September 11, 2002
Dear Mr. Carey: Below please find an AIDS cure patented by the United States in 1997. In November of last year I took the one-time injection. My life has drastically improved. The inventor, Dr. Marvin Antelman can be reached at 401-223-3000.
I am of the opinion the HIV enzyme was created in accordance with the 6,000 pages of the fifteeen progress reports of the U.S. Special Virus program. For some of the comments of some of the scientists on this list, please go to: www.boydgraves.com/comments .
According to Professor Lee, author of "AIDS: An Explosion of th eBiological Timebomb?", there was no HIV prior to this federal program. We have painstakingly pursued the Congressional Black Cause for review and investigation of this federal virus development program to no avail. We find NO ONE home in the security system of the American people to the detriment of African American and others.
There appears to be an entire section of this program that worked exclusively on cures and vaccine for the Special (AIDS) Virus. See, PHASE IV-A , 1971 "Research Logic" flowchart of the program.
In my opinion, we have found the wellspring of the genesis of AIDS. It is the U.S. Special Virus program. Specifically, the federal virus program "isolates" a human retrovirus and immediately inoculated non human primates. See, page 105, progress report #8 (1971), U.S. Special (AIDS) Virus program. Further, the program concedes that nazi visna had not yet been seen in human disease. id at 39. NOW, according to the Proceedings of the United States of America, the inhibition of visna is being studied to inhibit HIV. See, PROC NAS VOL 92, 3283 - 3287,Apirl 11, 1995.
In my opinion, the "identical match" sequences between HIV and VISNA can not be explained but for the recombinant genetics of this federal virus development program.
In 1926, the United States held a "Virus Cancer" Conference at M.I.T. The United States has known for the entire 20th Century that viruses cause cancer. An intensive effort was underway throughout the 20th Century to find an "ethnic biological weapon" which resulted in the United States concession they were attempting to develop "candidate human viruses". See, page 31, progress report #8 (1971).
A review of progress report #15 (1978) shows all of the "CREG's (Continuing Research Education Grants) are relevant to our modern day understanding oh HIV science.
In June of this year, the U.S. General Accounting Office (GAO) thwarted U.S. investigation of the program by bogusly concluding the federal virus program, that spent $550 million dollars, between 1964 and 1978, had nothing to do with the development of HIV. According to IADS ORIGIN researcher, Alan Cantwell, M.D., the federal virus program made 60,000 liters of HIV(and other viruses), ending in June 1978. Then, and only then, were there dueling epicenters of death in Africa and Manhattan.
According to Dr. Basil Wainwright, PhD, there will be no more Black Africans in 64 years. In this regard, I believe the United States will address every other issue except its secret, genocidal program aimed at people of color (and other alleged undesirables).
In light of the fact that the HIV is designed to seek out the CCR5 gene, known as the African American HIV entryway, I sincerely feel it behooves us to address the root cause of this biological disparity we call HIV/AIDS. In other words, we can not allow them to continue to kill us while we push to be re-paid. There will be none of us left to cash any check without our collective intellectual prowess firmly focused on the review and investigation of this mostly-secret federal virus development program. Boyd E. Graves, J.D.
for additional evidence: www.boydgraves.com
United States Patent 5,676,977
Antelman October 14, 1997
Method of curing AIDS with tetrasilver tetroxide molecular crystal devices
The diamagnetic semiconducting molecular crystal tetrasilver tetroxide (Ag.sub.4 O.sub.4) is utilized for destroying the AIDS virus, destroying AIDS synergistic pathogens and immunity suppressing moieties (ISM) in humans. A single intravenous injection of the devices is all that is required for efficacy at levels of about 40 PPM of human blood. The device molecular crystal contains two mono and two trivalent silver ions capable of "firing" electrons capable of electrocuting the AIDS virus, pathogens and ISM. When administered into the bloodstream, the device electrons will be triggered by pathogens, a proliferating virus and ISM, and when fired will simultaneously trigger a redox chelation mechanism resulting in divalent silver moieties which chelate and bind active sites of the entities destroying them. The devices are completely non-toxic. However, they put stress on the liver causing hepatomegaly, but there is no loss of liver function.
Inventors: Antelman; Marvin S. (Rehovot, IL)
Assignee: Antelman Technologies Ltd. (Providence, RI)
Appl. No.: 658955
Filed: May 31, 1996
Current U.S. Class: 424/618; 514/495
Intern'l Class: A61K 033/38
Field of Search: 424/618 514/495
Hi my name is Gregory Carey, president of Reparations
Central (http://www.reparationscentral.com) I am
wondering what the solution is to what you speak about,
now that you have each identified the cause and the
problem? I also would like to know where you stand on
the issue of reparations for African Americans. At this
time we are in the process of getting together the
right minded people that can help us put together a
National Congress on Reparations. Do you have
organizational skills that can be used?
Peace Be Upon You,
G. Carey >
PLEASE CONTACT YOUR CONGRESSMEN AND SENATORS.doc