Vaccines and Mitochondrial Dysfunction may cause harm. VaccinesPlusMD.htm
Vaccines + Mitochondrial Dysfunction (MD) + Scurvy è Neuropathy, ASD,
the causal conditions and processes are outlined for a conceptual proof that
Vaccines + Pre-existing-conditions cause disabilities and neuropathy associated
with the Autism Spectrum Disorders called ASD.
- The proof is general
and independent of individual case details.
- It is based on web
verifiable-knowledge, scientific principals and logic.
- I believe it is what is
argument might be used in the vaccine court show causality.
- The MMR vaccine-related
ASD claim-rate is less than the ASD epidemiological rate (~1/100)
- If the
time-linkage-window is enlarged to reflect actual illness durations it
might span 3 months.
- This would increase the
time-associated number of vaccine-disability cases.
- Then the court would be
able to decide ASD cases justly.
- This would mean the
claim-rate would grow to approach the current ASD rate of 1/100.
- With justice for
current claims and no new claims, the Vaccine Insurance Trust is out
- If the court fails to
deliver justice do the vaccine makers and the doctors have liability for
Who bears the responsibility for the
various causes of the harm?
The CDC for not considering the demographic statistics
of scurvy from chronic infections?
The CDC for not considering that scurvy and
vaccinations can kill and disable?
The government for not up-scaling vitamin C (AA)
- The parents for
trusting the government and not following the better advice available?
- The health media for
not advising that the nutrition rules are inadequate?
- The health media for
not publicizing the important best practices of ascorbate nutrition?
- The health media for
not publicizing how we all have scurvy at times and how oxides work?
- The government for
ignoring scurvy statistics’ long-tail & not mandating AA before &
- The government for not
properly accounting for adjuvants overload poisoning in single and
multiple vaccines administration?
- The FDA/CDC ignoring statistics long-tails and
mandating a harmful vaccinations schedule for dangerous vaccines they
approve for administration and
without AA protections?
causality is based on medical facts, confirmable by published reports.
- Oxidizing stress causes
mitochondrial dysfunction (MD).
- Many chronic
infections, microbial parasites, invade cells and cause oxidizing stress and
- Oxidizing stress in the
absence of enough antioxidants causes scurvy.
- Scurvy and vaccines
cause more oxidizing stress, inflammation cascading, then death, or
- If not death then:
Oxidizing stress in the scurvy state oxidizes fats
- Oxidized fats and
oxidized cholesterols are neurotoxins and myotoxins.
- Toxins, absent
antioxidants, cause permanent fast/slow neural poisoning, atrophy,
regression of neural growth, mental and physical disabilities.
- After the toxin
poisoning, the recovery is incomplete.
Leading to lifetime disabilities.
The child’s neural system fails to mature normally,
even in the presence of antioxidants and other therapeutic nutrition.
- Some of these neural
dysfunctions’ symptoms are called Autism and ASD.
- But they have many
other condition specific diagnoses: Neuropathy, ALS, Myopathy,….
leaders issue ignorant, conflicting “not the cause” pronouncements, to the
- Consensus medicine,
considering the costs of liability, helps to block justice for harmed
claim rate costs versus ASD incident rate:
- Not every ASD case can
make a vaccine related claim. A too-short time window excludes valid
claims. The course of scurvy
related vaccine harm takes weeks to months to do all the harm.
- ASD Vs. MMR number of claims per 1000
vaccinations is unknown.
- ASD incidence rate is
~1/100. One case per 100 in population group.
- A vaccine adverse
incident rate of ~1/100
vaccinations will bankrupt the Vaccine Insurance trust fund.
- To break even, claim
rate must be less than ~ 3/106 = .003/1000.
- With Obama care, the
insurance fund takes the ASD claims costs away from the Vaccine Insurance
- Vaccine makers may
still be liable if the Vaccine Court fails to provide justice and due
dysfunction (MD) as a cause
- Vaccines together with
“mitochondrial dysfunction” can cause ASD and related neural atrophy and
- The government in the
Hanna Poling case admits this.
