Thursday, May 16, 2019

Pet theories of Allopathy.

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For the modern medicos to become useful members of society, certain pet theories have to be ditched;


a) The body is a machine which can be fixed in parts. Removal of "problematic" parts can still allow the body to function normally
b) The body is a chemical factory that needs regular inputs of chemicals to keep going
c) The body does not know how to heal itself, the world would collapse without the increasing retinue of doctors and their interventions
d) The environment is an enemy conspiring to kill the body
e) Bacteria and viruses are always poised to attack the body
d) Acute diseases serve no purpose and all diseases must be tackled on a war footing. Lack of acute diseases is a desirable state.
e) Extreme toxins in material doses are extremely beneficial if prescribed by a doctor who is blissfully ignorant of toxicology and susceptibility.


Only after these huge fallacies are discarded can they begin to learn about health.

Wednesday, May 01, 2019

Vaccines: Where are the placebo controlled trials?

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The problem is that no true double blind inert placebo studies have ever been done period, not one on any vaccine or adjuvant! No one can provide you one. The ingredient thirmerosal has never had a double blind placebo controlled study done on it itself. The one done in 1929 gives no evidence to prove thimerosal is safe yet the government (CDC) uses it as the adjuvant anyway. That whole correlation does not equal causation claim just has to go out the window because there can’t be that many coincidences! You cannot study a drug using a adjuvant against another drug when the adjuvant itself is untested. The whole process was/is/has been a sham from the beginning! The CDC could never prove it to Congress. (See the video)Then going forward when they removed thimerosal, they used the old vaccines-to test the new versions, that isn’t science that just doesn’t work. The new adjuvant aluminum has never been tested. That’s the real debate here the prime underlying issue to this whole debate... 

From congressional testimony Monday 2002 the only adjuvant test ever done was in 1929

https://www.facebook.com/groups/VaccineResistanceMovement/permalink/2255270961178015?sfns=mo

The CDC has no inert placebo studies on any adjuvants and now they use aluminum and no inert placebo studies have ever been done on that adjuvant so you’re still in the same place. As the adjuvant itself may be causing the damage.

Congressional testimony. Problem is is now more people in Congress are bought off by the pharmaceutical companies.

https://www.govinfo.gov/content/pkg/CHRG-107hhrg82358/html/CHRG-107hhrg82358.htm

Here's a few examples of vaccine testing. They are not tested against placebos like you would think, they are tested against other vaccines :

DTaP
Daptacel tested against DTP and DT
https://www.vaccineshoppe.com/image.cfm?doc_id=11179... 

Infanrix tested againt Pediarix. Both groups administered varying combinations of HepB, IPV, HIB, PCV, MMR & Varicella vaccines at the same time.
https://www.gsksource.com/.../Infanrix/pdf/INFANRIX.PDF

Kinrix tested against Infanrix. Both groups also received IPV and MMR at same time.
https://www.gsksource.com/.../Presc.../Kinrix/pdf/KINRIX.PDF 

Pediarix
German study: test group =Pediarix AND HIB versus control group = Infanrix, HIB AND OPV.
USA study: test group = Pediarix, HIB, PCV versus control group = Infanrix, Hep B, IPV, HIB, PCV
https://www.gsksource.com/.../Pediarix/pdf/PEDIARIX.PDF

Pentacel (5 in 1: Dtap, Polio, HIB) tested against already licensed and non-licensed combinations of those vaccines. Both test and control groups also received PCV, HepB (and MMR at the last dose) at the same time. 
https://www.vaccineshoppe.com/image.cfm?doc_id=13799...

Quadracel (4 in 1: Dtap & Polio) tested against already approved Daptacel & IPOL vaccines. Both test and control groups also received mmr and varicella vaccines at same time. 
https://www.vaccineshoppe.com/image.cfm?doc_id=13791... 

__________

HIB 

ActHIB reactions observed after administering ActHib or ActHib plus Daptacel, IPOL & PCV. No group did not get ActHib at all. 
https://www.vaccineshoppe.com/image.cfm?doc_id=13692... 

