Reading things like that article leaves me with this desire to walk into labs all over the world offering up my blood and tissue and organs… Who are these people with ME/CFS that are being used in their samples? I can’t find a doctor that knows anything about this disease, let alone find anyone looking for research participants.
I agree – I would gladly offer bits of me and my blood for research, but like you said, I never see anywhere in my country that wants M.E. study participants/donors.
Rag and Bone Shop of the Heart 
That’s a good article. Thank you for sharing.
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Reading things like that article leaves me with this desire to walk into labs all over the world offering up my blood and tissue and organs… Who are these people with ME/CFS that are being used in their samples? I can’t find a doctor that knows anything about this disease, let alone find anyone looking for research participants.
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Great article. I was following this a lot in 2009. I agree..Mikovitz was wrong but she deserves credit for getting such huge attention to CFS.
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I agree – I would gladly offer bits of me and my blood for research, but like you said, I never see anywhere in my country that wants M.E. study participants/donors.
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