] |
I recall off hand what the exact test is to order for demyelination. I
think it is one of the lipid tests. I person in the know (medical professional) could easily answer this. The real question is or answer that they can't give is what is causing it and how to recover from it. I have been listening to Dr. Carley and the info has been extremely fascinating as the pieces fall into place. I am convinced that doing good detoxes, rebooting the system with colostrum and healing/ recovering with homeopathics are going to be the ticket for me. I am waiting for a call from Dr. Klinghardt's office right now to speak to one of their doctors, Dr. Kamiai. I am officially one of their patients (and paying $5 a minute by phone) and I'll tell you what she thinks. I plan on talking to Dr. Carley by phone to get her personal 2 cents as well. At least she is in the same state (NC) as I am. Please see > http://drcarley.com/ if you haven't read her stuff yet. Thank you, Andrew On Mar 18, 2009, at 4:30 PM, Stephanie Smith wrote: > Andrew how do you get tested for the demyelination? I don't mean to be > asking a silly question - because I know that a doctor would order it > - but how do you know whether it is worth testing for it? I ask this > because my doctor shows a marked reluctance to do tests - any tests - > when i ask for them. What symptoms would have to be presenting before > demyelination would be suspected? I'm interested in this because I > have been wondering about this for some time but haven't been well > enough to even research it on the computer. > > Best wishes > > Steph > > --- On Thu, 12/3/09, Andrew McAfee <[hidden email]> wrote: > > > From: Andrew McAfee <[hidden email]> > Subject: [eSens] demyelination/vaccines/autism/Lyme/colostrum > To: [hidden email] > Cc: [hidden email] > Date: Thursday, 12 March, 2009, 1:52 PM > > > ESENS group, > I just a found great website by Dr. Carley with more information on how > vaccines cause auto-immune diseases (and demyelination, which I have) > and much more. > I am glad to see that Dr. Carley is a proponent of bovine colostrum in > her protocol to recover from this condition (and autism). > My hunch is that electrical sensitivity is a demyelinating auto-immune > disorder caused by viruses (measles causes demyelination) in a vaccine > weakened immune system and stressed by an environmental overload > (radiation, toxins, chemicals, etc). > I hope more people with ES will get tested for demyelination and the > presence of auto-immune anti-bodies to confirm this relationship. > I will let you know more on the healing protocol if it works for me. > Andrew > > Excerpts from http://drcarley.com/ > > AUTISM IS SUBACUTE SCLEROSING PANENCEPHALITIS > > INOCULATIONS ARE CAUSING THE CORRUPTION OF THE IMMUNE SYSTEM LEADING TO > ALL AUTOIMMUNE DISEASE AND CANCER IN PEOPLE AND PETS. > > ....by directly injecting organisms into the body leads to a corruption > in the immune system...As a result, the pathogenic viruses or bacteria > cannot be eliminated by the immune system and remain in the body, where > they cause chronic disease and thus further grow and/or mutate as the > individual is exposed to ever more antigens and toxins in the > environment. > > In fact, the “prevention” of a disease via vaccination is, in reality, > an inability to expel organisms due to the suppression of the > cell-mediated response. Thus, rather than preventing disease, the > disease is actually prevented from ever being resolved. The organisms > continue circulating through the body, adapting to the hostile > environment by transforming into other organisms depending on acidity, > toxicity and other changes to the internal terrain of the body as > demonstrated by the works of Professor Antoine Béchamp. He established > this prior to the development of the “germ theory” of disease by Louis > Pasteur. Pasteur’s “germ theory” was a plagiarist’s attempt toreshape > the truth from Béchamp into his own “original” premise – the beLIEf > that germs are out to “attack” us, thereby causing dis-ease.. Thus, > treatment of infection with antibiotics as well as “prevention” of > disease with vaccines are both just corrupted attempts at cutting off > the branches of dis-ease, when the root of the cause is a toxic > internal environment combined with nutritional deficiency. However, > since Pasteur’s germ theory was conducive to the profits of the > burgeoning pharmaceutical cartels that only manage dis-ease, no mention > of the work of Professor Béchamp is made in medical school curricula. > > If components of the myelin sheath (the insulating covering of nerve > fibers which allows proper nerve conduction) or the actual > neurofilaments themselves are attacked by auto-antibodies, the > resultant condition is determined solely by the location of the damage > done. Such neurological conditions include but are not limited to > minimal brain dysfunction, ADD/ADHD, learning disabilities, mental > retardation, criminal behavior, the spectrum of pervasive developmental > disorders (including autism), multiple sclerosis, Parkinson’s disease, > Lou Gehrig’s disease, Guillen Barre’, seizure disorders, etc., etc. > etc. (Please note that other factors are also sometimes involved, such > as: the spirochete which causes Lymes disease, aspartame and mercury in > cases of MS; aspartame in seizures; or pesticides in cases of > Parkinson’s). Thus, when detoxing to reverse these diseases, these > other substances must also be removed to obtain a full recovery. > However, the corruption of the immune system caused by the injection of > vaccines is a key component in these disease states leading to immune > malfunction, and is the reason why an autistic child may also have > leaky gut or eczema, etc. Note that myelin production, for the most > part, does not begin until after birth. Most myelin is apparently laid > down by age 5 years and usually completed by age 10 years, judging by > the level of success at various ages in reversing autistic and other > neurological VIDS symptoms that this author has observed in hundreds of > children by detoxing the viruses with homeopathic nosodes5, and > repairing the immune corruption by simultaneous administration of > bovine colostrum (i.e., after 10 years of age, the ability to stop and > repair auto-antibody induced damage in the myelin sheath and > neurofilaments themselves is dramatically decreased). > > # The antigens present in the culture media itself cannot be completely > filtered and separated from the organisms cultured thereon. Thus, any > antibodies formed against antigens from the culture cells themselves > (for example myelin basic protein from chick embryos or the 13 vaccines > which now contain aborted human fetal cells) can cross-react to form an > autoimmune reaction against the myelin basic protein in your myelin > sheath, etc. See the package insert from Pfizer’s Rabies vaccine from > the “10th Edition of the Compendium of Veterinary Products” published > in 2007 posted on www.drcarley.com, which states “tissue origin > vaccines contain extraneous protein in addition to the [rabies] antigen > that can lead to autoimmune disease”. THIS IS TRUE FOR ALL VACCINES, > BUT THIS IS THE FIRST TIME I HAVE SEEN IT ADMITTED BY ANY VACCINE > MANUFACTURER. > > Although the symptoms of mercury poisoning have been described as > identical to the symptoms of autism, it should be noted that most > children who descend into the hellish state known as autism do so after > the MMR vaccine. The MMR vaccine is one of the few vaccines that do > not contain mercury; in fact, it has NEVER contained mercury. Thus, it > is self-evident that the removal of mercury will