This Is A Bio-Attack Alert, March 28, 1986
This results from an attempt by myself and my brother to form an Health Maintenance Organization. I had difficulty estimating the probable cost of the "Human Retroviruses" as related to premium costs and was led deeper and deeper into the literature of virology attempting to solve the problem.
At first I considered testing and
allowing individuals infected with the AIDS virus to form a special
group, associate, insure, and have sexual relations. The literature
reveals that plan will not work because the greater number of times one
is infected with "Human Retroviruses" the more quickly one dies. There
is a critical mass of infection which leads to reinfection of
associating individuals and accelerated death. (l), I abandoned that
Apparently, individuals in the
United States National Institute of Health and National Cancer Institute
have combined with the United Nation's World Health Organization to
attack the United States with Bio-Weapons. (6-8):
Congress whom I ask deliver this
to members of Congress as they deem appropriate.
In Volume 47 of the
Bulletin of The World Health Organization, pages 257 through 274 (1972)
, we find A. C. Allison with others including WHO officials and an NIH
bureaucrat recommend at page 259:(6)
(3): An attempt should be made to ascertain whether viruses can in fact
exert selective effects on immune function, e.g., by depressing 7S vs
19S antibody, or, by affecting T cell function as opposed to B cell
function (Allison et.. al., 1972). The possibility should also be looked
into that the immune response to the virus itself may be impaired if the
infecting virus damages more or less selectively the cells responding to
the viral antigens.
All their planning would be
worthless without willing bodies to do the work. The evidence of the
bodies is provided by the Seventh National Cancer Conference
Proceedings, sponsored by the American Cancer Society, Inc., and
the United States National Cancer Institute, published by the J. B.
Lippencott Company, Philadelphia and Toronto 1972. (8) It contains the
report on epidemiology by John Higginson, M.D., director of the
International Agency for Research on Cancer, Lyon, France, and a map on
page 681 indicating the world wide distribution of that agency's
programs. It is important that we remember that the date of the map is
1972, as we read the words of Doctor Higginson at page 680:
"......The complex biology of cancer makes it essential to approach observational studies in man with the same technical sophistication that characterizes animal experimentation. Thus, the Governing and Scientific Councils decided that the Agency's epidemiological studies should be fully integrated with recent developments in laboratory research and that a multidisciplinary team approach was essential to insure that the Agency would make full use of its unique international situation. The mere collection of numerical data --"nose-counting"-- is of no value per se, and descriptive epidemiology is only one of many disciplines concerned in the study of cancer causation. (Emphasis added)
Of course, descriptive epidemiology is merely the collection and analysis of numerical data. On the other hand the "technical sophistication that characterizes animal experimentation" involves the inoculation of disease into the research animals.
All we need to do to see the relationship between the "Governing and Scientific Councils," inoculation of disease, the AIDS virus, and its related Retroviruses is pincil in the homosexual cohorts from the Hepatitis B vaccine study reported in the Annals of Internal Medicine, Vol. 97, No. 3, (1982) pages 362-369, (31) on the map on page 681 of the Seventh National Conference Proceedings, (8) and we have marked the Retroviruses concentrations of the world as now known. The St. Louis and Chicago cohorts of the Hepatitis B Studies may have served as controls or got a dose of a slower acting cancer inducer like HTLV-I or HTLV-II. Robert C. Gallo and Flossie Wong-Stall reproduced the map for us at page 396 of their attack, "Human T-Lymphotropic Retroviruses", Nature, Vol. 317, October 3, 1985. (32) (maps enclosed)
THE CONFUSION OF TODAY
Writing in LANCET, January 11, 1986, (5) Doctor Robert J. Biggarof the United States National Institute of Health said:
"....The AIDS agent, a complicated Retroviruses with core proteins and a glycoprotein envelope, could not have originated de novo. The identification of the progenitor agent from which this agent either mutated or recombined has significant implications. First, the ancestor agent has not yet been identified. Its pattern of disease associations in man may differ from that of HTLV-III/LAV.... Secondly, the non-pathogenic progenitor could be a safe source of immunizing material if there is any neutralizing cross-reactivity between the two agents. (5)
I agree. I suggest:
(1) The World Health organization
asked for the AIDS virus HTLV-III/LAV/ARV) and it was supplied; (6-8)
(3) HTLV-II is bovine syncytial virus (BSV): in man; (14-17,24)
(4) HTLV-I is bovine leukemia virus (BLV), in man, is highly contagious, is vector borne, and is fomite born.(18-20,22,24)
I have also suggested that unless
the United States National Institute of Health has taken the advice of
Dr. Jacques Leibowitch given on page 97 of the English translation his
book, A Strange Virus of Unknown Origin (27), and had them stolen or
changed., Dr. Biggar should request the cell lines NBC-1 through NBC-13.
