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Its painful to bear views that make many think I’m an imbicile and dislike me. So please, if anybody has a rational argument why any of this is wrong, I beg to be enlightened. I’ve set up a diagram for the purpose that will support you to add your criticism exactly where it is pertinent. https://truthsift.com/graph/Are-Vaccines-Safe/406/0/-1/-1/0/0/0/0/0/0/0/0/0/0/0/0/0/0/0/0

(1) The National Academy’s Reviews Of Vaccine Safety
The Institute of Medicine of the National Academies has provided several multi-hundred page surveys studying the safety of vaccines, but rather than reassuring, these itemize some iatrogenic conditions being caused, and pronounce the scientific literature inadequate to say whether most others are. The 2011 Institute of Medicine (IOM) Review[1] looked at 146 vaccine-condition pairs for causality, reporting:

  • 14 for which the evidence is said to convincingly support causality, the vaccine is causing the condition.
  • 4 where the evidence is said to favor acceptance.
  • 5 where the evidence is said to favor rejection, including MMR causing autism.
  • 123 where the evidence is said insufficient to evaluate.

The 2003 IOM Review on multiple vaccines said[2]:
“The committee was unable to address the concern that repeated exposure of a susceptible child to multiple immunizations over the developmental period may also produce atypical or non-specific immune or nervous system injury that could lead to severe disability or death (Fisher, 2001). There are no epidemiological studies that address this.”
and:
“the committee concludes that the epidemiological and clinical evidence is inadequate to accept or reject a causal relationship between multiple immunization and an increased risk of allergic disease, particularly asthma.”

  • None of the IOM Safety Reviews[1][2][3][4] addressed the aluminum (for example whether the aluminum is causing autism), or mentioned contaminants, or discussed animal models although they had concluded as just quoted there is generally no epidemiological or clinical data worth preferring.

(2) The Aluminum.
Alum was added to vaccines back in the 1920’s, with no test of parenteral toxicity until recently[5], because it prods the immature immune system out of its normal operating range.[6] Maybe they figured aluminum is common in the environment, but injection bypasses half a dozen evolved sequential filters that normally keep it out of circulatory flow during development. Vaccines put hundreds of times as much aluminum into infants’ blood as they would otherwise get, and in an unnatural form that is hard for the body to remove.[7][8 (cfsec 4.2)][9]. The published empirical results indicate its highly toxic.

  • Bishop et al in NEJM 97 reported a Randomized Placebo Controlled(RPC) test on preemies.[10][11] Scaling the toxicity they measured to the 4000 mcg in the first six months projects the vaccine series’ aluminum as costing each recipient maybe 15 IQ points and bone density.[12]
  • Animal RPC experiments also show highly toxic[13][14][15][16]
  • The applicable epidemiology suggests its highly toxic.[8][18][19][20][21][22] Discussed more in point 8 below, basically every study that compares more to less finds less much better.
  • Numerous clinical publications, whole special issues, on ASIA (Autoimmune Syndrome Induced by Adjuvants)[23][24][25]
  • Any “placebo” controlled test I’ve ever found of an adjuvanted vaccine, the “placebo” contained an adjuvant.
  • Safety reviews ignore the issue. Search the pdfs. [1][2][3][4]
  • The FDA[26] cites a theory paper[27] that compares a published MRL based on dietary experiments in weaned rodents (thus completely uninformed about toxicity in early development) to a theoretical model of blood aluminum levels from the vaccines, and disdains all the above cited empirical evidence.

(3) The Safety Studies Ignore Confounding Patient Behavior
Since there are no Randomized Placebo Controlled (RPC) trials supporting vaccines, virtually all studies report on the association (or lack thereof) between vaccines and some iatrogenic condition. But parents who believe vaccines made their kids sick, stop vaccinating them, which systematically moves sick or vaccine damaged kids in the studies into the “low vaccine”, “low thimerisol”, or etc. bin. This invalidates most studies supporting safety (and the few remaining ones suck for other reasons). Numerous studies report incredible preventative effects for vaccines, presumably because of this corruption, like having more thimerisol or more MMR’s is strongly preventative of autism and other mental development issues[28][29][30], or like having more vaccines was strongly preventative of atopy, apparently even years before patients got the vaccines[31]. The fact this confounding factor is overlooked demonstrates extreme confirmation bias and is the defining factor of Cargo Cult Science according to R.P. Feynman.[32]

(4) The Animal Models
Animal models reliably and repeatably show in RPC tests (a) that vaccines at the wrong time in development damage the adult brain or behavior [33][34] and (b) that multiple vaccines cause autoimmune disease even in animals bred to be non-autoimmune[35][36]. The effects are said to be robust, and as we’ve already seen there isn’t good human data rebutting them.