- The science behind the
plaintiff’s case is sound, verifiable by published medical literature
- Prove persistent MD and
vaccine and reaction within allowed time-span
- This should then prove
legal causality for the court.
admission of the scientific facts
Department of Health and Human Services (HHS) concluded that the family of
Hannah Poling of Athens, GA is entitled to compensation from the federal
vaccine injury fund. The head of the agency testified to this before Congress.
MD incidence: A
mistake by HHS
maintained that the incidence of mitochondrial dysfunction is rare.
- This is
true if genetics is the only cause.
It is not. MD is
common. It is the main element of
ageing, it also comes from diseases and latent infections.
- There are
several, large population, non-genetic causes of MD and DNA mutations, low
AA or low oxygen to cells or scurvy increases vaccine risks: (Risk
caused by low AA diet and/or by persistent chronic parasitic infections (Yeast, Bacteria, Viral, protozoal or
other microbes) pleomorphic cell invading forms
Traumatic Brain Injury, altitude sickness, anemia,
illnesses, chronic fatigue, degenerative conditions. ALS/MS/MG etc.
key indicator of MD is a prior adverse reaction to a
most severe vaccine reactions occur after a prior adverse reaction.
- AA blood-half life of ½ hour means if ill or stressed:
Take AA every 2 hrs.
- Don’t mandate vaccination if MD is suspected (even if taking AA).
drugs, taken by millions, are killing thousands, slowly, by inducing MD,
- if they do not take a lot of AA
& CoQ10 at least daily.
- MD is not
rare, it can be created at will by a simple statin pill without the
- All you
have to do is do the same tests as for Hanna Poling to prove it.
- Over 15
million in USA and 25 million worldwide, estimated, are taking
- We are currently
creating millions of cases of premature senility, oxidizing their
improvement is not a total solution.
& CoQ10 are not al lthe essential molecules missing when we take
we wanted to save the government SSI money, we couldn’t find a better way to
speed up the ageing of our elder citizens.
Statins speed up ageing via the MD and oxidizing the DNA of their cells.
if they age quicker, they have much higher medical expenses and government has
offsetting higher end of life costs.
in the body a molecular-biochemistry summary:
block the action of the enzyme, HMG-CoA reductase,
in the mevalonate pathway at the point of action of the enzyme,
- There are other essential molecules
(nutrients) that are made in this pathway.
- Disabling the enzyme leads to
pathological shortages of the needed antioxidants:
- CoQ10 = ubiquinol, Heme-A and
- Other molecules essential to life
- CoQ10 is a key element in energy release
for all cells. It is also an
antioxidant protecting lipids.
- Heme-A, one function is as an
antioxidant to protect mitochondrial lipids and DNA from oxidization and
- Statins accelerate the deterioration if
accompanied by scurvy, oxidation stress, or chronic infections.
protect the mitochondria from oxidation.
- Vitamin C (AA), glutathione, CoQ10,
Heme-A, Vitamin E, and other nutrients.
- In their absence Statins induce
oxidation stress with high levels of ROS and RNS.
- These oxides attack lipids in the body
and rapidly turn them rancid.
- Rancid fats are toxic. Antioxidants normally neutralize
them. If scurvy they stay toxic.
- Cholesterol is a fat essential to our
brains, neurons, and the myelin sheaths that let neuron signals flow.
- Oxidize cholesterols and they become
- Induce low levels of needed cholesterol,
and poisoned cholesterol molecules of similar shapes are used as
- Statins produce cholesterol
starvation. This intensifies the
Action of Statins:
- Statins cause cholesterol starvation and the making of
antioxidant molecules is blocked.
- Statins cause oxidation stress, MD, and
pathology: muscle pain, destruction, enfeebling.
pathology: nerve pains, and slow loss of brain functions
and depression; reducing cellular energy, heart action, blood flow.
patent implies co-administration of nutritional supplementation of CoQ10.
The Lipitor drug patent
recommended dietary supplementation with “ubiquinol” to make up for the CoQ10
deficit that was caused by the enzyme blocking. This was to prevent (muscle deterioration) myopathy. We now know that neuropathy is also a
consequence if CoQ10 levels drop too low.
Do the prescribing doctors
follow the patent recommendation and supplement with CoQ10?
