Authenticself Acupuncture & Beyond

Wednesday, May 13, 2026

Amyotrophic Lateral Sclerosis Awareness Month

 So, Let’s Talk Awareness


Please notice the word “invention” with this patent for a new, original, innovative strain of mycoplasma. More will be said here about this invention as it relates to ALS.



In honor of “Amyotrophic Lateral Sclerosis Awareness Month” let’s talk about its possible cause and; though it’s against words on paper to say this word, its cure. Let’s have a different focus; something that gets us out of helplessness and victimhood, because knowing about the culprit CAN make a difference. When we can see the whole picture, we can make informed choices about resolving this issue, or perhaps even make our internal environment hostile to the culprit should we encounter it. Let’s embrace hope and true awareness that perhaps may end the attack of Amyotrophic Lateral Sclerosis (ALS) on humanity. I highly recommend that you read Amyotrophic Lateral Sclerosis by Donald and William Scott, especially if what you’ve read on the subject came from agents of the government. It’s this book that I mostly call on for the following message. At the end of their book, they have recommendations that just might help those suffering from ANY degenerative dis-easement. For what it’s worth, I’ll offer an article on non-mainstream ideas for balance with health soon.

Degenerative dis-easements aren’t innocent stories of “It just happened to her,” and “There’s nothing we can do about it.” Awareness about the prevalence of degenerative dis-easements isn’t where the focus needs to be during any month when something that plagues humans is spotlighted. Authentic awareness about what’s truly happening to those suffering from degenerative dis-easements—such as with ALS—needs to be understood for once and for all. So, let me give it to you straight at the risk of sounding like a broken record: the military/$cience/government/human/non-human faction is behind ALS and other degenerative dis-easements. When the criminals-that-believe-they-be are controlling the narrative about any dis-easement, the cure will be out of reach. This is why “numbers” of dis-easements is increasing, not decreasing despite all the public “research.”

In 1898, Nocard and Roux reported on a wall-less microorganism that seemed “a particle of bacterial DNA,” as the Scots state in their book, The Extremely Unfortunate Skull Valley Incident,1 about Brucella’s discovery. Great! A human will experience being defeated by this ancient bacterium and it may be known. A woman who suffers may receive a speedy diagnosis now that it’s been identified, and treatment shall start. Whoopee! Well, if any nation wants to turn this into a profound weapon, that plan doesn’t make sense. Everyone could figure out what the weapon is, as was explained on June 9, 1969 to the Senate during Dr. MacArthur’s testimony when he was seeking funds for a more stealth biological weapon. Earlier, and most importantly, by 1946, George W. Merck’s band of mad $cientists had taken Brucella and isolated “the active disease principle;” a toxin, mycoplasma, in “crystalline form.”2 Georgey-boy’s team of mad $cientists learned how to deliver the toxin of a bacterium without the bacterium itself! 3 They had weaponized something that was originally natural.

It took years to secure patents for various mycoplasma’s. Patent No. 5534413 is one. Please note in the patents listed at that link that it states, “The present invention…” when discussing this formerly natural thing, mycoplasma. Further, in “Pathogenic Mycoplasma Patent number 5242820,” the third one mentioned at the above link, it states, “The invention relates to a novel pathogenic mycoplasma isolated from patients with Acquired Immune Deficiency Syndrome (AIDS).” This weapon is called an invention, not simply something harvested from an ill person.

But, back to the delivery of a toxin of a bacterium without the bacterium itself…If average practitioners can’t locate a disease particle, then they can’t offer a profound treatment. They’ll tell you that there is nothing there. This means what they offer you is not help; not a cure. You’ll keep going back despite no diagnosis. They can’t see what’s plaguing you, but you’re a customer for life, which suits all involved behind the scenes just fine. If you’re exhausted and feeling broken, well, perhaps it’s high time to investigate the work of freelance scientists who hypothesize that weaponized mycoplasma may be the reason.

Donald W. Scott founded the Common Cause Medical Research Foundation (CCMRF) in 1998; it sadly became inactive with his death in 2011. While the foundation was active, despite much resistance, the independent CCMRF accomplished much, including linking Brucella abortus to causing ALS,4 and to an “especially dangerous mycoplasmal species”—mycoplasma fermentans—with those experiencing Gulf War Syndrome and to those “presenting with rheumatoid arthritis.”5 Notice that mycoplasma fermentans was patented in 1990. A purely natural thing may not be patented. They know what they have engineered.

