I used to be pro vaccine. I know the feeling of thinking others were just plain crazy and wrong for not vaccinating their children and themselves. ‘Irresponsible!’ I said when pointing my finger. I’d use the same old arguments about polio and small pox and how vaccines saved us from all those horrible diseases and just swallowing and regurgitating the propaganda I was brought up with. It was only recently, in 2009 that I started questioning my long held beliefs and began digging in to the history, efficacy and safety of vaccines. I was appalled at what I found and the recklessness of those government health agencies entrusted with our health and our children’s safety, and angry with myself that I had put my family’s health at risk by blind faith in others when I was ultimately responsible for the medical decisions of my family.
When I began to put this article together I specifically chose not to include research from or links to websites that are considered untrustworthy by most pro-vaxxers, sites such as Natural News, Mercola, etc. even though I personally trust those sites and much more than I would WebMd and for good reason [a]. Instead I chose to employ basic logic and also incorporate independent and .gov scientific studies-mostly peer review, journals, news from mainstream sources (that pro-vaxxers love and totally trust) and articles that link to other .gov scientific studies, as well as government statistical resources. So, I started writing down questions and then looking for answers. I’ll admit, some of these questions have already been asked by others, but I just expanded upon it to form a helpful list.
I hope the following information helps you in your lifelong journey in search of health, vitality and truth in your own lives and your children’s lives.
1. Why are newborn babies vaccinated on their first day of life against a disease that is primarily transmitted sexually and by needles in drug users?
(Pregnant women are already tested for STD’s prior to birth so there’s no reason to give it to an infant). Interesting to note, of the few vaccines that still are given to infants and STILL has thimerosol in it is Hep B and DipTet (and Flu shot recommended to pregnant women). So, the claim that it has been removed from all vaccines is a lie and misdirection. If they give it to all newborns then ALL the newborns are getting that thimerosol (mercury derivative). “It was removed from many child vaccines in 2002 but remains in some vaccines (e.g., hepatitis B virus and)” Page 21.
2. Why are babies given vaccines to produce antibodies when they do not produce antibodies until after the age of 3 to 6 months?
They get the required antibodies from breastfeeding. These preliminary shots don’t work anyway according to leading immunologists (video) @30 sec mark. The real reason for these early jabs is ‘parent training.’ (ibid)
3. Why does the government tell parents to delay breast feeding and get more vaccines when breast feeding babies produce higher levels of antibodies?
http://www.ncbi.nlm.nih.gov/pubmed/20442687
http://naturalsociety.com/scientists-say-delay-breastfeeding-to-improve-vaccine-potency/
4. Why aren’t vaccine manufacturers held responsible when their product injures your child? Why would these companies need to be protected from the effects of such wonderful products?
(Look into Vaccine Injury Compensation Program .gov and VAERS)
The Supreme Court ruling exempting the vaccine manufacturers from all liability is done under the explicit understanding that they fall under the category “unavoidably unsafe products.”
http://www.supremecourt.gov/opinions/10pdf/09-152.pdf
http://www.hrsa.gov/vaccinecompensation/index.html
https://vaers.hhs.gov/index
5. Why have no double blind, placebo, randomized controlled trials been done on any vaccines?
This is standard with any other drug.
6. Why are we following the US vaccination schedule? We are the most vaccinated population on the planet with the highest rates of infant deaths/SIDS in the western world?http://www.washingtonpost.com/blogs/wonkblog/wp/2014/09/29/our-infant-mortality-rate-is-a-national-embarrassment/
http://sm.stanford.edu/archive/stanmed/2013fall/article2.html
7. Why are disease outbreaks occurring in populations with 90%+ vaccination rates? What about that ‘Herd Immunity’ guys?
http://aje.oxfordjournals.org/content/139/1/77.short
http://www.ncbi.nlm.nih.gov/pubmed/8483623
http://wwwnc.cdc.gov/eid/article/6/5/00-0512_article
8. Why are children vaccinated against these diseases still catching and spreading them?
http://www.ncbi.nlm.nih.gov/pubmed/24076325
http://www.thehealthyhomeeconomist.com/studies-show-measles-vaccine-spreads-virus/(see Johns Hopkins paper)