(5) The Contaminants
Studies have repeatedly found contaminants such as viruses, retroviruses, circoviruses, and human DNA in vaccines seemingly whenever tested,
and I’ve found no reason to believe off the shelf vaccines are free[37][38][39][40][41]. Reported contaminants have included SV-40 in polio vaccines which were administered even though scientists knew the vaccines were contaminated and already had hunches and experiments indicating SV-40 causes cancer[41][42]. Chimpanzee Coryza Virus became known in humans as RSV and has killed many millions of infants and hospitalizes 100,000/yr in America today[43]. Contaminated polio vaccine is plausibly also the origin of HIV[44][41]. There are discovered viral contaminants in vaccines today[38][39], with unknown long term effects, as well as I expect many undiscovered contaminants.

(6) Studies Ask Whether Some One Vaccine Damages, and Thus Miss That Many Do.
Virtually every study not reporting damage compares kids who got numerous vaccines to kids who got numerous vaccines. Such studies wouldn’t show statistically significant results no matter how much damage the vaccines are doing, unless one vaccine or vector by itself is doing comparable or more damage than the rest put together. The studies more or less test the hypothesis one vaccine is invisibly damaging, the rest are fine, and the studies are all obscured in the presence of multiple problems, much less the kind of timing and interaction effects observed in animal models. The one study[45] often touted as proving “The Risk of Autism is Not Increased by ‘Too Many Vaccines Too Soon’”[46] in fact compares patients based on antigens, and since DTP had more than 3000 antigens and no other vaccine common among the study patients had more than a handful, effectively compared patients who’d had DTP and dozens of vaccines to patients who did not have DTP (many had DTaP instead) and dozens of vaccines. The only counterexamples to this I’ve found are contrived in bizarre ways to avoid reality, such as the study that withheld the 2 month vaccines till 3 months from a group of kids, and asked the mothers, who were terrified enough a bunch insisted on changing back to the early vaccination group, to record symptoms with no doctor even consulted, identifying the placebo effect as vaccine prevention of diseases. The authors wrote it would have been unethical to give a placebo at 2 months to the kids getting the vaccine at 3 months, in order to do the experiment blind, but apparently consider it ethical to inject dozens of vaccines into your kids with zero placebo controlled testing.[47] [48]

(7) The Extensive Evidence Indicating Flu Vaccines Damage Immune Systems, Particularly in Children.

  • RPC test reported child flu vaccine recipients getting 4 times the respiratory illnesses of placebo recipients[49]
  • Children seen at the Mayo Clinic 1996–2006 were 3 times as likely to be hospitalized if they had had a flu vaccine[50]
  • Prior receipt of 2008-09 TIV was associated with increased risk of medically attended pH1N1 illness during the spring–summer 2009 in Canada[51]
  • Multiple papers report flu vaccines damage CD8+ T Cells in both children and animal models[52][53][54]
  • Flu vaccine recipients’ blood produced less IFN-gamma in response to new flu than people not previously vaccinated[55].
  • The equation they use for flu vaccine “effectiveness” counts making recipients sick as effectiveness. Mathematically, if vaccine recipients get twice as many respiratory illnesses that counts the same as if they get half as many flu illnesses.[56][57] The published evidence of “effectiveness” is published evidence of collateral damage.

(8) The Epidemiological Studies That Aren’t Blatantly Confounded
All the credible ecological or epidemiological studies comparing people who got more vaccines to less indicate damage. For example,

  • a 1/1000 increase in Infant Mortality is associated with each 7 additional vaccines in a national series regressed over the developed nations [18].
  • An extra 680 ASD or Language impaired are associated with every 1% increase in compliance regressed over the 50 US states [19].
  • High correlation between and within nations of vaccine aluminum to autism.[8]
  • Two studies in Guinea-Bisseau that showed recipients of DTP died far more frequently than non-recipients, even though the recipients were from far more fortunate backgrounds[20][21].
  • Vaccine adverse event reports are far more likely to be fatal if they follow multiple vaccinations than two[58].
  • 1 in 10 girls is reported to make an ED visit within 42 days of receiving HPV vaccine[59][60].

Every empirical study I’ve read with a methodology that’s not clearly confounded consistently indicates vaccine damage.

(9) The Consistent Anecdotal and Informal Reports
Anecdotal and informal reports actually compare vaccinated and unvaccinated, unlike the contrived and confounded studies offered to support safety.