Mycoplasma is a “particle of bacterial nucleic acid” that has been confirmed to be the same genomically to Brucella abortus, which has also been known to us as Bang’s Disease.6 What’s shocking is that once this crystalline was grounded very finely, it could be delivered through the air—including via air conditioning units and mosquitoes*—and placed unnoticed into food and water supplies by governmental agents, for example, on any desired community,7 during war time or not. This should make you think twice about what COULD be placed in a vile vial.

As if no researcher speaks to another, in the 1950’s, researchers working with the U. S. Navy, such as Dr. Robert Huebner, noticed that recruits who were experiencing chronic pneumonia had mycoplasma present along with degenerated “lymphoid tissues of the adenoids,” so they moved their focus to finding a useful biological weapon from mycoplasma.8 Sane folks wouldn’t think scientists would be ecstatic finding a culprit that caused degeneration, outside finding a cure, that is. With the discovery of adenoid degeneration, these researchers were on their way, with other researchers working elsewhere, to harming the masses with few the wiser. After all, degenerating human cells as with ALS, Parkinson’s and Alzheimer’s could be a handy weapon to call on when needed.9

After being infected with mycoplasma, it may lay dormant until something traumatic occurs to the body.10 Trauma, such as Lou’s Gehrig’s broken hand any of the seventeen times, seems to set ALS, Parkinson’s, and many dis-easements into activated “degeneration” status through a series of events.11 After a trauma, the compromised cell starts up-taking pre-formed sterols, including cholesterol, and will eventually die, setting off a chain reaction of problems that most likely will lead to ALS, and the “bone-crushing fatigue” of degenerative dis-easements.12 A government grant contract PH 43-68-1256 within the Special Virus Cancer Program, was given to S. Rottem, E. A. Pfendt, and L. Hayflick, and it is their work that supported the Scott’s with their break-through to understanding what cascading events happened to someone after mycoplasma infected him, and after a trauma had occurred.13

After the death of a cell, its contents are discharged, leaving a “supply of glutamate from its own nucleus that is dumped.”14 With the release of glutamate and with the damaged cells, urea is eventually destroyed and after a whole process described in Amyotrophic Lateral Sclerosis by Donald and William Scott, ultimately, the glial cells “are deprived of their energy source” and die.15 As the Scotts say, “We are able to link the cholesterol requirements of the mycoplasma as established by Rottem et al. to the loss of synapses in the motor neurons because the glia-produced cholesterol wasn’t available for replacement as established by Mauch et al.”16† A synapse is a specially designed connection to send signals of information from the Central Nervous System (CNS) to muscles and glands, for instance, to have them respond appropriately. With ALS, Parkinson’s and other degenerative dis-easements, the messages stop flowing to the muscles, for example, and we can see how it results in abnormal outcomes.

Interestingly, depending on prerequisite factors, degenerative dis-easements appear when certain factors are present. Some may say genetics is the issue, and yes implants that are unknown to you may be pre-disposing one woman to an internal environment that would welcome problems from mycoplasma. Another may be able to raise his frequency, placing her body out of reach to any possible damage. To me, the former, in deciding that you’re ill because of genetics, makes you helpless. The latter, is more empowering because you have a way out no matter how long mycoplasma has been disabling you. To me, healthfulness is ultimately a choice once you may navigate the storm having been educated on the matter, and with the right kind of practitioner on your side.

That said, read about physiology and anatomy if you want to have an in-depth understanding of the following discovery, especially if your doctor has never mentioned any of this. ALS appears when motor neuron cells have been destroyed and messages from the cortex fail to get through the CNS [Central Nervous System] to the muscles.”17 Parkinson’s when dopamine production of the substantia nigra is gone because the substantia cells have been destroyed.18 Huntington’s Disease and multiple sclerosis appear when the putamen cells are killed.19 Research and patents on mycoplasma show that agents of the government are lying when they claim they don’t know why ALS and other degenerative dis-easements are occurring. The Scotts say it well: “In summary, the mycoplasma’s up-take of cholesterol is a source of cellular degeneration, and that is where amyotrophic lateral sclerosis, and the other degenerative diseases begin.”20

Folks may have learned that something mysterious occurs to the motor neurons in ALS, but were never led to look at what those neurons’ neighbors were doing.21 How about you? Have doctors informed you about what has been conveyed here? Well, testimony by Dr. Garth Nicolson saying that 83% of ALS and 100% of Gulf War Veterans with ALS have “systemic mycoplasmal infections” in their blood,22 might be further reason for you to read The Extremely Unfortunate Skull Valley Incident.

It seems that as with any stealth weapon that has been haphazardly or purposefully disseminated on a populace, mycoplasma is far-reaching in the problems it causes to the Genetic human body. Whether ALS sufferers were targeted on purpose or the crystalline mycoplasma simply found its way into an unsuspecting man or woman, I see degenerative dis-easements as a crime against humanity. The secrets and control of Officials makes it worse. The core cure is so simple that I wonder how many naturopathic doctors who have been killed or have disappeared found and implemented the answer: a homeopathic remedy made from mycoplasma fermentans itself.

