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 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.
Read moreInformation and news on specific primary immune deficiency diseases, referrals to major medical centers, patient support, etc.
Read moreInformation and materials about lupus and referrals to services for people with lupus and their families. Conducts education and research programs. Membership and newsletter available through local chapters.
Read morePromotes research and education into myasthenia gravis, a chronic neuromuscular disease. Supportive services for patients and families, information, referrals, newsletter, support groups, annual and scientific meetings, and patient registry.
Read moreDedicated to serving those with polymyositis, dermatomyositis, juvenile myositis, and inclusion body myositis. Education, newsletter, research reviews, literature, phone support, and annual conference.
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