Hiberix tested against previously licensed HIB vaccines and both groups given various combinations of pediarix, PCV, rotarix & HepB at the same time. https://www.gsksource.com/.../Pre.../Hiberix/pdf/HIBERIX.PDF

MenHibrix (Meningococcal & HIB) tested against a single licensed HIB vaccine. Both groups given various combinations of Pediarix, PCV, MMR or Varicella vaccines at the same time.https://gsksource.com/.../Pre.../Menhibrix/pdf/MENHIBRIX.PDF

PedVaxHib (Meningococcal & HIB) tested against another form of pedvaxhib or a placebo. All groups given DTP and OPV at the same time.http://www.merck.com/.../pi.../p/pedvax_hib/pedvax_pi.pdf

__________

Hep A

Havrix - all groups received Havrix. Group 1: Havrix Group, 2: Havrix and MMR, Group 3 Havrix and Varicella.
https://www.gsksource.com/.../Presc.../Havrix/pdf/HAVRIX.PDF

TwinRix (Hep A & Hep 
😎 tested against already approved Hep & and B vaccines given separately (Havrix & Engerix-B).
https://gsksource.com/.../Prescri.../Twinrix/pdf/TWINRIX.PDF 

__________

Hep B

Engerix-B given to all test subjects and observed for reactions. No control group was observed or compared. 
https://www.gsksource.com/.../Engerix-B/pdf/ENGERIX-B.PDF

Recombivax given to all test subjects. Infants and adults simply observed for reactions. Children compared the 2 vs 3 dose schedule. 
http://www.merck.com/.../r/recombivax_hb/recombivax_pi.pdf

__________

HPV

Gardasil tested against aluminum adjuvant or a "saline placebo". However, the saline placebo is made up of: water, 9.56mg sodium chloride, 0.78mg L-histidine and 50micrograms polysorbate-80.
http://www.merck.com/.../pi.../g/gardasil/gardasil_pi.pdf 

Gardasil 9 tested against regular Gardasil. 
https://www.merck.com/.../g/gardasil_9/gardasil_9_pi.pdf 

__________

Flu

All flu vaccines observed for reactions, no control group, and/or against other flu vaccines. 
http://www.immunize.org/fda/#flu

__________

MMR

MMRII, adverse event observation of those who receive MMR.
http://www.merck.com/.../pi_circulars/m/mmr_ii/mmr_ii_pi.pdf

ProQuad (mmr+varicela) tested against MMRII + Varivax given together.
http://www.merck.com/.../pi.../p/proquad/proquad_pi.pdf

__________

Meningococcal ACWY

Menactra tested against Menomune OR a group receiving PCV, MMRV and HepA instead. 
https://www.vaccineshoppe.com/image.cfm?doc_id=12580...

Menomune was tested against Menactra. 
https://www.vaccineshoppe.com/image.cfm?doc_id=10447...

Menvo was tested against groups getting typical childhood vaccines or a compararative vaccine.
https://gsksource.com/.../Prescribi.../Menveo/pdf/MENVEO.PDF

__________

Meningococcal B

Bexsero tested against either a meningococcal ACWY vaccine, Japanese encephalitis vaccine or an aluminum placebo.
https://gsksource.com/.../Prescri.../Bexsero/pdf/BEXSERO.PDF

Trumenba tested against groups getting other vaccines and/or a "saline placebo". However, the saline placebo is made up of: water, 9.56mg sodium chloride, 0.78mg L-histidine and 50 micrograms polysorbate-80. 
http://labeling.pfizer.com/ShowLabeling.aspx?id=1796...

__________

Pneumococcal (PCV13)

Prevnar 13 tested against the old prevnar: 
http://labeling.pfizer.com/showlabeling.aspx?id=501

__________

Polio

IPOL (Inactivated Polio) tested by observing subjects who got IPOL, DTP & Tripedia vaccines at same time.
https://www.vaccineshoppe.com/image.cfm?doc_id=5984...