Let me leave you with Donald Scott speaking in Canada in this video that was filmed about three years before his death.

And, The Role of Bioengineering in CFS, GWS & AIDS.

And, MYCOPLASMA The Linking Pathogen in Neurosystemic Diseases.

And, Eugenics Depopulation.

1The Extremely Unfortunate Skull Valley Incident by Donald W. Scott and William L. C. Scott, p. 114.

2Amyotrophic Lateral Sclerosis The Probable Cause A Possible Cure by Donald W. Scott and William L. C. Scott, p. 10.

3 Skull Valley, p. 114.

4 Amyotrophic Lateral Sclerosis The Probable Cause A Possible Cure, p. 12.

5 Ibid., p. 9, 20.

6 Ibid., p. 11, 19.

*On vectors being used to transmit a weapon: See page 74 of 1971 US Special Virus Cancer Program Progress Report 8 at this link, for instance; though, the whole paper may be enlightening. “Role of vectors in transmission, host range of tumor viruses.” (Please keep in mind “viruses” was not defined. Is it lab-tweaked microscopic weapons or the byproduct, the “exosomes” left after a cell attempts to balance itself?) “Studies on factors affecting horizontal transmission of tumor viruses.” (Also, they can’t sell a vaccine for viruses unless they make the public accept it as a natural, contagious infiltrator that caused cancer.) “Experimental and natural transmission of bovine leukemia.” On page 5, they state that breast cancer may be caused by a virus. It’s interesting that in 1898, when Nocard & Roux reported a wall-less microorganism that seemed “a particle of bacterial DNA” that it had been “labelled a ‘virus,’” which is not accurate and came to be called mycoplasma (Skull Valley, p. 114). So, were they experimenting with mycoplasma and cancer before 1971? Both commercialized $cientists and freelance scientists have thrown the word “virus” around to mean different things. But know this, there is no proof anywhere that a natural, contagious virus exists. Not even during 1918, nor 2020!

7 Amyotrophic Lateral Sclerosis The Probable Cause A Possible Cure, p. 11.

8 Ibid., p. 12.

9 Ibid., p. 12.

10 Ibid., p. 25.

11 Ibid., p. 3, 16.

12 Ibid., p. 28, 30.

13 Ibid., p. 13.

14 Ibid., p. 15, 28.

15 Ibid., p. 30.

16 Ibid., p. 30.

†For more of an understanding: ALS is a dis-easement due to nerve cells of the brain and spinal column being targeted in some way. Seven German researchers—and their important paper “CNS Synaptogenesis Promoted by Glia-Derived Cholesterol”—demonstrate “that the motor neurons themselves are too heavily burdened with the tremendous number of messages they must transport to have the resources necessary to maintain the synapses between the upper and alpha motor neurons and between the alpha neurons and the muscles to maintain those synapses on their own (ALS, p. 26). Usually, the glial cells support the motor neurons by producing “an external supply [of cholesterol] which is then transported to the frazzled motor neurons (ASL, p. 26-27). Cholesterol helps the motor neurons maintain and replace the necessary synapses [gaps between neurons], as well as to support the growth of mycoplasma (ALS, p. 27). Without cholesterol, without the support of the glial cells, communication between parts of the brain are stopped. Muscle twitching will become weak muscles. Speech will ultimately become slurred, and it will be hard to swallow. And like most dis-easements experienced by modern man, this one also is not known to have been started in a lab.

Further, on page 5 of this testimony, Dr. Garth Nicolson confesses, “The results support the suggestion that infectious agents may play a role in the pathogenesis and/or progression of ALS, or alternatively ALS patients are extremely susceptible to systemic mycoplasmal infections (ALS, p. 46). The mycoplasma weapon accesses “the glial cells that surround and support the motor neurons,” and though the bacteria that may house it may be killed, “the nucleic particle” can’t be destroyed so easily (ALS, p. 27-28).

17 Ibid., p. 15, 26.

18 Ibid., p. 15, 25.

19 Ibid., p. 15.

20 Ibid., p. 17.

21 Ibid., p. 15.

22 Ibid., p. 46.



 

Saturday, April 19, 2025

Experts Have Proven Autism Can Be Environmental Toxins

 

Experts Have Proven Autism Can Be Environmental Toxins



RFK, Jr. is not contradicting experts when he says Autism is due to environmental toxins. Published studies which show that ingredients in vaccines do indeed cause Autism (and other health issues) have been shown to us before. 