  • Virtually all the Amish who are autistic turn out to have been vaccinated, the large numbers of unvaccinated in certain communities having no ASD whatsoever.[61]
  • The Homestead Medical Practice in Chicago’s Dr. Mayer Eisenstein reports: ““My partners and I have over 35,000 patients who have never been vaccinated. You know how many cases of autism we have seen? ZERO, ZERO.” Also he reports virtually zero asthma.[61]
  • Southern religious homeschoolers were anecdotally reported to have very low vaccination rates, and similarly virtually no autism.[61]
  • An online survey of 13000 fully unvaccinated shows them to have less than a third of the prevalence of numerous conditions from allergies to skoliosis.[62](Figure 1.)
  • More than a thousand parents, some of them Doctors, have posted Youtube reports describing why they are confident they saw their child given autism by vaccines.[63]
    Figure 1: Online survey of 13,000 unvaccinated compared to peer-reviewed survey data of the German vaccinated population[62]. The peer-reviewed data shows the vaccinated population averaging better than one chronic ailment per person, the unvaccinated report less than a third of that. The unvaccinated survey is online, selection biased, and self-reported, but there is no trustworthy data rebutting it, and 10 reasons are given in the text to believe the unvaccinated may be much healthier.
    Figure 1: Online survey of 13,000 unvaccinated compared to peer-reviewed survey data of the German vaccinated population[62]. The peer-reviewed data shows the vaccinated population averaging better than one chronic ailment per person, the unvaccinated report less than a third of that. The unvaccinated survey is online, selection biased, and self-reported, but there is no trustworthy data rebutting it.

(10) The Authorities, Big Pharma, and Media Are Demonstrably Not Trustworthy.

  • All the above 9 points and more are readily observable, but you wouldn’t learn that from the media or in med school.
  • A Senior PhD CDC whistleblower has provided numerous documents and testified to congress about an explicit cover-up within CDC of a vaccine-autism connection,[64][65] and media whitewashed it.
  • The vaccine manufacturers are exempt from any liability for vaccine damage.
  • The same companies repeatedly plead guilty to marketing and safety violations and pay billions in fines.[66]
  • They pay vast sums to media and fund the medical schools and research and give boondoggles and perks and contracts to doctors and revolving door government officials.[67][68]
  • The authorities and big pharma never publicly commented while contaminated vaccines scientists expected to cause cancer and other dire problems were administered[41][42][43].
  • The way the authorities have averted their eyes from contrary results is again the defining factor of Cargo Cult Science[32].

To summarize 10 points in two: (A) the safety literature, wherever it doesn’t outright show vaccine damage, demonstrably is bollixed to where it doesn’t show much of anything. (B) Lots of peer reviewed publications cogently report lots of consistent damage that no published evidence rationally opposes, but are ignored by authorities and media.

The vaccine safety literature is laid out in considerable detail on this TruthSift diagram http://truthsift.com/search_view?topic=Are-Vaccines-Safe-?&id=406&nid=4083 where readers are invited to add more pertinent citations or arguments. Anybody who thinks I am confused on any point is invited to challenge any claim above and explain why[69]. Please feel free to ask your Pediatrician or other authority, and let me know what they say. I’ve submitted to 2 medical journals so far, but been unable to obtain a substantive review, a review citing any papers or making a case I’m wrong. As I receive no substantive rebuttal, it reaffirms what I have already concluded from extensive research, none exists.

If you’ve read the above, and are thinking: “you were right, I was deluded,” the next step is to ask yourself what else you may be deluded about, and what you can do about it. https://truthsift.com was designed to answer those questions.
If you think this post contains information that should be more widely known please share it.

