Posted by Andrew McAfee on
URL: https://www.es-forum.com/demyelination-vaccines-autism-Lyme-colostrum-tp1548713.html

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.