No they are not told to do
But even if you fix the
CoQ10 deficiency, you still have a shortage of Heme-A and that shortage causes
mitochondrial dysfunction, DNA mutations and who knows what other
dysfunctions. And then there are the
other molecules not made. And their deficiency dysfunctions.
There are also the real
effects of cholesterol starvation on brain function and regeneration. Even if
the oxidation stress was not present.
- Statins cause neuropathy by multiple
mechanisms, including MD = mitochondrial dysfunctions.
- This means that vaccinations and statins
together are contraindicated.
- Do we follow this in clinical
practice? No, we recommend
vaccines for seniors taking statins.
So what else causes
mitochondrial oxidation and dysfunction?
many years, and world wide, the answer has been well known. Scurvy causes MD. Scurvy has been ignored. We assume we all do not have scurvy because
we set the MRD too low.
We did not consider the pharmacokenetics; AA
lifetime =1/2 hour. Under suitable
stress that is all the time we need to shift from borderline-low to exponential
increases in histamine and runaway oxidation stress mode.
Allergic persons are borderline; so are those with
chronic infections. MRD is too low for
What else does scurvy cause?
- Mass vaccine related deaths.
- Shaken Baby Syndrome (SBS) and
- Sudden Infant Death Syndrome
- Scurvy causes sudden death, or with
better nutrition slow death, or life with disabilities.
- When you die of cancer you usually die
- It can come on quickly. It can be reversed quickly too, By AA
- Scurvy is the state induced by acute
infections, toxins, stress, allergens, cold, statins.
- When you feel sick you are feeling the
scurvy. You will feel better quickly if you take enough AA.
sudden infant deaths
- In Australia, scurvy once caused a ~50%
vaccination sudden death rate as reported in the book: Every Second Child, by Archie Kalokerinos.
- Scurvy plus vaccines caused the death of
the “Baby Yurkos”.
- Vaccines were injected into a
chronically sick child.
- Death involved medical malpractice,
based on professional ignorance.
- The father was convicted of SBS
- Conviction showed substantial
prosecutorial malpractice, and medical ignorance.
- Conviction was overturned, as have many
worldwide SBS convictions.
- Science knows the processes of scurvy. Do
medical practitioners? Not all do.
Many disbelieve the science.
- Clinical and emergency
room doctors may still be ignorant.
Some use AA but many do not when it is indicated.
- The reports of best
practices are out on the web. Historical
VitaminC Ascorbate Articles 1930s to
- Kalokerinos’ Yurkos autopsy analysis
describes the scurvy process in detail.
BabyYurkos Detail Postmortem Review showing vaccine induced scurvy leading
to Inflammation cascade then death
What is scurvy?
- It is, pure and simple, oxidative stress
running in a rapid histamine driven inflammation cascade.
- It is related to toxic shock, it is the
absence of AA in the blood.
- Many causes of stress apply:
Psychological dysfunctions, cold, colds, allergens, pain, toxins of every
kind, diseases & infections both acute and chronic, etc
- Too many ROS and NOS (peroxide and
nitrogen oxides) in our systems are created by immune cells.
- Oxides are associated with high
histamine levels and the allergic reactions.
What causes the
- Scurvy is caused in humans and a few
other mammals by a genetic defect that we all have.
- We do not make ascorbic acid (AA). AA is vitamin C.
- We need AA and burn it like a food. We must eat it; we do not make it. It is an essential molecule.
- We burn AA more when we are subject to
stress. Burning is also called
- After it is burned it acts as an
oxidant, so must be flushed away quickly. ½ hour and ½ is gone.
- With some chronic conditions we can burn
25, 50, even 150 grams per day.
But to get that much we must use IV infusions.
- 150 grams is a small steak. Steak is food.
So is AA.
- The FDA sets the Minimum Daily
Requirement (MDR) at about 100 milligrams.
- The MDR is for vitamins. AA is a food.
- The MDR is a joke. The concept MDR dulls
our thinking about crisis nutrition.
- It is not really a vitamin
because we need to burn it each day, to protect us from stress.
- Other animals make up to 15 grams per
day per 100 Kg of body weight.
- Sometimes they need more, especially
when they get sick. When we get
sick we can’t make AA.
- Wise nutritionists recommend much more,
3-20 grams each day.