References
[1] Adverse Effects of Vaccines: Evidence and Causality, Kathleen Stratton, Andrew Ford, Erin Rusch, and Ellen Wright Clayton, Editors; Committee to Review Adverse Effects of Vaccines; Institute of Medicine, The National Academies press 2011. 862pp.http://www.commed.vcu.edu/IntroPH/Communicable_Disease/2012/adverseffectsVaccines.pdf
[2] Immunization Safety Review: Multiple Immunizations and Immune Dysfunction Kathleen Stratton, Christopher B. Wilson and Marie C. McCormick, Editors, Immunization Safety Review Committee, Board on Health Promotion and Disease Prevention http://www.nap.edu/catalog/10306.html ISBN: 0−309−50866−5, 152 pages, 6 x 9, (2002) Institute of Medicine.
[3] Immunization Safety Review: Vaccines and Autism, Immunization Safety Review Committee, Institute of Medicine of the National Academies ISBN: 0−309−53275−2, 214 pages, 6 x 9, (2004) http://www.nap.edu/catalog/10997.html
[4] The Childhood Immunization Schedule and Safety: Stakeholder Concerns, Scientific Evidence, and Future Studies, Committee on the Assessment of Studies of Health Outcomes Related to the Recommended Childhood Immunization Schedule; Board on Population Health and Public Health Practice; Institute of Medicine ISBN 978−0−309−26702−1 230 pages (2013) http://www.nationalacademies.org/hmd/~/media/files/report%20files/2013/childhood-immunization-schedule/childhoodimmunizationscheduleandsafety_rb.pdf
[5] Conference report Workshop summary Aluminum in vaccines Vaccine 20 (2002) S1–S4 http://www.google.com/url?sa=t&rct=j&q=&esrc=s&source=web&cd=1&cad=rja&uact=8&ved=0CCoQFjAA&url=http%3A%2F%2Farchive.hhs.gov%2Fnvpo%2Fnvac%2Fdocuments%2FAluminumws.pdf&ei=nZQoU5eIIoX0oAT5pYGgCg&usg=AFQjCNG_Zx126W2-nIJIMyTvE9LZz47V1g&sig2=c8Nu9WKzK27SBfJENfQXMw&bvm=bv.62922401
[6] Neonatal and early life vaccinology. Siegrist CA. Vaccine. 2001 May 14;19(25-26):3331-46. http://www.ncbi.nlm.nih.gov/pubmed/11348697
[7] Infants’ exposure to aluminum from vaccines and breast milk during the first 6 months, Dórea JG, Marques RC, Journal of Exposure Science and Environmental Epidemiology Volume 20, Issue 7, November 2010, Pages 598-601 http://www.ncbi.nlm.nih.gov/pubmed/20010978
[8] Do aluminum vaccine adjuvants contribute to the rising prevalence of autism? Tomljenovic L, Shaw CA. J Inorg Biochem. 2011 Nov;105(11):1489-99 http://omsj.org/reports/tomljenovic%202011.pdf
[9] http://truthsift.com/search_view?topic=Are-Vaccines-Safe-?&id=406&nid=4083 See statement views for discussion and further citations
[10] Aluminum Neurotoxicity in Preterm Infants Receiving Intravenous-Feeding Solutions, Nicholas J. Bishop, M.D., Ruth Morley, M.B., B.Chir., J. Philip Day, Ph.D., and Alan Lucas, M.D. N Engl J Med 1997; 336:1557-1562May 29, 1997DOI: 10.1056/NEJM199705293362203 http://www.nejm.org/doi/full/10.1056/NEJM199705293362203#t=articleResults
[11] Aluminum exposure from parenteral nutrition in preterm infants: bone health at 15-year follow-up. Fewtrell MS, Bishop NJ, Edmonds CJ, Isaacs EB, Lucas A. http://www.ncbi.nlm.nih.gov/pubmed/19858156 Pediatrics. 2009 Nov;124(5):1372-9. doi: 10.1542/peds.2009-0783. Epub 2009 Oct 26. Erratum in Pediatrics. 2009 Dec;124(6):1709.
[12] http://truthsift.com/search_view?statement=Animal-Studies-report-results-tending-to-indicate-the-aluminum-is-toxic-in-the-quantities-administered-&id=406&nid=4133 See statement views for discussion and further citations
[13] Administration of aluminum to neonatal mice in vaccine-relevant amounts is associated with adverse long term neurological outcomes, C.A. Shaw, Y. Li , L. Tomljenovic, Journal of Inorganic Biochemistry, V 128, November 2013, Pages 237–244 http://www.sciencedirect.com/science/article/pii/S0162013413001773
[14] Slow CCL2-dependent translocation of biopersistent particles from muscle to brain, Zakir Khan, Christophe Combadière, François-Jérôme Authier, Valérie Itier, François Lux, Christopher Exley, Meriem Mahrouf-Yorgov, Xavier Decrouy, Philippe Moretto, Olivier Tillement, Romain K Gherardi BMC Medicine 201311:99 DOI: 10.1186÷1741−7015−11−99 http://bmcmedicine.biomedcentral.com/articles/10.1186/1741-7015-11-99
[15] http://truthsift.com/search_view?topic=Are-Vaccines-Safe-?&id=406 For discussion of other confirmatory citations
