https://homeopathyusa.org/about-aih-2/position-statements-letters-2/access-to-homeopathy-threatened-by-latest-fda-action.html

Access to Homeopathy Threatened by Latest FDA Action

The U.S. Food and Drug Administration (FDA) recently announced a new guidance that could lead to the end of homeopathy in America in less than three months.

The consequential action taken by the FDA involves the elimination of the administrative framework for homeopathy that the agency used for 30 years, one that allowed manufacturers of homeopathic remedies to thrive while ensuring the quality and purity of homeopathic medicines. We are referring to the withdrawal of Compliance Policy Guide (CPG) 400.400 which has served the industry and consumers well.

Homeopathic medicines are now in real danger. The newly revised Draft Guidance, if adopted as currently written, will be a recipe for the destruction of homeopathy as we know it in America.

Under the new guidance ALL homeopathic medicines will be considered illegal. This is because the Draft Guidance declares all homeopathic medicines to be “new drugs” which have not undergone the agency’s pre-market approval process known as a New Drug Application (NDA). This “new drug” designation makes this new guidance particularly damning for homeopathy. Homeopathic medicines cannot be patented and therefore cannot justify the enormous expenditures that an NDA entails. If the FDA insists that a homeopathic medicine be put through the NDA process, the agency will essentially be issuing a potential  ban on that medicine in the United States.

If the Draft Guidance is adopted unchanged ─ and especially if the designation of all homeopathic medicines as “new drugs” is allowed to stand ─ consumers will likely begin to see homeopathic medicines disappear from store shelves and practitioners’ offices as the FDA takes aim at one homeopathic medicine after another.

What’s more, if the Draft Guidance is finalized, the FDA will have little trouble defending its actions in any administrative procedure or court. The danger is real because the designation of homeopathic medicines as “new drugs” makes all of them illegal and the FDA can remove any illegal drug from the marketplace without notice and without additional justification merely because it is illegal.

It would be a simple matter for the American Institute of Homeopathy to produce evidence showing that homeopathy is extremely safe, with excellent clinical results backed by an extensive medical literature including hundreds of clinical trials which demonstrate its safety and effectiveness.  We could also point to the very real public health emergency around antibiotic resistance and the immense potential for homeopathy to save lives as reason alone to protect homeopathy.

Sadly, none of that will matter if those who support and rely on homeopathy do not immediately unite to seek a better framework from the FDA.

If you’d like to do your part to protect your access to this extraordinary system of medicine in America, please take these steps immediately:

  1. Submit a comment to the FDA docket about homeopathy telling the agency that we need a 180-day extension in order to respond adequately to the FDA’s latest proposed rules. When you’re ready to do that, click here: https://homeopathychoice.org/fda-comments-landing/
  2. Encourage all of your contacts, patients, and family members to also submit a comment to the docket by sending them a copy of this email.

We can and must save homeopathy in America but we must act now.

The Board of the American Institute of Homeopathy

Merry Christmas Text, Candle, Pine Tree Branches and Berries in Top Corner Over Rustic Wood

https://www.greenmedinfo.health/blog/vaccine-fail-whooping-cough-outbreak-closes-texas-school-despite-100-percent-vacc2?

Vaccine FAIL: “Whooping cough outbreak closes Texas school despite 100-percent vaccination rate: officials”

Written By:  GMI Reporter

“© [Sunday, December 22nd 2019] GreenMedInfo LLC. This work is reproduced and distributed with the permission of GreenMedInfo LLC. Want to learn more from GreenMedInfo? Sign up for the newsletter here //www.greenmedinfo.com/greenmed/newsletter.”

Despite a 100% vaccination rate, a Texas school closes early for winter break due to a whooping cough outbreak. Clearly the vaccine is failing to work as advertised. 

If ever there was convincing proof that vaccination does not equate to bona fide immunity, it is at St. Theresa Catholic School in Texas…

Reported by FoxNews.com on Dec. 19th, the school experienced an outbreak of whooping cough, causing them to close their doors and start their winter break early.

On Dec. 4th, St. Theresa Catholic School in Memorial Park, reported its first case to the Texas Department of State Health Services. Since then, the outbreak has continued to escalate — and not because of the abuse of religious and medical exemptions, and so-called “anti-vaxxer” parents. 

According to the FoxNews report, the school vaccine uptake rate was at 100%:

“Officials with the Archdiocese of Galveston-Houston said that 100 percent of students who attend St. Theresa Catholic School are vaccinated against the illness.”

This was confirmed by the following statement to parents sent by the school:

In response to this incident, Children’s Health Defense (CHD) posted an article titled, “Pertussis: Vaccine Failure, Not Failure to Vaccinate,” explaining how despite propaganda to the contrary, it is clearly not conscientious objectors to vaccination driving outbreaks like these (i.e. so-called “anti-vaxxers”), but a failing pertussis vaccine. 

In fact, according to CHD’s article the vaccine itself may be driving increased risk for whooping cough:

“Studies show that by five years after completion of the DTaP series, children were up to 15 times more likely to acquire pertussis compared to the first year after the series.” 

There are plenty of additional examples in the published literature of vaccination failure in highly vaccinated populations. View 30+ studies on the topic here.

There are also serious questions as to whether vaccines like DTaP are causing more harm than good. GreenMedInfo.com indexes peer-reviewed, published studies that confirm the unintended, adverse effects of vaccinations. You can view close to a thousand study abstracts on the subject on our Vaccination Database. The DTP vaccine has been linked to over 30 adverse health effects which you can viewed here: Vaccination: Diphtheria-Pertussis-Tetanus. 

Due to our advocacy on this subject, we have been systematically censored, including recent successful attempts to de-platform us from Mailchimp, Pinterest, and Google (learn more here). Please learn more and support our cause by becoming a member or donating, and celebrating our 10 year anniversary with us.