http://www.ncbi.nlm.nih.gov/pubmed/15954490
http://www.ncbi.nlm.nih.gov/pubmed/8483623
9. Why are we frightened of non-fatal illnesses that train a child’s immune system how to behave?
10. Why are vaccine manufacturers allowed to reduce antigens and insert cheap and toxic additives that aggravate the injection site?
11. Why do we need multi-dose vaccines if the number ONE priority of vaccine manufacturers is your child’s safety?
12. Why will no physician sign a written guarantee for a child’s safety prior to vaccinating them with products they insist you take and that they say are completely safe?
13. Why is there no outrage about the 3.1 billion dollars paid out in vaccine injury/death claims and yet they claim there is no correlation and they are perfectly safe?
http://www.hrsa.gov/vaccinecompensation/statisticsreport.pdf
14. Why don’t people recognize from history that the most widespread and lethal diseases in the last 200 years were reduced due to cleaner drinking water, improved sanitation, nutrition, less overcrowded areas and better living conditions?
Vaccines were introduced at points in time where every single disease was already declining, most almost completely gone. To give vaccines credit for global reductions in disease is like giving a band-aid credit for healing a wound that was already closing. Dr. Hans Rosling shows exactly how the health condition of nearly all countries of the world have improved with wealth, even 200 years ago, at the times where there no vaccines.
http://youtu.be/jbkSRLYSojo
https://childhealthsafety.wordpress.com/graphs/ (blog yes, but the links are amazing and historical data.)
http://www.columbia.edu/itc/hs/pubhealth/rosner/g8965/client_edit/readings/week_2/mckinlay.pdf
By the late 1950s, even before the introduction of measles vaccine, measles-related deaths and case fatality rates in the United States had decreased markedly, presumably as a result of improvement in health care and nutrition (Oxford Journal of Infectious Diseases).
15. Why do people keep parroting what they hear about ‘Herd Immunity?’
Herd immunity is a hilarious concept that assumes that 1) Vaccinated people are immune to the diseases for which they’ve been vaccinated, 2) Can not carry the diseases for which they are vaccinated/immune, 3) Because most of the people are vaccinated, other people around them can’t catch the disease. My favourite analogy for herd immunity is that if 95% of people in a building are wearing hard hats when the ceiling falls in, the 5% are protected. (credit Dr. Robert Murdoch)
16. Why are almost all pro-vaxxer adults we talk to not up to date on their adult vaccinations/boosters?
17. Why do pro-vaxxers ignore .gov scientific studies?
http://www.ncbi.nlm.nih.gov/pubmed/23902317
http://www.ncbi.nlm.nih.gov/pubmed/8483623
18. Why didn’t our government health agencies ever safety test thimerosol (a mercury derivative and adjuvant) since Lilly developed it in the 1920’s?
They used it in vaccines from 1930 to 2004! It still is in some vaccines such as the flu vaccine and others. Here is a 2 minute clip, from Congressional Hearings. The EPA themselves acknowledge the toxic effects of mercury:
http://www.epa.gov/hg/effects.htm
http://www.nytimes.com/2002/11/29/us/a-capitol-hill-mystery-who-aided-drug-maker.html