not make vaccines > “safe”. (This is why the mercury is the only thing being addressedat > all; because when the people reading this paper realize that the very > mechanism by which vaccines corrupt the immune system means that NO > vaccine is safe and effective; there will be an evolution of > consciousness where the structure of lies telling us vaccines are safe > and effective disintegrates.) > > The good news is that these VIDS can be reversed using natural > remedies (especially homeopathy) contained in the Hippocrates Protocol > (www.drcarley.com). > > the genocidal plan could drop anytime with activation of the Model > State Health Emergency Powers Act whenever the next fabricated > terrorist attack using biological agents occurs. The “bird flu” is > apparently going to be used as an excuse to inoculate the masses soon, > as predictions of a pandemic are being made by the media almost every > day. Little do people know that the 1918 Flu pandemic was actually > caused by inoculations given to soldiers in WW 1, as reported on p. 28 > of the book Vaccination the Silent Killer by Ida Honorof & E. McBean. > > [as recent evidence see: Vaccines as Biological Weapons? Live Avian Flu > Virus Placed in Baxter Vaccine Materials Sent to 18 Countries > http://www.naturalnews.com/025760.html] > > As stated in Harrison's Principles of Internal Medicine , 6th > edition, > p. 943: "RARELY IS PREVENTION OF INFECTION PER SE CONSIDERED TO BE AN > IMPORTANT GOAL OF VACCINATION. In fact, asymptomatic infection after > vaccination can serve to enhance and prolong the immune response." Of > course, if the immune response has been overwhelmed or corrupted, the > "asymptomatic infection" will become a CHRONIC DISEASE. In fact, on > the same page of Harrison's, in the following paragraph, it states the > following: > "PERSISTENCE AND LATENCY. Many viruses persist in host tissues for > months or years without causing overt disease. A FLARE-UP OF THESE > LATENT INFECTIONS MAY BE INDUCED BY TRAUMA, INTERCURRENT DISEASE, > DECLINE IN ANTIBODY TITERS, OR UNKNOWN STIMULI. Experiments with > tissue cultures and laboratory animals reveal that persistence of virus > in tissue results from an interplay of various factors peculiar to each > virus and its host. LATENCY IS PROMOTED BY THE PRESENCE OF ANTIBODY OR > OTHER VIRAL INHIBITORS THAT PREVENT EXTENSIVE CELL-TO-CELL SPREAD OF > VIRUS. IF ANTIBODY IS WITHDRAWN, VIRAL MULTIPLICATION OFTEN RESUMES, > WITH CONCOMITANT CELLULAR NECROSIS." > > In the same (6th) Edition of Harrison's Principles of Internal > Medicine , it is stated on page 975 in regards to the poliomyelitis > vaccine: "Vaccine virus multiplies in the intestinal tract and remains > at this site. LIVE VACCINE VIRUS SPREADS AND INFECTS CONTACTS OF > VACCINATED INDIVIDUALS. This type of immunization in the presence of > epidemic poliomyelitis may lead to REPLACEMENT OF THE "WILD" > PARALYTOGENIC STRAIN BY THE ONE IN THE VACCINE....." In direct > contradiction to this statement, the 1/1/2000 Vaccine Information > statement put out by the U.S. Department of Health & Human Services, > Centers for Disease Control and Prevention National Immunization > Program states that the "OPV (Oral Polio Vaccine) is better at keeping > the disease from spreading to other people. However, it does state in > this document that "OPV actually causes polio". > > The inoculation of organisms causes disease both by direct introduction > of organisms (including viruses that cause cancer) into the > bloodstream, as well as corruption of the immune system leading to > autoimmune disease (was posted on the CDC's own website and then > removed) OCSO - OPHR - CDC's Research Agenda - Starter List Comments , > where Dr. Carley's paper "Inoculation the True Weapons of Mass > Destruction causing an Epidemic of Genocide" was posted, and describes > the mechanism whereby corruption of the immune system occurs). In > this paper (which Dr. William Atkinson of the CDC's immunization > program has refused to respond to), it states that the hyperactivity of > the humeral arm of the immune system in autoimmune disease is caused by > adjuvants added just for that purpose. However, the damage caused by > the autoimmunity (i.e., antibody against self) has several mechanisms, > including the following: > > 1. The antigens present in the culture media itself cannot be > completely filtered and separated from the organisms cultured thereon. > Thus, any antibodies formed against antigens from the culture cells > themselves (for example myelin basic protein from chick embryos or the > 13 vaccines which now contain aborted human fetal cells) can > cross-react to form an autoimmune reaction against the myelin basic > protein in your myelin sheath, etc. causing DEMYELINATION. > > 2. Molecular mimicry is due to similarity of proteins contained > in organisms and mammals. (For example, the measles virus is made up > of proteins similar to myelin basic protein; thus, antibodies formed > against the measles virus antigens subsequently also cause an > auto-antibody attack against myelin basic protein in the myelin sheath > due to cross reactivity of these antibodies) causing DEMYELINATION > (leading to Autism, as proven below). > > In the aforementioned 6th edition of Harrison's > Principles of Internal Medicine on p. 1791, under the heading > "Multiple Sclerosis and other DEMYELINATING Diseases", it states the > following: "A large and important group of neurologic disorders are > termed the demyelinating diseases because they share the common > pathologic feature of foci of degeneration, involving the myelin sheath > of nerves. These foci vary in size, shape, distribution, and rate of > development in the different illnesses. The axis cylinder often > suffers damage, as does the myelin sheath, but the destruction of > myelin is considered the primary change...syndromes can be clearly > distinguished....(including) acute disseminated encephalomyelitis > (including post infectious and POSTVACCINAL ENCEPHALOMYELITIS)...(P. > 1798) - "the association of the neurologic disorder with vaccination or > inoculation usually leaves the diagnosis in little doubt, and the > characteristic combination of encephalitic and myelitic features will > help to distinguish the condition from meningitis, viral encephalitis, > and poliomyelitis". This self evident fact has been taken out of > subsequent editions of Harrison's Principles of Internal Medicine , > since as the vaccine schedule has dramatically increased over the > years, the incidence of vaccine induced demyelination has > correspondingly increased. This is most evident in the case of autism, > which has now risen to epidemic proportions in this country. Yet, > whereas there is almost no history of the disease in the families of > these children in most cases, and the parents report the onset of > symptoms after the child receives the MMR vaccine, the various arms of > the medical establishment (including the CDC) conclude that this is > just a "coincidence"; rather than that the association of the > neurologic disorder (autism) with vaccination or inoculation usually > leaves the diagnosis in little doubt. The way that the true etiology > of autism is hidden from doctors is by changing the name of the vaccine > induced disease. For example, SUB ACUTE SCLEROSING PAN ENCEPHALITIS > (SSPE) has been changed to AUTISM, as is demonstrated in the 10th > edition of Harrison's Principles of Internal Medicine where, on page > 2096, the following information about SSPE is included: > > "...The disease affects boys 3 to 10 times as frequently > as girls...Characteristically, they are entirely well until the disease > begins. The onset of usually insidious mental deterioration, often > expressed by a decline in the patient's schoolwork, is the presenting > symptom . Incoordination, ataxia, and myoclonic jerks develop within a > few months along with abnormalities of the pyramidal and extrapyramidal > motor systems....Elevated levels of measles antibody are found in the > serum and CSF....Measles virus is the etiologic agent....Staining of > brain tissue from patients with the disease demonstrates measles virus > antigen in the inclusions....A few reported cases have been related to > measles vaccination." Of course, the vaccine etiology has been deleted > from the 16th edition of Harrison's Principles of Internal Medicine , > although the age of onset has been changed to 2 years in that edition. > > What becomes SELF EVIDENT from these variouseditions of > Harrison's Principles of Internal Medicine (the "Bible" by which all > medical students learn about internal medicine) is that the source of > almost all of the viruses that cause demyelinating diseases is actually > VACCINES; and that the names of the diseases are changed to hide the > true etiology. Another example of this can be found on page 2104 of > the 10th edition of Harrison's Principles of Internal Medicine, under > the discussion of ACUTE NECROTIZING HEMORRHAGIC ENCEPHALOMYELITIS, > which is described as a "tissue destructive disease of the central > nervous system which occurs with explosive suddenness within a few days > of an upper respiratory infection. The pathologic findings are > distinctive. On sectioning the brain, much of the white matter of one > or both hemispheres is seen to be destroyed almost to the point of > liquefaction. The involved tissue is pink or yellowish-gray and > flecked with multiple small hemorrhages. Sometimes similar changes are > localized to the brainstem or spinal cord. As in acute disseminated > encephalomyelitis in showing perivenular foci of demyelination, all of > like age.....The cerebrospinal fluid examination discloses a more > intense reaction than in other demyelinating diseases....The etiology > of this disease is not established; however, the entire > clinical-pathologic entity bears a close resemblance to a hyper acute > form of EAE which can be induced in animals by administration of > endotoxin, PERTUSSIS VACCINE, or its histamine sensitizing factor > coincident with or shortly after injection of myelin in adjuvant. What > is self evident from this description is that this disease is actually > SIDS (Sudden Infant Death Syndrome) or many of the cases of Shaken Baby > Syndrome (the differentiation being whether the child has any evidence > of trauma that the prosecutor can use to make a case for shaken baby > and subsequently charge a parent with murder, as happened in the > well-known case of Alan Yurko in Florida). Thus, once again, the name > of the disease has been changed to conceal the fact that the pertussis > vaccine is the cause of SIDS and many cases of Shaken Baby Syndrome. > > > > ------------------------------------ > > Yahoo! Groups Links > > > > > > > > > [Non-text portions of this message have been removed] > > > > ------------------------------------ > > Yahoo! Groups Links > > > |
Administrator
|
> I am waiting for a call from Dr. Klinghardt's office right now to speak
> to one of their doctors, Dr. Kamiai. I am officially one of their > patients (and paying $5 a minute by phone) and I'll tell you what she > thinks. I saw the Kimai in person back in 2001... she scared me off, with her plans to inject procaine into my kidneys and then bind the mobilized heavy metals with DMPS... Marc |
I liked talking with her. She is hopeful that oral OSR will be close if
not as good as doing DMPS. According to my test results, she said I have high mineral depletion, a systemic infection, with low T-3 (typical with Lyme), and a very heavy toxic metal load (still). Recommended Magnesium Chloride (preferably by injection), some French Homeopathic and herbal remedies, and lots of other stuff that I'll report when I get her list. I thought it was a good call even though it will cost $225. Andrew On Mar 18, 2009, at 7:18 PM, Marc Martin wrote: >> I am waiting for a call from Dr. Klinghardt's office right now to >> speak >> to one of their doctors, Dr. Kamiai. I am officially one of their >> patients (and paying $5 a minute by phone) and I'll tell you what she >> thinks. > > I saw the Kimai in person back in 2001... she scared me off, with her > plans to inject procaine into my kidneys and then bind the mobilized > heavy metals with DMPS... > > Marc > > > ------------------------------------ > > Yahoo! Groups Links > > > |
Administrator
|
> I liked talking with her. She is hopeful that oral OSR will be close if
> not as good as doing DMPS. As I recall, Dr. Kimiai was quite impressive. But like I said, her suggested treatments scared me off. Who knows, maybe I would have done better if I had stayed with her. I don't recall her being that expensive, although I did see her in person. I'll be interested in seeing how you do following her advice, Andrew. She is always an option for me, as she's only a 15-minute drive away from my house... Marc |
Administrator
|
In reply to this post by Andrew McAfee
>> According to my test results, she said I have high mineral depletion
>> Recommended Magnesium Chloride (preferably by injection) By the way, is the Magnesium Chloride meant to counter the mineral depletion, or is it for some other purpose? I tried Magnesium chloride once, and didn't react well to it. I do much better with Magnesium citrate ("Natural Calm", to be precise) Marc |
Me too. I have never heard of taking the Chloride form and regularly
take the same "Natural Calm." I think it is to help with the mineral depletion. The issue is also that I am not ingestion or keeping minerals. This could be a intestinal auto-immune or the stuff that I do take or have taken (detox EDTA, DMSA, etc. some distilled water) has way over depleted my system. I take Cell Food and Ormus minerals but I guess not enough. She is prescribing Hydrochloric Acid as well to help absorption. I don't how that is going to be administered. Andrew On Mar 19, 2009, at 12:13 AM, Marc Martin wrote: >>> According to my test results, she said I have high mineral depletion >>> Recommended Magnesium Chloride (preferably by injection) > > By the way, is the Magnesium Chloride meant to counter the mineral > depletion, or is it for some other purpose? > > I tried Magnesium chloride once, and didn't react well to it. I do > much > better with Magnesium citrate ("Natural Calm", to be precise) > > Marc > > > ------------------------------------ > > Yahoo! Groups Links > > > |
In reply to this post by Andrew McAfee
Hi Andrew