If nothing else, please take away from looking over these studies how they were performed AFTER a problem arose, not BEFORE the product was put on the market as is the tyrants’ habit.

Having said that, let us take a look at what has already been studied and published by experts:

 

 

http://www.ncbi.nlm.nih.gov/pubmed/17674242

“A prospective study of thimerosal-containing Rho(D)-immune globulin administration as a risk factor for autistic disorders; 2007 May.

…This study evaluated the relationship between prenatal mercury exposure from thimerosal (49.55% mercury by weight)-containing Rho(D)-immune globulins (TCRs) and autism spectrum disorders (ASDs).

… Each ASD patient's mother was determined to have been administered a TCR [thimerosal] during her pregnancy.” (Autism in children from mother’s given a $hot during pregnancy.)

 

 

http://www.ncbi.nlm.nih.gov/pubmed/25198681

“A dose-response relationship between organic mercury exposure from thimerosal-containing vaccines and neurodevelopmental disorders; 2014 Sept.

…A hypothesis testing case-control study evaluated concerns about the toxic effects of organic-mercury (Hg) exposure from thimerosal-containing (49.55% Hg by weight) vaccines on the risk of neurodevelopmental disorders (NDs).

…the present study significantly associates organic-Hg exposure from T-HBV with an increased risk of an ND diagnosis.”

 

 

http://www.ncbi.nlm.nih.gov/pubmed/21993250

“Hypothesis: conjugate vaccines may predispose children to autism spectrum disorders; 2011 Dec.

…The first conjugate vaccine was approved for use in the US in 1988 to protect infants and young children against the capsular bacteria Haemophilus influenzae type b (Hib).

…There have been marked increases in the reported prevalence of autism spectrum disorders (ASDs) among children in the US beginning with birth cohorts in the late 1980s and in Denmark and Israel starting approximately 4-5 years later [after use in those countries].

…. The continuation of the trend toward increased rates of ASDs could be further explained by increased usage of the vaccine, a change in 1990 in the recommended age of vaccination in the US from 15 to 2 months, increased immunogenicity of the vaccine through changes in its carrier protein, and the subsequent introduction of the conjugate vaccine for Streptococcus pneumoniae. 

…the potential effects of conjugate vaccines on neural development merit close examination. 

…conjugate vaccines may have disrupted evolutionary forces that favored early brain development over the need to protect infants and young children from capsular bacteria.”

 

 

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3878266/

A two-phase study evaluating the relationship between Thimerosal-containing vaccine administration and the risk for an autism spectrum disorder diagnosis in the United States; 2013 Dec 19.

Results

In phase I, it was observed that there was a significantly increased risk ratio for the incidence of ASD reported following the Thimerosal-containing DTaP vaccine in comparison to the Thimerosal-free DTaP vaccine. In phase II, it was observed that cases diagnosed with an ASD were significantly more likely than controls to receive increased organic-Hg from Thimerosal-containing hepatitis B vaccine administered within the first, second, and sixth month of life.

Conclusions

…the present study provides new epidemiological evidence supporting an association between increasing organic-Hg exposure from Thimerosal-containing childhood vaccines and the subsequent risk of an ASD diagnosis.”

…The presence of Hg within brain cells is significant because it can induce cellular damage consistent with the neuronal damage observed in the brains of individuals diagnosed with ASD.”

 

 

http://www.ncbi.nlm.nih.gov/pubmed/17454560

“A case series of children with apparent mercury toxic encephalopathies manifesting with clinical symptoms of regressive autistic disorders; 2007 May.

…There was a significant dose-response relationship between the severity of the regressive ASDs observed and the total mercury dose children received from Thimerosal-containing vaccines/Rho (D)-immune globulin preparations.

….Evidence for mercury intoxication should be considered in the differential diagnosis as contributing to some regressive ASDs.”

 

 

 

http://www.ncbi.nlm.nih.gov/pubmed/24675092

“Transcriptomic analyses of neurotoxic effects in mouse brain after intermittent neonatal administration of thimerosal; 2014 June.

…Thimerosal is a vaccine antimicrobial preservative which has long been suspected an iatrogenic factor possibly contributing to neurodevelopmental disorders including autism. 

…Our results indicate that higher dose of neonatal thimerosal-mercury (20× higher than that used in human) is capable of inducing long-lasting substantial dysregulation of neurodevelopment, synaptic function, and endocrine system, which could be the causal involvements of autistic-like behavior in mice.”

 

 

http://www.ncbi.nlm.nih.gov/pubmed/22099159

“Do aluminum vaccine adjuvants contribute to the rising prevalence of autism? 2011 Nov.