__________

Tdap

Adacel tested against Td vaccine.
https://www.vaccineshoppe.com/image.cfm?doc_id=10437...

Boostrix tested against Td vaccine. Some participants also received meningococcal or flu vaccines at the same time. 
https://gsksource.com/.../Presc.../Boostrix/pdf/BOOSTRIX.PDF

__________

Td

TD Generic- states "Data on adverse reactions following fluid and adsorbed preparations of MassBiologics’ Td with various doses of the diphtheria and tetanus components have been reported in a series of studies." and also that it can be used to complete the dtap series but safety and efficacy has not been evaluated. Does not list study results.
https://www.fda.gov/.../ApprovedProducts/UCM164127.pdf

Tennivac tested against a vaccine called Decavac.
https://www.vaccineshoppe.com/image.cfm?doc_id=12609...

__________

Varicella

Varivax claims placebo based trials and later in the insert states no placebo based trials took place. Then describes trials with varying dosages of antigens and dosing schedules. 
http://www.merck.com/.../pi.../v/varivax/varivax_pi.pdf

__________

***Rotavirus and Pneumovax actually claim placebo studies but the contents of their placebo were undetermined.

https://m.facebook.com/knowthevax/photos/a.1628492207364814.1073741828.1628473224033379/1896308900583142/?type=3


Saturday, April 27, 2019

What vaccines have been linked to autism?


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What vaccines have been linked to autism?
- Hep B vaccine (CDC Verstraeten study lying unpublished, C M Gallagher et al)
- MMR vaccine (CDC DeStefano study exposed by co-author, directly and indirectly linked by several other studies)
- Chicken Pox vaccine (Dr Theresa Deisher)
- Thimerosal (mercury containing compound in vaccines, several studies). All non live virus vaccines contain this compound. 
- Aluminium adjuvant in vaccines (Dr Stephanie Seneff et al, Mathew Mold et al, Christopher Shaw). Contained in Hep A, Hep B, Tetanus, DPT, HPV, Hib, Pneumoccocal, Pentavalent, Hexavalent
- DPT vaccine (mentioned in package insert, now removed from FDA website)
- DNA material in vaccines (Helen V. Ratajczak). DNA material exists in MMR, Chicken pox, Hep A, Rotavirus, polio, adenovirus, rabies, and shingles vaccines
- Encephalopathy after vaccination with children suffering "autism like" symptoms - US Vaccine Court that has awarded compensation to 85 such children so far, Vaccine Court designated expert Dr Andrew Zimmermann.

Vaccine Nightmare: And yet, vaccinate at any cost!


