Author Archive

Did We Win Against the WHO?

https://standforhealthfreedom.com/interview/who-updates/

Did we win against the WHO?

WHO treaty and IHR update after WHA 75

​In the last few weeks, health advocates in the U.S. have seen massive wins in our stand against the rapid and coercive development of a global health governance. Thanks to your efforts to sound the alarm, the U.S. Congress has come alive with new bills, new sponsors on existing bills, and letters from the House and the Senate reminding the president that the Constitution is the supreme law of the land and no international agreement will push that aside.

So where are we now with the global health agenda? Read on for updates to the U.S. involvement with the World Health Organization so you can keep the momentum going!

What happened with the proposed US IHR amendments?

In January 2022, the United States, along with approximately 40 other countries, proposed amendments to 13 articles of the existing WHO International Health Regulations.[i] At WHA 75 in Geneva from May 22 through 28, 2022,[ii] the Assembly adopted a resolution to substantially amend one article of the International Health Regulations regarding timelines for amendments to the IHR, along with “necessary” changes to four additional articles to reinforce those major changes. Member States of the World Health Organization will have the opportunity to reject or accept the amendments with reservations (explained below). The other 12 amendments proposed by the U.S. are not off the table — these will now be addressed by the new Working Group on IHR Amendments which will report to the World Health Assembly in 2024, the same year the pandemic treaty is planned to be voted on.

The final version of the amendment was negotiated in “informal discussions” outside of the WHA meetings. U.S. Deputy Secretary Colin McIff of the HHS Office of Global Affairs explained on the record that, “Member States decided to commence a Member-State led process to consider proposed amendments2 to the International Health Regulations (2005) beyond those adopted below.” [iii] That footnote you see mid-sentence is in a WHA document and refers to the 12 proposed amendments rumored to be withdrawn. It refers to “Including the other proposed amendments set out in the annex of Document A75/18, as well as other amendments which have or may be submitted by other IHR (2005) States Parties or the Director-General, including through the above-mentioned Member State-led process.” (emphasis added) Document A75/18 includes the amendments as submitted by the U.S. to the WHO. So not only are all of the U.S. amendments still proposed for consideration, more amendments from other Member States are invited as well.

Details on the adopted amendment

The amendment adopted at the WHA to Article 59: Entry into force; period for rejection or reservations, regarding the timeline for new amendments to the IHR to be adopted and become legally binding on Member States was the one never thought to be withdrawn.

The U.S. wanted to reduce the timeline for adoption of new amendments from a 2-year process to a 6-month process. Right now, after notification of an adopted amendment, countries have 18 months to reject or make reservations, and an additional 6 months before those amendments go into force. The proposal adopted by WHA 75 decreases that timeline to 10 months instead of 18 months to reject or reserve, and two additional months for effect, shortening the entire timeline by a year.

Amendment to Section 59 adopted by the Assembly,[iv] along with additional language changes to Articles 55, 61, 62, 63, having to do with the amendment process, rejections and reservations, and the timeline for amendments to go into force was proposed to reinforce the changes proposed to Article 59. These additional articles were not in the original U.S. proposal but were deemed necessary after informal negotiations.[v]

Throughout the Assembly, countries voiced opposition to, or concern with, changes to WHO authority and reach by way of amending the IHR and creating a new pandemic treaty. Notably, Brazil President Jair Bolsanaro stated Brazil would have no part of a pandemic treaty[vi] (and has been on record since 2020 considering leaving the WHO entirely[vii]). Other countries expressing concern included Botswana, Iran, Bangladesh, Namibia, India, Brunei, the Russian Federation,[viii] and several African states.[ix]

What to watch for now?

Health Advocates can keep an eye on the WHO process through 2024, but pay attention to what is happening in the WHO’s backyard which will eventually come knocking.

WHA created two new WHO groups to work on IHR changes.

The Assembly agreed to the creation of two new groups in the WHO to work on updating the IHR. The Working Group on IHR Regulations (WGIHR) will meet over the next two years to collect, discuss, and propose “targeted” amendments to the IHR at the 77th World Health Assembly in 2024.[x] The WGIHR will be helped by a new IHR Review Committee to focus on “technical recommendations” (changes that are not considered substantial enough to be amendments but bring the IHR in line with amendments and goals for strengthening the WHO).

