CFSgate = AIDSgate = GWSgate
The medical establishment will have you believe that Chronic Fatigue Syndrome/Myalgic Encephalomyelitis (CFS/ME) is some sort of mysterious illness, but it’s no mystery to me; CFS/ME leads to HIV-Negative AIDS, idiopathic CD lympocytopena (ICL), a clinical diagnosis that I possess.
How can the AIDS establishment continue with a stale "it's caused by HIV" theory when there are ICL cases cited in medical journals dating back to 1992? While millions of ailing immunodeficient CFS/ME patients get belittled and neglected, perfectly healthy HIV+ people are allocated billions of dollars in taxpayer money. How can it make sense to anyone?
In the U.S. this year, the NIH spent $2.9 Billion of our tax money drugging perfectly healthy HIV+ people. Sick, ailing immunodeficienct (some of us dying) CFIDS patients received $4 Million. How can it make sense to you? source: http://report.nih.gov/rcdc/categories/
It's so easy to see that the medical establishment simply has these paradigms (CFIDS, HIV) inverted. AIDS patients are simply more CFIDS patients, who also happen to harbor a seemingly harmless virus, HIV. AIDS patients are just the tip of the CFIDS iceberg, and it's already well-documented that HIV is not the cause of CFS/ME.
How else do you explain why there is no CFS/ME pandemic in the HIV+ population? CFS/ME does not discriminate. The answer is that there is; any otherwise perfectly healthy HIV+ person that is: 1) symptomatic, 2) better on ARV's, and/or 3) severely immunosuppressed (AIDS)...
...is a CFIDS patient.
Putting causal pathogens aside (for a minute), simply rename CFS, ME, and AIDS all to be "low natural killer cell disease" and only diagnosis patients with "low NK cells" with it. Everyone would clearly see that:
CFIDS + ME + AIDS = low NK cell disease = one catastrophic pandemic *
* not caused by HIV
Allied government sold-out global public health for sake of profit --> industry, oil, and Orwellian greed. If I weren't only 25% alive, I often wonder if I should 'Occupy' the White House.
Now that the mystery has been solved, could we please stop wasting time and re-allocate ALL HIV funding into CFS/ME/AIDS research?
I demand a revolution!
7 Step Plan to resolving our World’s catastrophic public health disaster:
1. Demand research funding parity for CFIDS with AIDS.
2. Suggest that CFIDS & AIDS be researched together by scientists rather than as separate entities.
4. Urge that AIDS organizations (like AmfAR) include CFS under their umbrellas so that CFS advocates don’t have to reinvent the wheel.
5. Demand that the White House, Fauci and the Director of NIH make a public statement that (just from what we know today) in terms of the immune dysfunction and human suffering, CFIDS is just as serious a public health problem as AIDS.
6. Request that an annual international joint CFIDS/AIDS conference be held by the World Health Organization.
7. Suggest that next December 1st be declared the first “World CFS/AIDS Day.”
If it takes courage to think and to say the things that I do, I hope that there will be a miraculous outbreak of bravery from coast-to-coast.
I stopped fighting for myself a long, long time ago.
I fight for humanity.
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If you are moved, disturbed, horrified and/or inspired by my medical plight, please write a letter to your representative(s) demanding that all HIV funding be halted and entirely re-allocated into CFS/AIDS research.
The government works for you (not vice versa)!
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.


7 Comments:
Hallo my name is Alex.
I'd like to contact you because i'm having the same problem.
Please contact me.
Thanks
I am having the same problems and i cannot get the doctors to understand my problems they keep telling me that it is in my head.
I know that there is something wrong with me and everybody that sees me know that there is something wrong,but the doctors cant see it.
All of my blood work is normal except my absolute lymphocytes have dropped a 1000 points from 3400 to 2400 in about two years, and they say thats ok because it is in the normal range.
Call me crazy but I would like to know why did they drop.
I live in the atlanta ga area and I would love to know if you know of any support groups down here.
Thanks
ms1
I think I may have this too. I will join the yahoo group now.
Hi,
1 in 4 sexually active teenagers become infected with an STD every year, in the United States alone. Now, more than ever, we need to join together to fight this growing issue. As I read through your website, it is clear that you share the same passion for STD/STI awareness. We here, at Disease.com, understand the importance of STD/STI prevention and treatments. If you could, please list us as a resource or host our social book mark button, it would be much appreciated. We can not reach every teenager, but together we can try.
If you need more information please mail me with the subject line as your URL.
Thnak You,
Sharon Vegoe
Disease.com
Well done!............................................................
感謝您願意分享您的生活經驗~~支持您的更新哦!............................................................
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