On February 12, the federal “Vaccine Court” in Washington issued a sweeping ruling in three highly touted “test cases” against families who claimed that their childrens’ autism had been caused by vaccines. The Special Masters in those three cases found that Petitioners failed to establish causation between MMR vaccines, the mercury-laced vaccine preservative thimerosal, and autism (the court decision, which is under appeal, deferred any finding on a thimerosal-only theory of causation). The rulings could have a significant precedential impact on some 5,000 families who opted to bring their cases in the Omnibus Autism Proceedings (OAP) hoping that the vaccine court would officially hold that the MMR vaccine or thimerosal had caused autism in their children.

The New York Times joined the government Health Agency (HRSA) and its big pharma allies hailing the decisions as proof that the scientific doubts about vaccine safety had finally been “demolished.” The US Department of Health and Human services said the rulings should “help reassure parents that vaccines do not cause autism.” The Times, which has made itself a blind mouthpiece for HRSA and a leading defender of vaccine safety, joined crowing government and vaccine industry flacks applauding the decisions like giddy cheerleaders, rooting for the same court that many of these same voices viscously derided just one year ago, after Hannah Poling won compensation for her vaccine induced autism.

But last week, the parents of yet another child with autism spectrum disorder (ASD) were awarded a lump sum of more than $810,000 (plus an estimated $30-40,000 per year for autism services and care) in compensation by the Court, which ruled that the measels-mumps-rubella (MMR) vaccine had caused acute brain damage that led to his autism spectrum disorder.

The family of 10-year-old Bailey Banks won their case quietly and without fanfare in June of 2007, but the ruling has only now come to public attention. In the remarkably clear and eloquent decision, Special Master Richard Abell ruled that the Banks had successfully demonstrated that “the MMR vaccine at issue actually caused the conditions from which Bailey suffered and continues to suffer.”

Bailey’s diagnosis is Pervasive Developmental Disorder — Not Otherwise Specified (PDD-NOS) which has been recognized as an autism spectrum disorder by CDC, HRSA and the other federal health agencies since at least the 1990s.

In his conclusion, Special Master Abell ruled that Petitioners had proven that the MMR had directly caused a brain inflammation illness called acute disseminated encephalomyelitis (ADEM) which, in turn, had caused the autism spectrum disorder PDD-NOS in the child:

The Court found that Bailey’s ADEM was both caused-in-fact and proximately caused by his vaccination. It is well-understood that the vaccination at issue can cause ADEM, and the Court found, based upon a full reading and hearing of the pertinent facts in this case, that it did actually cause the ADEM. Furthermore, Bailey’s ADEM was severe enough to cause lasting, residual damage, and retarded his developmental progress, which fits under the generalized heading of Pervasive Developmental Delay, or PDD [an autism spectrum disorder]. The Court found that Bailey would not have suffered this delay but for the administration of the MMR vaccine, and that this chain of causation was… a proximate sequence of cause and effect leading inexorably from vaccination to Pervasive Developmental Delay.

The Bailey decision is not an isolated ruling. We now know of at least two other successful ADEM cases argued in Vaccine Court. More significantly, an explosive investigation by CBS News has found that since 1988, the vaccine court has awarded money judgments, often in the millions of dollars, to thirteen hundred and twenty two families whose children suffered brain damage from vaccines. In many of these cases, the government paid out awards following a judicial finding that vaccine injury lead to the child’s autism spectrum disorder. In each of these cases, the plaintiffs’ attorneys made the same tactical decision made by Bailey Bank’s lawyer, electing to opt out of the highly charged Omnibus Autism Proceedings and argue their autism cases in the regular vaccine court. In many other successful cases, attorneys elected to steer clear of the hot button autism issue altogether and seek recovery instead for the underlying brain damage that caused their client’s autism.



The Pentagon — A Voice of Reason on Vaccines and Autism?

The Pentagon — A Voice of Reason on Vaccines and Autism?

