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My cause is an #MECFS diagnostic blood test so that :   No ME/CFS patient will be sectioned or starved again So friends and family, doctors and hospitals will believe us  The FDA will vote yes to treatments  Medical education will improve   ME/CFS research funding will increase  We will gain allies  NIH will study ME/CFS from an ImmunoBiological basis  If we focus on funding and finding a ME/CFS diagnostic test so many issues will be solved!

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About me, with ME/CFS
I am a Severe ME/CFS patient. I am bedridden, and I cannot speak. ME/CFS biomarkers are important to me because I would like to see a validated biomarker become a ME/CFS diagnostic blood test that changes the world for ME/CFS patients worldwide.
I think that can only happen by focusing on ME/CFS biomarkers, advocating for them, fundraising for them, fighting for them. We need to see biomarkers as they are developing without walls and siloes, and become aware of the issues within ME/CFS biomarkers so we can address them before someone at a regulatory agency does.


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