The National CFIDS Foundation is compiling this list of people with CFIDS/ME that haved. In doing so, we hope to make people especially those in the medical community, media and goverment more fully aware of the seriousness of CFIDS/ME.. - This is the Patient and Physician Information page of the National CFIDS Foundation website. It contains information on anesthesia, education, employment, prescriptions, tissue donation, a symptom checklist and information for young patients.. - The links page of the National CFIDS Foundation contains links to valuable resources for patients of Chronic Fatigue Immune Dysfunction Syndrome/ M.E. Support Launched in 2001, M.E. Support is one of the leading Websites on Myalgic Encephalomyelitis providing information, advice and support..
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The National CFIDS Foundation is compiling this list of people with CFIDS/ME that haved. In doing so, we hope to make people especially those in the medical .
Full list of all local, national and international organizations for Chronic Fatigue Syndrome.
Trying to stigmatize a patient with a chronic illness such as MS or CFS with sentences like: "you are sick because of your personality, is your fault" is really .