> 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.
>  
>
>
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