David Kirby

Recently, several documents have been brought to my attention which, when viewed together, suggest that the Department of Defense has legitimate concerns about vaccine injuries and their possible connection to autism, perhaps more so than other branches of the Federal Government.

These documents raise several questions that I am currently trying to get answered from DOD officials:

1) Autism may be an “adverse event” of Tripedia (DTaP) use

According to the website of the Vaccine Healthcare Centers Network, run by DOD and CDC, autism is listed as an “adverse event” associated with use of the Tripedia triple vaccine for diphtheria, tetanus and pertussis.

My questions are: Why does autism appear here? Does VHC consider autism to be a possible adverse event of DTaP use, or has it simply been reported that way by parents?

2) Patients who have bad vaccine reactions should avoid multiple vaccines in the future

According to this VHC slide, any patient who has a “Systemic Event” following immunization – defined as “symptoms and signs of illness after vaccination” and “any reaction that does not involve the injection site” – should avoid multiple vaccines in the future, if possible.

My questions are: Is that standard DOD policy? Is there an alternative schedule for these patients? Does this advice apply to children of service members as well? Why is this information not shared with civilian doctors and pediatricians?

3) Patients who develop serious neurological diseases might need vaccine exemptions in the future

This VHC slide says that a patient who develops a severe neurologic disease following vaccination might need temporary or permanent exemption from future vaccines. Such diseases include peripheral neuropathy, encephalopathy (including autism, presumably) Guillain-Barré syndrome and progressive focal neurologic disease. Such patients should be given temporary exemptions from future vaccinations.

Meanwhile, risks for recurrent reactions should be assessed before additional doses are given, and “permanent vaccine exemption may be required.”

Again, is this DOD policy? Are such exemptions given? Because autism is listed as a “severe neurological disease,” would those patients (ie, children of service members) also be exempt from future vaccinations? And, on a related note, does VHC consider autism to be a “neurological disease,” as opposed to a developmental/behavioral disorder?

4) Mercury, and possibly thimerosal may cause autism and dementia

According this slide (#22) on the vaccine preservative thimerosal, from the Armed Forces Institute of Pathology (AFIP), “exposure to mercury in utero and children may cause mild to severe mental retardation and mild to severe motor coordination impairment.” The slide also seems to indicate that autism and dementia might questionably be “health effects” of mercury or thimerosal exposure.

My question is: Why does autism appear on a list of health effects on a slide about thimerosal, even if it is followed by a question mark?

5) Alternative biomedical treatments may be prescribed for thimerosal exposure

The same slide says that “treatments” for thimerosal exposure include: “Methyl-B12, ointment DMPS, & glutathione (GSH).” These are all alternative (some would say fringe, radical and dangerous) treatments being used today by thousands of autism parents and their children’s physicians, with varying degrees of success (including reports of full recovery).

Methyl-B12 – has been shown to repair damage to the process of methylation, and to restore methionine and glutathione levels in patients with autism to within normal ranges.

DMPS – is a sulfur-based amino acid used in the process of chelation – in which sulfur molecules bind with heavy metals such as mercury, and eliminate them from the system.

Glutathione – is a sulfur-based protein that binds with heavy metals and eliminates them from the system. It is also a powerful anti-oxidant. Many children with autism show signs of glutathione depletion, heavy metal accumulation and oxidative stress.

My questions are: Was the speaker simply refering to treatments that some people have tried, or is the AFID endorsing these treatments for thimerosal toxicity and/or autism? On what evidence is this based? Are Methyl B-12 and GSH, like chelation, considered standard of care in the military for mercury toxicity? Can you explain why autism families in the military have these treatments covered, (at thousands of dollars a year), even if they also have an autism diagnosis? Is this why military insurance will pay for visits to doctors in the Defeat Autism Now network, which advocates the use of these non-traditional treatments?

I eagerly await the replies from VHC and AFID officials, and will update this blog as soon as I hear anything.