Disclaimer: This article is not intended to provide medical advice, diagnosis or treatment. Views expressed here do not necessarily reflect those of GreenMedInfo or its staff.
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Former Merck scientists sued Merck Alleging MMR Vaccine Efficacy Fraud back in 2010.  These whistleblowers were threatened with jail if they alerted the FDA that they were forced to add rabbit antibodies to human samples to increase efficacy of Merck’s mumps vaccine (which is currently only available in the combination MMR vaccine and conveniently the ONLY manufacturer licensed by the FDA to sell it in the U.S.). This addition increased pre-vaccine blood from 10% positive to 80% positive:  https://ahrp.org/former-merck-scientists-sue-merck-alleging-mmr-vaccine-efficacy-fraud/
Mainstream media failed to report that in 2014 a judge ruled in favor of the whistleblowers.  
When The Wall Street Journal did cover it in 2012, it was removed 3 days later.

One of the lead authors on a CDC published study in 2004 has also become a whistleblower, stating that the CDC withheld data from the public linking the MMR vaccine to a higher rate of autism among some children, specifically African American boys.  http://healthimpactnews.com/2014/judge-lawsuit-against-mercks-mmr-vaccine-fraud-to-continue/

A FEDERAL JUDGE HAS RULED THE CASE WILL PROCEED DESPITE THE MEDIA NOT TOUCHING THIS WITH A 10 FOOT POLE.
OOPS, WELL THAT’S AN INCONVENIENT TRUTH.

 

 

Approx. 7 Min.

Dr. Janet Kern on the Dangers of Thimerosal

From the UNEP Intergovernmental Negotiating Committee meeting

Neuroscientist Janet K. Kern, PhD, speaks in this video about the connection between thiomersal in vaccines and autism. Thiomersal, commonly known in the U.S. as thimerosal, is an organomercury compound. Dr. Kern gave this talk for the UNEP Intergovernmental Negotiating Committee in Punta del Este, Uruguay, in July, 2012. She is a director of the Council for Nutritional and Environmental Medicine (CONEM), and the chairman of the CONEM US Autism Research Group.

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For more:  https://madisonarealymesupportgroup.com/2016/12/08/mercury-and-autism/

Excerpt:

In 1999 studies began to surface showing that multi-dose vial vaccines, such as the MMR and hepatitis B vaccines, contained enough thimerosal to expose vaccinated children to 62.5 ug of mercury per visit to the pediatrician. This is one hundred times the dose considered safe by the Federal Environmental Protection Guidelines for infants!

https://madisonarealymesupportgroup.com/2018/09/28/toxic-metal-pollution-linked-with-development-of-autism-spectrum-disorder/

https://madisonarealymesupportgroup.com/2019/01/21/exposure-to-heavy-metals-linked-to-autism-in-children-and-vaccines-still-contain-mercury/

https://madisonarealymesupportgroup.com/2019/07/08/autism-affecting-up-to-1-in-36-children-in-america/

https://www.sciencedirect.com/science/article/pii/S0946672X19305784?via%3Dihub

Acute exposure and chronic retention of aluminum in three vaccine schedules and effects of genetic and environmental variation

Under a Creative Commons license
open access

Abstract

Like the mechanisms of action as adjuvants, the pharmacodynamics of injected forms of aluminum commonly used in vaccines are not well-characterized, particularly with respect to how differences in schedules impact accumulation and how factors such as genetics and environmental influences on detoxification influence clearance. Previous modeling efforts are based on very little empirical data, with the model by Priest based on whole-body clearance rates estimated from a study involving a single human subject.

In this analysis, we explore the expected acute exposures and longer-term whole-body accumulation/clearance across three vaccination schedules: the current US Centers for Disease Control and Prevention (CDC) schedule, the current CDC schedule using low aluminum or no aluminum vaccines, and Dr. Paul Thomas’ “Vaccine Friendly Plan” schedule. We then study the effects of an implicit assumption of the Priest model on whether clearance dynamics from successive doses are influenced by the current level of aluminum or modeled by the assumption that a new dose has its own whole-body dynamics “reset” on the day of injection. We model two additional factors: variation (deficiency) in aluminum detoxification, and a factor added to the Priest equation to model the potential impact of aluminum itself on cellular and whole-body detoxification. These explorations are compared to a previously estimated pediatric dose limit (PDL) of whole-body aluminum exposure and provide a new statistic: %alumTox, the (expected) percentage of days (or weeks) an infant is in aluminum toxicity, reflecting chronic toxicity.

We show that among three schedules, the CDC schedule results in the highest %alumTox regardless of model assumptions, and the Vaccine Friendly Plan schedule, which avoids >1 ACV per office visit results in the lowest (expected) %alumTox. These results are conservative, as the MSL is derived from data used by FDA to estimate safety of aluminum in adult humans. These results demonstrate high potential utility of modeling variation in patient responses to aluminum. More empirical data from individuals who are suspected of being intolerant of aluminum from vaccines, evidenced by high aluminum retention, neurodevelopmental disorders and/or a myriad of chronic illnesses would help answer questions on whether the model predictions can be used to estimate parameter values tied to genetic factors including genomic sequence variation and family history of chronic illnesses tied to aluminum exposure.

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**Comment**

According to James Lyons Weiler, one of the study authors,

New research conducted by IPAK shows that children on the CDC pediatric vaccine schedule may be spending over 70% of their days in aluminum toxicity in the first seven months of life. This level of chronic exposure is far higher than that experienced by infants whose parents choose to follow the Vaccine Friendly Plan. The study, building on prior research, was published following blinded peer review in the Journal of Trace Elements in Medicine and Biology.