- Much more & frequently if sick or
Pharmacokenetics of Vitamin
The pharmacokenetics of a
drug or molecule measures the lifetime of the molecule in our bodies.
How long does AA
- Recent Pub Med abstract (2011) gives AA
half lifetime in the blood as ½ hour. 30 minutes.
- The idea of a single AA daily dose
doesn’t work for disease or with oxidizing stress.
- Most AA can be gone in two hours to 1/16th
of its starting concentration.
- In 6 hours it can be (1/212)th
of the starting level, when we are sick.
- So when we are sick we need more AA and
every 2 to 3 hours.
- Do we ever do this? Some of us do, but most do not and
The Scurvy State:
- When we run out of AA we have a
condition like that caused by the statins.
- We have the same oxidizing stress that
causes the mitochondrial dysfunctions of the Hanna Poling case.
- So if we have any latent chronic
infection, like CFS , CFIDS, Lime disease, etc, or an acute infection, or
allergies, we can have scurvy on the borderline.
- Doctors find it hard to recognize the
subtle symptoms of latent, chronic (sub clinical) infections.
- The AA burn rate is already high with
- A vaccination intensifies the AA burn
rate; multiple vaccines adjuvants turn on the immune system increasing
- The AA level in the blood drops rapidly to zero and he
suffers, the induced allergy cascades and the baby dies. Too often we do
not give babies enough/any AA.
- Or if the baby does not die, the poisonous
lipid-oxide toxins may permanently disable him. Or he may recover,
partially. No one can tell what a
genius he might have become.
Standard Vaccine Practices
that might help outcomes:
- Is it standard practice to test AA
levels before vaccination? No it
is not. We should give AA tablet
several days beforehand unless allergic to it. If allergic or cranky, we should not vaccinate.
- Is it standard practice to administer
supplemental AA before and after vaccinations? No. Who is responsible?
- Is it standard practice to test/review
for chronic infections blood markers before vaccinations? Check patient’s records ask
parents. If history of repeated
- Is it standard practice to test for
T-cell, B-cell, macrophage or other immune dysfunctions before
vaccinations? Check patient’s records for this.
- Do clinicians follow the CDC
Vaccination Contraindications Guide procedures for immune impaired
persons? They should.
- Do Docs know that many persistent
infections’ microbes invade & disable immune system cells? They should
- If they knew this, tested for this, and
applied the rules in the tables, a lot of damage would be eliminated.
- Should vaccines be mandatory ahead of
need or maturity of the immune system?
- Do we routinely make vaccination
mandatory and too early and too many at a time? Do we pressure parents to
vaccinate? Do we tell them they
don’t have to? Yes, All the time.
- Can we do better than we are doing? Yes. Some improvements should be
- Do we know that live virus vaccines
cause chronic infections in some persons?
- Do we know that these chronic vaccine
induced infections cause scurvy? We should.
- Do we know that the next vaccination
(booster) with scurvy and chronic infections and MD will be high risk of
harmful reactions? Most do; a few
are ignorant or ignore the consequences.
Is our current medical
Only a tiny bit; but
multiply by 280 million, and you will get a fair number of failures.
- It is not surprising that vaccines can
accelerate scurvy; it is surprising that we ignore it. Persons are harmed
and persons are responsible.
- It is now admitted that vaccines,
oxidative stress and MD can and will cause disablement. This is a start.
- One can deduce, from searching the
global medical knowledge on the web, that:
Low AA levels, oxidation stress & MD plus vaccines
can induce a scurvy cascade leading to death or disablement.
MD and vaccines/infections and scurvy oxidation stress
oxidize cholesterols into neurotoxins.
Polio may work this way; caused by a virus; Klenner used AA, to cure polio for many patients.
- Klenner’s methods were consistent with
AA’s pharmacokenetics. Repeated:
high-frequency & high-dosages.
- All the failed AA experiments were not
consistent with AA’s pharmacokenetics. That’s why they failed. ½ hour
lifetime; low doses; single doses; wrong way to administer; it’s not a
- All the years since Jungeblut (1936),
and we don’t use
AA correctly as an antibiotic and cure illnesses
- We cannot even get the
trials approved. Stupid stonewalling? 1977: After $billions, Still no AA
studies. A third disapproval of a 2 times Nobel researcher. You might
think they were afraid he might be successful and this might change the
medical delivery system.