Thanks for this information - I will check out this site and will be interested to know how you get on with Dr Kamiai. Best wishes Steph --- On Wed, 18/3/09, Andrew McAfee <[hidden email]> wrote: From: Andrew McAfee <[hidden email]> Subject: Re: [eSens] demyelination/vaccines/autism/Lyme/colostrum To: [hidden email] Date: Wednesday, 18 March, 2009, 11:10 PM I recall off hand what the exact test is to order for demyelination. I think it is one of the lipid tests. I person in the know (medical professional) could easily answer this. The real question is or answer that they can't give is what is causing it and how to recover from it. I have been listening to Dr. Carley and the info has been extremely fascinating as the pieces fall into place. I am convinced that doing good detoxes, rebooting the system with colostrum and healing/ recovering with homeopathics are going to be the ticket for me. I am waiting for a call from Dr. Klinghardt's office right now to speak to one of their doctors, Dr. Kamiai. I am officially one of their patients (and paying $5 a minute by phone) and I'll tell you what she thinks. I plan on talking to Dr. Carley by phone to get her personal 2 cents as well. At least she is in the same state (NC) as I am. Please see > http://drcarley.com/ if you haven't read her stuff yet. Thank you, Andrew On Mar 18, 2009, at 4:30 PM, Stephanie Smith wrote: > Andrew how do you get tested for the demyelination? I don't mean to be > asking a silly question - because I know that a doctor would order it > - but how do you know whether it is worth testing for it? I ask this > because my doctor shows a marked reluctance to do tests - any tests - > when i ask for them. What symptoms would have to be presenting before > demyelination would be suspected? I'm interested in this because I > have been wondering about this for some time but haven't been well > enough to even research it on the computer. > > Best wishes > > Steph > > --- On Thu, 12/3/09, Andrew McAfee <[hidden email]> wrote: > > > From: Andrew McAfee <[hidden email]> > Subject: [eSens] demyelination/vaccines/autism/Lyme/colostrum > To: [hidden email] > Cc: [hidden email] > Date: Thursday, 12 March, 2009, 1:52 PM > > > ESENS group, > I just a found great website by Dr. Carley with more information on how > vaccines cause auto-immune diseases (and demyelination, which I have) > and much more. > I am glad to see that Dr. Carley is a proponent of bovine colostrum in > her protocol to recover from this condition (and autism). > My hunch is that electrical sensitivity is a demyelinating auto-immune > disorder caused by viruses (measles causes demyelination) in a vaccine > weakened immune system and stressed by an environmental overload > (radiation, toxins, chemicals, etc). > I hope more people with ES will get tested for demyelination and the > presence of auto-immune anti-bodies to confirm this relationship. > I will let you know more on the healing protocol if it works for me. > Andrew > > Excerpts from http://drcarley.com/ > > AUTISM IS SUBACUTE SCLEROSING PANENCEPHALITIS > > INOCULATIONS ARE CAUSING THE CORRUPTION OF THE IMMUNE SYSTEM LEADING TO > ALL AUTOIMMUNE DISEASE AND CANCER IN PEOPLE AND PETS. > > ....by directly injecting organisms into the body leads to a corruption > in the immune system...As a result, the pathogenic viruses or bacteria > cannot be eliminated by the immune system and remain in the body, where > they cause chronic disease and thus further grow and/or mutate as the > individual is exposed to ever more antigens and toxins in the > environment. > > In fact, the “prevention” of a disease via vaccination is, in reality, > an inability to expel organisms due to the suppression of the > cell-mediated response. Thus, rather than preventing disease, the > disease is actually prevented from ever being resolved. The organisms > continue circulating through the body, adapting to the hostile > environment by transforming into other organisms depending on acidity, > toxicity and other changes to the internal terrain of the body as > demonstrated by the works of Professor Antoine Béchamp. He established > this prior to the development of the “germ theory” of disease by Louis > Pasteur. Pasteur’s “germ theory” was a plagiarist’s attempt to reshape > the truth from Béchamp into his own “original” premise – the beLIEf > that germs are out to “attack” us, thereby causing dis-ease.. Thus, > treatment of infection with antibiotics as well as “prevention” of > disease with vaccines are both just corrupted attempts at cutting off > the branches of dis-ease, when the root of the cause is a toxic > internal environment combined with nutritional deficiency. However, > since Pasteur’s germ theory was conducive to the profits of the > burgeoning pharmaceutical cartels that only manage dis-ease, no mention > of the work of Professor Béchamp is made in medical school curricula.. > > If components of the myelin sheath (the insulating covering of nerve > fibers which allows proper nerve conduction) or the actual > neurofilaments themselves are attacked by auto-antibodies, the > resultant condition is determined solely by the location of the damage > done. Such neurological conditions include but are not limited to > minimal brain dysfunction, ADD/ADHD, learning disabilities, mental > retardation, criminal behavior, the spectrum of pervasive developmental > disorders (including autism), multiple sclerosis, Parkinson’s disease, > Lou Gehrig’s disease, Guillen Barre’, seizure disorders, etc., etc. > etc. (Please note that other factors are also sometimes involved, such > as: the spirochete which causes Lymes disease, aspartame and mercury in > cases of MS; aspartame in seizures; or pesticides in cases of > Parkinson’s). Thus, when detoxing to reverse these diseases, these > other substances must also be removed to obtain a full recovery. > However, the corruption of the immune system caused by the injection of > vaccines is a key component in these disease states leading to immune > malfunction, and is the reason why an autistic child may also have > leaky gut or eczema, etc. Note that myelin production, for the most > part, does not begin until after birth. Most myelin is apparently laid > down by age 5 years and usually completed by age 10 years, judging by > the level of success at various ages in reversing autistic and other > neurological VIDS symptoms that this author has observed in hundreds of > children by detoxing the viruses with homeopathic nosodes5, and > repairing the immune corruption by simultaneous administration of > bovine colostrum (i.e., after 10 years of age, the ability to stop and > repair auto-antibody induced damage in the myelin sheath and > neurofilaments themselves is dramatically decreased). > > # The antigens present in the culture media itself cannot be completely > filtered and separated from the organisms cultured thereon. Thus, any > antibodies formed against antigens from the culture cells themselves > (for example myelin basic protein from chick embryos or the 13 vaccines > which now contain aborted human fetal cells) can cross-react to form an > autoimmune reaction against the myelin basic protein in your myelin > sheath, etc. See the package insert from Pfizer’s Rabies vaccine from > the “10th Edition of the Compendium of Veterinary Products” published > in 2007 posted on www.drcarley.com, which states “tissue origin > vaccines contain extraneous protein in addition to the [rabies] antigen > that can lead to autoimmune disease”. THIS IS TRUE FOR ALL VACCINES, > BUT THIS IS THE FIRST TIME I HAVE SEEN IT ADMITTED BY ANY VACCINE > MANUFACTURER. > > Although the symptoms of mercury poisoning have been described as > identical to the symptoms of autism, it should be noted that most > children who descend into the hellish state known as autism do so after > the MMR vaccine. The MMR vaccine is one of the few vaccines that do > not contain mercury; in fact, it has NEVER contained mercury. Thus,it > is self-evident that the removal of mercury will not make vaccines > “safe”. (This is why the mercury is the only thing being addressed at > all; because when the people reading this paper realize that the very > mechanism by which vaccines corrupt the immune system means that NO > vaccine is safe and effective; there will be an evolution of > consciousness where the structure of lies telling us vaccines are safe > and effective disintegrates.) > > The good news is that these VIDS can be reversedusing natural > remedies (especially homeopathy) contained in the Hippocrates Protocol > (www.drcarley.com). > > the