Meanwhile, regardless of the Pentagon’s positions on the above questions, we know for certain that DOD is concerned about the risk of injury from multiple vaccines.

In fact, it may even need to reconsider the practice.

“We have preliminary findings from one of our many on-going research studies that suggest a relationship between adverse events and multiple vaccinations exist,” US Army Colonel Renata J. M. Engler, MD, director of the VHC, (a “collaborative network” of the Defense Department and the CDC), wrote to Rep. Carolyn Maloney (D-NY). “These findings will require validation, but heighten our concern for the current clinical practice of multiple vaccinations.”

“The more drugs one is exposed to, the greater the likelihood of having an adverse event so as vaccine numbers increase, and (sic) we will see more people who have efficacy or safety issues,” Col. Engler said. “The standard of care (ie, in the context of mixing vaccines) is to minimize drug exposures because of the recognition that the more drugs being used, the greater the chance of a reaction and potentially a serious adverse event.”

I wonder when the CDC and America’s pediatricians will issue an equally thoughtful and cautionary statement, instead of their usual reassurance that small children can easily get 100,000 shots at once, without a single “serious adverse event” among them.


Age of Autism

VHCN  _the page that is now under revision you can view here.

Building a Baby from the Foundation Upwards:

                                Building a Baby from the Foundation Upwards:

Neurological Issues Can Start From Conception If the Conditions Are Right


 Genetics, nutrition, environmental toxins, vaccines, and their combined impact on the immune system, can all play a role in Autism spectrum disorders. Think of it as a pyramid with the child at the top and all the damaging features underneath starting in utero. Some children don’t need vaccines to tip them over the edge if the child was born at the top or near the top of the pyramid to begin with. Other children who are close to the top, all they would need is a major mineral imbalance combined with one or two vaccines to tip them over the edge.

Think about this quote in the United States Senate on May 12, 1999 by Dr. Bonnie Dunbar, a Professor of Immunobiology:

“I would challenge any colleague, clinician or research scientist to claim that we have a basic understanding of the human newborn immune system. It is well established in studies in animal models that the newborn immune system is very distinct from the adolescent or adult. In fact, the immune system of newborns in animal models can easily be perturbed to ensure that it cannot respond properly later in life.”


Children who have gone into an immediate regressive autism after vaccines are the ones who may have been able to cope, and not tipped over the edge, if they had more time to mature their immature immune systems.  Others, without vaccines, were just too close to the top of the pyramid at birth or in utero.


Birth Control Pill Use:


Anything that affects hormones enough to stop a lining shedding could cause issues. The use of hormones disrupts mineral balance, and further disturbs the normal running of metabolic pathways. If enough are disturbed, then it could contribute to an unstable foundation for a baby. The pill can strip out magnesium, zinc, B6, folic acid and EFA’s from the body.

The pill can skew the hormone system long-term and changes vascular circulation permanently, and further trashes the body’s supply of magnesium, zinc, B vitamins, folic acid and essential fatty acids. All these things lay the foundation for a pregnancy in which fetal nutrient absorption comes from a deficit position right at the outset.

Dr. Ellen Grant wrote a book called Sexual Chemistry which explains it. She was involved in the original large trials on what the pill does to the body.


…”Our studies in 1981 and 1989 found significantly higher concentrations of copper and cadmium in hair in dyslexic children compared with matched controls.1,2 Sweat zinc was severely deficient in the dyslexic children, being 66% lower than that for control children. However, the control children in 1989 had much lower average zinc level than the children tested for laboratory reference range purposes 10 years before in 1979.2,3 Zinc deficiency allows accumulation of toxic metals which may be important causes of the increase in autism, asthma, dyslexia and hyperactivity in the past few decades.4,5

