CFIDS/ME Patients with ICL

HIV-Negative AIDS (ICL) cases, like mine, are the bridge that connects the CFS and AIDS paradigms. I often wonder: if "AIDS" had been named "low natural killer cell disease," rather than having it's present day man-made definitional construct, if the true nature of the relationship between AIDS & CFS would have been seen 2 decades ago?
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Request to retract Gallo's 1984 Science Magazine papers: http://www.imeassoc.com/Request_to_Science_mag.html
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CFIDS/CFS, FMS, GWI, MCS, and related illnesses: http://www.ncf-net.org/forum/HopewithICL-Fall05.htm
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I remain infuriated by my government's betrayal of her people. Most CFS/ME patients believe that their government has their best interest at heart, and sadly that is 100% false. So, to a lesser extent, I remain bothered that CFS/ME patients' do not question authority.

I think it's lovely that CFS/ME patients like to chit-chat amongst themselves in web forums. CFS is not science, however. CFS is not a disease...a syndrome is a syndrome (not a disease). CFS is 100% a political paradigm, and in order to make progress with CFS research "getting political" is the only solution.

To this day, I continue to write at least 12 letters per day. Here are some examples of responses that I've received: http://cfsstraighttalk.blogspot.com/2005/07/few-highlights-of-my-plight.html

The doorways keep opening for me. I can only imagine the profound possibilities of what would happen if every CFS/ME patient started doing the same thing.

If one person can change the world, imagine what 1,000 can do!

Please feel free to use this SAMPLE LETTER: http://cfsstraighttalk.blogspot.com/2006/10/potential-hope-for-cfidsme-patients.html

U.S. reps can be found here:
http://www.senate.gov/general/contact_information/senators_cfm.cfm http://www.house.gov/representatives/
http://www.whitehouse.gov/contact/
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Good night. God Bless. And God Bless America.