The WGIHR must coordinate with the Intergovernmental Negotiating Body (INB), “as both the International Health Regulations (2005) and the new instrument are expected to play central roles in pandemic prevention, preparedness, and response in the future.”[xi]

Timeline as of June 1, 2022 (all subject to change)

  • TBD – Official notice from the WHO Director-General of adoption of resolution to amend Articles 59, 55, 61, 62 and 63 of the IHR, which starts the clock ticking for reservations or rejections
  • TBD — Member States must reject or take reservation. By law, States should have 18 months, per the existing and legally binding regulations in force now. Some wonder, however, if the DG will impose the newly adopted timeline even though it is not yet in force. (In other words, the U.S. will have 10 to 18 months to respond to the amendments.)
  • June 16-17 — Second meeting of INB to inform drafting of pandemic treaty[xii]
  • August 2022 — First draft of pandemic treaty expected
  • September 30, 2022 — Deadline for proposed amendments to IHR
  • October 1, 2022 — Deadline for creation of IHR Review Committee for technical recommendations to proposed amendments and to inform the work of the WGIHR
  • November 15, 2022 — Deadline for first meeting of WGIHR
  • January 15, 2023 — Requested deadline for IHR Review Committee to submit a report to the DG, who will transfer it to the WGIHR immediately
  • May 2023 — World Health Assembly 76
  • May 2024 — World Health Assembly 77 to consider targeted amendments to IHR as well as pandemic treaty.

The IHR and treaty are not the only way to move a global health agenda forward.

Outside of these documents, meetings, and negotiations, there are other agreements strategically being put into place. The World Bank is setting up accounts for a new global health security fund for pandemic preparedness, which already has over $3.2 billion pledged by countries around the globe.[xiii] The WHO opened a new global hub for pandemic and epidemic intelligence in Germany for “data, surveillance, and analytics innovation…the largest network of global data to predict, prevent, detect, prepare for, and respond to pandemic and epidemic risks worldwide.”[xiv] The WHO also has ongoing research, pilot programs, and guidance regarding digital documentation of COVID-19 tests and vaccination certificates.[xv] Switzerland is home to the new WHO BioHub where countries can rapidly share novel biological materials and pathogens.[xvi] Negotiations to share intellectual property (patent rights) for pandemic medical products have been ongoing at the World Trade Organization.[xvii] Right now all of these agreements and negotiations are voluntary, but all of these issues are expected to be addressed and become legally binding through the pandemic treaty.

In America there are state and federal laws, bills, and regulations either aligning with or rejecting the WHO. Stand for Health Freedom already reported on the 2017 CDC quarantine regulation updates that included the WHO definition of public health emergency.[xviii] State legislatures started seeing bills referencing WHO definitions as well, including the Mental Health Parity Act that did not pass the Georgia House this past session.[xix] The Biden administration created an Office of Climate Change and Health Equity in 2021, [xx] and added to it an Office of Environmental Justice, within the Health and Human Services agency. [xxi] This new creation is in line with the “One Health” approach of the WHO for the new pandemic treaty, which includes humans, animals, and the environment together in public health.

Here’s the great news.

Americans have seen lawmakers wake up and start opposing WHO takeover of U.S. public health decisions.

Since the launch of the SHF action to support HR 419, No Taxpayer Funding for the WHO Act, there have been 39 new cosponsors! Two senators[xxii] as well as House members of the Freedom Caucus[xxiii] sent letters to the White House insisting the U.S. reform their relationship with the WHO or pull out altogether. Some representatives have been making public statements against WHO involvement, like Mary Miller from Illinois.[xxiv] Candidates for governor are speaking out against WHO overreach after witnessing two years of federal overreach and promising to stand strong to protect the health of their constituents.[xxv] State legislators, like in Louisiana, are voicing opposition as well![xxvi]

Additionally, in just one week three new bills were introduced in Congress to protect U.S. sovereignty in public health matters. Senator Rick Scott of Florida introduced S4305 on May 25, a bill to limit the authority of the WHO on the U.S. and oppose amendments not approved by Congress.[xxvii] Senator Ron Johnson announced his introduction of a bill, “No WHO Pandemic Preparedness Treaty Without Senate Approval Act.”[xxviii] And Representatives Rogers and Massie introduced HR 7806, the American Sovereignty Restoration Act,” which expands congressional oversight beyond the WHO to its parent organization the United Nations.[xxix]

Because of your voice, our lawmakers are taking action, and quickly!