[16] Examination of the safety of pediatric vaccine schedules in a non-human primate model: assessments of neurodevelopment, learning, and social behavior. Curtis B, Liberato N, Rulien M, et al. 2015. Environ Health Perspect 123:579–589; http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4455585/
[18] Infant mortality rates regressed against number of vaccine doses routinely given: is there a biochemical or synergistic toxicity? Miller NZ, Goldman GS, Hum Exp Toxicol. 2011 Sep;30(9):1420-8. doi: 10.1177÷0960327111407644. Pub 2011 May 4. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170075/
[19] A positive association found between autism prevalence and childhood vaccination uptake across the U.S. population. Delong G. J Toxicol Environ Health A. 2011;74(14):903-16. http://www.ncbi.nlm.nih.gov/pubmed/21623535
[20] Routine vaccinations and child survival: follow up study in Guinea-Bissau, West Africa Commentary: an unexpected finding that needs confirmation or rejection, Ines Kristensen, Peter Aaby, Henrik Jensen, BMJ 2000; 321 dos: http://dx.doi.org/10.1136/bmj.321.7274.1435
[21] Oral polio vaccination and low case fatality at the paediatric ward in Bissau, Guinea-Bissau. Aaby P, Rodrigues A, Biai S, et al ‚Vaccine. 2004 Aug 13;22(23-24):3014-7. http://www.ncbi.nlm.nih.gov/pubmed/15297050
[22] http://truthsift.com/search_view?id=406&nid=4144 See for further discussion and citations
[23] Special Issue ASIA – Autoimmune Syndrome Induced by Adjuvants, Lupus February 2012; 21 (2) http://lup.sagepub.com/content/21/2.toc
[24] Biopersistence and brain translocation of aluminum adjuvants of vaccines Front. Neurol., 05 February 2015 |http://dx.doi.org/10.3389/fneur.2015.00004
http://journal.frontiersin.org/article/10.3389/fneur.2015.00004/full
[25] Chronic fatigue syndrome and fibromyalgia following immunization with the hepatitis B vaccine: another angle of the ‘autoimmune (auto-inflammatory) syndrome induced by adjuvants’ (ASIA). Agmon-Levin N1, Zafrir Y, Kivity S, Balofsky A, Amital H, Shoenfeld Y. Immunol Res. 2014 Dec;60(2–3):376–83. doi: 10.1007/s12026-014‑8604-2.
[26] Study Reports Aluminum in Vaccines Poses Extremely Low Risk to Infants (2015−2016) http://www.fda.gov/BiologicsBloodVaccines/ScienceResearch/ucm284520.htm
[27] Updated aluminum pharmacokinetics following infant exposures through diet and vaccination, Mitkus RJ, King DB, Hess MA, Forshee RA, Walderhaug MO., Vaccine 29(51) 9538-43 2011. http://www.ncbi.nlm.nih.gov/pubmed/22001122
[28] Thimerosal Exposure in Infants and Developmental Disorders: A Retrospective Cohort Study in the United Kingdom Does Not Support a Causal Association, Nick Andrews; Elizabeth Miller; Andrew Grant et al, Pediatrics September 2004, VOLUME 114 / ISSUE 3 http://pediatrics.aappublications.org/content/114/3/584.full-text.pdf
[29] Prenatal and Infant Exposure to Thimerosal From Vaccines and Immunoglobulins and Risk of Autism, Cristofer S. Price, William W. Thompson, Barbara Goodson,et al, Pediatrics October 2010, VOLUME 126 / ISSUE 4 http://pediatrics.aappublications.org/content/126/4/656
[30] Autism Occurrence by MMR Vaccine Status Among US Children With Older Siblings With and Without Autism, Anjali Jain; Jaclyn Marshall; Ami Buikema; et al. JAMA. 2015;313(15):1534-1540. doi:10.1001/jama.2015.3077. http://jama.jamanetwork.com/article.aspx?articleid=2275444
[31] Transient suppression of atopy in early childhood is associated with high vaccination coverage, Gruber, C., S. Illi, S. Lau, R. Nickel, J. Forster, W. Kamin, C.P. Bauer, V. Wahn, U. Wahn, and the MAS-90 Study Group. 2003. . Pediatrics 111(3):e282-e288. http://pediatrics.aappublications.org/content/111/3/e282
[32] CARGO CULT SCIENCE (adapted from Caltech Commencement Address 1974), Richard P Feynman https://www.lhup.edu/~DSIMANEK/cargocul.htm
[33] Peripheral immune challenge with viral mimic during early postnatal period robustly enhances anxiety-like behavior in young adult rats.
Konat GW, Lally BE, Toth AA, Salm AK.Metab Brain Dis. 2011 Sep;26(3):237-40. doi: 10.1007/s11011-011-9244-z http://www.ncbi.nlm.nih.gov/pubmed/21643765
[34] Postnatal Inflammation Increases Seizure Susceptibility in Adult Rats, Michael A. Galic, Kiarash Riazi, James G. Heida, et al, The Journal of Neuroscience, 2 July 2008, 28(27): 6904-6913; doi: 10.1523/JNEUROSCI.1901-08.2008 http://www.jneurosci.org/content/28/27/6904.full
