Public education about aphasia. Information for patients and families, referrals to local groups, and young people’s network for people ages 13 to 21 with acquired aphasia. Networks parents to share information. Newsletter and manual for starting new grou
Read moreAdvocacy and education for men concerned about circumcision. Discussion groups for affected men and for men undergoing restoration. Information, referrals, newsletter, literature, and assistance in starting groups.
Read moreThe Speak Easy International Foundation, Inc., a self-help/mutual aid group dedicated to assisting people who stutter. The organization provides a network of friendship and understanding to stutterers, and offers encouragement, motivation, and support in dealing with their disfluency.
Chapter meetings are held bi-weekly, and are chaired by individual members on a voluntary rotating basis.
Read moreSupport for persons with Cushing’s Disease through information and referrals, advocacy, scientific research, and education. Regional get-togethers, conferences, phone support, pen pals, newsletter, and assistance in starting local groups.
Read moreImproving the lives of people with all forms of Hypoparathyroidism, a rare medical disorder, by maintaining a worldwide network of family support, and promoting public, as well as professional, awareness.
Read moreResource and Groups online. Information on self-help groups, therapy, and referrals to professionals. Meetings led by members with professionals as sponsors. Newsletter and group development guidelines.
ANAD is a donation-based recovery community. We believe eating disorder support should be affordable and accessible to all. To continue offering our services for free, we rely on
Read moreInformation and educational materials on rosacea, a chronic, acne-like condition of the facial skin.
Read moreOUR MISSION: To enhance the quality of life for those children having a life-threatening disorder by granting their special wish.
Read moreInformation and resources about Dandy-Walker Syndrome for families.
Read moreInformation, Education, Research, Resources, and Advocacy for those with different types of ectodermal dysplasias and their families. Connection to other families like yours.
Read more