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A team at Purdue University
School of Veterinary Medicine conducted several studies (1,2) to determine if
vaccines can cause changes in the immune system of dogs that might lead to
life-threatening immune-mediated diseases. They obviously conducted this
research because concern already existed. It was sponsored by the Haywood
Foundation which itself was looking for evidence that such changes in the human
immune system might also be vaccine induced. It found the evidence.
The vaccinated, but not the
non-vaccinated, dogs in the Purdue studies developed autoantibodies to many of
their own biochemicals, including fibronectin, laminin, DNA, albumin, cytochrome
C, cardiolipin and collagen.
This means that the vaccinated
dogs -- ”but not the non-vaccinated dogs”-- were attacking their own fibronectin,
which is involved in tissue repair, cell multiplication and growth, and
differentiation between tissues and organs in a living organism.
The vaccinated Purdue dogs also
developed autoantibodies to laminin, which is involved in many cellular
activities including the adhesion, spreading, differentiation, proliferation and
movement of cells. Vaccines thus appear to be capable of removing the natural
intelligence of cells.
Autoantibodies to cardiolipin are
frequently found in patients with the serious disease systemic lupus
erythematosus and also in individuals with other autoimmune diseases. The
presence of elevated anti-cardiolipin antibodies is significantly associated
with clots within the heart or blood vessels, in poor blood clotting,
haemorrhage, bleeding into the skin, foetal loss and neurological conditions.
The Purdue studies also found
that vaccinated dogs were developing autoantibodies to their own collagen. About
one quarter of all the protein in the body is collagen. Collagen provides
structure to our bodies, protecting and supporting the softer tissues and
connecting them with the skeleton. It is no wonder that Canine Health Concern's
1997 study of 4,000 dogs showed a high number of dogs developing mobility
problems shortly after they were vaccinated (noted in my 1997 book, What Vets
Don't Tell You About Vaccines).
Perhaps most worryingly, the
Purdue studies found that the vaccinated dogs had developed autoantibodies to
their own DNA. Did the alarm bells sound? Did the scientific community call a
halt to the vaccination program? No. Instead, they stuck their fingers in the
air, saying more research is needed to ascertain whether vaccines can cause
genetic damage. Meanwhile, the study dogs were found good homes, but no
long-term follow-up has been conducted. At around the same time, the American
Veterinary Medical Association (AVMA) Vaccine-Associated Feline Sarcoma Task
Force initiated several studies to find out why 160,000 cats each year in the
USA develop terminal cancer at their vaccine injection sites.(3) The fact that
cats can get vaccine-induced cancer has been acknowledged by veterinary bodies
around the world, and even the British Government acknowledged it through its
Working Group charged with the task of looking into canine and feline
vaccines(4) following pressure from Canine Health Concern. What do you imagine
was the advice of the AVMA Task Force, veterinary bodies and governments? "Carry
on vaccinating until
we find out why vaccines are killing cats, and which cats are most likely to
die."
In America, in an attempt to
mitigate the problem, they're vaccinating cats in the tail or leg so they can
amputate when cancer appears. Great advice if it's not your cat amongst the
hundreds of thousands on the "oops" list.
But other species are okay -
right? Wrong. In August 2003, the Journal of Veterinary Medicine carried an
Italian study which showed that dogs also develop vaccine-induced cancers at
their injection sites.(5) We already know that vaccine-site cancer is a possible
sequel to human vaccines, too, since the Salk polio vaccine was said to carry a
monkey retrovirus (from cultivating the vaccine on monkey organs) that produces
inheritable cancer. The monkey retrovirus SV40 keeps turning up in human cancer
sites.
It is also widely acknowledged
that vaccines can cause a fast-acting, usually fatal, disease called autoimmune
haemolytic anaemia (AIHA). Without treatment, and frequently with treatment,
individuals can die in agony within a matter of days. Merck, itself a
multinational vaccine manufacturer, states in The Merck Manual of Diagnosis and
Therapy that autoimmune haemolytic anaemia may be caused by modified live-virus
vaccines, as do Tizard's Veterinary Immunology (4th edition) and the Journal of
Veterinary Internal Medicine.(6) The British Government's Working Group, despite
being staffed by vaccine-industry consultants who say they are independent, also
acknowledged this fact. However, no one warns the pet owners before their
animals are subjected to an unnecessary booster, and very few owners are told
why after their pets die of AIHA.
A Wide Range of
Vaccine-induced Diseases
We also found some worrying
correlations between vaccine events and the onset of arthritis in our 1997
survey. Our concerns were compounded by research in the human field.