He will most likely find the progenitor he seeks in NBC-6, NBC-8,
NBC-10, or NBC-13 . (2 8,29) He should start with NBC-13.
GIVEN THE REACTION OF THE MEDICAL JOURNALS TO WHICH THESE SUGGESTIONS WERE SUBMITTED, I MAY BE CORRECT IN MY IDENTIFICATION OF THE AGENTS INVOLVED. I enclose copies of my letters and the journals' replies. HOWEVER, I SUGGEST TO YOU THAT MY IDENTIFICATION OF THE PROGENITOR IS UNNECESSARY BECAUSE THE AIDS VIRUS ITSELF REPRESENTS THE FRUITION OF THE MURDER PLAN OUTLINED ABOVE.
THE OBJECTIVE OF THE ATTACK
The purpose of the attack may be to prepare America by infection with immune depressing virus for a fast bio-attack. If that is true, it was started in the homosexuals in America because the enemy correctly judged that most Americans would not be alarmed by a homosexual disease. I wasn't alarmed by the "Homosexual" disease until I started my virology literature search. The disease will inexorably spread to the heterosexual population. The lies of the United States National Institute of Health in this regard reveal its Participation in the attack. AIDS is not merely a homosexual disease and the NIH knows it.
In war the objective of each contesting side is to inflict death and wounds upon the other. The method chosen by the enemy will preserve American land and structures for the victors. Their action is calculated to demonstrate that right lies in their might, and freedom, impossible.
The enemy hopes to impose despotic rule by the few and cry of the population to abandon the rights of others including the infected to save themselves. This is an attempt to exhaust America with hatred, struggle, want, confusion, and inoculation of disease. The enemy intends to control our population with disease, make us dependent upon their remedies, engineer each birth, and reduce America to a servant of the Supreme Soviet. All this, even though America has repeatedly abandon any attempt at world domination when such was easily within its power. It is not, repeat not, too late to thwart this plan.
THE BATTLE STATUS
This is being fought slowly. Few know that it is going on. Does D. Carlton Gajdusek, now chief of the National Institute of Health's laboratory of Central Nervous System Studies and Labatory of Slow, Latent and Temperate Virus Infections know? At page 106 of Omni, March, 1986, (34) in response to the question, "Isn't Fort Detrick in Maryland such a Biological-Warfare Research Facility", he answers:
"No, emphatically no! There is no defensive or offensive warfare microbiology done at Fort Detrick today. It is the national cancer research facility of NIH. In this facility I have a building where more good and loyal Communist scientists from the USSR and laboratories than Americans. With bright working U.S. citizens and foreign Communist investigators here, obviously there is no "secret" bacterial warfare activity going on. Even the Army's infectious-disease unit is loaded with foreign workers not always friendly nationals. It is a valid basic research unit on worldwide problems of infectious diseases in which no classified or secret activities unfold....."
Of course, there are no secret activities unfolding. They, the virologists of WHO, NCI, and the NIH, have written in plain english their plan for conquest of America and are presently executing it disguised as cancer research.
Gentleman, we are under attack. We must act. If Dr. Gajdusek is correct, only a few loyal Communist scientists will be required to conclude the enemy's assault. Obviously, this might be done by contamination of American scientists experiments or despoiling vaccine cultures. At present only an estimated 2 million Americans are infected. We can deal with that amount, but, we must halt these induced diseases' spread. We are losing population to the AIDS virus at a rate of 2000 per week infected all of which will die prematurely.