genocidal plan could drop anytime with activation of the Model > State Health Emergency Powers Act whenever the next fabricated > terrorist attack using biological agents occurs. The “bird flu” is > apparently going to be used as an excuse to inoculate the masses soon, > as predictions of a pandemic are being made by the media almost every > day. Little do people know that the 1918 Flu pandemic was actually > caused by inoculations given to soldiers in WW 1, as reported on p. 28 > of the book Vaccination the Silent Killer by Ida Honorof & E. McBean. > > [as recent evidence see: Vaccines as Biological Weapons? Live Avian Flu > Virus Placed in Baxter Vaccine Materials Sent to 18 Countries > http://www.naturalnews.com/025760.html] > > As stated in Harrison's Principles of Internal Medicine , 6th > edition, > p. 943: "RARELY IS PREVENTION OF INFECTION PER SE CONSIDERED TO BE AN > IMPORTANT GOAL OF VACCINATION. In fact, asymptomatic infection after > vaccination can serve to enhance and prolong the immune response." Of > course, if the immune response has been overwhelmed or corrupted, the > "asymptomatic infection" will become a CHRONIC DISEASE. In fact, on > the same page of Harrison's, in the following paragraph, it states the > following: > "PERSISTENCE AND LATENCY. Many viruses persist in host tissues for > months or years without causing overt disease. A FLARE-UP OF THESE > LATENT INFECTIONS MAY BE INDUCED BY TRAUMA, INTERCURRENT DISEASE, > DECLINE IN ANTIBODY TITERS, OR UNKNOWN STIMULI. Experiments with > tissue cultures and laboratory animals reveal that persistence of virus > in tissue results from an interplay of various factors peculiar to each > virus and its host. LATENCY IS PROMOTED BY THE PRESENCE OF ANTIBODY OR > OTHER VIRAL INHIBITORS THAT PREVENT EXTENSIVE CELL-TO-CELL SPREAD OF > VIRUS. IF ANTIBODY IS WITHDRAWN, VIRAL MULTIPLICATION OFTEN RESUMES, > WITH CONCOMITANT CELLULAR NECROSIS." > > In the same (6th) Edition of Harrison's Principles of Internal > Medicine , it is stated on page 975 in regards to the poliomyelitis > vaccine: "Vaccine virus multiplies in the intestinal tract and remains > at this site. LIVE VACCINE VIRUS SPREADS AND INFECTS CONTACTS OF > VACCINATED INDIVIDUALS. This type of immunization in the presence of > epidemic poliomyelitis may lead to REPLACEMENT OF THE "WILD" > PARALYTOGENIC STRAIN BY THE ONE IN THE VACCINE....." In direct > contradiction to this statement, the 1/1/2000 Vaccine Information > statement put out by the U.S. Department of Health & Human Services, > Centers for Disease Control and Prevention National Immunization > Program states that the "OPV (Oral Polio Vaccine) is better at keeping > the disease from spreading to other people. However, it does state in > this document that "OPV actually causes polio". > > The inoculation of organisms causes disease both by direct introduction > of organisms (including viruses that cause cancer) into the > bloodstream, as well as corruption of the immune system leading to > autoimmune disease (was posted on the CDC's own website and then > removed) OCSO - OPHR - CDC's Research Agenda - Starter List Comments , > where Dr. Carley's paper "Inoculation the True Weapons of Mass > Destruction causing an Epidemic of Genocide" was posted, and describes > the mechanism whereby corruption of the immune system occurs). In > this paper (which Dr. William Atkinson of the CDC's immunization > program has refused to respond to), it states that the hyperactivity of > the humeral arm of the immune system in autoimmune disease is caused by > adjuvants added just for that purpose. However, the damage caused by > the autoimmunity (i.e., antibody against self) has several mechanisms, > including the following: > > 1. The antigens present in the culture media itself cannot be > completely filtered and separated from the organisms cultured thereon. > Thus, any antibodies formed against antigens from the culture cells > themselves (for example myelin basic protein from chick embryos or the > 13 vaccines which now contain aborted human fetal cells) can > cross-react to form an autoimmune reaction against the myelin basic > protein in your myelin sheath, etc. causing DEMYELINATION. > > 2. Molecular mimicry is due to similarity of proteins contained > in organisms and mammals. (For example, the measles virus is made up > of proteins similar to myelin basic protein; thus, antibodies formed > against the measles virus antigens subsequently also cause an > auto-antibody attack against myelin basic protein in the myelin sheath > due to cross reactivity of these antibodies) causing DEMYELINATION > (leading to Autism, as proven below). > > In the aforementioned 6th edition of Harrison's > Principles of Internal Medicine on p. 1791, under the heading > "Multiple Sclerosis and other DEMYELINATING Diseases", it states the > following: "A large and important group of neurologic disorders are > termed the demyelinating diseases because they share the common > pathologic feature of foci of degeneration, involving the myelin sheath > of nerves. These foci vary in size, shape, distribution, and rate of > development in the different illnesses. The axis cylinder often > suffers damage, as does the myelin sheath, but the destruction of > myelin is considered the primary change...syndromes can be clearly > distinguished....(including) acute disseminated encephalomyelitis > (including post infectious and POSTVACCINAL ENCEPHALOMYELITIS)...(P. > 1798) - "the association of the neurologic disorder with vaccination or > inoculation usually leaves the diagnosis in little doubt, and the > characteristic combination of encephalitic and myelitic features will > help to distinguish the condition from meningitis, viral encephalitis, > and poliomyelitis". This self evident fact has been taken out of > subsequent editions of Harrison's Principles of Internal Medicine , > since as the vaccine schedule has dramatically increased over the > years, the incidence of vaccine induced demyelination has > correspondingly increased. This is most evident in the case of autism, > which has now risen to epidemic proportions in this country. Yet, > whereas there is almost no history of the disease in the families of > these children in most cases, and the parents report the onset of > symptoms after the child receives the MMR vaccine, the various arms of > the medical establishment (including the CDC) conclude that this is > just a "coincidence"; rather than that the association of the > neurologic disorder (autism) with vaccination or inoculation usually > leaves the diagnosis in little doubt. The way that the true etiology > of autism is hidden from doctors is by changing the name of the vaccine > induced disease. For example, SUB ACUTE SCLEROSING PAN ENCEPHALITIS > (SSPE) has been changed to AUTISM, as is demonstrated in the 10th > edition of Harrison's Principles of Internal Medicine where, on page > 2096, the following information about SSPE is included: > > "...The disease affects boys 3 to 10 times as frequently > as girls...Characteristically, they are entirely well until the disease > begins. The onset of usually insidious mental deterioration, often > expressed by a decline in the patient's schoolwork, is the presenting > symptom . Incoordination, ataxia, and myoclonic jerks develop within a > few months along with abnormalities of the pyramidal and extrapyramidal > motor systems....Elevated levels of measles antibody are found in the > serum and CSF....Measles virus is the etiologic agent....Staining of > brain tissue from patients with the disease demonstrates measles virus > antigen in the inclusions....A few reported cases have been