IOJ Files IMPORTANT HHS DoD FOIA Appeal. Give Us The Records On Covid Vaccine Countermeasure Experiment Records. No More Loopholes and Semantics To Pretend The EXPERIMENT Is Not Investigational DoD!
Ok DoD/HHS we get it. You are playing the game of SPELLing & terms of art to pretend there is no experiment with biological agents on civilians. Is there an ATTACK HHS? We need more information dammit
Folks - the next round of IOJ lawsuits are coming quicker than you may think. Lets start here with HHS and DoD getting all crazy and rolling out covid vaccine countermeasure experiments with NO human rights protections. We filed an appeal last night to HHS regarding DoD countermeasures and required reports and agreements between DoD & HHS for the covid vaccine rollout, delegation of authority to export covid vaccines and more which HHS pretends all of it does not exist.
The only way we can sue HHS and DoD for the non vaccine experiments with no human rights protections is to file the appeal. Read the appeal below.
We asked for some KEY INFO A WHILE BACK AND HHS SAYS IT CANT BE FOUND. NONE OF IT?
Fishy? Yes.
How it all began:
![HHS Says Our FOIA Request Is "Unusual & Will Need More Time" For The Covid-19 Vaccine Reports Regarding The Military Plans To Rollout Experimental Countermeasure [non]Vaccines.](https://substackcdn.com/image/fetch/w_280,h_280,c_fill,f_webp,q_auto:good,fl_progressive:steep,g_auto/https%3A%2F%2Fsubstack-post-media.s3.amazonaws.com%2Fpublic%2Fimages%2F755c88e6-26c2-43d0-9992-6489b7c506f3_768x432.gif)
Where we are now is having to appeal and ask HHS to find the reports we asked for, or please explain why DoD is exempt from the required reports that include Congress intent for human rights requirements for experiments on civilians:
Read Our Appeal:
Freedom of Information Act Appeal
TO: William H. Holzerland
Deputy Agency Chief FOIA Officer
U.S. Department of Health and Human Services
Office of the Assistant Secretary for Public Affairs
RE: Case No. 2023-*****-FOIA-OS -
Sent via email: Response from HHS FOIA - 10/23/2023 6:21 AM
Dustin Bryce
Public Relations
Interest Of Justice
Dear Friends,
This is an appeal under the Freedom of Information Act. My request was assigned the following identification number: 2023*****-FOIA-OS . On 10/23/2023 6:21 AM, I received a response to my request in a letter signed by Arianne Perkins, Director, Initial FOIA Requests, FOI/Privacy Acts Division.
I appeal the denial of my information request sent March 10, 2023.
The documents that were "not found" must be disclosed under the FOIA because they are statutorily required reports for initiating DoD & HHS experimentation that must be in existence prior to the human research (experiments) using covid-19 vaccines or exports.
Our organization is not aware of any exemption to these required records, and if the DoD and HHS used an exemption or waiver to evade responsibility for issuing the reports we requested then we would like to know precisely which laws or authorities allow DoD and HHS to not have the requested reports.
Semantics and legal loopholes do not change the fact that under US and international law all clinical and non clinical research on humans are properly labelled as "experimentation" or biomedical research "experiments".
The covid-19 vaccines at the time of rollout were not approved and other than Corminarty which was recklessly and outrageously approved despite unfavorable risk to benefit ratio, all are still not approved, therefore the non approved covid-19 vaccines were and still are investigational under many laws and the word means experimental.
see: https://www.fda.gov/patients/learn-about-expanded-access-and-other-treatment-options/understanding-investigational-drugs#:~:text=An%20investigational%20drug%20can%20also,be%20used%20in%20that%20disease. An investigational drug can also be called an experimental drug and is being studied to see if your disease or medical condition improves while taking it. Scientists are trying to prove in clinical trials:
If the drug is safe and effective.
How the drug might be used in that disease.
How much of the drug is needed.
Information about the potential benefits and risks of taking the drug.
and see: https://www.fda.gov/news-events/expanded-access/expanded-access-information-physicians#:~:text=Sometimes%20called%20%E2%80%9Ccompassionate%20use%E2%80%9D%2C,trials%20when%20no%20comparable%20or Investigational medical products have not yet been approved or cleared by FDA and FDA has not found these products to be safe and effective for their specific use. Furthermore, the investigational medical product may, or may not, be effective in the treatment of the condition, and use of the product may cause unexpected serious side effects.
