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Toxic MMR - vaccination forced on UK toddlers = autism?
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outsider
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PostPosted: Sat Mar 09, 2019 1:14 am    Post subject: Reply with quote

'DISTURBING reality: Only about 1% of vaccine injury cases are ever reported':
https://naturalnews.com/2019-02-20-only-about-1-of-vaccine-injury-case s-are-reported.html#
'Children vaccinated in accordance with CDC guidelines are exposed to 25 TIMES the amount of aluminum necessary to cause autism
Another often-overlooked factor in the vaccine debate is the sheer amount of chemicals that children are exposed to when they receive the dozens of vaccines on the official CDC schedule within the first few years of their lives.

A mere 25 micrograms (mcg) of aluminum for adults, and 10 mcg of aluminum for children, is considered the maximum threshold after which physical damage, and possibly even death, can occur. And yet, children vaccinated in accordance with CDC guidelines receive at least 250 mcg of aluminum in their bodies – or 25 times the “safe” level for children.

“Injecting neurotoxins into the human body is NOT ‘safe’ or ‘effective.’ It’s just wrong,” Schmidt concludes. “We, as concerned citizens, must educate ourselves and (always) make informed decisions about our healthcare......”

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outsider
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PostPosted: Sat Mar 09, 2019 1:37 am    Post subject: Reply with quote

'Vaccine injury payouts exceed $4 billion, yet most people remain uninformed about the risks linked to vaccinations':
https://www.naturalhealth365.com/vaccine-injury-2788.html

'...Payouts from a vaccine injury compensation fund have now exceeded $4 billion, and this reflects the government’s own assessment that just one percent of all vaccine injuries are reported....'
'...The reason why vaccines cause problems like, autism and autoimmune disorders
According to ‘conventional wisdom,’ adults should not receive more than 25 micrograms (mcg) of aluminum at one time; infants or children – no more than 10 micrograms. Yet, while adhering to a typical vaccine schedule, small children will be exposed to at least 250 mcg on their first day of life! (plus, much more before the age of 3)

In addition to neurological problems, autoimmune disorders and autism, many vaccine side effects include: chronic aches and pain, paralysis and even sudden premature death. Regulatory agencies and the drug companies themselves need to start focusing on better ways to protect our society from disease.

Injecting neurotoxins into the human body is NOT ‘safe’ or ‘effective.’ It’s just wrong....'

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outsider
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PostPosted: Tue Mar 19, 2019 2:09 am    Post subject: Reply with quote

'‘I will never get over feeling I killed my son’: Anti-vaccination activists refuse to be 'silenced':
https://www.rt.com/news/454052-vaccination-activists-side-effects-/
'....Vaccination Liberation, an activist group from Idaho, believes that as the battle intensifies, this will become a civil rights issue, particularly as ever more hardline measures are handed down from above.

"The presumed and unconstitutional authority of legislators to mandate vaccines, a form of medical rape, has not abated in the face of two generations of extremely unhealthy children and adults," says its founder, Ingri Cassel.

And having spent years fighting their cause on the margins, they are not about to stop now.

"They are trying to suppress the wrong group of people. Parents who have lost their children are the last group you want to silence. They will only get louder and fight harder," says Cordingley.'

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PostPosted: Thu Apr 25, 2019 8:05 pm    Post subject: Reply with quote

Bump!

TonyGosling wrote:
Infanrix hexa and sudden death: a review of the periodic safety update reports submitted to the European Medicines Agency.
Puliyel J, et al. Indian J Med Ethics. 2018 Jan-Mar.
https://www.ncbi.nlm.nih.gov/m/pubmed/28918379/

Abstract
There have been a number of spontaneous reports of sudden unexpected death soon after the administration of Infanrix hexa (combined diphtheria, tetanus, acellular pertussis, hepatitis B, inactivated poliomyelitis and Haemophilus influenza type B vaccine). The manufacturer, GlaxoSmithKline (GSK), submits confidential periodic safety update reports (PSURs) on Infanrix hexa to the European Medicines Agency (EMA). The latest is the PSUR 19. Each PSUR contains an analysis of observed/expected sudden deaths, which shows that the number of observed deaths soon after immunisation is lower than that expected by chance. This commentary focuses on that aspect of the PSUR which has a bearing on policy decisions. We analysed the data provided in the PSURs. It is apparent that the deaths acknowledged in the PSUR 16 were deleted from the PSUR 19. The number of observed deaths soon after vaccination among children older than one year was significantly higher than that expected by chance once the deleted deaths were restored and included in the analysis. The manufacturer must explain the figures that have been submitted to the regulatory authorities. The procedures undertaken by the EMA to evaluate the manufacturer's claims in the PSUR need to be reviewed. The Drugs Controller General of India nearly automatically accepts drugs and vaccines approved by the EMA. There is a need to reappraise the reliance on due diligence by the EMA.#


https://www.ncbi.nlm.nih.gov/m/pubmed/28918379/

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outsider
Trustworthy Freedom Fighter
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Joined: 30 Jul 2006
Posts: 5868
Location: East London

PostPosted: Sat Apr 27, 2019 11:47 pm    Post subject: Reply with quote

TonyGosling wrote:
Bump!

TonyGosling wrote:
Infanrix hexa and sudden death: a review of the periodic safety update reports submitted to the European Medicines Agency.
Puliyel J, et al. Indian J Med Ethics. 2018 Jan-Mar.
https://www.ncbi.nlm.nih.gov/m/pubmed/28918379/

Abstract
There have been a number of spontaneous reports of sudden unexpected death soon after the administration of Infanrix hexa (combined diphtheria, tetanus, acellular pertussis, hepatitis B, inactivated poliomyelitis and Haemophilus influenza type B vaccine). The manufacturer, GlaxoSmithKline (GSK), submits confidential periodic safety update reports (PSURs) on Infanrix hexa to the European Medicines Agency (EMA). The latest is the PSUR 19. Each PSUR contains an analysis of observed/expected sudden deaths, which shows that the number of observed deaths soon after immunisation is lower than that expected by chance. This commentary focuses on that aspect of the PSUR which has a bearing on policy decisions. We analysed the data provided in the PSURs. It is apparent that the deaths acknowledged in the PSUR 16 were deleted from the PSUR 19. The number of observed deaths soon after vaccination among children older than one year was significantly higher than that expected by chance once the deleted deaths were restored and included in the analysis. The manufacturer must explain the figures that have been submitted to the regulatory authorities. The procedures undertaken by the EMA to evaluate the manufacturer's claims in the PSUR need to be reviewed. The Drugs Controller General of India nearly automatically accepts drugs and vaccines approved by the EMA. There is a need to reappraise the reliance on due diligence by the EMA.#


https://www.ncbi.nlm.nih.gov/m/pubmed/28918379/


Looks like they introduced yet another version of the 6-in-1 baby vaccine early in January this year:
'FDA Approves VAXELIS Combo Vaccine Despite Infant Mortality':
https://thetruthaboutcancer.com/vaxelis-merck-combo-vaccine/

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'And he (the devil) said to him: To thee will I give all this power, and the glory of them; for to me they are delivered, and to whom I will, I give them'. Luke IV 5-7.
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