related to > measles vaccination." Of course, the vaccine etiology has been deleted > from the 16th edition of Harrison's Principles of Internal Medicine, > although the age of onset has been changed to 2 years in that edition. > > What becomes SELF EVIDENT from these various editions of > Harrison's Principles of Internal Medicine (the "Bible" by which all > medical students learn about internal medicine) is that the source of > almost all of the viruses that cause demyelinating diseases is actually > VACCINES; and that the names of the diseases are changed to hide the > true etiology. Another example of this can be found on page 2104 of > the 10th edition of Harrison's Principles of Internal Medicine, under > the discussion of ACUTE NECROTIZING HEMORRHAGIC ENCEPHALOMYELITIS, > which is described as a "tissue destructive disease of the central > nervous system which occurs with explosive suddenness within a few days > of an upper respiratory infection. The pathologic findings are > distinctive. On sectioning the brain, much of the white matter of one > or both hemispheres is seen to be destroyed almost to the point of > liquefaction. The involved tissue is pink or yellowish-gray and > flecked with multiple small hemorrhages. Sometimes similar changes are > localized to the brainstem or spinal cord. As in acute disseminated > encephalomyelitis in showing perivenular foci of demyelination, all of > like age.....The cerebrospinal fluid examination discloses a more > intense reaction than in other demyelinating diseases....The etiology > of this disease is not established; however, the entire > clinical-pathologic entity bears a close resemblance to a hyper acute > form of EAE which can be induced in animals by administration of > endotoxin, PERTUSSIS VACCINE, or its histamine sensitizing factor > coincident with or shortly after injection of myelin in adjuvant. What > is self evident from this description is that this disease is actually > SIDS (Sudden Infant Death Syndrome) or many of the cases of Shaken Baby > Syndrome (the differentiation being whether the child has any evidence > of trauma that the prosecutor can use to make a case for shaken baby > and subsequently charge a parent with murder, as happened in the > well-known case of Alan Yurko in Florida). Thus, once again, the name > of the disease has been changed to conceal the fact that the pertussis > vaccine is the cause of SIDS and many cases of Shaken Baby Syndrome. > > > > ------------------------------------ > > Yahoo! Groups Links > > > > > > > > > [Non-text portions of this message have been removed] > > > > ------------------------------------ > > Yahoo! Groups Links > > > ------------------------------------ Yahoo! Groups Links [Non-text portions of this message have been removed] |
In reply to this post by Andrew McAfee
Hi Andrew and Steph, There may be other tests which show demyelination, but the ones I had were MRIs. Diane --- On Wed, 3/18/09, Andrew McAfee <[hidden email]> wrote: > From: Andrew McAfee <[hidden email]> > Subject: Re: [eSens] demyelination/vaccines/autism/Lyme/colostrum > To: [hidden email] > Date: Wednesday, March 18, 2009, 7:10 PM > I recall off hand what the exact test is to order for > demyelination. I > think it is one of the lipid tests. I person in the know > (medical > professional) could easily answer this. > The real question is or answer that they can't give is > what is causing > it and how to recover from it. > I have been listening to Dr. Carley and the info has been > extremely > fascinating as the pieces fall into place. > I am convinced that doing good detoxes, rebooting the > system with > colostrum and healing/ recovering with homeopathics are > going to be the > ticket for me. > I am waiting for a call from Dr. Klinghardt's office > right now to speak > to one of their doctors, Dr. Kamiai. I am officially one of > their > patients (and paying $5 a minute by phone) and I'll > tell you what she > thinks. > I plan on talking to Dr. Carley by phone to get her > personal 2 cents as > well. At least she is in the same state (NC) as I am. > Please see > > http://drcarley.com/ > if you haven't read her stuff yet. > Thank you, > Andrew > > On Mar 18, 2009, at 4:30 PM, Stephanie Smith wrote: > > > Andrew how do you get tested for the demyelination? I > don't mean to be > > asking a silly question - because I know that a doctor > would order it > > - but how do you know whether it is worth testing for > it? I ask this > > because my doctor shows a marked reluctance to do > tests - any tests - > > when i ask for them. What symptoms would have to be > presenting before > > demyelination would be suspected? I'm interested > in this because I > > have been wondering about this for some time but > haven't been well > > enough to even research it on the computer. > > > > Best wishes > > > > Steph > > > > --- On Thu, 12/3/09, Andrew McAfee > <[hidden email]> wrote: > > > > > > From: Andrew McAfee <[hidden email]> > > Subject: [eSens] > demyelination/vaccines/autism/Lyme/colostrum > > To: [hidden email] > > Cc: [hidden email] > > Date: Thursday, 12 March, 2009, 1:52 PM > > > > > > ESENS group, > > I just a found great website by Dr. Carley with more > information on how > > vaccines cause auto-immune diseases (and > demyelination, which I have) > > and much more. > > I am glad to see that Dr. Carley is a proponent of > bovine colostrum in > > her protocol to recover from this condition (and > autism). > > My hunch is that electrical sensitivity is a > demyelinating auto-immune > > disorder caused by viruses (measles causes > demyelination) in a vaccine > > weakened immune system and stressed by an > environmental overload > > (radiation, toxins, chemicals, etc). > > I hope more people with ES will get tested for > demyelination and the > > presence of auto-immune anti-bodies to confirm this > relationship. > > I will let you know more on the healing protocol if it > works for me. > > Andrew > > > > Excerpts from http://drcarley.com/ > > > > AUTISM IS SUBACUTE SCLEROSING PANENCEPHALITIS > > > > INOCULATIONS ARE CAUSING THE CORRUPTION OF THE IMMUNE > SYSTEM LEADING TO > > ALL AUTOIMMUNE DISEASE AND CANCER IN PEOPLE AND PETS. > > > > ....by directly injecting organisms into the body > leads to a corruption > > in the immune system...As a result, the pathogenic > viruses or bacteria > > cannot be eliminated by the immune system and remain > in the body, where > > they cause chronic disease and thus further grow > and/or mutate as the > > individual is exposed to ever more antigens and toxins > in the > > environment. > > > > In fact, the “prevention” of a disease via > vaccination is, in reality, > > an inability to expel organisms due to the suppression > of the > > cell-mediated response. Thus, rather than preventing > disease, the > > disease is actually prevented from ever being > resolved. The organisms > > continue circulating through the body, adapting to the > hostile > > environment by transforming into other organisms > depending on acidity, > > toxicity and other changes to the internal terrain of > the body as > > demonstrated by the works of Professor Antoine > Béchamp. He established > > this prior to the development of the “germ theory” > of disease by Louis > > Pasteur. Pasteur’s “germ theory” was a > plagiarist’s attempt to reshape > > the truth from Béchamp into his own “original” > premise – the beLIEf > > that germs are out to “attack” us, thereby causing > dis-ease.. Thus, > > treatment of infection with antibiotics as well as > “prevention” of > > disease with vaccines are both just corrupted attempts > at cutting off > > the branches of dis-ease, when the root of the