[35] Vaccine model of antiphospholipid syndrome induced by tetanus vaccine, L Dimitrijevi, I ivkovi, M Stojanovi, V Petrui, S ivanevi-Simonovi dos: 10.1177÷0961203311429816 Lupus February 2012 vol. 21 no. 2 195-202 http://lup.sagepub.com/content/21/2/195.abstract
[36] Self-Organized Criticality Theory of Autoimmunity, Ken Tsumiyama, Yumi Miyazaki, Shunichi Shiozawa 2009 DOI: 10.1371/journal.pone.0008382
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0008382
[37] Some oral poliovirus vaccines were contaminated with infectious SV40 after 1961. Cutrone R, Lednicky J, Dunn G, et al. Cancer Res. 2005 Nov
15;65(22):10273-9. http://www.ncbi.nlm.nih.gov/pubmed/16288015
[38] Viral Nucleic Acids in Live-Attenuated Vaccines: Detection of Minority Variants and an Adventitious Virus, J. G. Victoria, C. Wang, M. S. Jones,et al. J. Virol. June 2010 vol. 84 no. 12 6033-6040 http://jvi.asm.org/content/84/12/6033
[39] Viruses and Virus Nucleic Acid Contaminate Many Vaccines: Risks of cancer and creation of new pathogens should not be underplayed by regulators Prof. Joe Cummins http://www.i-sis.org.uk/Viruses_and_Virus_Nucleic_Acid_Contaminate_Vaccines.php
[40] Impact of environmental factors on the prevalence of autistic disorder after 1979, Theresa A. Deisher, Ngoc V. Doan, Angelica Omaiye, et al. Journal of Public Health and Epidemiology Vol. 6(9), pp. 271-284, 2014 DOI: 10.5897/JPHE2014.0649 http://soundchoice.org/scpiJournalPubHealthEpidem092014.pdf
[41] https://www.youtube.com/watch?v=13QiSV_lrDQ Dr. Maurice Hillman, The Merck Chief Scientist, discusses how the polio vaccine was administered although they knew it was contaminated with SV-40, which they strongly believed caused cancer. According to the tape, the monkeys from which the vaccine was being grown, were being kept in epidemic conditions crowded into cages, so they were all sick with a variety of viruses which then contaminated the vaccine stock. As Hillman discusses, SIV could very well have entered the human population this way as well.
[42] Association between simian virus 40 and non-Hodgkin lymphoma. Vilchez RA, Madden CR, Kozinetz CA, et al. Lancet. 2002 Mar 9;359(9309):817-23. http://www.ncbi.nlm.nih.gov/pubmed/11897278
[43] Polio eradication: a complex end game, Viera Scheibner, BMJ 2012;344:e2398 http://www.bmj.com/content/344/bmj.e2398/rapid-responses
[44] Polio vaccines and the origin of AIDS: some key writings, http://www.uow.edu.au/~bmartin/dissent/documents/AIDS/
[45] Increasing Exposure to Antibody-Stimulating Proteins and Polysaccharides in Vaccines Is Not Associated with Risk of Autism, Frank DeStefano, MD,MPH, Cristofer S. Price, ScM, Eric S. Weintraub, MPH DOI: http://dx.doi.org/10.1016/j.jpeds.2013.02.001
[46] The Risk of Autism is Not Increased by “Too Many Vaccines Too Soon”, Editorial of The Journal of Pediatrics http://www.jpeds.com/content/JPEDSDeStefano
[47] General Non-specific Morbidity is Reduced After Vaccination Within the Third Month of Life – the Greifswald Study, S. Otto, B. Mahner, I. Kadow, J. F. Beck, S. K.W. Wiersbitzky and R. Bruns, Journal of Infection (2000) 41, 172–175 doi: 10.1053/jinf.2000.0718, available online at http://www.idealibrary.com
[48] http://truthsift.com/node_info?nid=5340&superNode=No&subNode=No&isFlagged=No&probability=1&likelihoodEstimateT=0.5&likelihoodEstimateF=0.5&likelihoodEstimate=0.5&rating=TE
[49] Increased risk of noninfluenza respiratory virus infections associated with receipt of inactivated influenza vaccine. Cowling BJ, Fang VJ, Nishiura H, Chan KH, Ng S, Ip DK, Chiu SS, Leung GM, Peiris JS. Clin Infect Dis. 2012 Jun;54(12):1778-83. doi: 10.1093/cid/cis307. Epub 2012 Mar 15. http://www.ncbi.nlm.nih.gov/pubmed/22423139
[50] Effectiveness of trivalent inactivated influenza vaccine in influenza-related hospitalization in children: a case-control study. Joshi AY, Iyer VN, Hartz MF, Patel AM, Li JT. Allergy Asthma Proc. 2012 Mar-Apr;33(2):e23-7. doi: 10.2500/aap.2012.33.3513. http://www.ncbi.nlm.nih.gov/pubmed/22525386
[51] Association between the 2008-09 Seasonal Influenza Vaccine and Pandemic H1N1 Illness during Spring–Summer 2009: Four Observational Studies from Canada, Danuta M. Skowronski , Gaston De Serres, Natasha S. Crowcroft, et al.PLOS(2010), http://dx.doi.org/10.1371/journal.pmed.1000258