The traitors have destroyed 14 years of virus research by lying in their research papers and inoculating subjects. Yet, we allow the enemy abide on these shores.
Read Ralph Kinney Bennett' characterization of the United Nations. He claims the U.N. has become:
An organization that sanctions the violent overthrow of sovereign governments;
One of the Soviet Union's most important espionage posts in the West;
A political base, a source of funds and a propaganda organ for terrorist organizations;
The advocate of a new "World Order" amounting to global socialism;
A forum for anti-American, anti-Western, anti-free-enterprise activity. (30)
He is correct. We have allowed
the United Nations World Health Organization to combine with traitors in
the United States National Institute of Health to start a Soviet Union
The Correct Response
America has always been poised
between the pit of anarchy and the abyss of despotic rule. We are
delicately balanced on the ledge of liberty.
Unknowing Africans, (sibships
inoculated) hemophiliacs, (contaminated blood transfusions) southern
poor, (free shots) homosexuals, (Hepatitis B inoculations) and unwarned
heterosexuals trusted and died. You are next. Those groups were selected
for initial attack because the enemy hoped no one would attempt to
defend until it was too late. We must:
2. Mobilize national guard to prepare quarentine hospitals and hospices for the infected individuals. Note that some of these institutions must be quite large. We need not leave our wounded in the field.
3. Inform the American people that the nation has been attacked and the enemy is ashore and advancing. Inform all scientists concerning the true nature of the disease and its origin. Someone may have a cure.4. Arrest the immediately identifiable individual's for murder and submit their cases to grand juries for indictment. Include all culpable members of IARC, NIH, NCI, and WHO presently in this country. Locate other culpable individuals and return them for trial.
5. Seize all the records in the
CDC and NIH of the inoculation projects. We will need them for the
prosecutions. Attach the U.N. building and all U.N. funds including
6. Try the culpable individuals. But, note that some scientists will have been confused and tricked by the Governing and Scientific councils. We will have to sort carefully.
7. Alert remaining doctors to be on guard against other ordered diseases. See 47 WHO Bull. Organize for quarantine. Hopefully, quarantine won't be needed, but, we must act quickly.
8. Be on guard against
vaccination projects. Merck is the company that made the Hepatitis
vaccine that went into the American homosexual cohorts. AIDS is not
progressing quickly enough to-satisfy the murderers or to hide their
.... a sexually
transmitted disease needs a "portal of entry" in order to affect a
group. For example, if half a dozen promiscuous students returned to a
college campus carrying the virus in the fall, the virus would have
achieved a "portal of entry" to that campus.
10. The enemy wants us to abandon
our wounded, abandon liberty, abandon due process of law, and submit to
their despotic rule while they cull and kill. That is the only way that
these diseases have been controlled in bovines. If we wait much longer,
we all will be infected and reinfection each other. That is the enemy's
goal. There are presently drugs which may inhibit the progress of these
diseases and the NIH may be hiding them. (36,37) We need not fear the
enemy. We shall cull the enemy from our midst and deal with these
murders as provided by law. We need not live enslaved in chains of
tyranny. Neither need we leave our children to these bastards' tender
mercies. AIDS is not a homosexual disease and the NIH knows it.
In my judgment we should respond as a United States not as individual States. Our response need not be based on institutionalized lies. In the time after you receive this warning, you should decide for yourself whether or not I am correct by consulting the listed references. Make sure that any experts consulted are not working for or supported by. grants of the WHO NIH, CDC, or NCI.
The Department of Defense must be prepared to respond to an attack originating elsewhere. If the President does not lead the nation in response to the attack, the Governors of the several states must act to protect their state's residents by alerting them to it and taking such action as is within their power if Any are convinced I am correct.
If the President fails to act and the Governors are convinced that I am correct, the Governors should act. We have to restructure the U.N., NCI, and NIH.
All that 14 years of research has done is institutionalize fraud and murder as national policy, move disease from cows to men, and speed the Soviet Union toward its goal of world domination. We are far from any cancer cure other than hype reported to the community.