Steps You Can Take Now:

You are making a difference! Our lawmakers are hearing your message about protecting our rights and our Constitution when it comes to health. Let’s keep the momentum going!

Step 1: Tell your lawmakers about the WHO’s plans for global health governance. Your representatives can support HR 419, and your senators can make sure they are doing their constitutional duty to advise and approve of any international treaties. Our campaign makes it easy to get in touch with email and phone scripts that you can use or adapt to send a message.

Step 2: We can stop medical tyranny by voting people into office who will stand for health freedom! To have good candidates on the ballot in November, we must vote now in the primaries. Check out where your candidates stand using our Vote for Health Freedom Guide for your state! Go to our Vote for Health Freedom page, or Text the letters VHF to 52886, to learn about candidates in your area!

Step 3: Please support our work in bringing this information to light. Every penny counts toward exposing the global health agenda and educating our lawmakers into action!

References & Sources

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**Comment**

According to an article written last year, the U.S. is on course to become a ‘digital dictatorship’ under a proposed biomedical research agency. This agency would merge national security with public health, a perfect formula for a dangerous agenda that would destroy medical freedom as we know it.

This agency would “use both physical and mental health ‘warning signs’ to prevent outbreaks of disease or violence before they occur. Such a system is a recipe for a technocratic ‘pre-crime’ organization with the potential to criminalize both mental and physical illness as well as ‘wrongthink.’”

This article proves the political interference at HHS as well as the fact governments are working in lockstep to bring in digital I.D.s & a social credit system.

The CDC already rules both research and the medical profession with an iron fist and medical freedom is increasingly under fire.
All of this sounds like a perfect prelude to global “vaccine” passports.

For more:

News Report: Tiny Terror – The Truth About Ticks

https://www.localsyr.com/living-with-lyme/living-with-lyme-tiny-terror/  News Video Here (Approx. 24 Min)

Tiny Terror: The Truth About Ticks

SYRACUSE, N.Y. (WSYR-TV) Ticks are in our yards and they’re saturating Central New York. One bite can change everything. Most people do not know Central New York is an epicenter for tick-borne disease. Most recent data indicates a 439% increase in Central New York between 2008 and 2018.

What are some of the symptoms of Lyme disease?

  • Brain fog
  • Headaches
  • Joint Pain
  • Extreme Fatigue
Doctors and scientists struggle to agree on how to get this under control.

(See link for video and story)

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SUMMARY:

  • The reason Lyme/MSIDS patients are not treated appropriately is due to the faulty, unscientific, and fraudulent CDC Lyme guidelines which serve as an Iron Curtain in the medical community.
  • It is imperative to get to a Lyme literate (LLMD) doctor trained by ILADS, a group of medical professionals who recognize the faulty, unreliable testing and ineffective CDC guidelines.
  • The quote from a doctor in the news story that taking a single or double dose of doxycycline reducing the risk of transmission has been completely and utterly debunked.
    • Based on animal studies, ILADS recommends that known blacklegged tick bites be treated with 20 days of doxycycline (barring any contraindications).
    • Given the low success rates in trials treating EM rashes for 20 or fewer days, ILADS recommends that patients receive 4-6 weeks of doxycycline, amoxicillin or cefuroxime. A minimum of 21 days of azithromycin is also acceptable, especially in Europe. All patients should be reassessed at the end of their initial therapy and, when necessary, antibiotic therapy should be extended.
    • ILADS recommends that patients with persistent symptoms and signs of Lyme disease be evaluated for other potential causes before instituting additional antibiotic therapy.
    • ILADS recommends antibiotic retreatment when a chronic Lyme infection is judged to be a possible cause of the ongoing manifestations and the patient has an impaired quality of life.
  • Lyme survivor Brenna Osmun, who lost her ability to walk, is interviewed on the report.  Two months of IV antibiotics saved her life. She suffered years of relapses until she saw a LLMD, a specialist rarely covered by insurance.  She also had Babesia and Bartonella and was treated with more than a dozen herbs and antibiotics.  She says this to patients:

“It gets better. It really, really does. And my life changed for the better I wanna say. Even though I was really sick, it does get better. And having that support really helps you. Don’t give up. Please don’t give up. I didn’t and I’m still alive.” ~ Brenna Osmu

  • Executive Director of the Central New York Lyme and Tick-Borne Disease Alliance, Royale Scuderi became infected years ago when doctors treating this were scarce.  She had to drive to Long Island for year to get appropriately treated.
  • Journalist and host of the news program, Nicole Sommavilla became septic with her organs shutting down.  Years later she was diagnosed with Lyme disease and required a dozen drugs to treat Lyme, Babesia, and Anaplasmosis

“I went from years of oral medications and injections to just one medication I’m on now and just a lot of maintenance with diet and knowing when not to push myself past my limit, it’s a lot of self-awareness.” ~ Nicole Sommavilla

A MESSAGE FROM NICOLE:

If you’re fighting Lyme right now, please don’t give up.

Don’t quit in the darkness. Most days it may feel easier to give in, but hang on. Lean into your support system and keep fighting. Because joy and healing are coming. ~ Nicola Sommavilla

For more:

Nearly 15% of the World Has Lyme Disease, According to First Global Estimate (Which is Still Low)

https://www.dailymail.co.uk/health/article-10910857/Nearly-15-CENT-world-Lyme-disease-according-global-estimate

Nearly 15 PER CENT of world has Lyme disease, according to first global estimate

  • 900 Britons and 30,000 Americans are diagnosed with Lyme disease annually
  • Experts say figures are an underestimate and not clear how common globally
  • Now, researchers estimate 14.5% people worldwide have had the condition

Up to one in seven people worldwide may have had Lyme disease, according to new estimates.

For decades, researchers have been clueless as to exactly how widespread the tick-borne illness was.

The new findings could open up avenues to tackle the bacterial infection, which can cause sufferers symptoms such as headaches, muscle and joint pain and fatigue that can last for years.

Singer Justin Bieber and model Bella Hadid are just two celebrities who have spoken out about their plight with Lyme.

Academics from China examined blood sample data from studies involving 150,000 people.
Results showed 14.5 per cent had antibodies indicating Lyme disease.

(See link for article)

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**SUMMARY**

  • Chinese researchers utilized previous studies that relied upon antibody blood test results.  It is commonly known to everyone that these tests are completely unreliable and miss a preponderance of cases, therefore all numbers are a complete stab in the dark.  Further, a third of the studies only used one type of test to confirm a diagnosis.
  • Blood testing can not confirm whether a person is currently infected or has been previously.
  • The authors state some of the studies used were conducted in endemic regions and may over-estimate cases, but please remember they used faulty testing rendering ALL numbers essentially meaningless. 
  • They recommend a global “standard” testing method to confirm cases, which in my opinion, if done would only doom even more patients to a lifetime of suffering. Current CDC 2-tiered testing already misses anywhere from 70-86% or more of cases. Due to CDC conflicts of interest in owning patents on testing, vaccines, and more, mainstream doctors and organizations vilify CLIA-certified labs which are more sensitive because they compete with CDC testing.
  • Pushing a “global”, centralized approach to medicine is not the answer.  Lyme/MSIDS has been in a juggernaut for over 40 years due to a literal Cabal controlling the research, and conflict-riddled public health ‘authorities’ only doling out research money to those who tout the accepted narrative. So, no, we do not want a global testing”standard” or any medical monopoly. 
Patients and the doctors who dare treat them need MORE choices not less.