The New England Journal of
Medicine, for example, reported that it is possible to isolate the rubella virus
from affected joints in children vaccinated against rubella. It also told of the
isolation of viruses from the peripheral blood of women with prolonged arthritis
following vaccination.(7)
Then, in 2000, CHC's findings
were confirmed by research which showed that polyarthritis and other diseases
like amyloidosis, which affects organs in dogs, were linked to the combined
vaccine given to dogs.(8) There is a huge body of research, despite the paucity
of funding from the vaccine industry, to confirm that vaccines can cause a wide
range of brain and central nervous system damage. Merck itself states in its
Manual that vaccines (i.e., its own products) can cause encephalitis: brain
inflammation/damage. In some cases, encephalitis involves lesions in the brain
and throughout the central nervous system. Merck states that "examples are the
encephalitides following measles, chickenpox, rubella, smallpox vaccination,
vaccinia, and many other less well defined viral infections".
When the dog owners who took part
in the CHC survey reported that their dogs developed short attention spans,
73.1% of the dogs did so within three months of a vaccine event. The same
percentage of dogs was diagnosed with epilepsy within three months of a shot
(but usually within days). We also found that 72.5% of dogs that were considered
by their owners to be nervous and of a worrying disposition, first exhibited
these traits within the three-month post-vaccination period.
I would like to add for the sake
of Oliver, my friend who suffered from paralysed rear legs and death shortly
after a vaccine shot, that "paresis" is listed in Merck's Manual as a symptom of
encephalitis. This is defined as muscular weakness of a neural (brain) origin
which involves partial or incomplete paralysis, resulting from lesions at any
level of the descending pathway from the brain. Hind limb paralysis is one of
the potential consequences. Encephalitis, incidentally, is a disease that can
manifest across the scale from mild to severe and can also cause sudden death.
Organ failure must also be
suspected when it occurs shortly after a vaccine event. Dr Larry Glickman, who
spearheaded the Purdue research into post-vaccination biochemical changes in
dogs, wrote in a letter to Cavalier Spaniel breeder Bet Hargreaves:
"Our ongoing studies of dogs
show that following routine vaccination, there is a significant rise in the
level of antibodies dogs produce against their own tissues. Some of these
antibodies have been shown to target the thyroid gland, connective tissue such
as that found in the valves of the heart, red blood cells, DNA, etc. I do
believe that the heart conditions in Cavalier King Charles Spaniels could be
the end result of repeated immunisations by vaccines containing tissue culture
contaminants that cause a progressive immune response directed at connective
tissue in the heart valves. The clinical manifestations would be more
pronounced in dogs that have a genetic predisposition [although] the findings
should be generally applicable to all dogs regardless of their breed."
I must mention here that Dr Glickman believes that vaccines are a necessary
evil, but that safer vaccines need to be developed.
Meanwhile, please join the queue
to place your dog, cat, horse and child on the Russian roulette wheel because a
scientist says you should.
Vaccines Stimulate an
Inflammatory Response
The word "allergy" is synonymous
with "sensitivity" and "inflammation". It should, by rights, also be synonymous
with the word "vaccination". This is what vaccines do: they sensitise (render
allergic)an individual in the process of forcing them to develop antibodies to
fight a disease threat. In other words, as is acknowledged and accepted, as part
of the vaccine process the body will respond with inflammation. This may be
apparently temporary or it may be longstanding.
Holistic doctors and
veterinarians have known this for at least 100 years.
They talk about a wide range of inflammatory or "-itis" diseases which arise
shortly after a vaccine event. Vaccines, in fact, plunge many individuals into
an allergic state. Again, this is a disorder that ranges from mild all the way
through to the suddenly fatal. Anaphylactic shock is the culmination: it's where
an individual has a massive allergic reaction to a vaccine and will die within
minutes if adrenaline or its equivalent is not administered.
There are some individuals who
are genetically not well placed to withstand the vaccine challenge. These are
the people (and animals are "people", too) who have inherited faulty B and T
cell function. B and T cells are components within the immune system which
identify foreign invaders and destroy them, and hold the invader in memory so
that they cannot cause future harm. However, where inflammatory responses are
concerned, the immune system overreacts and causes unwanted effects such as
allergies and other
inflammatory conditions.
Merck warns in its Manual that
patients with, or from families with, B and/or T cell immunodeficiencies should
not receive live-virus vaccines due to the risk of severe or fatal infection.