http://www.ncbi.nlm.nih.gov/pubmed/21350943
http://www.ncbi.nlm.nih.gov/pubmed/20803069
http://www.ncbi.nlm.nih.gov/pubmed/21549155
19. Why is it that only 40% of health professionals receive the flu shot each year? They must not believe in it.
http://abcnews.go.com/Health/ColdandFluNews/story?id=6418974&page=1
http://articles.mercola.com/sites/articles/archive/2000/07/30/doctors-death-part-one.aspx
http://www.worldlawdirect.com/article/749/medical-malpractice-basic-information.html
http://www.cnbc.com/id/102473744
http://www.nc.cdc.gov/eid/article/6/5/00-0512_article
With all the big pharma fraud cases, Merck, Glaxo Smith Kline, etc. and all the class action suits that come out several times a year for death/injury you see on tv commercials every week, combine that with the VICP and VAERS .gov statistics, and Iatrogenic Death statistics, why do people still trust their government health agencies when they say vaccines are perfectly safe? Having said that, why is government trusted at all since Democide statistics (death by government) show that nearly 300 million in this last century were killed by the state. Those are non-combatants.
University of Hawaii Study: https://www.hawaii.edu/powerkills/20TH.HTM
23. Why do they put aborted fetal cells in Vaccines? Also DNA from monkeys, chickens, human tumour cells?
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4202242/ (Go to Section 1.2. The Toxic Effects of Aluminum as a Vaccine Adjuvant. One of many aluminum studies)
When they put toxic ingredients in vaccines, food, drugs, water and our sky that have no long term safety studies by any government health agency, that is tantamount to human experimentation. It’s a crime under the Geneva Convention, Nuremberg Code and our own constitution, and against medical informed consent laws.
• Al Gore admits government experimentation
• Bill Clinton apology for secret human experimentation
• http://www.nbcnews.com/id/41811750/ns/health-health_care/t/ugly-past-us-human-experiments-uncovered/#.VQDefeEYGgg
• http://www.bibliotecapleyades.net/sociopolitica/esp_sociopol_depopu28.htm
• http://www.ncbi.nlm.nih.gov/pubmed/12656420 (government study admitting experimentation of large populaces with aerosol vaccines)
Here’s a few more studies:
• Abnormal measles-mumps-rubella antibodies and CNS autoimmunity in children with autism. http://www.ncbi.nlm.nih.gov/pubmed/12145534
“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.
….over 90% of MMR antibody-positive autistic sera were also positive for MBP autoantibodies, suggesting a strong association between MMR and CNS autoimmunity in autism. 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.”
• Serological association of measles virus and human herpes virus-6
with brain auto-antibodies in autism. http://www.ncbi.nlm.nih.gov/pubmed/9756729
This study is the first to report an association between virus serology and brain auto antibody in autism; it supports the hypothesis that a virus-induced autoimmune response may play a causal role in autism.
• Hypothesis: conjugate vaccines may predispose children to autism spectrum disorders. http://www.ncbi.nlm.nih.gov/pubmed/21993250
“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 favoured early brain development over the need to protect infants and young children from capsular bacteria.”
• Effects of diphtheria-tetanus-pertussis or tetanus vaccination on allergies and allergy-related respiratory symptoms among children and adolescents in the United States.
http://www.ncbi.nlm.nih.gov/pubmed/10714532
“The odds of having a history of asthma was twice as great among vaccinated subjects than among unvaccinated subjects. The odds of having had any allergy-related respiratory symptom in the past 12 months was 63% greater among vaccinated subjects than unvaccinated subjects. The associations between vaccination and subsequent allergies and symptoms were greatest among children aged 5 through 10 years.”
• Neurological Complications of Pertussis Immunization
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2025848/#reference-sec
Review is made of 107 cases of neurological complications of pertussis inoculation reported in the literature. The early onset of neurological symptoms was characteristic, with changes of consciousness and convulsions as the most striking features. The question of aetiology is considered and contraindications are discussed….as is the grave danger of further inoculations when a previous one has produced any suggestion of a neurological reaction.
• Hepatitis B vaccination of male neonates and autism diagnosis, NHIS 1997-2002.
http://www.ncbi.nlm.nih.gov/pubmed/21058170
“Findings suggest that U.S. male neonates vaccinated with the hepatitis B vaccine prior to 1999 (from vaccination record) had a threefold higher risk for parental report of autism diagnosis compared to boys not vaccinated as neonates during that same time period. Nonwhite boys bore a greater risk.”