Al in vaccines and ASD may be causal.”

 

 

 

http://www.ncbi.nlm.nih.gov/pubmed/21623535

“A positive association found between autism prevalence and childhood vaccination uptake across the U.S. population; 2011.

The results suggest that although mercury has been removed from many vaccines, other culprits may link vaccines to autism. Further study into the relationship between vaccines and autism is warranted.”  

  

 

 

http://www.ncbi.nlm.nih.gov/pubmed/25377033

Commentary--Controversies surrounding mercury in vaccines: autism denial as impediment to universal immunization; 2014 Oct-Dec.

In 2004, the US Center for Disease Control (CDC) published a paper showing that there is no link between the age at which a child is vaccinated with MMR and the vaccinated children's risk of a subsequent diagnosis of autism. One of the authors, William Thompson, has now revealed that statistically significant information was deliberately omitted from the paper. Thompson first told Dr S Hooker, a researcher on autism, about the manipulation of the data. Hooker analysed the raw data from the CDC study afresh. He confirmed that the risk of autism among African American children vaccinated before the age of 2 years was 340% that of those vaccinated later.

 

 

http://www.ncbi.nlm.nih.gov/pubmed/24995277

“Methodological issues and evidence of malfeasance in research purporting to show thimerosal in vaccines is safe; 2014.

The purpose of this review is to examine these six publications and analyze possible reasons why their published outcomes are so different from the results of investigations by multiple independent research groups over the past 75+ years.”

First, divide your scientists into freelance scientists and commercialized, university $cientists supported by Big Pharma. The question in the Abstract may already be answered.

 

 

http://www.ncbi.nlm.nih.gov/pubmed/12145534

“Abnormal measles-mumps-rubella antibodies and CNS autoimmunity in children with autism; 2002 Jul-Aug.

Autoimmunity to the central nervous system (CNS), especially to myelin basic protein (MBP), may play a causal role in autism, a neurodevelopmental disorder. Because many autistic children harbor elevated levels of measles antibodies, we conducted a serological study of measles-mumps-rubella (MMR) and MBP autoantibodies.

ELISA analysis showed a significant increase in the level of MMR antibodies in autistic children. 

…Stemming from this evidence, we suggest that an inappropriate antibody response to MMR, specifically the measles component thereof, might be related to pathogenesis of autism.”

 

 

http://www.ncbi.nlm.nih.gov/pubmed/21058170

Hepatitis B vaccination of male neonates and autism diagnosis, NHIS 1997-2002

This is on the former Hep B vax.

 

 

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364648/

“What is regressive autism and why does it occur? Is it the consequence of multi-systemic dysfunction affecting the elimination of heavy metals and the ability to regulate neural temperature? 2009 July.

This article explores the issues and concludes that sensory dysfunction and systemic failure, manifested as autism, is the inevitable consequence arising from subtle DNA alteration and consequently from the overuse of vaccines.”

 

 

http://www.ncbi.nlm.nih.gov/pubmed/19106436

“A comprehensive review of mercury provoked autism; 2008 Oct.

…Hg has been found to cause immune, sensory, neurological, motor, and behavioural dysfunctions similar to traits defining/associated with ASDs, and that these similarities extend to neuroanatomy, neurotransmitters, and biochemistry.

…the overwhelming preponderance of the evidence favors acceptance that Hg exposure is capable of causing some ASDs.”

 

 

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3774468/

“Thimerosal Exposure and the Role of Sulfation Chemistry and Thiol Availability in Autism; 2013 Aug .

…The associated behavioral and developmental outcomes found in ASD are plausible as a manifestation of Hg toxicity, since the brain is a target organ for TM’s [Thimerosal’s] toxic effects as well as a target organ for the bioaccumulation of the toxic, long-retained Hg species derived from injected Et-Hg compound exposures.

…With the rate of children diagnosed with an ASD in the US now exceeding 1 in 50 children and the rate of children with neurodevelopmental/behavioral disorders in the US now exceeding 1 in 6 children, and the preceding evidence showing that there is vulnerability to TM that would not be known without extensive testing, the preponderance of the evidence indicates that TM should be removed from all vaccines.”

 

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3697751/

“B-Lymphocytes from a Population of Children with Autism Spectrum Disorder and Their Unaffected Siblings Exhibit Hypersensitivity to Thimerosal; Jun 9;2013.

…certain individuals with a mild mitochondrial defect may be highly susceptible to mitochondrial specific toxins like the vaccine preservative thimerosal.”

 

 

http://www.ncbi.nlm.nih.gov/pubmed/21299355

“Theoretical aspects of autism: causes--a review; 2011 Jan-Mar.