cause > is a toxic > > internal environment combined with nutritional > deficiency. However, > > since Pasteur’s germ theory was conducive to the > profits of the > > burgeoning pharmaceutical cartels that only manage > dis-ease, no mention > > of the work of Professor Béchamp is made in medical > school curricula. > > > > If components of the myelin sheath (the insulating > covering of nerve > > fibers which allows proper nerve conduction) or the > actual > > neurofilaments themselves are attacked by > auto-antibodies, the > > resultant condition is determined solely by the > location of the damage > > done. Such neurological conditions include but are > not limited to > > minimal brain dysfunction, ADD/ADHD, learning > disabilities, mental > > retardation, criminal behavior, the spectrum of > pervasive developmental > > disorders (including autism), multiple sclerosis, > Parkinson’s disease, > > Lou Gehrig’s disease, Guillen Barre’, seizure > disorders, etc., etc. > > etc. (Please note that other factors are also > sometimes involved, such > > as: the spirochete which causes Lymes disease, > aspartame and mercury in > > cases of MS; aspartame in seizures; or pesticides in > cases of > > Parkinson’s). Thus, when detoxing to reverse these > diseases, these > > other substances must also be removed to obtain a full > recovery. > > However, the corruption of the immune system caused by > the injection of > > vaccines is a key component in these disease states > leading to immune > > malfunction, and is the reason why an autistic child > may also have > > leaky gut or eczema, etc. Note that myelin > production, for the most > > part, does not begin until after birth. Most myelin is > apparently laid > > down by age 5 years and usually completed by age 10 > years, judging by > > the level of success at various ages in reversing > autistic and other > > neurological VIDS symptoms that this author has > observed in hundreds of > > children by detoxing the viruses with homeopathic > nosodes5, and > > repairing the immune corruption by simultaneous > administration of > > bovine colostrum (i.e., after 10 years of age, the > ability to stop and > > repair auto-antibody induced damage in the myelin > sheath and > > neurofilaments themselves is dramatically decreased). > > > > # The antigens present in the culture media itself > cannot be completely > > filtered and separated from the organisms cultured > thereon. Thus, any > > antibodies formed against antigens from the culture > cells themselves > > (for example myelin basic protein from chick embryos > or the 13 vaccines > > which now contain aborted human fetal cells) can > cross-react to form an > > autoimmune reaction against the myelin basic protein > in your myelin > > sheath, etc. See the package insert from Pfizer’s > Rabies vaccine from > > the “10th Edition of the Compendium of Veterinary > Products” published > > in 2007 posted on www.drcarley.com, which states > “tissue origin > > vaccines contain extraneous protein in addition to the > [rabies] antigen > > that can lead to autoimmune disease”. THIS IS TRUE > FOR ALL VACCINES, > > BUT THIS IS THE FIRST TIME I HAVE SEEN IT ADMITTED BY > ANY VACCINE > > MANUFACTURER. > > > > Although the symptoms of mercury poisoning have been > described as > > identical to the symptoms of autism, it should be > noted that most > > children who descend into the hellish state known as > autism do so after > > the MMR vaccine. The MMR vaccine is one of the few > vaccines that do > > not contain mercury; in fact, it has NEVER contained > mercury. Thus, it > > is self-evident that the removal of mercury will not > make vaccines > > “safe”. (This is why the mercury is the only > thing being addressed at > > all; because when the people reading this paper > realize that the very > > mechanism by which vaccines corrupt the immune system > means that NO > > vaccine is safe and effective; there will be an > evolution of > > consciousness where the structure of lies telling us > vaccines are safe > > and effective disintegrates.) > > > > The good news is that these VIDS can be > reversed using natural > > remedies (especially homeopathy) contained in the > Hippocrates Protocol > > (www.drcarley.com). > > > > the genocidal plan could drop anytime with activation > of the Model > > State Health Emergency Powers Act whenever the next > fabricated > > terrorist attack using biological agents occurs. The > “bird flu” is > > apparently going to be used as an excuse to inoculate > the masses soon, > > as predictions of a pandemic are being made by the > media almost every > > day. Little do people know that the 1918 Flu > pandemic was actually > > caused by inoculations given to soldiers in WW 1, as > reported on p. 28 > > of the book Vaccination the Silent Killer by Ida > Honorof & E. McBean. > > > > [as recent evidence see: Vaccines as Biological > Weapons? Live Avian Flu > > Virus Placed in Baxter Vaccine Materials Sent to 18 > Countries > > http://www.naturalnews.com/025760.html] > > > > As stated in Harrison's Principles of Internal > Medicine , 6th > > edition, > > p. 943: "RARELY IS PREVENTION OF INFECTION PER > SE CONSIDERED TO BE AN > > IMPORTANT GOAL OF VACCINATION. In fact, asymptomatic > infection after > > vaccination can serve to enhance and prolong the > immune response." Of > > course, if the immune response has been overwhelmed or > corrupted, the > > "asymptomatic infection" will become a > CHRONIC DISEASE. In fact, on > > the same page of Harrison's, in the following > paragraph, it states the > > following: > > "PERSISTENCE AND LATENCY. Many viruses persist > in host tissues for > > months or years without causing overt disease. A > FLARE-UP OF THESE > > LATENT INFECTIONS MAY BE INDUCED BY TRAUMA, > INTERCURRENT DISEASE, > > DECLINE IN ANTIBODY TITERS, OR UNKNOWN STIMULI. > Experiments with > > tissue cultures and laboratory animals reveal that > persistence of virus > > in tissue results from an interplay of various factors > peculiar to each > > virus and its host. LATENCY IS PROMOTED BY THE > PRESENCE OF ANTIBODY OR > > OTHER VIRAL INHIBITORS THAT PREVENT EXTENSIVE > CELL-TO-CELL SPREAD OF > > VIRUS. IF ANTIBODY IS WITHDRAWN, VIRAL > MULTIPLICATION OFTEN RESUMES, > > WITH CONCOMITANT CELLULAR NECROSIS." > > > > In the same (6th) Edition of > Harrison's Principles of Internal > > Medicine , it is stated on page 975 in regards to the > poliomyelitis > > vaccine: "Vaccine virus multiplies in the > intestinal tract and remains > > at this site. LIVE VACCINE VIRUS SPREADS AND INFECTS > CONTACTS OF > > VACCINATED INDIVIDUALS. This type of immunization in > the presence of > > epidemic poliomyelitis may lead to REPLACEMENT OF THE > "WILD" > > PARALYTOGENIC STRAIN BY THE ONE IN THE > VACCINE....." In direct > > contradiction to this statement, the 1/1/2000 Vaccine > Information > > statement put out by the U.S. Department of Health > & Human Services, > > Centers for Disease Control and Prevention National > Immunization > > Program states that the "OPV (Oral Polio > Vaccine) is better at keeping > > the disease from spreading to other > people. However, it does state in > > this document that "OPV actually causes > polio". > > > > The inoculation of organisms causes disease both by > direct introduction > > of organisms (including viruses that cause cancer) > into the > > bloodstream, as well as corruption of the immune > system leading to > > autoimmune disease (was posted on the CDC's own > website and then > > removed) OCSO - OPHR - CDC's Research Agenda - > Starter List Comments , > > where Dr. Carley's paper "Inoculation the > True Weapons of Mass > > Destruction causing an Epidemic