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  • National Eosinophilia-Myalgia Syndrome Network
    Supporting EMS sufferers and their families and working to increase public awareness of the illness caused by consumption of contaminated L-tryptophan supplements.
    www.nemsn.org
  • Take the Lead
    Take the Lead is a nonprofit organization "dedicated to provide direct services, support and care for all qualified participants in the sport of dogs who suffer from the devastating realities of life-threatening or terminal illnesses."
    www.takethelead.org
  • Friends' Health Connection
    Connects people who are currently experiencing or who have overcome the same disease, illness, handicap or injury in order to communicate for mutual support.
    www.48friend.org
  • Nevus Network
    Home of the Congenital Nevus Support Group. Offers educational material and emotional support for those with congenital nevi and/or neurocutaneous melanosis (NCM).
    www.nevusnetwork.org
  • Melungeon Health Education and Support Network, The
    Dedicated to the health of Melungeon descendants who have one or more of the five major Mediterranean illnesses, including Behçet's Syndrome and Sarcoidosis.
    www.melungeonhealth.org
  • Australian Pituitary Foundation
    Supports research and disseminates information for the medical community, the public, pituitary patients, and their families. Includes news and contacts.
    www.pituitary.asn.au
  • Wobblers Anonymouse
    Support group for those damaged by gentamicin. Symptoms include oscillopsia and loss of balance.
    www.wobblers.com
  • Cody Unser First Step Foundation
    Not-for-profit corporation aimed at raising research funds to fight paralysis and build awareness of Transverse Myelitis.
    www.codysfirststep.org
  • Canadian Bacterial Diseases Network
    www.cbdn.ca
  • Beryllium Support Group
    Information about chronic beryllium disease (CBD).
    www.beryllium.org
  • Myoclonus Research Foundation
    www.myoclonus.com
  • Children Afflicted With Lymphatic Malformations - CALM
    Organization of parents and children afflicted with lymphatic malformations. Offers information, support, medical references, and encourages research to improve treatment.
    www.staycalm.org
  • Stevens Johnson Syndrome Foundation
    Provides information and support to the medical communities and the public.
    www.stevensjohnsonsyndrome.net
  • Pituitary Society, The
    Seeks to further the understanding of diseases of the pituitary gland.
    pituitarysociety.med.nyu.edu
  • Lois Joy Galler Foundation
    Acquires the funds needed to conduct research and develop methods of preventing or curing Hemolytic Uremic Syndrome (HUS).
    www.loisjoygaller.org
  • Disfigurement Guidance
    Information on treatments, literature, compensation and other services and facilities concerning disfigurement guidance and skin camouflage.
    www.timewarp.demon.co.uk
  • Langer-Giedion Syndrome Association
    International support organization for people and families living with Langer-Giedion Syndrome and related disorders.
    lgsa.net
  • Worldwide Society of Wolfram Syndrome Families
    Support group for a rare disease.
    www.wolframsyndrome.org
  • Sotos Syndrome Support Association
    Provide a social support environment for professionals and families of individuals affected by Sotos Syndrome so they can meet, exchange ideas and help one another cope with the condition
    www.well.com/user/sssa
  • International Society for the Study of Cough
    Promotes research in cough and encourages the exchange of ideas and information.
    www.issc.info
 


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