Elsewhere, it lists features of B and T cell immunodeficiencies as food
allergies, inhalant allergies, eczema, dermatitis, neurological deterioration
and heart disease. To translate, people with these conditions can die if they
receive live-virus vaccines. Their immune systems are simply not competent
enough to guarantee a healthy reaction to the viral assault from modified
live-virus vaccines.
Modified live-virus (MLV)
vaccines replicate in the patient until an immune response is provoked. If a
defence isn't stimulated, then the vaccine continues to replicate until it gives
the patient the very disease it was intending to prevent.
Alternatively, a deranged immune
response will lead to inflammatory conditions such as arthritis, pancreatitis,
colitis, encephalitis and any number of autoimmune diseases such as cancer and
leukaemia, where the body attacks its own cells.
A new theory, stumbled upon by
Open University student Gary Smith, explains what holistic practitioners have
been saying for a very long time. Here is what a few of the holistic vets have
said in relation to their patients:
Dr Jean Dodds: "Many
veterinarians trace the present problems with allergic and immunologic diseases
to the introduction of MLV vaccines..." (9)
Christina Chambreau, DVM:
"Routine vaccinations are probably the worst thing that we do for our animals.
They cause all types of illnesses, but not directly to where we would relate
them definitely to be caused by the vaccine." (10)
Martin Goldstein, DVM: "I think
that vaccines...are leading killers of dogs and cats in America today."
Dr Charles E. Loops, DVM:
"Homoeopathic veterinarians and other holistic practitioners have maintained for
some time that vaccinations do more harm than they provide benefits." (12)
Mike Kohn, DVM: "In response to
this [vaccine] violation, there have been increased autoimmune diseases
(allergies being one component), epilepsy, neoplasia [tumours], as well as
behavioural problems in small animals." (13)
A Theory on Inflammation
Gary Smith explains what
observant healthcare practitioners have been saying for a very long time, but
perhaps they've not understood why their observations led them to say it. His
theory, incidentally, is causing a huge stir within the inner scientific
sanctum. Some believe that his theory could lead to a cure for many diseases
including cancer. For me, it explains why the vaccine process is inherently
questionable.
Gary was learning about
inflammation as part of his studies when he struck upon a theory so
extraordinary that it could have implications for the treatment of almost every
inflammatory disease -- including Alzheimer's, Parkinson's, rheumatoid arthritis
and even HIV and AIDS.
Gary's theory questions the
received wisdom that when a person gets ill, the inflammation that occurs around
the infected area helps it to heal. He claims that, in reality, inflammation
prevents the body from recognising a foreign substance and therefore serves as a
hiding place for invaders. The inflammation occurs when at-risk cells produce
receptors called All (known as angiotensin II type I receptors). He says that
while At1 has a balancing receptor, At2, which is supposed to switch off the
inflammation, in most diseases this does not happen.
"Cancer has been described as the
wound that never heals," he says. "All successful cancers are surrounded by
inflammation. Commonly this is thought to be the body's reaction to try to fight
the cancer, but this is not the case.
"The inflammation is not the body
trying to fight the infection. It is actually the virus or bacteria deliberately
causing inflammation in order to hide from the immune system [author's
emphasis]." (14)
If Gary is right, then the
inflammatory process so commonly stimulated by vaccines is not, as hitherto
assumed, a necessarily acceptable sign. Instead, it could be a sign that the
viral or bacterial component, or the adjuvant (which, containing foreign
protein, is seen as an invader by the immune system), in the vaccine is winning
by stealth.
If Gary is correct in believing
that the inflammatory response is not protective but a sign that invasion is
taking place under cover of darkness, vaccines are certainly not the friends we
thought they were. They are undercover assassins working on behalf of the enemy,
and vets and medical doctors are unwittingly acting as collaborators. Worse, we
animal guardians and parents are actually paying doctors and vets to unwittingly
betray our loved ones.
Potentially, vaccines are the
stealth bomb of the medical world. They are used to catapult invaders inside the
castle walls where they can wreak havoc, with none of us any the wiser. So
rather than experiencing frank viral diseases such as the 'flu, measles, mumps
and rubella (and, in the case of dogs, parvovirus and distemper), we are
allowing the viruses to win anyway - but with cancer, leukaemia and other
inflammatory or autoimmune (self-attacking) diseases taking their place.
The Final Insult
All 27 veterinary schools in
North America have changed their protocols for vaccinating dogs and cats along
the following lines; (15) however, vets in practice are reluctant to listen to
these changed protocols and official veterinary bodies in the UK and other
countries are ignoring the following facts.
Dogs' and cats' immune systems
mature fully at six months. If modified live-virus vaccine is giver after six
months of age, it produces immunity, which is good for the life of the pet. If
another MLV vaccine is given a year later, the antibodies from the first vaccine
neutralise the antigens of the second vaccine and there is little or no effect.