of Genocide" was > posted, and describes > > the mechanism whereby corruption of the immune system > occurs). In > > this paper (which Dr. William Atkinson of the > CDC's immunization > > program has refused to respond to), it states that the > hyperactivity of > > the humeral arm of the immune system in autoimmune > disease is caused by > > adjuvants added just for that purpose. However, the > damage caused by > > the autoimmunity (i.e., antibody against self) has > several mechanisms, > > including the following: > > > > 1. The antigens present in the culture media > itself cannot be > > completely filtered and separated from the organisms > cultured thereon. > > Thus, any antibodies formed against antigens from the > culture cells > > themselves (for example myelin basic protein from > chick embryos or the > > 13 vaccines which now contain aborted human fetal > cells) can > > cross-react to form an autoimmune reaction against the > myelin basic > > protein in your myelin sheath, etc. causing > DEMYELINATION. > > > > 2. Molecular mimicry is due to similarity > of proteins contained > > in organisms and mammals. (For example, the measles > virus is made up > > of proteins similar to myelin basic protein; thus, > antibodies formed > > against the measles virus antigens subsequently also > cause an > > auto-antibody attack against myelin basic protein in > the myelin sheath > > due to cross reactivity of these antibodies) causing > DEMYELINATION > > (leading to Autism, as proven below). > > > > In the aforementioned 6th > edition of Harrison's > > Principles of Internal Medicine on p. 1791, under > the heading > > "Multiple Sclerosis and other DEMYELINATING > Diseases", it states the > > following: "A large and important group of > neurologic disorders are > > termed the demyelinating diseases because they share > the common > > pathologic feature of foci of degeneration, involving > the myelin sheath > > of nerves. These foci vary in size, shape, > distribution, and rate of > > development in the different illnesses. The axis > cylinder often > > suffers damage, as does the myelin sheath, but the > destruction of > > myelin is considered the primary change...syndromes > can be clearly > > distinguished....(including) acute disseminated > encephalomyelitis > > (including post infectious and POSTVACCINAL > ENCEPHALOMYELITIS)...(P. > > 1798) - "the association of the neurologic > disorder with vaccination or > > inoculation usually leaves the diagnosis in little > doubt, and the > > characteristic combination of encephalitic and > myelitic features will > > help to distinguish the condition from meningitis, > viral encephalitis, > > and poliomyelitis". This self evident fact has > been taken out of > > subsequent editions of Harrison's Principles of > Internal Medicine , > > since as the vaccine schedule has dramatically > increased over the > > years, the incidence of vaccine induced demyelination > has > > correspondingly increased. This is most evident in > the case of autism, > > which has now risen to epidemic proportions in this > country. Yet, > > whereas there is almost no history of the disease in > the families of > > these children in most cases, and the parents report > the onset of > > symptoms after the child receives the MMR vaccine, the > various arms of > > the medical establishment (including the CDC) conclude > that this is > > just a "coincidence"; rather than that the > association of the > > neurologic disorder (autism) with vaccination or > inoculation usually > > leaves the diagnosis in little doubt. The way that > the true etiology > > of autism is hidden from doctors is by changing the > name of the vaccine > > induced disease. For example, SUB ACUTE SCLEROSING > PAN ENCEPHALITIS > > (SSPE) has been changed to AUTISM, as is demonstrated > in the 10th > > edition of Harrison's Principles of Internal > Medicine where, on page > > 2096, the following information about SSPE is > included: > > > > "...The disease affects > boys 3 to 10 times as frequently > > as girls...Characteristically, they are entirely well > until the disease > > begins. The onset of usually insidious mental > deterioration, often > > expressed by a decline in the patient's > schoolwork, is the presenting > > symptom . Incoordination, ataxia, and myoclonic > jerks develop within a > > few months along with abnormalities of the pyramidal > and extrapyramidal > > motor systems....Elevated levels of measles antibody > are found in the > > serum and CSF....Measles virus is the etiologic > agent....Staining of > > brain tissue from patients with the disease > demonstrates measles virus > > antigen in the inclusions....A few reported cases have > been related to > > measles vaccination." Of course, the vaccine > etiology has been deleted > > from the 16th edition of Harrison's Principles > of Internal Medicine , > > although the age of onset has been changed to 2 years > in that edition. > > > > What becomes SELF EVIDENT from > these various editions of > > Harrison's Principles of Internal Medicine (the > "Bible" by which all > > medical students learn about internal medicine) is > that the source of > > almost all of the viruses that cause demyelinating > diseases is actually > > VACCINES; and that the names of the diseases are > changed to hide the > > true etiology. Another example of this can be found > on page 2104 of > > the 10th edition of Harrison's Principles of > Internal Medicine, under > > the discussion of ACUTE NECROTIZING HEMORRHAGIC > ENCEPHALOMYELITIS, > > which is described as a "tissue destructive > disease of the central > > nervous system which occurs with explosive suddenness > within a few days > > of an upper respiratory infection. The pathologic > findings are > > distinctive. On sectioning the brain, much of the > white matter of one > > or both hemispheres is seen to be destroyed almost to > the point of > > liquefaction. The involved tissue is pink or > yellowish-gray and > > flecked with multiple small hemorrhages. Sometimes > similar changes are > > localized to the brainstem or spinal cord. As in > acute disseminated > > encephalomyelitis in showing perivenular foci of > demyelination, all of > > like age.....The cerebrospinal fluid examination > discloses a more > > intense reaction than in other demyelinating > diseases....The etiology > > of this disease is not established; however, the > entire > > clinical-pathologic entity bears a close resemblance > to a hyper acute > > form of EAE which can be induced in animals by > administration of > > endotoxin, PERTUSSIS VACCINE, or its histamine > sensitizing factor > > coincident with or shortly after injection of myelin > in adjuvant. What > > is self evident from this description is that this > disease is actually > > SIDS (Sudden Infant Death Syndrome) or many of the > cases of Shaken Baby > > Syndrome (the differentiation being whether the child > has any evidence > > of trauma that the prosecutor can use to make a case > for shaken baby > > and subsequently charge a parent with murder, as > happened in the > > well-known case of Alan Yurko in Florida). Thus, > once again, the name > > of the disease has been changed to conceal the fact > that the pertussis > > vaccine is the cause of SIDS and many cases of Shaken > Baby Syndrome. > > > > > > > > ------------------------------------ > > > > Yahoo! Groups Links > > > > > > > > > > > > > > > > > > [Non-text portions of this message have been removed] > > > > > > > > ------------------------------------ > > > > Yahoo! Groups Links > > > > > > > > > > ------------------------------------ > > Yahoo! Groups Links > > > |
Free forum by Nabble | Edit this page |