HHS exports the experimental products to Costa Rica (apparently with no Delegation of Authority on record?), and the law there is clear: 9234: ARTICLE 1.- Object of the law The purpose of this law is to regulate biomedical research with human beings in health matters, in the public and private sectors. Definitions Article 2: Experimental, clinical or interventional biomedical research: any scientific research in the area of health in which a preventive, diagnostic or therapeutic intervention is applied to human beings, in order to discover or verify the clinical, pharmacological or pharmacodynamic effects of an experimental product, a medical device or a clinical or surgical procedure; or that attempts to identify any adverse reaction to an experimental product, device, or procedure; or study the absorption, distribution, metabolism and excretion of an experimental product, in order to assess its safety and efficacy or assess the outcome of an unproven psychological intervention. For the purposes of this law, all references to clinical research shall be understood as experimental, clinical or interventional biomedical research in human beings in the area of health.
We write on behalf of our organization Interest of Justice as well as for the best interest of the Comptroller of Costa Rica, who has tasked us the responsibility of investigating the irregularity of the covid-19 vaccine imports and use. We all require the requested information from the US government.
Disclosure of the documents we requested in is in the public interest because the information is likely to contribute significantly to public understanding of the operations or activities of government and is not primarily in any commercial interest.
We kindly request that you locate every item on the list of requested reports and immediately release any withheld documents not withstanding their exempt status, which must be explained in detail with HHS authority and reason for the exempt status.
The public interest in their release outweighs the public interest in withholding them because the Congress intent is to have the required records we requested issued prior to any research/experimentation using biological agents, which covid vaccines meet the exact definition of a biological agent and therefore, the requested reports must exist as a matter of HHS statutory obligations!
We need the records to be located and released or the precise reasons why DoD and HHS are not required to have them.
The information is required by Congress as a way to protect the welfare, safety and human rights of the people using HHS and DoD countermeasure products.
We require the requested reports to be provided promptly, or in the alternative, if they really do not exist (which is doubtful) we require HHS to explain point by point why each requested report does not exist in the record as it should be as a matter of law.
For instance, considering the sheer volume of exports of covid-19 vaccines from US to developing countries and COVAX, one would think the delegation of authority to export covid-19 vaccines should be a locatable record, as well as the other reasonable requests.
How could HHS and DoD have no agreement on record to roll out covid-19 vaccines using peacetime authority? Are we in war? The lack of these required records makes no sense and seems like a cover up. HHS cant find a single document out of our 3 easy FOIA requests.
Obviously there is a HUGE legal problem if these records are truly not in existence and HHS would owe detailed explanations why they are exempt from the statutory requirements and records we are requesting. The records are required in order for us to fulfill our mission to defend and protect human rights by holding government to account for their duties.
If you need to discuss this request, I can be reached at +1-323-***-****. Thank you for your consideration of this appeal.
Cordially,
Dustin Bryce
Public Relations
Interest Of Justice
Related Reading (subject of next HHS Dod FOIA Appeal and LAWSUIT COMING SOON):
If you don’t want the WHO pandemic agreement, tell HHS how you feel about it sign the protest and request for a science integrity hearing below:
Just a reminder.... Mistakes are/were NOT made.....They have been at this for decades..... we need to educate everyone.....
Back in 1969, Dr Richard Day made some astonishing predictions about where the world would be today https://henrithibodeau.wordpress.com/2015/06/08/back-in-1969-dr-richard-day-made-some-astonishing-predictions-about-where-the-world-would-be-today/
How to Fake Pandemics in 4 Easy Steps A masterclass by the DOD showman, James Giordano. https://sashalatypova.substack.com/p/how-to-fake-pandemics-in-4-easy-steps
...hard to believe that this level of evil exists in our world....
WORLD WIDE PEOPLE IN UNITY, UNITE WITH GOD AND LIKE MINDED WARRIORS TO RID EVILS BACK TO THE DARK CLOSETS THEY CRAWLED FROM