[52] Vaccination with whole inactivated virus vaccine affects the induction of heterosubtypic immunity against influenza virus A/H5N1 and immunodominance of virus-specific CD8+ T-cell responses in mice. Bodewes R, Kreijtz JH, Hillaire ML, Geelhoed-Mieras MM, Fouchier RA, Osterhaus AD, Rimmelzwaan GF. , J Gen Virol. 2010 Jul;91(Pt 7):1743-53. doi: 10.1099/vir.0.020784-0. Epub 2010 Mar 24. http://www.ncbi.nlm.nih.gov/pubmed/20335492
[53] Vaccination against human influenza A/H3N2 virus prevents the induction of heterosubtypic immunity against lethal infection with avian influenza A/H5N1 virus. Bodewes R, Kreijtz JH, Baas C, Geelhoed-Mieras MM, de Mutsert G, van Amerongen G, van den Brand JM, Fouchier RA, Osterhaus AD, Rimmelzwaan GF. PLoS One. 2009;4(5):e5538. doi: 10.1371/journal.pone.0005538. Epub 2009 May14. http://www.ncbi.nlm.nih.gov/pubmed/19440239
[54] Annual vaccination against influenza virus hampers development of virus-specific CD8+ T cell immunity in children. Bodewes R, Fraaij PL, Geelhoed-Mieras MM, van Baalen CA, Tiddens HA, van Rossum AM, van der Klis FR, Fouchier RA, Osterhaus AD, Rimmelzwaan GF., J Virol. 2011 Nov;85(22):11995-2000. doi: 10.1128/JVI.05213-11.Epub 2011 Aug 31. http://www.ncbi.nlm.nih.gov/pubmed/21880755
[55] Difference in immune response in vaccinated and unvaccinated Swedish individuals after the 2009 influenza pandemic, Isabelle Magalhaes Mikael Eriksson, Charlotte Linde, Rashid Muhammad, Lalit Rane, Aditya Ambati, Rebecca Axelsson-Robertson, Bahareh Khalaj, Nancy Alvarez-Corrales, Giulia Lapini, Emanuele Montomoli, Annika Linde, Nancy L Pedersen,3 and Markus Maeurer BMC Infect Dis. 2014; 14: 319.Published online 2014 Jun 11. doi: 10.1186÷1471−2334−14−319 PMCID: PMC4067073 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4067073/
[56] “Vaccine effectiveness was estimated as 100% x (1 — odds ratio [ratio of odds of being vaccinated among outpatients with influenza-positive test results to the odds of being vaccinated among outpatients with influenza-negative test results])”, Center for Disease Control, Early Estimates of Seasonal Influenza Vaccine Effectiveness — United States, January 2015 Weekly January 16, 2015 / 64(01);10-15 http://www.cdc.gov/mmwr/preview/mmwrhtml/mm6401a4.htm
[57] http://truthsift.com/node_info?nid=2823&superNode=No&subNode=No&isFlagged=No&probability=1&likelihoodEstimateT=0.5&likelihoodEstimateF=0.5&likelihoodEstimate=0.5&rating=TE for more discussion
[58] Combining Childhood Vaccines at One Visit Is Not Safe, Neil Z. Miller, Journal of American Physicians and Surgeons Volume 21 Number 2 Summer 2016 http://www.jpands.org/vol21no2/miller.pdf
[59] Adverse events following HPV vaccination, Alberta 2006–2014, Xianfang C. Liu, , Christopher A. Bell, , Kimberley A. Simmonds, , Lawrence W. Svensona, Margaret L. Russell, Vaccine Volume 34, Issue 15, 4 April 2016, Pages 1800–1805 http://www.sciencedirect.com/science/article/pii/S0264410X16002036
[60] For further data analysis and discussion see http://truthsift.com/node_info?nid=5196&superNode=No&subNode=No&isFlagged=No&probability=1&likelihoodEstimateT=0.5&likelihoodEstimateF=0.5&likelihoodEstimate=0.5&rating=TE
[61] http://www.vaccinationcouncil.org/2009/05/22/a-pretty-big-secret/
[62] http://www.vaccineinjury.info/survey/results-unvaccinated/results-illnesses.html
[63] https://www.youtube.com/results?search_query=%23hearthiswell
[64] http://www.morganverkamp.com/august-27-2014-press-release-statement-of-william-w-thompson-ph-d-regarding-the-2004-article-examining-the-possibility-of-a-relationship-between-mmr-vaccine-and-autism/
[65] https://sharylattkisson.com/cdc-scientist-we-scheduled-meeting-to-destroy-vaccine-autism-study-documents/
[66] http://projects.propublica.org/graphics/bigpharma
[67] http://www.washingtonsblog.com/2015/06/editors-in-chief-of-worlds-most-prestigious-medical-journals-much-of-the-scientific-literature-perhaps-half-may-simply-be-untrue-it-is-simply-no-longer-poss.html
[68] http://www.nybooks.com/articles/2009/01/15/drug-companies-doctorsa-story-of-corruption/
[69] http://truthsift.com/search_view?topic=Are-Vaccines-Safe-?&id=406