• Immunological findings in autism.
http://www.ncbi.nlm.nih.gov/pubmed/16512356
“The immunopathogenesis of autism is presented schematically in Fig. 1. Two main immune dysfunctions in autism are immune regulation involving pro-inflammatory cytokines and autoimmunity. Mercury and an infectious agent like the measles virus are currently two main candidate environmental triggers for immune dysfunction in autism.”
Aluminum Studies:
• Do aluminum vaccine adjuvants contribute to the rising prevalence of autism?
http://www.ncbi.nlm.nih.gov/pubmed/22099159
“Our results show that: (i) children from countries with the highest ASD prevalence appear to have the highest exposure to Al from vaccines; (ii) the increase in exposure to Al adjuvants significantly correlates with the increase in ASD prevalence in the United States observed over the last two decades; and (iii) a significant correlation exists between the amounts of Al administered to preschool children and the current prevalence of ASD in seven Western countries, particularly at 3-4 months of age.”
• Aluminum hydroxide injections lead to motor deficits and motor neuron degeneration.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2819810/?tool=pubmed
“…A second series of experiments was conducted on mice injected with six doses of aluminum hydroxide. Behavioural analyses in these mice revealed significant impairments in a number of motor functions as well as diminished spatial memory capacity.”
• Aluminum Vaccine Adjuvants: Are they Safe?
http://www.ncbi.nlm.nih.gov/pubmed/21568886
Experimental research, clearly shows that aluminum adjuvants have a potential to induce serious immunological disorders in humans. In particular, aluminum in adjuvant form carries a risk for autoimmunity, long-term brain inflammation and associated neurological complications and may thus have profound and widespread adverse health consequences. click for entire study
• Aluminum-Induced Entropy in Biological Systems: Implications for Neurological Disease.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4202242/
• Mechanisms of aluminum adjuvant toxicity and autoimmunity in pediatric populations.
http://www.ncbi.nlm.nih.gov/pubmed/22235057
• Aluminum adjuvant linked to Gulf War illness induces motor neuron death in mice.
http://www.ncbi.nlm.nih.gov/pubmed/17114826
The findings suggest a possible role for the aluminum adjuvant in some neurological features associated with GWI and possibly an additional role for the combination of adjuvants (Synergistic Toxicity).
• Aluminum in the central nervous system (CNS): toxicity in humans and animals, vaccine adjuvants, and autoimmunity.
http://www.ncbi.nlm.nih.gov/pubmed/23609067
• Biopersistence and brain translocation of aluminum adjuvants of vaccines.
http://www.ncbi.nlm.nih.gov/pubmed/25699008
“We previously showed that poorly biodegradable aluminum-coated particles injected into muscle are promptly phagocytosed in muscle and the draining lymph nodes, and can disseminate within phagocytic cells throughout the body and slowly accumulate in brain. This strongly suggests that long-term adjuvant biopersistence within phagocytic cells is a prerequisite for slow brain translocation and delayed neurotoxicity.”
• Autoimmune/inflammatory syndrome induced by adjuvants (Shoenfeld’s syndrome): clinical and immunological spectrum.
http://www.ncbi.nlm.nih.gov/pubmed/23557271
“The activation of the immune system by adjuvants, a desirable effect, could trigger manifestations of autoimmunity or autoimmune disease. Recently, a new syndrome was introduced, autoimmune/inflammatory syndrome induced by adjuvants (ASIA), that includes postvaccination phenomena, macrophagic myofasciitis, Gulf War syndrome and siliconosis. This syndrome is characterized by nonspecific and specific manifestations of autoimmune disease. The main substances associated with ASIA are squalene (Gulf War syndrome), aluminum hydroxide (postvaccination phenomena, macrophagic myofasciitis) and silicone with siliconosis. Mineral oil, guaiacol and iodine gadital are also associated with ASIA.”
