An Open Letter to President Donald J. Trump
Please help to bring this open letter to the attention of President Trump.
FOR COMPLETE DETAILS: NotSafeAndNotEffective.com
Please watch all 5 videos below:
December 12, 2020
https://www.youtube.com/watch?v=-io8Ufsq67A
Tucker Carlson / Deborah Birx
Dr. Paul Alexander
https://x.com/harryfisherEMTP/status/1879223466190413897
An Open Letter to President Donald J. Trump
December 27, 2024
Dear President Donald J. Trump,
Upon your inauguration as the 47th President of the United States on January 20, 2025, you have the opportunity to make amends for the mistakes that were made during your first administration.
I call upon you to take the actions necessary to REVOKE the FDA licenses for the COVID-19 mRNA “vaccines” from Pfizer and Moderna, REMOVE the mRNA biological products from the marketplace and call for a halt to all clinical trials involving this technology.
Please hear this loud and clear:
Operation Warp Speed was NOT a success. From a health perspective, it was an absolute disaster, and as President you bear personal responsibility for the harm, devastation and death that has been inflicted upon millions of Americans and billions of people around the world.
Because of political pressure that you proudly claim to have exerted upon the FDA, the mRNA injectable biological products that were a result of Operation Warp Speed were not subjected to the required tests to ensure safety. As a result, they have caused unprecedented harm while providing absolutely no benefit. They do not fit the definition of a “vaccine,” but they do fit the definition of a biological weapon.
During your first term in office you proclaimed that there was an emergency and that immediate and decisive action needed to be taken.
By now, you must certainly know the following:
The Centers for Data Concealment (CDC) manipulated their data in order to create a fraudulent COVID-19 “casedemic” and they are ignoring VAERS, V-safe and DMED data while also manipulating the analyses of death certificates in order to hide the evidence that a massive number of deaths have been caused by the mRNA injections.
The pharmaceutical companies committed fraud by hiding very important data from the FDA and from the American people which clearly show that the mRNA injections are NOT safe and NOT effective.
Pfizer performed a “bait and switch” tactic in which they used one manufacturing method (“process 1”) to make the biological products that were used in the clinical trials in order to gain Emergency Use Authorization (EUA). Pfizer then switched to a different manufacturing method (“process 2”) to make the biological products that have been injected into billions of people worldwide. The biological products made via “process 2” have been shown to be adulterated with turbo-cancer-causing SV40 promoter sequences in amounts that are far beyond the regulatory limit. This is potentially an absolutely unmitigated disaster.
The hurried and pressured manner in which the mRNA products were brought to market did not stop or even slow down the so-called COVID-19 pandemic. Quite to the contrary, the more injections people have received the more likely they are to be diagnosed with COVID-19, as well as a whole host of vaccine-acquired immuno-deficiency diseases (VAIDS). By working at "warp speed," without concern for long- term safety and with blatant disregard for the fundamental rights of people and the principles of informed-dissent, our government colluded with the pharmaceutical hospital emergency industrial complex and the mainstream media to create an actual pandemic of long-term, chronic, horrifically disabling and enormously costly diseases.
Well over 1,000 VAERS reports have been filed on behalf of women who lost their unborn children on the very same day that they received the mRNA injections.
Over 38,000 VAERS reports have been filed documenting the deaths that are likely to have been caused by the mRNA injections.
The FDA has been captured by the pharmaceutical industry and has approved additional mRNA products without requiring the necessary long-term safety testing that has historically been required.
The FDA, the Environmental Protection Agency (EPA) and the Occupational Safety and Health Administration (OSHA) have absolutely failed to require the proper monitoring of the environment within research and manufacturing facilities. Everyone involved in such work is at risk of exposure to gene-altering and cancer-causing substances during the course of their research, clinical trials, manufacture and administration of the mRNA products. Due to the process known as “shedding,” it is believed that workers who may have been exposed to these experimental biological products may then spread contagion to their close family members as well as other members of their community. In essence, “lab leaks” may be occurring throughout America and the world on a daily basis due to the transmissibility of these experimental gene-based products.
I call upon you to take the following actions IMMEDIATELY upon taking office.
SEIZE
Immediately stop this biological warfare by directing the Attorney General to seek an emergency injunction and warrants to seize the biological weapons that are masquerading as COVID-19 mRNA “vaccines.”
RECALL
Direct the Secretary of the Department of Health and Human Services to recall any and all mRNA “vaccines” that have been approved or authorized by the FDA.
REVOKE
Instruct the Commissioner of the FDA to revoke the biological licenses and Emergency Use Authorizations that have been granted to Pfizer and Moderna to market their mRNA gene-based biological products.
INSPECT
Direct the EPA and OSHA to thoroughly examine the facilities related to the research, manufacture and administration of the mRNA products and treat them as the hazardous biological weapons sites that they are.