Biolab Medical Unit offers analyses of all toxic metal levels in blood, metal sensitivity tests and the effects of toxic metal substitution on proteins and some binding sites.6,7 Dr John McLaren- Howard presented the results of testing 61 autistic children at a Biolab Workshop for Doctors in June 2004, as he was attempting to find out which nutritional tests should be recommended. Among the 42 boys and 19 girls most were deficient in zinc and magnesium. Many were also deficient in copper, chromium, manganese, molybdenum and B vitamins. Therefore, essential fatty acids were also likely to be deficient. 16 children had DNA-adducts in leucocytes to malondialdehyde, 12 to cadmium, 9 to nickel. Three of the 61 children had DNA-adducts to mercury and one had DNA- adducts to lead. 37 children had antigliadin IgG antibodies, while 30 children had malabsorption detected by a D-xylose test. Malabsorption was most common in those with Asperger’s type syndrome, 16 out of 18 children.

The zinc and magnesium lowering effects of maternal use of progesterones and oestrogens, parental smoking and alcohol use and parental dental mercury and other dental metal levels like nickel and tin, need to be looked at in larger studies. Mercury is a toxic metal whether it is in dental amalgams or in vaccines. If 5% of autistic children show evidence of signs of mercury exposures, this still means large numbers of children have been adversely affected. Clearly the increasing incidence of childhood diseases needs proper biochemical scientific investigations.”



Pollutants ‘in children’s blood’  

Toxic metals for vegetable fruit sprays, like Arsenate of copper and Arsenate of Mercury, DDT used to be used. Now, sprays are different, but are they really better? Our stolen future  and Chem Trails.  




The vaccine becomes the bullet for many children. They start out seemingly healthy, even with perhaps a shaky foundation. But once the bullet (vaccine) is injected, they begin to spiral downwards. Symptoms are pathway dysfunction, not illness.


Diet and Nutrition/Minerals:


Copper and zinc are important because if they are out of sync the enzymes that create neurotransmitters, that the brain cells use to transmit their messages from one brain cell to another, won’t work properly. B6 works with those. Proper balance is what is needed because if you get the copper and zinc right, you can modulate the brains regulation of mood and reaction to stress. These enzymes also need B6; as B6 often helps in treating depression. In women, low zinc and high copper can be linked to ‘rage’ episodes during PMS.

Suphur has a key interaction with selenium. Selenium is good for skin, hair, nails, to build certain amino acids in the cells and brain, and make sulfonated compounds for the joints.  When there is a deficiency, there is a reduction in the activity of the enzyme gluthathione peroxidase. This results in reduced immune function, which has its greatest effect on the helper T dependent cells,  and production of Ig.M is impaired. IgM is one of the front line Th1 antibodies which are made in the early stages of an infection. Children suffering from malnutrition fail to grow when given a recuperative diet, if it remains selenium deficient because selenium is necessary for protein synthesis. While it protects against the toxic effects of the pollutant cadmium, and mercury from all sources, it also increases the effectiveness of vitamin E, and it reduces the chances of all types of cancer. In communities where selenium intake is low, the cancer rate is high.

Maternal selenium nutrition and neonatal immune system development.

Skeletal muscle disorders associated with selenium deficiency in humans.
Deficiency in selenium or Vitamin E also shows reduced natural killer cell activity. With regard to the enzymes; Glutathione is essential for:
-detoxification and liver function
-effective immune response
-antioxidant defense
-male fertility (low sperm counts)

-blood sugar metabolism
-blood pressure regulation
-tumor inhibition
-inhibition of thrombus formation in diabetes
-prevention of neurodegenerative disorders like Alzheimer’s disease, Parkinson disease, Huntington’s chorea, stroke and brain trauma.

Effective Glutathione is important for T cell proliferation, development of large CD8+ T cells, cytotoxic T cell activity and production of CD16+ natural killer cells. Glutathione protects and repairs liver tissue under severe acute and chronic alcohol exposure.

Selenium protects against the toxic effects of the pollutants cadmium, and mercury. It helps prevent chromosome breakage in tissue culture. It is the basis of the unique enzyme system Glutathione peroxidase, which destroys peroxides before they can attack cellular membranes, while the vitamin E acts within the membrane itself preventing the oxidation of membrane lipids.