• Long-term Persistence of Vaccine-Derived Aluminum Hydroxide is Associated with Chronic Cognitive Dysfunction.
http://www.sciencedirect.com/science/article/pii/S0162013409001895
• Long-term follow-up of cognitive dysfunction in patients with aluminum hydroxideinduced macrophagic myofasciitis (MMF).
http://www.sciencedirect.com/science/article/pii/S0162013411002194
Thimerosal studies:
• Integrating experimental (in vitro and in vivo) neurotoxicity studies of low-dose thimerosal relevant to vaccines.
http://www.ncbi.nlm.nih.gov/pubmed/21350943
There is a need to interpret neurotoxic studies to help deal with uncertainties surrounding pregnant mothers, newborns and young children who must receive repeated doses of Thimerosal-containing vaccines (TCVs).
Information extracted from studies indicates that: (a) activity of low doses of Thimerosal against isolated human and animal brain cells was found in all studies and is consistent with Hg neurotoxicity; (b) the neurotoxic effect of ethylmercury has not been studied with co-occurring adjuvant-Al in TCVs; (c) animal studies have shown that exposure to Thimerosal-Hg can lead to accumulation of inorganic Hg in brain, and that (d) doses relevant to TCV exposure possess the potential to affect human neuro-development.
• Neurodevelopmental disorders following thimerosal-containing childhood immunizations: a follow-up analysis.
http://www.ncbi.nlm.nih.gov/pubmed/15764492
“The present study provides additional epidemiological evidence supporting previous epidemiological, clinical and experimental evidence that administration of thimerosal-containing vaccines in the United States resulted in a significant number of children developing NDs.”
• Neonatal administration of thimerosal causes persistent changes in mu opioid receptors in the rat brain.
http://www.ncbi.nlm.nih.gov/pubmed/20803069
“These data document that exposure to thimerosal during early postnatal life produces lasting alterations in the densities of brain opioid receptors along with other neuropathological changes, which may disturb brain development.”
• Persistent behavioural impairments and alterations of brain dopamine system after early postnatal administration of thimerosal in rats.
http://www.ncbi.nlm.nih.gov/pubmed/21549155
“These data document that early postnatal THIM administration causes lasting neurobehavioral impairments and neurochemical alterations in the brain, dependent on dose and sex. If similar changes occur in THIM/mercurial-exposed children, they could contribute do neurodevelopmental disorders.”
• Maternal Thimerosal Exposure Results in Aberrant Cerebellar Oxidative Stress, Thyroid Hormone Metabolism, and Motor Behaviour in Rat Pups; Sex- and Strain-Dependent Effects.
http://www.ncbi.nlm.nih.gov/pubmed/22015705
“Thimerisol exposure also resulted in a significant increase in cerebellar levels of the oxidative stress marker 3-nitrotyrosine… This coincided with an increased (47.0%) expression of a gene negatively regulated by T3… Our data thus demonstrate a negative neurodevelopmental impact of perinatal thimerisol exposure.”
• 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
Thimerosal, a mercury-containing vaccine preservative, is a suspected factor in the etiology of neurodevelopmental disorders. We previously showed that its administration to infant rats causes behavioral, neurochemical and neuropathological abnormalities similar to those present in autism.
Flu Vaccine during Pregnancy:
• Influenza Vaccination during Pregnancy.
http://www.jpands.org/vol11no2/ayoub.pdf
The ACIP’s recommendation of influenza vaccination during pregnancy is not supported by citations in its own policy paper or in current medical literature. Considering the potential risks of maternal and fetal mercury exposure, the administration of Thimerosal during pregnancy is both unjustified and unwise. Also, take note of the 71 references at the end of this study.