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While you are dreaming, the dream seems real to you. After you awake you are amazed at how you could consider it real. You look around at sleeping people and know they too are trapped in their dream worlds. You wait for them to wake up. Vaccination is that dream which takes time to break as it promises an Utopian world free from death, disease and suffering.
However when those very things hit you as you submit to that dream you suffer a rude awakening. Vaccination is not a good idea. This practice targets infants and children and suffers huge ethical issues. Ethics does not recommend indiscriminate medical interventions particularly on healthy subjects. These subjects being infants and children the issue becomes even more perplexing.
Consider this against the practices of other systems of medicine. Let alone medicate the healthy, they are extremely cautious even while treating sick children. While ayurveds frown on rural practices like giving a drop of honey to infants at intervals claiming it improves the immune system, classical homeopaths will balk at giving remedies directly to infants and give it to the breastfeeding mother who can then pass it on to the child along with the breast milk.
Even mainstream science does not advocate anything except breast milk to an infant. Not even water. One wonders how the many vaccines, containing seriously debatable ingredients, are injected during such a sensitive period. Scientific studies now stress on the benefits of natural childhood illnesses and how breastfeeding and natural exposures lead to a strong immune system and a healthy microbiome - a sine qua non for a healthy life.
There are many studies now to prove that vaccines irreversibly affect the immune system balance and can cause serious autoimmune disorders. These and other serious damage from vaccine ingredients are listed in vaccine package inserts and in confidential reports submitted by vaccine manufacturers to the federal agencies who sit on them doing nothing.
Vaccines are never adequately tested for safety - the safety tests being rigged by manufacturers to show that they are safe. They are not tested against any inert placebo but against the same vaccine minus the antigen - a process that defies logic. Vaccines are given in bunches - a procedure that has never been tested. The effects of the entire schedule are never tested. Long term studies are never done.
There are no studies to compare the health status of vaccinated vs the not vaccinated. Agencies are sitting on studies that reflect great harm from vaccines. The state of health of today’s children abundantly reflects that harm.
Vaccines are actually tested only after they are marketed. Considering that post marketing administration is a phase iv clinical trial, all rules are thrown to the winds as there is no apparatus to track that harm and rather adverse effects are termed 'coincidence'. Rules for reporting of adverse effects have been tweaked so that vaccines cannot be linked to the harm they inflict.
Doctors, nurses and health care workers are ticked off for reporting adverse events so as not to 'alarm the public'.
The chronic disease and cancer epidemics can be described in three words; autoimmune, inflammatory, immunotoxic. Vaccines cause exactly this! Thus vaccines are the only medical intervention that can be connected with all disease states we witness today.
Vaccines are now being made mandatory. Schemes are afoot to make them mandatory for adults too. Under these circumstances the public should not wait for the experts to declare harm. These experts have been bought. The industry rules the game. It is time for mass protests. It is time for non cooperation. It is time to protect our children. It is time to protect our health.

And yet, vaccinate at any cost!

The aim is to vaccinate each and every child regardless of opposition and consequences. Those engaged in this task know very well that there is serious opposition to vaccination based on science and that they have industry sponsored trash in their hands with which they are countering the opposition. There is no attempt to sit and and answer or even consider the points put forward by the doctors and scientists who have critically examined the issue. 

The constant vilification of those raising critical questions serves to sideline the growing anger and continue vaccinating the children. Even Court orders are being ignored. Since 1942 it is known that vaccines cannot prevent disease. Today as per their own records vaccines are connected to 248 serious diseases and disorders including death. Children are today seriously ill and childhood is lost. Research shows most childhood illnesses serve a purpose and that they are beneficial for the child. 

Yet vaccination does not stop. Why? What is even more disconcerting is that independent investigations find lack of the antigens in vaccines people are supposed to build antibodies against, or the quantity of antigens is so low it cannot provoke the body to produce antibodies. The whole thing appears very sinister. What is the purpose behind injecting every child with known and decidedly dangerous toxins? Why are governments participating in this genocide? Why are doctors groups silent and even justifying this mass poisoning? What the heck is going on?


Friday, April 19, 2019

Herd immunity does not exist.

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Junk Science Week: Vaccinating the 'herd'

Mass vaccination advocates rely on 'herd immunity' to make their case. But it doesn’t exist