INVESTIGATE
Call for an independent investigation into the crimes that have been perpetrated due to collusion among public officials, pharmaceutical companies and mainstream media outlets in their efforts to defraud and harm millions of Americans as well as billions of people around the world.
INDICT
Instruct the Department of Justice to file indictments and bring criminal charges for fraud, mislabeling of products, violations of fundamental human rights and many other far more serious crimes against humanity that have been perpetrated by a wide range of people, corporations and organizations.
REPEAL
Call upon Congress to repeal the protections from liability that were unconstitutionally granted via the PREP Act and the Childhood Vaccine Injury Act.
Your approval ratings and your reputation will suffer every single day that you delay in removing these biological weapons from the marketplace.
Your legacy will be strengthened by taking strong, bold and well-informed action.
I pray that you look into your heart and do the right thing.
God bless you. God bless America. God bless the people of the world.
Sincerely,
James Roguski
310-619-3055
Please do NOT follow Bill Gates’s advice.
https://www.youtube.com/watch?v=JNe1ixzOXA0
Dr. Phil Outraged as RFK Jr. Exposes NIH Kickbacks from Moderna Vaccine
The Pharmaceutical Companies are Serial Felons, and They Have Captured the Health Agencies
RFK Jr: Our regulatory agencies have now become captured
https://rumble.com/v5dju7x-rfk-jr-our-regulatory-agencies-have-now-become-captured.html
Recommendations from Paul Alexander
1) NIH
NIH (National Institutes of Health): must initiate and implement research studies and programs that examine the Malone, Bourla, Bancel ,Weissman, Sahin et al. mRNA technology vaccine injures that have accumulated.
NIH must join and partake with CDC etc. acute surveillance of Malone, Bourla, Bancel, Weissman, Sahin et al. mRNA technology vaccine harms and deaths across time.
NIH must revisit all the COVID Operation Warp Speed (OWS) related studies (it funded) and convene an expert panel to examine the research protocols, the methods, the statistics used, the findings, and the funding approved. Findings are to be made known to the public in 6 months of the new NIH Director taking lead.
There is no existing randomized placebo-controlled study, double blinded or triple blinded, that shows that the COVID mRNA gene vaccines reduced hospitalization, death, ICU, severe illness etc. in children or adults, elderly etc. The NIH Director must reveal to the public what studies the NIH (past and existing under new leadership) uses to support that statement that the mRNA vaccine reduced hospitalization and death and was beneficial to the public, e.g. in the elderly.
NIH must also initiate a review of all ethics review panels and input that was used to authorize the COVID related studies and findings made known to the public in 6 months of the new NIH Director taking lead.
NIH must immediately stop all gain-of-function (GoF) or related research in any US affiliated or funded or operated biolab anywhere in the world. NIH must stop its involvement (direct or indirectly) in all bioweapons biological research in US laboratories and anywhere globally that the US is affiliated. No US tax-payer money must be used for any such research anywhere in the world.
The NIH Director must IMMEDIATELY call for the end of any mRNA technology gene-based vaccine research.
The NIH Director must call (with the new FDA Commissioner) for the Malone et al. mRNA gene vaccine to be removed from market, completely, and immediately upon swearing in. None to be made available to infants, children, teens, adults, elderly. No moratorium.
The NIH Director must ensure that any studies for mRNA vaccines touted under ‘new and improved’ ‘minor adjustments’ etc. must run for at least 20 years of proper duration, sample size, patient-important outcomes, gold-standard trustworthy research methods, and with all the necessary safety follow-up. Any such study must have proper ethical debate and accompanied by cost-effectiveness analyses. Drugs and vaccines and medical devices must not only meet safety and effectiveness thresholds but there must be a dedicated examination of if the drug or vaccine is NEEDED, necessary.
NIH must return to the 1972/1975 Nixon era and agreements (1969 to 1976 Nixon era, the Biological Weapons Convention (BWC), or Biological and Toxin Weapons Convention (BTWC) 1975 relating to weapons of mass destruction) and renounce the use of lethal biological agents and weapons, and all other methods of biological warfare. Renounce its role in such lethal biological agents and weapons. NIH will confine its biological research to defensive measures such as immunization and safety measures and work with the Department of Defense in disposing of existing stocks of bacteriological or any such weapons or specimens. The same posture for NIH in use or research in and of lethal chemical weapons.
NIH must end any conflicted relationship (real, perceived etc.) with the pharmaceutical industry as it relates to approval of any of its funded studies.
NIH is to take no funding or donations from any pharmaceutical industry parties etc.
NIH must have no contact whatsoever (direct or indirect) with the Chief of Staff Suzie Wiles of the Trump administration.
NIH’s new Director must move to abolish DEI ‘woke’ hiring at the agency and return to a pure merit based.