91 Peer Review Studies on The Dangers of Vaccines:
http://adventuresinautism.blogspot.com/2007/06/no-evidence-of-any-link.html
• Methodological Issues and Evidence of Malfeasance in Research Purporting to Show Thimerosal in Vaccines Is Safe.
http://www.hindawi.com/journals/bmri/2014/247218/
• Research below represents under-reported, minimized and otherwise overlooked peer-reviewed data on adverse effects associated with vaccination.
http://www.greenmedinfo.com/guide/health-guide-vaccine-research
• Neurologic adverse events following vaccination.
http://www.rescuepost.com/files/prog-health-sci-2012-vol-2-no1-neurologic-adverse-events-vaccination.pdf
Why are most of the links broken? Very frustrating read.
Hey Katherine,
Try deleting your cache and cookies and refresh your browser – the links were recently fixed. They all work for me!
I'm afraid this is a classic case of a little bit of knowledge being dangerous. As someone educated in the sciences, I can tell you your understanding of how vaccines are developed and tested is lacking. I can also tell you that your interpretation of the data and information you are passing on is biased and, due to your lack of any real knowledge of the subject, it is dangerous to flaunt your opinion as fact.
An example is your highlighting of the lack of testing on pregnant women. This is because medicine and vaccines are not generally not tested on pregnant women as it may not be safe. Therefore, these treatments are not recommended for pregnant women, and these warnings are present on packaging as a precaution only, not because they are actually given to pregnant women.
Another point raised was that people receiving the vaccine for chicken pox shouldn't mix with immune compromised people. A vaccine is a weakened form of the disease, so of course you shouldn't spread it to other people. Only logical, right? But even without taking a vaccine you can be a disease carrier, so this really is a moot point.
I am not a fan, personally, of putting unnecessary chemicals in the body. I am a fan of preventing myself and my family from life threatening/debilitating diseases. Do not believe blindly. Do educate yourself, but not by reading a few factoids and thinking you have a PhD.
So are you saying its safe to administer a product to a pregnant woman that has never been tested on pregnant women? Currently, pregnant women are recommended to get the DTaP vaccine and Flu vaccine, none of which have been studied for safety for use during pregnancy and also since the years it has been recommended has no correlated with any less "outbreaks" or better fetal outcomes which the US ranks in at one of the lowest for compared to other developed countries with less aggressive vaccine use.
Great points Jessica 🙂
Jessica – The DTaP has been tested on pregnant women. It was not done before the vaccine's package insert was created and approved, but studies were done later.
Here's SEVENTY-SIX articles for you.
http://www.ncbi.nlm.nih.gov/pmc/?term=DTaP+safety+pregnancy
Sara, the post is TITLED '25 QUESTIONS.' As someone educated in reading comprehension, I can tell that you aren't interested in answering legitimate questions. You are simply attempting to force people to live by your beliefs without regards to their own personal safety.
actually, vaccines are being tested on pregnant women and i think its criminal: Maternal immunization in Argentina: A storyline from the prospective of a middle income country. (http://www.ncbi.nlm.nih.gov/pubmed/26277071)
I'm "old fashion" doctor who was tough in med school that pregnant women should have variate of goods, the food should be nutritionally dense and free of chemicals. and here we are: inject them with chemicals!
some doctors are saying that we need to protect their babies from pertussis, but i want to ask them: who created this problem? why 2 month old gets the pertussis?
we (doctors and big pharma) created this problem! we immunize kids and shift the disease burden to too young ( to young to be immunized) kids. also, they should be protected by maternal antibodies (from the milk), but we immunized mothers when they were 15 y.o. and by the time they are pregnant antibodies from the vaccination are gone. they are not protected, neither their babies! Epidemiologists were talking about it many ears ago. we just ignored their warnings. now we are trying to install " family vaccination "program… its just does not make any sense!
ups. correction: too young ( to young to be immunized) and injecting (inject them with chemicals!)
