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politics and CFS

Information, Symptoms, Treatments and Resources

Posts on politics and CFS (90)

I am going to post a similiar poll in the fibro/CFS forum. How many of you believe that p...
Remember that politics played a role in this illness... the same politics I suppose that ar...
How many of you believe that politics play a role with your diagnosis of fibro or CFIDS (AK...
If this kind of action appeals to you, the Cfids Association of America (at www.cfids.org ...
Its a shame that the CDC didn't discover this and that many CFS patients believe that the...
I discovered this site www.fibroandfatigue.com in researching info on CFS. It appears to be...
I am 18 and female. I got mono this past september during my first semester at college and ...
I am at wk 11 of tx.The dose of both meds were reduced due to severe drops in both WBC and ...
I usually only post links to new items or writings that support chronic Lyme. But as Sun T...

Journals about politics and CFS(1)

Epidemic Myalgic Encephalomyelitis: A Demand for Urgent Action and Accountability‏


by PlateletGal, May 22, 2009 12:50PM - 20 Comments
Permission to repost To the CFSAC: Epidemic Myalgic Encephalomyelitis: A Dem...