It is good to see production costs v. value add return comparisons with drugs as part of an ongoing drive to create drugs cheaper and making them cheaper to patients. However, lets do not sacrifice quality (especially in areas like cancer, MS, etc.) for costs of development/ cost savings. Value of life is priceless.


Defining the value of a drug in relation to its cost and benefit is an emerging theme in cancer care but remains untested.

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A new UK study has identified a gene signature that predicts poor survival from ovarian cancer. The study also identified genes which help the cancer develop resistance to chemotherapy — offering a new route to help tackle the disease.

The study, published in the International Journal of Cancer, examined the role of HOX genes in ovarian cancer resistance and whether a drug known as HXR9 which targets HOX, could help prevent the resistance from developing.

The HOX gene family enables the remarkably rapid cell division seen in growing embryos. Most of these genes are switched off in adults, but previous research has shown that in several cancers, including ovarian cancer, HOX genes are switched back on, helping the cancer cells to proliferate and survive.

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Glad they are doing something on this because my biggest concern on biometrics and systems storing other people’s DNA/ bio information is criminals hacking in and collecting bio information on people and reselling it on the Dark Web. With this type of information; criminals can do many interesting things especially if they have access to a gene editing kit, or 3D printers, etc. We have seen how easy it is to create gene editing kits and selling them on the net for $129 each. And, how 3D printers can replicate synthetic skin, contacts mimicking eye structures, etc. So, criminals can do some amazing things once they have access to anyone’s biometrics information.


A biometric system to verify travelers exiting the country could be in effect as soon as 2018.

By Kayla Nick-Kearney.

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Excellent start in using GPU for mapping and predictive analysis on brain functioning and reactions; definitely should prove interesting to medical & tech researchers and engineers across the board should find this interesting.


MIS Asia offers Information Technology strategy insight for senior IT management — resources to understand and leverage information technology from a business leadership perspective.

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Results from quantitative MRI and neuropsychological testing show unprecedented improvements in ten patients with early Alzheimer’s disease (AD) or its precursors following treatment with a programmatic and personalized therapy. Results from an approach dubbed metabolic enhancement for neurodegeneration are now available online in the journal Aging.

The study, which comes jointly from the Buck Institute for Research on Aging and the UCLA Easton Laboratories for Neurodegenerative Disease Research, is the first to objectively show that memory loss in patients can be reversed, and improvement sustained, using a complex, 36-point therapeutic personalized program that involves comprehensive changes in diet, brain stimulation, exercise, optimization of sleep, specific pharmaceuticals and vitamins, and multiple additional steps that affect brain chemistry.

“All of these patients had either well-defined mild cognitive impairment (MCI), subjective cognitive impairment (SCI) or had been diagnosed with AD before beginning the program,” said author Dale Bredesen, MD, a professor at the Buck Institute and professor at the Easton Laboratories for Neurodegenerative Disease Research at UCLA, who noted that patients who had had to discontinue work were able to return to work and those struggling at their jobs were able to improve their performance. “Follow up testing showed some of the patients going from abnormal to normal.”

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Hawking repeats Zoltan Istvan’s worries:

“Governments seem to be engaged in an AI arms race, designing planes and weapons with intelligent technologies,” Hawking told veteran interviewer Larry King. “The funding for projects directly beneficial to the human race, such as improved medical screening, seems a somewhat lower priority.”


British physicist Stephen Hawking sees signs that the applications for artificial intelligence are already going down the wrong track.

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Definitely been seeing great research and success in Biocomputing; why I have been looking more and more in this area of the industry. Bio/ medical technology is our ultimate future state for singularity. It is the key that will help improve the enhancements we need to defeat cancer, aging, intelligence enhance, etc. as we have already seen the early hints already of what it can do for people, machines and data, the environment and resources. However, a word of caution, DNA ownership and security. We will need proper governance and oversight in this space.


undefined © iStock/ Getty Images undefined How much storage do you have around the house? A few terabyte hard drives? What about USB sticks and old SATA drives? Humanity uses a staggering amount of storage, and our needs are only expanding as we build data centers, better cameras, and all sorts of other data-heavy gizmos. It’s a problem scientists from companies like IBM, Intel, and Microsoft are trying to solve, and the solution might be in our DNA.

A recent Spectrum article takes a look at the quest to unlock the storage potential of human DNA. DNA molecules are the building blocks of life, piecing our genetic information into living forms. The theory is that we can convert digital files into biological material by translating it from binary code into genetic code. That’s right: the future of storage could be test tubes.

In April, representatives from IBM, Intel, Microsoft, and Twist Bioscience met with computer scientists and geneticists for a closed door session to discuss the issue. The event was cosponsored by the U.S. Intelligence Advanced Research Projects Activity (IARPA), who reportedly may be interested in helping fund a “DNA hard drive.”

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A “huge” stash of helium discovered in East Africa could ease a decades-long shortage of the rare and valuable gas.

Researchers in the United Kingdom and Norway say the newly discovered helium gas field, found in the East African Rift Valley region of Tanzania, has the potential to ease a critical global shortage of helium, a gas that is vital to many high-tech applications, such as the magnetic resonance imaging (MRI) scanners used in many hospitals.

The researchers say the discovery is the result of a new approach to searching for helium that combines prospecting methods from the oil industry with scientific research that reveals the role of volcanic heat in the production of pockets of helium gas. [Elementary, My Dear: 8 Elements You Never Heard Of].

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In new experiments using bird embryos, U.S. scientists have successfully converted cells of the lower-body region into facial tissue that makes cartilage.

The researchers of the California Institute of Technology discovered a “gene circuit”, composed of just three genes, that can alter the fate of cells destined for the lower bodies of birds, turning them instead into cells that produce cartilage and bones in the head.

Reporting in the latest issue of the journal Science, published on June 24, the researchers say the results could eventually lead to therapies for conditions where facial bone or cartilage is lost. For example, cartilage destroyed in the nose due to cancer is particularly hard to replace.

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