How Vaccines and Mitochondrial Dysfunction may cause harm. VaccinesPlusMD.htm

Vaccines + Mitochondrial Dysfunction (MD) + Scurvy è Neuropathy, ASD, Ageing.

All 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 really happening.

This 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 of money.
• If the court fails to deliver justice do the vaccine makers and the doctors have liability for the harm?

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) nutritional requirements?

• 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 & after vaccinations?
• 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?

The 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 MD.
• 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,….
• Medical/Political leaders issue ignorant, conflicting “not the cause” pronouncements, to the press.
• Consensus medicine, considering the costs of liability, helps to block justice for harmed families.

Vaccine 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 fund.
• Vaccine makers may still be liable if the Vaccine Court fails to provide justice and due process.

Detail Process Description:

Mitochondrial dysfunction (MD) as a cause

• Vaccines together with “mitochondrial dysfunction” can cause ASD and related neural atrophy and dysfunction.
• 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.

Legal admission of the scientific facts

U.S. 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

• 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 factors overlap)
• Scurvy caused by low AA diet and/or by persistent chronic parasitic infections (Yeast, Bacteria, Viral, protozoal or other microbes) pleomorphic cell invading forms
• Statin drug reactions.
• Stroke, Traumatic Brain Injury, altitude sickness, anemia, malaria, etc.
• Acute illnesses, chronic fatigue, degenerative conditions. ALS/MS/MG etc.
• A key indicator of MD is a prior adverse reaction to a vaccination.
• Many 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).

Statins cause MD:

• Statin 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 protective supplements.
• 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 statins.
• We are currently creating millions of cases of premature senility, oxidizing their mitochondria.
• Dietary improvement is not a total solution.
• AA & CoQ10 are not al lthe essential molecules missing when we take statins.

· If 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.

· But if they age quicker, they have much higher medical expenses and government has offsetting higher end of life costs.

Statins in the body a molecular-biochemistry summary:

• Statins 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 mutations.
• Statins accelerate the deterioration if accompanied by scurvy, oxidation stress, or chronic infections.

Antioxidant molecules 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 toxic, neurotoxins.
• Induce low levels of needed cholesterol, and poisoned cholesterol molecules of similar shapes are used as substitutes.
• Statins produce cholesterol starvation. This intensifies the toxins’ harm.

The Action of Statins:

• Statins cause cholesterol starvation and the making of antioxidant molecules is blocked.
• Statins cause oxidation stress, MD, and toxic lipids.

· Muscle pathology: muscle pain, destruction, enfeebling.

· Nerve pathology: nerve pains, and slow loss of brain functions

· Fatigue and depression; reducing cellular energy, heart action, blood flow.

Lipitor 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 so.

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 Conclusion:

• 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? SCURVY.

For 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 them.

What else does scurvy cause?

• Mass vaccine related deaths.
• Shaken Baby Syndrome (SBS) and
• Sudden Infant Death Syndrome (SIDS).
• Scurvy causes sudden death, or with better nutrition slow death, or life with disabilities.
• When you die of cancer you usually die of scurvy.
• It can come on quickly. It can be reversed quickly too, By AA injection.
• 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.

Scurvy causes 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 murder.
• 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 1990s
• Kalokerinos’ Yurkos autopsy analysis describes the scurvy process in detail. See ---
• DrKalokarinos: 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 state?

• 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 metabolizing.
• 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 stressed.

Pharmacokenetics of Vitamin C:

The pharmacokenetics of a drug or molecule measures the lifetime of the molecule in our bodies.

How long does AA last?

• 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 1/16^th 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 suffer needlessly.

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 chronic infections.
• A vaccination intensifies the AA burn rate; multiple vaccines adjuvants turn on the immune system increasing stress.
• 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? Parents.
• Is it standard practice to test/review for chronic infections blood markers before vaccinations? Check patient’s records ask parents. If history of repeated illnesses, beware.
• 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 know it.
• 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? No.
• 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 practical.
• Do we know that live virus vaccines cause chronic infections in some persons? Not widely.
• 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 system dysfunctional?

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 vitamin!
• All the years since Jungeblut (1936), and we don’t use AA correctly as an antibiotic and cure illnesses like cancer.
• 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 $225.
• The claims for $ 225 in taxes would be about $896K 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 problem vaccinations?
• 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 better.
• 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.

These changes would save huge medical system future costs:

A 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 day.

And 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.

(Strong 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)

Early Clinical Usage of Vitamin C. –Klenner.

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Vaccine Claims Spreadsheet PDFs Source: Public Records from Vaccine injury Compensation Program

Vaccine Claims Summary Spreadsheet

Vaccine Vs Claims Spreadsheet

Vaccine Vs Claims89-11 Spreadsheet (2011 data)