Very truly yours,
Theodore A. Strecker
334 North Central Ave. Suite 101
Glendale CA 91203 USA
1. Goedert JJ. Biggar RJ. Weiss SH. et al. Three-Year Incidence of AIDS in Five Cohorts of HTLV-III--Infected Risk Group Members. Science 1986; 231:992-5.
2. Barre-Sinoussi F. Nugeyre MT.
Chermann JC. Resistance of AIDS Virus at Room Temperature. Lancet 1985;
iii:721-2. (Sept. 28, 1985)
8. Higginson J. The Epidemiological Program of the International Agency for Research on Cancer. In: Seventh National Cancer Conference Proceedings. Los Angeles: American Cancer Society, Inc. and National Cancer Institute. 1972:679-684. (Note the map on page 681 as it relates to the epidemiology of AIDS in reference No.'s 32 and 33.)
9. Georgiades JA. Billiau A. Vanderschueren B. Infection of Human Cell Cultures with Bovine Visna Virus. J Gen Vir 1978;38:375-81
10. Van Der Matten MJ. Booth AD. Seger CL. Isolation of a Virus From Cattle With Persistent Lymphocytosis. JNCI 1972; 49:1649-57.
11. Booth AD. Van Der Matten MJ.
Ultrastructural Studies of a Visna-Like Syncytia-Producing virus from
Cattle with Lymphocytosis. J
12. Van Der Matten MJ. Miller JM. Booth AD. Replicating Type-C Virus Particles in Monolayer Cell Cultures of Tissues From Cattle With Lymphosaarcoma. JNCI 1974; 52:491-4.
13. Dodds JA. Hamilton RI. Structural Interactions Between Viruses as a Consequence of Mixed Infections. In: Advances in VIRUS RESEARCH. ed Lauffer MA. Bang FB. Maramorosch K. Smith KM. New York: Academic Press, 1976:33-86. (vol 20);
14. Malmquist WA. Van Der Matten
MJ. Booth AD. et al. Isolation, Immunodif fusion, Immunofluorescence,
and Electron Microscopy of a Syncytial Virus of Lymphosarcomatous and
Apparently Normal Cattle. Can
15. Dermott E. Clark JK. Samuels J. et al. The Morphogenesis and Classification of Bovine Syncytial Virus. J Gen Vir 1971, 12:105-19.
16. Parks WP. Todaro GJ. Biological Properties of Syncytium-Forming ('Foamy'): Viruses. Virology 1972; 47:673-83.
17. Gallagher RE. Gallo RC. Type C RNA Tumor Virus Isolated from Cultured Human Acute Myelogenous Leukemia Cells. Science 1975; 187:350-3. (Note designation of patient as HL-23.)
18. Van der Matten MJ. Miller JM. Serological Evidence of Transmission of Bovine Leukemia Virus to Chimpanzees'. Vet Micro 1976; 1:1351-7.
19. Miller JM. Miller LD. Olson C. Gillette KG. Virus-Like Particles in Phytohemagglutinin-Stimulated Lymphocyte Cultures With Reference to Bovine Lymphosarcoma. JNCI 1969; 43:1297-305.
20. Burny A. Bruck C.. Chantrenne
H. et al. Bovine Leukemia Virus: Molecular Biology and Epidemiology. In:
Viral Oncology Ed. Klein G. 1980 Raven Press. (See particularly page
232, Table 1; Note BLV and BSV disease characteristics in cows which are
duplicated in humans for
21, Sodroske J. Rosen C. Wong-Stall F. et al. Trans-Acting Transciptional Regulation of Human T-Cell Leukemia Virus Type III Long Terminal Repeat. Science 1985, 1227:171-3.
22. Corneo G. Nelli LC. Medica II
CdP. et al. Could Bovine Leukemia
23. Biggar RJ. Melbye M. Sarin PS. et al. ELISA HTLV Retrovirus Antibody Reactivity Associated with Malaria and immune Complexes in Healthy Africans. Lancet; ii:520-3.(Sept- 7, 1985).
24. Gallo RC. Essex ME. Gross L.
Ed. Human T-Cell Leukemia/Lymphoma
25. Blattner WA. Gallo RC. Epidemiology of Human Retroviruses. Leuk Res 1985; 9:697-8. (Note that a tool is man-made instrument for work.)