Mass vaccination advocates rely on ‘herd immunity’ to make their case. But it doesn’t exist
Cracked beaker“When vaccination rates are very high, as they still are in the nation as a whole, everyone is protected,” explained USA Today in a recent editorial entitled “Vaccine opt-outs put public health at risk.”
“This ‘herd immunity’ protects the most vulnerable, including those who can’t be vaccinated for medical reasons, infants too young to get vaccinated and people on whom the vaccine doesn’t work. But herd immunity works only when nearly the whole herd joins in. When some refuse vaccinations and seek a free ride, immunity breaks down and everyone is more vulnerable.”
The concept of “herd immunity” first materialized in the 1930s, when Johns Hopkins University’s Arthur Hedrich discovered that, after 55% of Baltimore’s population acquired measles (and thus immunity to measles), the rest of the population, or “herd,” became protected. This concept provides today’s rationale for insisting that everyone be vaccinated.
Measles outbreaks occur even when the vaccinated population exceeds 95%
“If you only risked your own health by not getting vaccinated, that would be your business,” mass vaccination advocates state. “But when your failure to get vaccinated endangers me or my child, that becomes my business.” It’s a powerful argument, except for one thing — herd immunity in vaccinated populations has been repeatedly disproven.
In November 1966, in announcing a mass vaccination program for measles that would exceed the 55% level reached in Baltimore, the U.S. Public Health Service confidently announced that “Effective use of these vaccines during the coming winter and spring should insure the eradication of measles from the United States in 1967.”
When measles failed to be eradicated, public health experts decided that a 70% or 75% vaccination rate would secure herd immunity. When that proved wrong, the magic number rose to 80%, 83%, 85%, and then it became 90%, according to a 2001 Health Services Research report. Later health experts commonly cited 95%.
But that too was insufficient — measles outbreaks occur even when the vaccinated population exceeds 95%, leading some to say a 98% or 99% vaccination rate is needed to protect the remaining 1% or 2% of the herd. But even that may fall short, since outbreaks occur in fully vaccinated populations.
“The target would be to have 100% of the population vaccinated,” Dr. Gregory Taylor of the Public Health Agency of Canada recently told CBC, voicing an increasingly common perspective among public health professionals. At that point, the balance of the herd that would be protected through mass vaccination would be precisely 0.
But even vaccinating 100% of the population wouldn’t be enough, say scientists at the Mayo Clinic’s Vaccine Research Group, because the measles vaccine is a dud with some people, offering no protection at all, and its effectiveness wanes with others, even if they get boosters. According to Tetyana Obukhanych of Stanford University’s School of Medicine, the measles vaccine works as planned with only 25% of the population, leaving the majority of adults who have been vaccinated as children with little or no protection. Up to half of today’s cases involve adults.
Unlike childhood measles, adult measles is dangerous: 25% of cases require hospitalization. Measles is especially dangerous when contracted by expectant mothers — studies of hospital outcomes in Los Angeles and Houston found that most suffered serious complications, some died, and their babies often died in the womb.
The dangers extend to infants who, as USA Todaypoints out, are too young to be vaccinated. These entirely helpless members of “the herd” depend on antibodies inherited from their mothers. Yet previously vaccinated mothers have few antibodies to pass on, depriving their babies of protection. The only tried-and-true way for mothers to safeguard their infants — those most at risk of death from measles — remains nature’s way: by ensuring that the mother had previously contracted natural measles.
In fact, herd immunity — so elusive today — fully existed prior to the vaccine’s introduction. Virtually 100% of the population then contracted measles, typically as children, giving everyone lifelong immunity — and future mothers the means to protect their offspring. In mass vaccinating us, scientists of the 1960s didn’t realize that infecting us with the measles vaccine — a weak version of the natural measles virus — would give us a weak version of the defenses our bodies develop to the real thing.
Ironically, the Public Health Service considered measles generally benign in the pre-vaccine era. “Complications are infrequent and, with adequate medical care, fatality is rare…. Immunity following recovery is solid and lifelong in duration,” its chief of epidemiology, Alexander Langmuir, acknowledged in “Epidemiologic basis for eradication of measles in 1967.”
Why, then, did he decide to eradicate this generally harmless and beneficial disease? “To those who ask me, ‘Why do you wish to eradicate measles,’ I reply with the same answer that Hilary used when asked why he wished to climb Mt. Everest. He said, ‘Because it is there.’ To this may be added, ‘…and it can be done.’”
Herd immunity sounds fine in theory. But as Stanford’s Dr. Obukhanych concluded, “As with any garbage in-garbage out type of theory, the expectations of the herd-immunity theory are bound to fail in the real world.”
Lawrence Solomon is research director of Consumer Policy InstituteLawrenceSolomon@nextcity.com

Thursday, April 18, 2019

JAMA: Sanitation reduced mortality from infectious diseases


Tacit admission vaccines were not responsible for fall in disease and mortality rates. JAMA analysis clearly shows infectious diseases were in the decline before vaccines were introduced. Ascribes this to better living conditions, sanitation and medical care. Vaccines not mentioned.