Despite COVID Vax Destroying Female Reproductive Systems & Killing Youth, FDA Rubberstamps Moderna 2-Dose Shot for Kids Based on Insufficient Evidence

https://thenewamerican.com/covid-vax-destroying-female-reproductive-systems-killing-kids-toxicologist-warns/  Video Here (Approx. 20 Min)

Covid Vax Destroying Female Reproductive Systems & Killing Kids, Toxicologist Warns

Audio Playe

The experimental Covid injections forced on millions by the Biden administration are killing people and wreaking havoc on female reproductive organs and other body systems, warned toxicologist Dr. Janci Lindsey in this interview on Conversations That Matter with The New American magazine’s Alex Newman. Dr. Lindsey, who holds PhDs in biochemistry and molecular biology and serves as director of Toxicology and molecular biology for a toxicology firm, worked on Rockefeller-funded research into fertility regulating vaccines in the 1990s. Among other concerns, she warned that the shots are causing all sorts of toxic effects on the human body. Within the next 6 months, humanity should expect to see another “plandemic” to bring in more medical tyranny, she warned. Dr. Lindsey urged everyone to refuse to comply.

At 11:30 Dr. Lindsey discusses minocycline as a therapeutic to ameliorate COVID “vaccine” injury as well as glutathione, NAC, proper diet, and vitamin C.  She also discussed how the spike protein hangs out in the lymph nodes and that ivermectin & HCQ may help this as well as the dangers blood clotting.

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https://childrenshealthdefense.org/defender/fda-moderna-two-dose-covid-vaccine-kids/

Breaking: FDA Panel Recommends Moderna Two-Dose COVID Vaccine for Kids Ages 6 to 17 Despite Serious Safety Concerns

The U.S. Food and Drug Administration’s vaccine advisory panel on Tuesday voted 22 – 0 to authorize Moderna’s COVID-19 vaccines for children ages 6 to 11 and 12 to 17 despite the lack of short- and long-term safety data and no evidence children are at risk of serious illness.

By Megan Redshaw

6/14/22

The U.S. Food and Drug Administration’s (FDA) vaccine advisory panel today voted unanimously to recommend Moderna’s COVID-19 vaccine for children ages 6 to 17 after determining the benefits of the vaccine outweigh the risks for use.

The Vaccines and Related Biological Products Advisory Committee (VRBPAC) voted 22 to 0 to recommend Moderna’s two-dose vaccine for 6- to 11-year-olds at half the strength of the adult version, and 22 to 0 in favor of authorizing the shot for 12- to 17-year-olds at the same strength as adults.

The FDA’s vaccine advisors will meet again on Wednesday to discuss amending Emergency Use Authorization (EUA) for Moderna’s COVID-19 vaccine to include the “administration of the primary series to infants and children 6 months through 5 years of age.”

(See link for article)

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https://popularrationalism.substack.com/p/fda-rubberstamps-the-moderna-covid?

FDA Rubberstamps the Moderna COVID-19 Vaccine for Kids Aged 6-17 Based on Insufficient Evidence

Yesterday, the vote was in 100% in favor of “approval” of the vaccine for kids 6 to 17. None of the votes were based on Science.

This article is dedicated to the parents of the children not yet harmed or killed by COVID-19 vaccines. We are trying to warn you that the FDA and CDC are whole-heartedly engaged in fraud.

Dr. Toby Rogers deserves credit for sitting through a grueling, “heart-braking” nine hours of FDA rubber-stamping COVID-19 vaccines based on clinically trivial endpoints. This rubber-stamp is based on data showing no serious cases of COVID19 in children (no hospitalizations). Here I review most of his interview with Steve Kirsch. (Link to video).

Under EUA rules, an emergency must be in place. Yesterday, I pointed out the vanishingly small number of cases since March 2020.  (See link for Weiler’s point by point detailing of the FDA’s “political theatre.”

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**COMMENT**

There was a public comment session during the meeting where many expressed serious concern over recommending a gene therapy injection to an age group that has almost a ZERO risk of experiencing severe illness or death from COVID.

Dr. Harvey Klein, orthopedic surgeon, mechanical engineer and yes, even a rocket scientist said he is appalled at the FDA’s arrogance in even “thinking of vaccinating healthy children with outdated, highly toxic COVID vaccines,” and that have a 99.998% recovery rate with no sequelae.

Pharmacologist, pharmacist, FDA and healthcare policy oversight fellow and FDA reform advocate at the Ethics and Public Policy Center in Washington, D.C., Dr. David Gortler states the FDA and the advisory panel have “maintained a highly non-scientific and casual attitude toward approving a vaccine whose short- and long-term effects on children are unclear.”  After reminding the FDA of the need for parents to be informed of “vaccine” safety, he stated the FDA has failed to address genotoxicity, teratogenicity, oncogenicity of COVID-19 vaccines and cardiovascular risk following “vaccination”, potential fertility issues and clinical effects of spike proteins in donated or transfused blood.  He ended by stating that four million doses must be administered to children 5 to 11 years of age to prevent a single ICU admission in the same age group.