When discussing epigenetics; they know demethylation is carried down through the generations and they know it can be reversed.

 This is the list of tests a DAN doctor may perform:

*Complete blood count w/ differential and platelet count
*Serum metabolic assay (complete)
*Thyroid profile (T3, T4 and TSH)
*Amino acid profile (plasma)
*Organic acid profile (urine)
*Ammonia level
*Lactic acid level
*Pyruvic acid level (pyruvate)
*Heavy metal profile (lead, mercury, arsenic and cadmium), blood
*Vitamin A level
*Zinc and copper (serum)
*Measles, mumps and rubella antibody IGG titers
*Fragile X
*IgG, A, M, E
*IGG subclasses
*T cell function tests
*Myelin basic protein and neural axon filament antibodies

 But other minerals should be tested as well such as:







Immunologist have begun to test for a genetic variant in an enzyme called  Methylenetetrahydrofolate reductase (MTHFR) and  Glutathione.  
Diseases that can occur because of MT protein dysfunction include:
· Psoriasis and eczema
· ADD and ADHD
· Autism
· Schizophrenia and Obsessive Compulsive disorder
· Anorexia
· Alcoholism
· Chronic fatigue syndrome
· Alzheimer’s

Metallothionine protein disorder is thought to be a genetic defect involving more than one gene. This disorder results in a decreased ability of the MT protein to function normally. Metallothionine protein helps regulate zinc and copper levels in the blood,  withdrawal heavy metals as they enter the body, help development and continued functioning of the immune system, help development and pruning of brain cells, (neurons), help prevent  yeast overgrowth in the intestines, aid in the production of enzymes that break down casein and gluten, aid in the production of hydrochloric acid by stomach cells, help taste and texture discrimination by the tongue, and aid in the behavior control and development of memory and social skills.

In 2000, William Walsh, Ph.D. of the Pfeiffer Treatment Center discovered that the majority of autistic patient’s exhibit MT dysfunction and the classic signs of autism can be explained by a MT dysfunction. There are four primary types of MT proteins and each has an important role in the body.

MT-I and II are present in all cells throughout the body. They regulate copper and zinc, are involved in cell transcription, detoxify heavy metals, play a role in the immune function, and are involved in a variety of G.I. tract functions.

MT-III is found primarily in the brain and functions as a gross inhibitory factor in the brain. MT-III is located primarily in the central nervous system with small amounts present in the pancreas and intestines. It plays a major role in the development, organization and programmed death of brain cells.

MT-IV is found in the skin and upper G.I. tract. They help regulate stomach acid pH, taste and texture discrimination of the tongue and help protect against sunburn and other skin traumas.

Theories for the Pathophysiology of Autism:

Brain autoimmunity
Deficits in sulfur metabolism
Abnormal liver detoxification
Gastrointestinal abnormalities


Possible Causes of Immune Injury or Alterations:


A genetic weakness (C4B null allele) and/or predisposition, combined with one or more of the following:
1) Shortened or absent breast-feeding preventing the full development of transferred cellular immunity. (Fudenberg)

2) Early gluten (usually wheat) introduction prior to one year of age. Wheat has been genetically manipulated in the last 100 years to increase the gluten content.

3) Early use of cow’s milk or casein based formulas. (Allergenic and altered)

4) Immunizations with live viruses, especially the MMR after 1978. There is frequent regression after the MMR vaccine that has been observed and published (Wakefield). Other vaccinations and the resulting effects on interleukin or autoimmunity. (Singh) DPT (especially if whole cell pertussis is used) and HepB (not live viruses) may also play a role in immune alterations.

