In Partnership with AOL
See also:
  • Alison Hunter Memorial Foundation - Myalgic encephalopathy and chronic fatigue syndrome information for patients and medical professionals.
    [!]
  • Association of Young People with ME - Includes phone helpline, assistance with study problems, and guide to request a disabled students allowance. A UK-based charity.
    [!]
  • CFIDS Association of America - Funds research studies towards accurate diagnosis and treatment. Also offers support and advocacy resources, including a grassroots on-line action center.
    [!]
  • CFIDS/Fibromyalgia Self-Help - American non-profit organization that provides online self-management courses. Also furnishes a library of articles on coping, pacing, stress management and treatment.
    [!]
  • Connecticut CFS/FM Association - Provides email and telephone support, online library of medical articles, and quarterly newsletter.
    [!]
  • FM-CFS Canada - National registered-charity that provides guides for doctors and pharmacists, nursing, assessment and treatment of patients, and guidelines for support groups.
    [!]
  • Hummingbirds Foundation for ME - Provides an overview of known medical facts, diagnosis and basic treatment, comprehensive symptom list, research and advocacy information, and a monthly newsletter
    [!]
  • Invest in ME - Independent UK charity campaigning for biomedical research. Offers conference reports, research news, media corner, and guestbook.
    [!]
  • Massachusetts CFIDS/FM Association - Articles on diagnosis, coping, advocacy, treatment, and disability. Assists patients with referrals to health care providers and gives guidance on disability issues.
    [!]
  • The ME Association - Practical help is offered by this UK national charity, including information on benefits and other sources of assistance.
    [!]
  • ME Association of Ontario - Canadian charity that offers info, tips, and support to those coping with CFS and related illnesses, including youth and parents.
    [!]
  • ME Research UK - National charity that funds scientific investigation into causes and treatment. Offers educational literature, reports of conferences and workshops, and a bi-annual magazine.
    [!]
  • ME/CFS Australia - Nationwide non-profit with resources on diagnosis, possible causes, symptoms, treatment and management. Also helps patients to find a local support group.
    [!]
  • ME/CFS Society of NSW - Australian registered charity that provides information and support to sufferers and their carers. Features support groups, brochures and fact sheets, forum, and newsletter.
    [!]
  • National CFIDS Foundation - American non-profit that funds research and provides information, education, and support to patients.
    [!]
  • National ME/FM Action Network - Includes a quarterly newsletter, online library of articles, list of support groups, and discusses active projects. A Canadian registered charity.
    [!]
  • Pandora - American patient advocacy group for CFS and other neuroendocrineimmune disorders. Provides scientific articles, support and educational resources, newsletters.
    [!]
  • Sussex ME/CFS Society - UK registered charity offering support through newsletters, meetings, and telephone contacts to patients in East Sussex, West Sussex, and Kent.
    [!]
  • Waterloo Wellington ME Association - Canadian registered charity offering coping and self-help strategies, and help with finding a physician.
    [!]
  • Wisconsin ME/CFS Association - Online library with medical articles and resources for children. Access to support groups, phone support and their quarterly newsletter is for members only.
    [!]
Volunteer to edit this category.
[Mozilla Genie]
Copyright © 1998-2014 AOL Inc. Terms of Use
Visit our sister sites  mozilla.org | MusicMoz | Wikipedia

Last update: August 8, 2014 at 6:35:09 UTC - edit