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.