This means that if you assume two doses per child, two MILLION children must risk potentially serious side-effects and/or death to prevent a single child from entering the ICU.

But the real clincher came from Kathy Dopp and Dr. Stephanie Seneff’s analysis which highlighted the following:
  • Children under 18 are 51 more times more likely to die from the injection than they are to die from COVID if not “vaccinated.”
  • The COVID injection actually increases a child’s risk of dying from COVID.

It was also pointed out that instead of breaking down the data per age group, the “vaccine” manufacturer lumped all the age groups together to “massage” the data.  When each group is looked at separately, the shot fails in each category according to Dr. Toby Rogers. He also points out that Moderna created 20 adverse event tables allowing it to simply eliminate or hide data is didn’t like. Please also see this important paper written by Dr. Rogers on how the FDA is set to decide on Pfizer’s jab for kids based on unethical trial data that makes the data functionally useless for making decisions.

Again, it can not be over emphasized that science is now being done by press release and the very people doing the “science” are selling the products. 

Lastly, despite the CDC’s narrowed case definition of “myocarditis,” which excludes cases of cardiac arrest, ischemic strokes and deaths due to heart problems that occur before one has the chance to go to the emergency department, 635 cases of myocarditis in the 5 to 17 age group have been confirmed. Imagine the numbers if the case definition were more realistic and accurate. Lyme/MSIDS patients should be well aware of the CDC’s shenanigans with “case definitions” by now.

It doesn’t take a rocket scientist to see something is rotten in Denmark.
Take a stand and tell the FDA to get their hands off our children.

For more:

The global experiment must stop.
Millions have already been adversely affected by these clot shots and nobody knows what the future holds for those who received these gene therapy shots that have caused more adverse reactions and death than any other vaccine in the history of VAERS.

31 Weeks to Protect Freedom in the U.S.

https://popularrationalism.substack.com/p/please-read-we-have-31-weeks-to-protect?

31 Weeks to Protect Freedom in the United States

IPAK-EDU is partnering with CloutHub and will focus on Scientific Freedom and Freedom in Education

If you have never heard of Fundfreely.com, you will. When GoFundMe and the government of Canada conspired to steal funds donated to Canadian Truckers, Jeff Brain of CloutHub created a new, secure platform for crowdsource funding.

Better yet, Jeff and a few close associates have decided to take a highly proactive approach to terminate the erosion of individual rights and freedom in the United States. They have decided to conduct a major raise to defend freedom. In doing so, they chose a handful of carefully selected organizations (“pillars”) to receive an equal portion of their $100M goal.

IPAK-EDU has been selected as one of those pillars.

Our charter is to work to promote Freedom in Science and Freedom in Education.

This is very real; the contracts are signed, and fundraising is underway. I won’t go into great detail on what strategies and tactics we will be taking, but be assured, they will be measured and we will be aiming for lasting, hopefully permanent, impact. I can tell you this: per the contract, this initiative is NOT political. We expect that support will begin flowing into IPAK-EDU next month. We all collectively have 31 months to do as much to support Jeff’s raise as possible. His goal is $100M; we expect to receive 1/4 of that.

The link to the initiative is https://www.fundfreely.com/go

There you’ll see supporting quotes from Dr. Peter McCullough, Robert F. Kennedy, Jr., yours truly, and others.

Please consider supporting this cause – and please consider using FundFreely.com for your own crowdsource campaigns.

Yours in Science and Education,

-James Lyons-Weiler, PhD

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**Comment**

Lyme/MSIDS patients are already stretched financially, but often wonder what they can do with the pennies they have left over.  Protecting freedom in Science and Education is one such worthy place to put those pennies.  For far too long our corrupt government has used sick patients to fund their own manipulated, biased research, which has only served to hurt patients.  Time for change.  Time to put money toward scientific honesty and transparency, and time to hold corrupt public health ‘authorities’ accountable.  They have lined their pockets for far too long on our dime.