…The inflammation could be caused by a defective placenta, immature blood-brain barrier, the immune response of the mother to infection while pregnant, a premature birth, encephalitis in the child after birth, or a toxic environment.”

(Searched information since 1943 only.)

 

 

http://www.ncbi.nlm.nih.gov/pubmed/21907498

Conjugate vaccines and autism; 2011 Dec.

https://pubmed.ncbi.nlm.nih.gov/21993250/

“Hypothesis: conjugate vaccines may predispose children to autism spectrum disorders; 2011 Dec.

…Conjugate vaccines fundamentally change the manner in which the immune systems of infants and young children function by deviating their immune responses to the targeted carbohydrate antigens from a state of hypo-responsiveness to a robust B2 B cell mediated response. This period of hypo-responsiveness to carbohydrate antigens coincides with the intense myelination process in infants and young children, and conjugate vaccines may have disrupted evolutionary forces that favored early brain development over the need to protect infants and young children from capsular bacteria.”

 

 

 

http://www.ncbi.nlm.nih.gov/pubmed/11339848

“Autism: a novel form of mercury poisoning; 2001 April.

…autism may affect 1 in 150 US children.

…Thimerosal, a preservative added to many vaccines, has become a major source of mercury in children who, within their first two years, may have received a quantity of mercury that exceeds safety guidelines.” 

 

 

http://www.ncbi.nlm.nih.gov/pubmed/15780490

“The potential importance of steroids in the treatment of autistic spectrum disorders and other disorders involving mercury toxicity; 2005.

it is imperative that further research should be conducted to understand mercury-testosterone toxicity.”

 

 

http://www.ncbi.nlm.nih.gov/pubmed/12933322

“Reduced levels of mercury in first baby haircuts of autistic children; 2003 Jul-Aug.

…One possible factor underlying these increases is increased exposure to mercury through thimerosal-containing vaccines.”

 

 

 

http://www.ncbi.nlm.nih.gov/pubmed/16870260

“Cultured lymphocytes from autistic children and non-autistic siblings up-regulate heat shock protein RNA in response to thimerosal challenge; 2006 Sept.

…Determining cellular response, at the level of gene expression, has important implications for the understanding and treatment of conditions that result from exposure to neurotoxic compounds.”

 

 

http://www.ncbi.nlm.nih.gov/pubmed/19043938

“A possible central mechanism in autism spectrum disorders, part 1; 2008 Nov-Dec.

…This mechanism explains the link between excessive vaccination, use of aluminum and ethylmercury as vaccine adjuvants, food allergies, gut dysbiosis, and abnormal formation of the developing brain.”

 

 

 

http://www.ncbi.nlm.nih.gov/pubmed/12142947

The role of mercury in the pathogenesis of autism; 2002.

https://pubmed.ncbi.nlm.nih.gov/18829819/

“Mercury levels in newborns and infants after receipt of thimerosal-containing vaccines; 2008 Oct.

…the inorganic mercury likely being formed as a result of the dealkylation of the ethyl or methyl mercury in the brain.”

 

 

 

FDA concludes vaccines cause Autism

http://www.getcancercure.com/fda-announce-that-dtap.../

..."the present study provides new epidemiological evidence supporting an association between increasing organic-Hg exposure from Thimerosal-containing childhood vaccines and the subsequent risk of an ASD diagnosis"...

.A two-phase study evaluating the relationship between…

Autism spectrum disorder (ASD) is defined by…

NCBI.NLM.NIH.GOV

https://search.brave.com/search?q=the+present+study+provides+new+epidemiological+evidence+supporting+an+association+between+increasing+organic-Hg+exposure+from+Thimerosal-containing+childhood+vaccines+and+the+subsequent+risk+of+an+ASD+diagnosis%22...+.A+two-phase+study+evaluating+the+relationship&source=desktop&summary=1&conversation=304f43a47a451257a1d292

“Thimerosal and ASD Study

A two-phase study evaluated the relationship between Thimerosal-containing vaccine administration and the risk for an autism spectrum disorder (ASD) diagnosis in the United States. The study found that there was a significantly increased risk ratio for the incidence of ASD reported following the Thimerosal-containing Diphtheria-Tetanus-acellular-Pertussis (DTaP) vaccine in comparison to the Thimerosal-free DTaP vaccine. In the second phase, it was observed that cases diagnosed with an ASD were significantly more likely than controls to receive increased organic-Hg from Thimerosal-containing hepatitis B vaccines administered within the first, second, and sixth month of life.245