The litre is no "boosted", nor are more memory cells induced.
Not only are annual boosters
unnecessary, but they subject the pet to potential risks such as allergic
reactions and immune-mediated haemolytic anaemia.
In plain language, veterinary
schools in America, plus the American Veterinary Medical Association, have
looked at studies to show how long vaccines last and they have concluded and
announced that annual vaccination is unnecessary.(16-19)
Further, they have acknowledged
that vaccines are not without harm. Dr Ron Schultz, head of pathobiology at
Wisconsin University and a leading light in this field, has been saying this
politely to his veterinary colleagues since the 1980s. I've been saying it for
the past 12 years. But change is so long in coming and, in the meantime,
hundreds of thousands of animals are dying every year - unnecessarily.
The good news is that thousands
of animal lovers (but not enough) have heard what we've been saying. Canine
Health Concern members around the world use real food as Nature's supreme
disease preventative, eschewing processed pet food, and minimise the vaccine
risk. Some of us, myself included, have chosen not to vaccinate our pets at all.
Our reward is healthy and long-lived dogs.
It has taken but one paragraph to
tell you the good and simple news. The gratitude I feel each day, when I embrace
my healthy dogs, stretches from the centre of the Earth to the Universe and
beyond.
About the Author:
Catherine O'Driscoll runs
Canine Health Concern which campaigns and also delivers an educational
program, the Foundation in Canine Healthcare. She is author of Shock to the
System (2005; see review this issue), the best-selling book What Vets Don't
Tell You About Vaccines (1997, 1998), and Who Killed the Darling Buds of May?
(1997; reviewed in NEXUS 4/04).
She lives in Scotland with her partner, Rob Ellis, and three Golden
Retrievers, named Edward, Daniel and Gwinnie, and she lectures on canine
health around the world.
For more information,
contact Catherine O'Driscoll at Canine Health Concern, PO Box 7533, Perth PH2
1AD, Scotland, UK, email catherine@carsegray.co.uk , website http://www.canine-health-concern.org.uk.
Shock to the System is available in the UK from CHC, and worldwide from
Dogwise at http://www.dogwise.com.
Endnotes
1. "Effects of Vaccination on the Endocrine and Immune Systems of Dogs, Phase
II", Purdue University, November 1,1999, at http://www.homestead.com/vonhapsburg/haywardstudyonvaccines.html.
2. See www.vet.purdue.edu/epi/gdhstudy.htm.
3. See http://www.avma.org/vafstf/default.asp.
4. Veterinary Products Committee
(VPC) Working Group on Feline and Canine Vaccination, DEFRA, May 2001.
5. JVM Series A 50(6):286-291,
August 2003.
6. Duval, D. and Giger,U. (1996).
"Vaccine-Associated Immune-Mediated Hemolytic Anemia in the Dog", Journal of
Veterinary Internal Medicine 10:290-295.
7. New England Journal of
Medicine, vol.313,1985.
See also Clin Exp Rheumatol 20(6):767-71, Nov-Dec 2002.
8. Am Coll Vet Intern Med
14:381,2000.
9. Dodds, Jean W.,DVM, "Immune
System and Disease Resistance", at http://www.critterchat.net/immune.htm.
10. Wolf Clan magazine, April/May
1995.
11. Goldstein, Martin, The Nature
of Animal Healing, Borzoi/Alfred A. Knopf, Inc., 1999.
12. Wolf Clan magazine, op. cit.
13. ibid.
14. Journal of Inflammation
1:3,2004, at http://www.journal-inflammation.com content/1/1/3.
15. Klingborg, D.J., Hustead, D.R.
and Curry-Galvin, E. et al., "AVMA Council on Biologic and Therapeutic Agents'
report on cat and dog vaccines", Journal of the American Veterinary Medical
Association 221(10):1401-1407, November 15,2002,
http://www.avma.org/policies/vaccination.htm.
16. ibid.
17. Schultz, R.D., "Current and
future canine and feline vaccination programs", Vet Med 93:233-254,1998.
18. Schultz, R.D., Ford, R.B.,
Olsen, J. and Scott, P., "Titer testing and vaccination: a new look at
traditional practices", Vet Med 97:1-13, 2002 (insert).
19. Twark, L. and Dodds, W.J.,
"Clinical application of serum parvovirus and distemper virus antibody liters
for determining revaccination strategies in healthy dogs", J Am Vet Med Assoc
217:1021-1024,2000. |