5) Use of antibiotics and resulting yeast and pathogenic bacteria infection or overgrowth, with resulting immune modification and toxic exposure. (Shaw, Fudenberg, Wuepper)

6) Maternal allergy, chronic fatigue syndrome, or leaky gut problems that caused the child to be pre-sensitized in the womb. (Fudenberg)

7) Leaky gut from any number of the above or also related to parasites or GI infections in the child that allow gluten and casein to leak into the bloodstream. Once in the body, the body alters them into toxic substances. Sucrose (table sugar) also leaks in and it is an abnormal sugar in the blood stream that causes a host of problems.

8) Defect in the detoxification pathway of the brain, Phenol Sulfur-Transferase or PST enzyme defect. Inadequate intake of sulfur compounds. (Rosemary Waring, Birmingham University, England).

9) They develop autoantibodies to Myelin Basic Protein (Singh, Fudenberg, and Gupta) and other brain components. Measles is known to induce MBP antibodies. I’ll talk about this a lot more later.

10) Defective cellular immunity, especially in the NK cell activity towards self and pathogens. (Fudenberg, Gupta). And the probable elevation of Interleukin-2 and 12.


Jeff Bradstreet, M.D., FAAFP
The International Child Development Resource Center  
Let’s break each one above down…

1. Breast milk creates the right probiotics which absorb minerals the right way, and provide the foundation for cellular immunity and nutrient absorption. The gut makes up 70 % of the immune system.  It also plays a role in e-coli endotoxin production.

2. It has nothing to do with the gluten. Salivary fluid has an enzyme in it, to break down grains when the molar teeth cut. Celiac for example isn’t caused by too much gluten. It’s caused by lack of the enzyme opening the pathway to those with epigenetic susceptibility. Before 1900’s, celiac was pretty much unheard of. More gluten isn’t good for some people.

3. Unpasteurized animal milk worked well versus pasteurized.

4.  True, but you only know what you have looked at. What about the others?

5.  Antibiotics cause immune modification all on their own, not necessarily as a result of the resulting yeast and pathogenic bacteria infection and overgrowth. What about e.coli?

6.  What caused the maternal allergy? If you look at minerals and other, you may be able to eliminate the allergy.

7.  Leaky gut would not be a problem if the foundation was laid right and a change in nutrition better understood.

8.  If you have an inadequate intake of sulfur compounds and/or an inadequate intake of other minerals such as magnesium, zinc, selenium.

9.  That is not the cause, but the end result. The cause needs to be worked out.

10.  See # 9.

Fever Reducers
Fever reducers lower glutathione levels. When glutathione levels are reduced, you increase the level of the hormones. They also suppress the immune system further.

 Also See:

 Autism – the vaccine connection 
The lutein free diet, a treatment option for autism. Review of lutein as it relates to autism. 
The Thoughtful House (2005 Conference)


David Kirby and Mark Blaxill Slide Presentations

HERE is David Kirby’s slide presentation from the Vaccine/Autism meeting in DC. 9/28

Mark Blaxill, briefing on Capitol Hill. HERE are slides from his presentation, titled, Why the Autism Crisis Has Become So Controversial and Why Families Need Your Help.

New Link Between Vaccines and Autism Rates

The charts and notes (HERE)

I used the “Autism Rates by Birth Years” data from TACA Now and compared it to public records about vaccine histories.  I found that since the DTP vaccine in 1949 the ONLY time period with NO increase in autism cases is also the only time period with NO vaccines added to the CHILDHOOD schedule. The hep b was licensed during this time but it was not given to children until 1990.  Also, the Hib was reformulated for infants in 1987, but due to a shortage, it was not added to the schedule until 1990 (There was a HUGE jump in autism rates in 1990).  See for yourself.

This link also includes information about the NNii (National Network for Immunization Information) conceding that after vaccinations children’s aluminum levels are above the minimal risk, but they say it’s no big deal.  I disagree.  The CDC says that aluminum toxicity causes neurological delays and thin bones, and the CDC cites a study named “Thin Bones Seen in Boys with Autism.”  No one else is talking about this correlation, so I’m trying to tell everyone whom I think can help.