The study provides new epidemiological evidence supporting an association between increasing organic-Hg exposure from Thimerosal-containing childhood vaccines and the subsequent risk of an ASD diagnosis.245 This conclusion was reached using a two-phased, hypothesis-generating and hypothesis-testing, epidemiological analytical methodology in two separate databases. The study emphasized the importance of an adequate follow-up period to ensure that individuals were appropriately classified with respect to their exposures and outcomes, thus helping to ensure the potential for a cause-and-effect relationship between exposure and outcome was not biased or confounded.245

However, it is important to note that the results of this study differ from several other cohort studies that failed to find an association between ASD and organic-Hg exposure from Thimerosal-containing childhood vaccines. These differences may be due to variations in childhood vaccine schedules, diagnostic criteria for outcomes, and the epidemiological methods employed, particularly with respect to the issue of follow-up period for individuals in the cohorts examined.245

Routine childhood vaccination remains an important public health tool to reduce the morbidity and mortality associated with infectious diseases.”

 

 

 

https://pubmed.ncbi.nlm.nih.gov/28595786/

“Increased risk for an atypical autism diagnosis following Thimerosal-containing vaccine exposure in the United States: A prospective longitudinal case-control study in the Vaccine Safety Datalink; 2017 July.

The present study provides important epidemiological evidence significantly associating increasing Hg exposure from Thimerosal-containing childhood vaccines and the subsequent risk of atypical autism diagnosis, and suggests that Thimerosal should be eliminated from vaccines.

 

 

 

https://pubmed.ncbi.nlm.nih.gov/25382662/

“A case-control study evaluating the relationship between thimerosal-containing haemophilus influenzae type b vaccine administration and the risk for a pervasive developmental disorder diagnosis in the United States; 2014 Nov.

…the present study provides new epidemiological evidence of a significant relationship between increasing organic Hg exposure from Thimerosal-containing vaccines and the subsequent risk of PDD [pervasive developmental disorder] diagnosis in males and females.”

 

 

 

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1646939/

A positive association found between autism prevalence and childhood vaccination uptake across the U.S. population.

(Been scrapped from the internet. Scrap: discarded waste material. That’s how they see information on Vax & Autism correlation. It is waste material for the waste basket. Naturally, being papers on studies that did happen, they can be found somehow/where.)

 

 

 

 

http://www.ncbi.nlm.nih.gov/pubmed/21623535 (Been scrapped)

Hepatitis B vaccination of male neonates and autism diagnosis, NHIS 1997-2002.

 

 

http://www.ncbi.nlm.nih.gov/pubmed/21058170 (Been scrapped)

Abnormal measles-mumps-rubella antibodies and CNS autoimmunity in children with autism.

 

http://www.ncbi.nlm.nih.gov/pubmed/12145534 (Been scrapped)

The plausibility of a role for mercury in the etiology of autism: a cellular perspective

 

http://jcm.asm.org/content/46/3/1101.long (Been scrapped)

A case series of children with apparent mercury toxic encephalopathies manifesting with clinical symptoms of regressive autistic disorders.

 

http://www.uscfc.uscourts.gov/.../ABELL.ZELLER073008.pdf

Vaccine-caused autism here in this federal court case  (Been scrapped.)

 

http://www.eurekalert.org/pub.../2010-06/kp-cmv062310.php (Been scrapped)

Impact of environmental factors on the prevalence of autistic disorder after 1979

 

https://www.facebook.com/flx/warn/? (Been scrapped)

 Here are 127 separate studies linking vaccines and autism. 

 

 

PLUS

 

https://pubmed.ncbi.nlm.nih.gov/17092614/

“DTP with or after measles vaccination is associated with increased in-hospital mortality in Guinea-Bissau;2007 Jan.

…We examined in-hospital mortality of children having received DTP with or after measles vaccine.

…The case fatality was increased for children who had received DTP with or after measles vaccine compared with children who had received measles vaccine as the most recent vaccine, the ratio being 2.53 (1.37-4.67) and 1.77 (0.92-3.41) in the two periods, respectively.”

 

http://www.ncbi.nlm.nih.gov/pubmed/16126512

“Infection, vaccines and other environmental triggers of autoimmunity; 2005 May

…Vaccines, in several reports were found to be temporally followed by a new onset of autoimmune diseases.”

 

http://www.ncbi.nlm.nih.gov/pubmed/22531966

“Relative trends in hospitalizations and mortality among infants by the number of vaccine doses and age, based on the Vaccine Adverse Event Reporting System (VAERS), 1990-2010

Is infant immunization a risk factor for childhood asthma or allergy?”

 

http://www.ncbi.nlm.nih.gov/pubmed/22423139

“Effectiveness of trivalent inactivated influenza vaccine in influenza-related hospitalization in children: a case-control study; 2012 June.