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Wednesday, April 17, 2019

Mercury in Vaccines: History & Toxicity.

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Mercury in Vaccines: History & Toxicity.

Wasn’t mercury removed from vaccines? Is mercury in vaccines safe? These are questions that parents typically have when they begin to research vaccines.
“In some states, if a doctor takes that multi dose vial [flu vaccine] and drops it by mistake on the floor, and it breaks, he is required by law to evacuate the building and to bring in hazmat crews to clean it up before the building can be reoccupied.”
– RFK Jr, The Truth About Vaccines (Epidode 4)

History:

Mercury has been added to vaccines to preserve and prevent bacterial contamination of multi-dose shots (1,2). It is in vaccines in the form of a compound called thimerosal, and once injected into the body via intramuscular injection, it is rapidly broken down into thiosalicylate and ethylmercury (1). Ethylmercury is an organic toxic mercury compound and the focus of the debate over mercury in vaccines.
To re-state: Mercury in vaccines is in the form of a compound called thimerosal, which breaks down into ethylmercury.
In 1999, the American Academy of Pediatrics and the Public Health Service called for mercury to be taken out of vaccines because they discovered that the amount of mercury in certain vaccines which were given to infants far exceeded the EPA reference dose or exposure threshold for how much mercury that any individual should be exposed to in one day.
EPA Reference Dose = 0.1 mcg/kg/day (2,3,4).
Please note that the EPA reference dose is based on the compound methylmercury, not ethylmercury. The safety level of ethylmercury has never been scientifically determined, so federal agencies and the World Health Organization use methylmercury instead.
Though the thimerosal content of most vaccines was reduced to “trace amounts” (0.3-1.0mcg mercury per dose) or eliminated after 1999, unfortunately, the total amount of mercury a child from 6 months to 18 years of age will receive through the recommended CDC vaccination schedule, has actually increased since the AAP called for its removal (6). The reason for this was that in 2002, the CDC began recommending that pregnant women and infants as young as 6 months get annual flu shots at 1-2 doses each season.

Toxicity:

Question: Is the amount of mercury in flu and meningococcal vaccines toxic?
Vaccines which contain mercury are multi-dose influenza vaccines (though independent tests have suggested other vaccines may be contaminated).
Thimerosal-preserved “multi-dose” flu shots contain 25mcg mercury per dose. Surprisingly, even some vaccines labeled “preservative free” (“thimerosal free” or “no mercury”) – actually still contain trace amounts of mercury (2). Children from 6 months to 35 months of age receive a half-dose of the flu shot. Children three years of age or older, and adults, receive a full dose (cdc.gov). 21-36 million multi-dose flu shots have been produced for the US in the 2017-2018 season. 
In one multi-dose flu shot, a six-month-old receives 12.5mcg mercury (a half dose) which is over 16x the safe dose per the EPA (calculations below). A three-year-old receives 25mcg mercury via the flu shot, which is almost 18x the safe dose per the EPA. In one mutli-dose meningococcal vaccine, an 11-12 year-old receives over 6x the safe dose of mercury per the EPA. At 25mcg mercury per dose, an individual would have to weigh over 550lbs to approach the safe exposure level.
Therefore, the multi-dose flu shot is toxic to every person who receives it.
Calculations:
Average 6-month-old infant weight = 16.5lbs or 7.5kg
EPA reference dose or allowable limit for average 6-month-old:
7.5kg (0.1mcg/kg/day) = 0.75mcg/day
1/2 dose flu shot for children ages 6-35 months contains 12.5mcg mercury.
(12.5mcg) / (0.75mcg) = 16.67
The amount of mercury in your infant’s flu shot is over 16x the “safe” limit.