NIH new Director must work with academia, academic publishing, academic journals to rework, redo the journal editor standards and peer-review process for scientific writing and publishing. Medical journal peer review is dead, lost its independence as has EBM given their capitulation to pushing lockdowns and mRNA vaccine and the fraud pandemic and must be revamped moving forward; NIH has the power to forge this in the USA.
2) FDA
The Food and Drug Administration (FDA) must disband the current drug and vaccine research and related EUA and BLA panels, decision groups, advisory boards, external and internal boards and make know to the public all the decisions and what went into them across COVID for all COVID decisions.
The FDA commissioner must IMMEDIATELY call for the withdrawal of any and all mRNA technology related vaccines e.g. Pfizer, Moderna etc.; complete; this must include a complete removal from market with witnessed destruction of any supplies.
The FDA commissioner must IMMEDIATELY call for the end of any mRNA technology gene-based vaccine research. Complete.
FDA Commissioner (incoming) must commit to end the revolving door between itself (Commissioners) and BIG Pharma, that he himself/herself will accept no position within BIG Pharma for at least 5 years post leaving the FDA post.
The FDA commissioner must state immediately that there will not be any FAST TRACK approvals of any future products especially vaccines that come to it for approval.
The FDA commissioner must initiate a public open examination of all EUAs granted to Pfizer and Moderna etc. as it relates to all COVID mRNA vaccines, DNA viral vector, any drugs e.g. Paxlovid etc. In fact, any and all medications and vaccines and any sort of ‘countermeasure’ that the FDA gave EUA approval for up to this date.
The FDA must initiate new and proper vaccine and drug advisory boards within 2 weeks of the new FDA lead taking over.
The FDA must make available to the public (in at most 6 months after approval of the incoming Commissioner) all the data, evidence, submissions, everything, that all organizations and entities submitted to it across COVID up to present, including all data and submissions that went into the FDA’s approval (EUAs) of the Pfizer and Moderna mRNA gene vaccines. All.
The FDA must call for an urgent meeting of all the vaccine companies e.g. CEOs Bourla, Bancel, Sahin etc. and all mRNA technology inventors e.g. Malone, Weissman, Tureci, Kariko etc. and especially those vaccine makers that manufactured Malone et al. mRNA gene vaccines e.g. Pfizer, Moderna, BioNTech etc. and in live open door public meetings, display all the harms, adverse event, death data it has (they have in possession) and allow all relevant external experts to attend to produce all the harms, adverse event, and death data that has accumulated since the roll-out of the mRNA vaccine. All aspects of the mRNA vaccine must be reviewed in public and all made available to the public within 6 months of the new FDA Commissioner taking office.
There is no existing randomized placebo-controlled study double blinded, or triple blinded that shows that the COVID mRNA gene vaccines reduced hospitalization, death, ICU, severe illness etc. in children or adults, elderly etc. The FDA Commissioner must reveal to the public what studies the FDA (past and existing under new leadership) uses to support that statement that the mRNA vaccine reduced hospitalization and death and was beneficial to the public, e.g. in the elderly.
The FDA must cease and desist any and all promotion of the mRNA gene vaccine for COVID.
All senior officials of FDA must be removed and re-assigned to other agencies. 25% of the FDA’s workforce must be fired within 2 months of the new FDA Commissioner taking office.
FDA must end any conflicted relationship (real, perceived etc.) with the pharmaceutical industry as it relates to approval of any of its funded studies or decisions, advisory boards etc.
FDA is to take no funding or donations or financial support of any kind from any pharmaceutical industry parties etc.
FDA must have no contact whatsoever (direct or indirect) with the Chief of Staff Suzie Wiles of the Trump administration.
The new FDA Commissioner under Trump 2.0 must work with head agency HHS Secretary and CDC and NIH etc. to reverse the 1986 Childhood vaccine ACT; National Childhood Vaccine Injury Act (NCVIA) of 1986 (42 U.S.C. §§ 300aa-1 to 300aa-34) was signed into law by United States President Ronald Reagan; NCVIA's purpose was to eliminate the potential financial liability of vaccine manufacturers due to vaccine injury claims; so that anyone harmed in the future by vaccines can sue the vaccine makers and all involved
The new FDA Commissioner under Trump 2.0 must work with head agency HHS Secretary and CDC and NIH etc. to end and make retroactive the LIABILITY PROTECTION under PREP Act that Azar helped implement (Feb/March 2020) and enforce/activate for the fraud PCR manufactured COVID; this so that those harmed by the mRNA vaccine can enter courts for financial redress.
The new FDA Commissioner under Trump 2.0 must make available to the public all data related to COVID, all, all linked to the mRNA vaccines that FDA, CDC, NIH etc. has in possession. Bourla, Bancel etc. All.
The new FDA Commissioner under Trump 2.0 with CDC, HHS etc. must work immediately with POTUS Trump to end the woke TRANSGENDER madness and brutal transgender surgeries and puberty blockers on our children.
