The ongoing support group offers patients and their supporters a place to go for shelter and comfort in dealing with myeloma. Many myeloma patients benefit by meeting with peers, sharing information, and learning from one another’s experiences. Please join our community and tell us stories of your journey and accomplishments.
Read moreThe Reeve Foundation’s Living with Paralysis and Caring for a Family Member Living with Paralysis support groups provide an opportunity for members to connect with others who understand what they are going through and to gain support, insight and guidance. Separate groups are held for individuals living with quadriplegia, those living with paraplegia, and family
Read morePromotes the welfare of persons with Scleroderma and their families. Education, support groups, peer counseling, referrals, fundraising, newsletter, educational materials, and group development guidelines.
Read moreSSF provides patients with practical information and coping strategies that minimize the effects of Sjögren’s. In addition, the Foundation is the clearinghouse for medical information and is the recognized national advocate for Sjögren’s.
Read moreMutual support helping patients with scleroderma and their families cope with the illness. Funds research. Literature, medical reference lists, assistance in starting groups, conferences, newsletter, information, and referrals.
Read moreHealth organization for patients with life-threatening Wegener’s granulomatosis and related vascular diseases. Information and newsletter for patients and physicians. Educates families, friends, and the public about effects, symptoms, and treatment.
Read moreTo cure tinnitus through the development of resources that advance tinnitus research. Support groups are offered via telephone and email.
Visit website for resources and support group information: http://www.ata.org/
Read moreEmotional support, visitation, and education for people affected by Guillain-Barre Syndrome. Promotes education and research. Newsletter, pen pals, phone network, group development guidelines, and international symposium.
Read moreSupport and education for families affected by primary immune deficiency diseases. Newsletter, handbook, videotape, and educational materials for public and medical professionals. Scholarships and fellowship programs. Group development guidelines.
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