Methyl vs. Ethyl.
There are several different forms of mercury that we might encounter, and the type and route of exposure dictates its toxicity. The different routes of exposure are dermal, inhalation, ingestion, and injection. For example, the mercury in a thermometer is elemental mercury and won’t readily absorb through the skin. But if you were to burn that amount of mercury and inhale the vapors, it would be toxic to internal organs. That same amount of mercury in an organic form would quickly absorb through the skin, into your body, and reach your bloodstream. Organic mercury can pass through the placenta, exposing a developing fetus. Therefore, the form of mercury and route of exposure is important (7,8).
Methylmercury and ethylmercury are organic mercury compounds. Methylmercury has been extensively studied as a result of its accumulation in fish. The FDA even advises against eating too much of certain species in order to reduce our exposure. But when it comes to ethylmercury, the CDC claims that the amount of ethylmercury in vaccines is safe. The CDC website covers the topic of thimerosal (and ethylmercury) in vaccines, yet lists only one scientific study from the past decade. It’s stated that ethylmercury in vaccines is “cleared from the body more quickly than methylmercury, and is therefore less likely to cause any harm” (1). When the CDC makes this statement, what they’re referring to is that the amount of ethylmercury in the blood – after it’s injected through a vaccine – drops more quickly than methylmercury would (9). The problem with this statement is that they’re allowing readers to make the assumption that blood levels of ethylmercury drop because it’s being eliminated from the body, and no longer poses the threat of toxicity. Unfortunately, this is a half-truth. Blood levels drop because much of it is quickly going to the brain and other organs, where it gets converted to inorganic mercury, gets trapped, and becomes difficult to remove. It’s also been found that ethylmercury ends up depositing twice as much inorganic mercury into the brain than would an equal amount of methylmercury from consuming contaminated fish (10). Therefore, the CDC’s statement that ethylmercury is safer than methylmercury is misleading at best. A reference dose for ethylmercury based on injection, not ingestion, should be determined based on finding the NOEL (No Observed Effect Level), considering the fact that vaccination targets our most sensitive populations – infants, children, and the developing fetus (11).
Evidence of toxicity.
Contrary to what the CDC has to say about the safety of mercury or thimerosal in vaccines, over 165 scientific studies have been published on thimerosal and found it to be harmful (12). These studies have found that exposure to thimerosal has been associated with: neurotoxicity (13,14) and excitotoxic brain injury (15,16), lasting neuropathological changes (17), neurodevelopmental disorders and autism (14,16,18,19), immune system stimulation and inducing autoimmunity (20,21), kidney toxicity (22), modification of hormone levels (16), mitochondria toxicity (23), fetal toxicity (24,25,26), DNA damage (27), and more. When it comes to child development, thimerosal exposure has also been found to be a risk factor for tics, speech delay, language delay, neurodevelopmental delay, delayed startle response, decreased motor learning, and attention deficit disorder (12,25,26,28).

References:

1. CDC > Vaccine Safety > Thimerosal in Vaccines
http://www.cdc.gov/vaccinesafety/concerns/thimerosal/
2. FDA > Vaccines, Blood, & Biologics > Thimerosal in Vaccines
https://www.fda.gov/BiologicsBloodVaccines/SafetyAvailability/VaccineSafety/UCM096228
3. CDC > Morbidity and Mortality Weekly Report > Notice to Readers: Thimerosal in Vaccines: A Joint Statement of the American Academy of Pediatrics and the Public Health Service.
http://www.cdc.gov/mmwr/preview/mmwrhtml/mm4826a3.htm
4. EPA > National Center for Environmental Assessment > Risk Assessment > Reference Dose for Methylmercury
https://cfpub.epa.gov/ncea/risk/recordisplay.cfm?deid=20873&CFID=56744553&CFTOKEN=98271626
5. Medscape > Influenza virus vaccine trivalent (Rx) > Dosing & Uses > Pediatric
http://reference.medscape.com/drug/fluzone-afluria-influenza-virus-vaccine-trivalent-343153
6. “Ten Lies” told about Mercury in Vaccines
http://traceamounts.com/ten-lies-told-about-mercury-in-vaccines/
7. CDC > Environmental Health Document > Mercury > 2009
http://www.cdc.gov/biomonitoring/pdf/Mercury_FactSheet.pdf
8. Agency for Toxic Substances & Disease Registry (ATSDR) > Toxic Substances Portal – Mercury > Public Health Statement on Mercury, March 1999.
https://www.atsdr.cdc.gov/PHS/PHS.asp?id=112&tid=24
9. Neurotoxic character of thimerosal and the allometric extrapolation of adult clearance half-time to infants.
http://www.ncbi.nlm.nih.gov/pubmed/12884410
10. Comparison of blood and brain mercury levels in infant monkeys exposed to methylmercury or vaccines containing thimerosal.
http://www.ncbi.nlm.nih.gov/pubmed/16079072
11. EXTOXNET > Toxicology Information Brief > Dose-Response Relationships in Toxicology
http://pmep.cce.cornell.edu/profiles/extoxnet/TIB/dose-response.html
12. Methodological issues and evidence of malfeasance in research purporting to show thimerosal in vaccines is safe.
http://www.ncbi.nlm.nih.gov/pubmed/24995277
13. Integrating experimental (in vitro and in vivo) neurotoxicity studies of low-dose thimerosal relevant to vaccines.
http://www.ncbi.nlm.nih.gov/pubmed/21350943
14. Transcriptomic analyses of neurotoxic effects in mouse brain after intermittent neonatal administration of thimerosal.
http://www.ncbi.nlm.nih.gov/pubmed/24675092
15. Administration of thimerosal to infant rats increases overflow of glutamate and aspartate in the prefrontal cortex: protective role of dehydroepiandrosterone sulfate.
http://www.ncbi.nlm.nih.gov/pubmed/22015977
16. A possible central mechanism in autism spectrum disorders, part 2: immunoexcitotoxicity.
http://www.ncbi.nlm.nih.gov/pubmed/19161050
17. Lasting neuropathological changes in rat brain after intermittent neonatal administration of thimerosal.
http://www.ncbi.nlm.nih.gov/pubmed/21225508
18. A dose-response relationship between organic mercury exposure from thimerosal-containing vaccines and neurodevelopmental disorders.
http://www.ncbi.nlm.nih.gov/pubmed/25198681
19. The biological basis of autism spectrum disorders: Understanding causation and treatment by clinical geneticists.
http://www.ncbi.nlm.nih.gov/pubmed/20628444
20. Immunosuppressive and autoimmune effects of thimerosal in mice.
http://www.ncbi.nlm.nih.gov/pubmed/15808517
21. Ethylmercury and Hg2+ induce the formation of neutrophil extracellular traps (NETs) by human neutrophil granulocytes.
http://www.ncbi.nlm.nih.gov/pubmed/25701957
22. A systematic study of the disposition and metabolism of mercury species in mice after exposure to low levels of thimerosal (ethylmercury).
http://www.ncbi.nlm.nih.gov/pubmed/25173055
23. Thimerosal-Derived Ethylmercury Is a Mitochondrial Toxin in Human Astrocytes: Possible Role of Fenton Chemistry in the Oxidation and Breakage of mtDNA
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3395253/
24. The effect of ethylmercury on fetal development and some essential metals levels in fetuses and pregnant female rats.
http://www.ncbi.nlm.nih.gov/pubmed/24257943
25. Low-dose mercury exposure in early life: relevance of thimerosal to fetuses, newborns and infants.
http://www.ncbi.nlm.nih.gov/pubmed/23992327
26. Maternal thimerosal exposure results in aberrant cerebellar oxidative stress, thyroid hormone metabolism, and motor behavior in rat pups; sex- and strain-dependent effects.
http://www.ncbi.nlm.nih.gov/pubmed/22015705
27. Thimerosal Induces DNA Breaks, Caspase-3 Activation, Membrane Damage, and Cell Death in Cultured Human Neurons and Fibroblasts.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1892749/
28. Exposure to Mercury and Aluminum in Early Life: Developmental Vulnerability as a Modifying Factor in Neurologic and Immunologic Effects.             http://www.mdpi.com/1660-4601/12/2/1295/htm