The new FDA Commissioner under Trump 2.0 must work with head agency HHS Secretary and CDC and NIH etc. to set up a victim compensation fund for all those hurt by the COVID fraud OWS lockdowns and the Malone et al. mRNA vaccine.
FDA’s new Commissioner must move to abolish DEI ‘woke’ hiring at the agency and return to a pure merit based.
FDA’s new Commissioner must work with NIH as the co-leads, and together force academia, academic publishing, academic journals to rework, to redo the journal editor standards and peer-review process for scientific writing and publishing. Medical journal peer review is dead, lost its independence as has EBM given their capitulation to pushing lockdowns and mRNA vaccine and the fraud pandemic and must be revamped moving forward; NIH and FDA has the power to forge this in the USA.
3) CDC
The CDC must immediately disband the MMWR (Morbidity and Mortality Weekly Report) it produces (especially during COVID) given its lack of scientific rigor, merit, substance and the politicization of the MMWR. The MMWR in COVID (and prior) operated as a political tool to damage POTUS Trump and it tantamounts to pseudo-science and NOT proper academic research or publishing. This may be replaced by an independent, unbiased public health report.
The CDC must cease and desist any and all promotion of the mRNA technology gene vaccine for COVID.
The CDC Director must call for an immediate stoppage of the mRNA technology and mRNA gene vaccine, that it must not be made available to the public.
CDC Director (incoming) must commit to end the revolving door between itself and BIG Pharma, that he himself/herself will accept no position within BIG Pharma for at least 5 years post leaving the CDC position.
All senior officials of CDC must be removed and re-assigned to other agencies. 25% of the CDC’s workforce must be fired within 2 months of the new CDC Director taking office.
The CDC must immediately disband the VAERS vaccine adverse event database surveillance system and replace it with an updated acute surveillance system to track and report on mRNA vaccine harms and deaths with a focus on the upcoming 25 years.
CDC must immediately stop all gain-of-function (GoF) or related research in any US affiliated or funded or operated biolab anywhere in the world. CDC must stop its involvement (direct or indirectly) all bioweapons biological research in US laboratories and anywhere globally that the US is affiliated to. No US tax-payer money must be used for any such research anywhere in the world.
CDC must end any conflicted relationship (real, perceived etc.) with the pharmaceutical industry as it relates to approval of any of its funded studies or decisions, advisory boards etc.
CDC is to take no funding or donations or financial support of any kind from any pharmaceutical industry parties etc.
CDC must have no contact whatsoever (direct or indirect) with the Chief of Staff Suzie Wiles of the Trump administration.
CDC’s new Director must move to abolish DEI ‘woke’ hiring at the agency and return to a pure merit based.
4) NIAID
NIAID must immediately stop all gain-of-function (GoF) or related research in any US affiliated or funded or operated biolab anywhere in the world. NIAID must stop its involvement (direct or indirectly) all bioweapons biological research in US laboratories and anywhere globally that the US is affiliated to. No US tax-payer money must be used for any such research anywhere in the world. NIAID must return to the 1972/1975 Nixon era and agreements (1969 to 1976 Nixon era, the Biological Weapons Convention (BWC), or Biological and Toxin Weapons Convention (BTWC) 1975 relating to weapons of mass destruction) and renounce the use of lethal biological agents and weapons, and all other methods of biological warfare. Renounce its role in such lethal biological agents and weapons. NIAID will confine its biological research to defensive measures such as immunization and safety measures and work with the Department of Defense in disposing of existing stocks of bacteriological or any such weapons or specimens. The same posture for NIAID in use or research in and of lethal chemical weapons.
NIAID must end any conflicted relationship (real, perceived etc.) with the pharmaceutical industry as it relates to approval of any of its funded studies or decisions, advisory boards etc.
NIAID is to take no funding or donations or financial support of any kind from any pharmaceutical industry parties etc.
NIAID must have no contact whatsoever (direct or indirect) with the Chief of Staff Suzie Wiles of the Trump administration.
NIAID’s new Director must move to abolish DEI ‘woke’ hiring at the agency and return to a pure merit based. If possible, shut down NIAID as an entity and place key components within other existing science and research agencies.
SOURCE:
https://palexander.substack.com/p/i-have-noticed-some-in-the-anti-covid
James Roguski
310-619-3055
JamesRoguski.substack.com/archive
ControlBloodSugarNaturally.com
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This is Fantastic James, so glad you have reached out to President Trump. I have tried in the past and it went nowhere, but now a really good chance to get the message across to him! I'm working on getting the flyer printed on one side, with the "open letter" on the other side in a 950 subscribers News Paper. I'm pretty confident that it will work. Thank you James for Never Giving Up on Our Country!!
God Bless You and Yours Always!!!!