TIV [the vaccinated group] recipients had an increased risk of virologically-confirmed non-influenza infections.”

 

https://pubmed.ncbi.nlm.nih.gov/7494055/

 Detection of measles virus RNA in urine specimens from vaccine recipients; 1995 Sept.

…Overall, measles virus RNA was detected in 10 of 12 children.” 

(Environmental: vaccine toxins shed)

 

 

http://www.ncbi.nlm.nih.gov/pubmed/9345669 (Been scraped.)

Infant mortality rates regressed against number of vaccine doses routinely given: Is there a biochemical or synergistic toxicity? 

 

 

https://www.law.cornell.edu/supct/html/09-152.ZD.html  February, 2011. Convoluted:13 words from the statutory text, including the key term ‘unavoidable.’” Such an unavoidably unsafe] product, properly prepared, and accompanied by proper directions and warning, is not defective.” “…There would have been no need for Congress to include the additional 13 words ‘the injury or death resulted from side effects that were unavoidable even though.’ See TRW Inc. v. Andrews 534 U. S. 1931 (2001) (noting “cardinal principle of statutory construction that a statute ought, upon the whole, to be so construed that, if it can be prevented, no clause, sentence, or word shall be superfluous, void, or insignificant”

 

https://www.scribd.com/.../124-Research-Papers-Supporting... (Been scrapped.)

 

And here page 2 http://www.uscfc.uscourts.gov/.../CAMPBELL-SMITH.MOJABI... (Been scraped.)

 

https://ecf.cofc.uscourts.gov/cgi-bin/show_public_doc... (Been scraped.)

 

Here are 83 cases reviewed by lawyers http://digitalcommons.pace.edu/cgi/viewcontent.cgi... (Been scraped.)

 

Oh, look here's a dead kid compensated https://ecf.cofc.uscourts.gov/cgi-bin/show_public_doc... (Been scraped.)

 

https://www.law.cornell.edu/supct/cert/09-152 (Been scraped.)

Read this about Hannah Brusewitz case and how she was harmed by DTP

 

 

Supreme Court Unavoidably Unsafe http://www.supremecourt.gov/opinions/10pdf/09-152.pdf (Been scraped.)

http://www.ncbi.nlm.nih.gov/pubmed/25198681 (Been scraped.)

A dose-response relationship between organic mercury exposure from thimerosal-containing vaccines and neurodevelopmental disorders.

 

http://www.ncbi.nlm.nih.gov/pubmed/9345669 (Been scraped.)

Relative trends in hospitalizations and mortality among infants by the number of vaccine doses and age, based on the Vaccine Adverse Event Reporting System (VAERS), 1990-2010.

 

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170075/ (Been scraped.)

DTP with or after measles vaccination is associated with increased in-hospital mortality in Guinea-Bissau. But I found one posted above.

 

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3173748/ (Been scraped)

Detection of RNA of Mumps Virus during an Outbreak in a Population with a High Level of Measles, Mumps, and Rubella Vaccine Coverage

 

http://www.ncbi.nlm.nih.gov/pubmed/17454560 (Been scrapped)

Aluminum in the central nervous system (CNS): toxicity in humans and animals, vaccine adjuvants, and autoimmunity.

 

http://www.ncbi.nlm.nih.gov/pubmed/23609067 (Been scrapped)

Unvaccinated Children are Healthier

 

 

http://www.mednat.org/vaccini/dannivacc_study.pdf (Been scrapped)

Self-Organized Criticality Theory of Autoimmunity

 

http://www.plosone.org/.../10.1371/journal.pone.0008382 (Been scrapped)

Combination MMRV vaccine linked with 2-fold risk of seizures

 

http://www.ms.academicjournals.org/.../article1409245960...(Been scrapped)

Increased risk of non-influenza respiratory virus infections associated with receipt of inactivated influenza vaccine

 

http://www.ncbi.nlm.nih.gov/pubmed/22525386 (Been scrapped)

Speciation of methyl- and ethyl-mercury in hair of breastfed infants acutely exposed to thimerosal-containing vaccines.

 

http://www.ncbi.nlm.nih.gov/pubmed/21575620 (Been scrapped)

Comparison of VAERS fetal-loss reports during three consecutive influenza seasons

 

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3888271/ (Been scrapped)

---------

 

If you ever need a lawyer http://www.mctlawyers.com/vaccine-injury/cases/

 

https://time.com/2888403/u-s-health-care-ranked-worst-in-the-developed-world/?fbclid=IwAR1oYtP21IPE9JrvEFAiXp7CR57MLeCHnqLrF1jPyWbACzUsz0wl_E2Beyk

US Health; June 17, 2014. (Has healthfulness improved here among the vaccinated?)