The NNii also says that aluminum has been used in vaccines for 75 years.  I don’t know what vaccine they are talking about.  In 1949 DTP was the first vaccine (on the current Childhood schedule) to contain aluminum and was licensed during the first significant increase in autism rates.  Also FYI, according to Wikipedia, mercury thermometers are not even allowed on some airliners because mercury reacts with aluminum. Many childhood vaccines contain(ed) both aluminum and mercury. 

Read On..


Are Some Cases of Autism Actually Subclinical, Congenital Attenuated Rubella Syndrome?



  • F. Edward Yazbak, MD, FAAP, found a link between mothers’ rubella susceptibility in pregnancy and their having children with autism spectrum disorders. He described 60 previously vaccinated women who were considered “rubella susceptible” during their routine prenatal OB/GYN visits. All of these women were revaccinated in the post partum period due to their not having antibodies to rubella. Each of these women could be described as having failed to seroconvert to an previous vaccination or having rubella immunity that declined over time.





  • A few ideas and questions are warranted on WHY some females may unknowingly be serving as hosts to a persistent rubella infection and why the RA27/3 vaccine strain of rubella virus might be particularly well adapted to persist undetected in females.





  • Information provided by the FDA in Appendix A on the history of the development of rubella vaccines used in the US prompts many questions about the safety of RA27/3 strain of rubella vaccine and its use in females. Per the FDA, the rubella virus used in the vaccine originated from a fetus that was aborted in 1964. It was isolated in and recovered from fetal tissue. It was attenuated through 25 passages through human fetal cells, and it is grown in human fetal cells.

















19 Year Old Sues His Own Parents For Vaccine Damage Leading To His Autism

A 19 year old boy is suing his parents for contributing to his Autism. The boy’s name has been kept confidential pending the outcome of the trial and a gag order has been put on everyone related to this court hearing, including the judge. We will refer to the boy as John Doe.
John filed suit on his parents for vaccinating him as a youth. John received the CDC recommended schedule of 62 doses of 17 different vaccinations before the age of 5 years old. He alleges his parents directly caused his illness by not practicing informed consent when they had him injected with multiple viruses, sometimes up to 10 shots at one time, in this landmark case.
The pharmaceutical companies who manufacture the vaccines are protected under the government laws as are the doctors from any liability relating to vaccine injury. The National Injury Compensation Program is now rejecting all cases of Autism although there are confirmed studies linking Autism to vaccinations. There isn’t enough money to pay all the victims. We will see more and more children left with no choice but to sue their parents for vaccine damage.
Okay, this story is fictional but doesn’t it make you think? What will our world be like in 20 more years when more and more children become autistic, ill and sick with autoimmune disorders? Will they end up having to sue their own parents because there is no other recourse? I mean, it’s the parents obligation to make informed decisions on the safety of vaccines. The parents who don’t make informed decisions regarding their children’s health should be held responsible. This includes researching vaccines and making sure they are safe enough to be injected in to their children in the first place.
We, as parents, need to stand up and say enough is enough. We should have the right to reject these vaccinations because we don’t feel they are safe! Do people not see we are slowly losing our freedoms for the so called greater good? Please google gunpoint medicine and see how many parents (and people in general) are being threatened with jail time and arrested, then FORCED to undergo medical treatments they object to. Don’t let this happend with vaccines. Don’t let us lose what exemptions we do have! We need a philosophical exemption in every single state for those who can’t morally claim a religious exemption. We need to protect the homeschooled (scape goats) rights to avoid being forced to inject vaccines not proven to work and full of neurotoxins, aborted fetal tissues, and animal DNA, especially in those states with only a medical exemption.
We are allowing our government to make our children sick and KILL THEM with these vaccines. Those who allow their children to be injected with vaccines and never research or question the safety will only have themselves to blame. I apologize if the truth hurts.
Copyright ©Safer Shots 2008