- Linus Pauling: The
[In-]Effectiveness of the National Cancer Institute
- 2011, Still not the
right studies with proper dosage methods, monitoring AA levels, as Klenner
did, and consistent with AA pharmacokenetics,
and maintaining effective blood levels.
- The statistics of the statin-caused neuropathies
show about 50% partial recovery and 50% no recovery, like polio.
- However the study showed, in part, that
our best nutritional knowledge relating to recovery is not being used by
the treating doctors, so there is some hope of improving the recovery
outcomes. Polio history says
massage helps. HBOT?
- Recovery nutrition: AA,CoQ10, Lysine,
Proline, Omega 3 EPA+DHA, Vitamins, HGH. Cod liver oil, HBOT. Plus massage as was done successfully
for polio? Best practices need to
be described on the web.
- It is not surprising that our public
health mantra is that the VaccineàASD connection is unproven. Billions
in liabilities are at stake.
- If they admitted it, all the ASD claims in
the Vaccine court would have to be paid to serve justice.
- This would bankrupt the Vaccines
Insurance fund. Stonewalling in
the court has stopped the claims; not the harms.
- Unspent money in the fund is earmarked
by legislation to feed the bureaucracy, as if it were a surplus.
Vaccine fund is
not workable for ASD so why do we keep vaccinating with high-risk vaccines?
- ASD rates are ~1/100 cases of harm.
Worst case, if vaccine causes all ASD, è one claim per 100 vaccinations.
- The tax collected is 100 x $ 2.25 per MMR vaccination or
- The claims for $ 225 in taxes would be
for the MMR vaccine.
- If the Vaccine Court is bankrupt due to
the ASD epidemic. It can only deliver injustice, or unequal justice.
- So, why do we not stop/slow all the
- Why do we not give AA before and after
vaccinations, delay til older like Japan, and stretch them out. I hear HHS
is thinking about doing this.
- Don’t mandate vaccinations. Many
vaccine-harm skeletons hide in government closets.
- Why are we in such a reckless hurry to
jab our babies?
- Why are we ever giving
them a live microbe soup (possibly contaminated) that some babies cannot
tolerate? We are “perfecting” our
gene-pool at a tragic expense to our families?
We can do and need to do
better than what we are doing now.
- We have some very smart people out
there. They can help us to do
- There are some Effective
Modalities from medical history we have almost forgotten.
- But many have not listened to others who
have said important things.
- Google the web! It is all out there in the worldwide
medical tribal knowledge and history.
- It’s a pity all medical history and
articles are not on-line to search openly and freely.
- You arrogant ones, please try to keep an
open mind, read widely, think deeply, seek full understanding, you might
change your minds and the minds of others.
changes would save huge medical system future costs:
lot of social and medical costs & misery could be saved:
- If ascorbic acid (AA) was administered
before and after every vaccination.
- If the AA MDR were replaced by
guidelines to fight scurvy and cancer saying:
AA is a necessary food; eat 3 grams AA 3 times per
a lot of people did it.
- If AA were added to lots of junk food,
we would not even have to think about eating enough separately. We really can’t eat enough of it.
- If CoQ10 were added as a supplement to
some foods, like butter and margarines and salad dressings.
- If coconut
oil and palm kernel oils were used in all margarines sold.
antiviral AIDS/COPD microbe killing properties)
- If statins were not taken off the
market, just highly-restricted, as a
sometimes-harmful drug, and fish oil EPA & DHA & various
vitamin E’s from palm oils were substituted.
- If adequate AA, CoQ10, Lysine, Proline,
fish oil, vitamin E and EGCG were used against heart
disease and cancer.
- If AA was taken 3-6 grams
every 2-3 hours whenever we feel sick, have allergies, drug reactions,
headaches and body pains, rashes, colds, flu, sprains, surgery, sunburn,
jellyfish stings, poison ivy, spider bites, pneumonia, etc. More “high
level” AA, by injection, frequently, plus oral AA for
many viral infections. (West Nile)
Clinical Usage of Vitamin C.
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