Not very good examples to support your rather blanket complaint. The point that you took issue with on a person's ability to shed virus and infect others demonstrates you don't understand the reference. The issue taken here deals with the faulty logic of herd immunity (specifically concerning the modern rendition). Under the logic of herd immunity as it's applied to artificial immunization, it's asserted that by being immunized, you can protect the smaller part of the population made up of people who cannot be immunized (the thicker the barrier, the less likely one is to come into contact with the infectious agents). As the author points out, most vaccines aren't even designed to keep you from being infected by, carry and even spread that pathogen to others. Thus, the herd immunity hypothesis fails.
Thanks Josh for your understanding 🙂
I'm a parent who is vaccine injured and I have family and friends that are vaccine injured also, I'm not sure the point in your comment except that I think you are saying that we as parents cannot have questions and we are incapable of understanding scientific studies that are meant for the layman and average person. I don't need a PhD to read a vaccine insert, studies, or to read up on vaccine injury and death statistics through VICP and VAERS .gov programs.
I don't believe I flaunted any opinion, in fact I backed up most (if not all) of my claims/questions with NIH or other studies. You say that medicines are not tested on pregnant women, but that isn't true, they have been experimenting on pregnant women, children, ..all of us since the 1930's because there were NO safety tests on thimerosal, or etHg and meHg in combination with Al (aluminum) for it's synergistic toxicological and neurological effects. Hearings on thimerosal (2 min): https://www.facebook.com/RageAgainstVaccines/videos/vb.341081422696435/511368319001077/?type=2&theater
Any live virus vaccines sheds, it's not a moot point, you can find this information from the CDC, the FDA, the EPA, there are NO studies saying that just because it's a weakened form of the disease that somehow it is less contagious, they DO shed to the unvaccinated. Any newly vaccinated child or adult should be quarantined. My question to you since you have also chosen to use some scientific language, do you have a PhD?
Further Sarah, the best way for you to prevent life threatening illnesses from affecting your family is to eat very well and take care of yourselves, that is the best way. Vaccines did not save us from any disease, and if you had read my article in full, you would have seen how that is documented and is the truth.
~Blessings
Sarah jones, are you aware that there has never been a blind trial of a vaccine?
Oh yes, they do give the vaccines to pregnant women. Pregnancy used to be a contraindication. My hairdresser's daughter-in-law "had to" get the flu vaccine while pregnant because she was a nurse. Her son has been plagued with the most horrific case of eczema since birth; he's now a toddler, with always a beet-read, splotchy face; he spent most of his babyhood with mittens on to keep him from scratching.
But Sarah, we fully understand WHY testing on pregnant women is not done for these vaccines, but they ARE RECOMMENDED FOR PREGNANT WOMEN. Every pregnant woman is told to get the flu and the DTap vaccine and the vast majority do as their doctor tells them, no questions asked. They most certainly are given to pregnant women DESPITE them not being tested b/c the testing would be "unsafe". Do you hear how crazy that is? It seems that you are the one lacking knowledge on that subject.
I think this article has a lot of potential but lacks organization. The first link was broken, for instance. I would like to see commentary too under each of the the questions, not just links.
Thanks!
I think LLF has fixed that.
I just mailt this article to a senator who's staff asked this evening
on FACEBOOK page of "NO FORCED VACCINATIONS "
the following
"URGENT CALL TO ACTION – District 46 Assemblymember request for information
#sb277 #cdcwhistleblower #parental rights ******URGENT Constituents of ASM NAZARIAN their
staff is asking for us to send over letters with articles /info that you want him to read TODAY !
I just spoke to Talene her email is [email protected] I hope he will read it thoroughly
This was the best I could send him such a brilliant piece of work 🙂 thanks Brian Rogers
Thank you, I'll be posting an article about Synergistic Toxicity and Vaccine Safety with lots of links real soon if LLF chooses to publish it. 🙂