26. Hino S. Yamaguchi K. Katamine S. et al. Mother-to-Child Transmission of Human T-Cell Leukemia Virus Type-I. Jpn J Can Res (Gann)- 1985: 76:474-80.
27. Leibowitch, J. A Strange Virus of Unknown Origin. trans. Howard R. (UN VIRUS ETRANGE VENU D'AILLEURS. Grasset et Fasquelle 1984) New York: Ballentine Books 1985:97.
28. Ferrer JF. Stock ND. Lin P. Detection of Replicating C-Type Virus in Continous Cell Cultures Established From cows with-Leukemia: Effect of the Culture Medium. JNCI 1971; 47:613-621.
29. McClure HM. Keeling ME. Custer RP. Marshak RR. Abt DA. Ferrer JF. Esytholeukemia in Two-Infant Chimpanzees Fed Milk from Cows Naturally Infected with the Bovine C-Type Virus. Can Res 1974; 34:2745-57. (This is just a brand of AIDS in chimps!)
30. Bennett RK. The Broken Promise of the United Nations. Reader's Digest 1983; October: 117-124.
31. Francis DP. Hadler SC. Thompson SE. et al. The Prevention of Hepatitus B with Vaccine. Annls Int Med 1982; 97:362-6.
32. Wong-Stall F. Gallo RC. Human T-Lymphotropic Retroviruses. Nature 1985; 317;395-403. (Compare the map on 396 to map on page 681 of reference No. 8.)
33. Wong-Stall F. Gallo RC. The Family of Human T-Lymphotropic Leukemia Viruses: HTLV-I as the Cause of Adult T-Cell Leukemia and HTLV-III as the Cause of Acquired Immunodeficiency Syndrome. Blood 1985; 65:25363. (No. 2 Feb.) (Compare the map on page 254 to map in reference No. 8.).
34. Moseley B. Interview of D. Carlton Gajdusek. OMNI 1986; March: 62 et al.,at page 106
35. Slaff JI. Brubaker JK. The Aids Epidemic. How You Can Protect Yourself and Your Family-Why You Must-." 1985; Warner Books Edition.
36. Guyton JR. Rosenberg RD. Clowes AW. Karnovsky MJ. Inhibition of Rat Arterial Smooth Muscle Cell Proliferation by Heparin. Cir Res 1980; 46:625-633 (No. 5 May) Muller WEG. Zahn RK. Seidel HJ. Inhibitors acting on Nucleic Acid Synthesis in an Oncogenic RNA Virus. Nature New Biology 1971; 232:143-5. (August 4)
37. Torrence PF. Biological response Modifiers: New Approaches to Disease Intervention. 1985: New York: Academic Press, Inc. Harcourt Brace Javanovich.
38.Klatzmann D. Barre-Sinoussi F. Nugeyre MT. et al. Selective Tropism of Lymphadenopathy Associated Virus (LAV) for Helper-Inducer T Lymphocytes; Science 1984; 225:59-63.
39. Chiu I. Callahan R. Tronick SR. et al. Major 221 Gene Progenitors in-the Evolution of Oncoviruses. Science 1985; 223:364-70.
AMERICAN COLLEGE OF PHYSICIANS
4200 PINE ST
We all know it is easier for a king to have a lie believed than a beggar to spread the truth. Well, we are spreading the truth about AIDS. Unfortunately, it isn't pretty. But the fact is you are not being told the truth by the government or the so-called AIDS experts. The media, for reasons of their own, will not present information contradicting the official propaganda. So you can choose to go along with the same people who gave us brain cancer (SV- 40) virus) as a result of their contaminated polio vaccines in the early 1960's; a polio-like disease from their contaminated Swine Flu vaccine in the 1970's; and AIDS from their smallpox and hepatitis B vaccines; or, you can at least make yourself aware of the clear and present dangers that we all face by watching "The Strecker Memorandum." The cost of the DVD is nominal, but we submit that remaining ignorant can cost infinitely more.
Get a copy of this powerful video on DVD and share it with your friends.