Spinal Muscular Atrophy Foundation
The mission of the SMA Foundation is to accelerate the development of a treatment for spinal muscular atrophy, the number one genetic killer of infants and toddlers.
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The mission of the SMA Foundation is to accelerate the development of a treatment for spinal muscular atrophy, the number one genetic killer of infants and toddlers.
Find information about myasthenia gravis (MG), including living with MG, community support, research and how you can help.
The American Society of Plastic Surgeons (ASPS) offers information about cleft lip and cleft palate repairs.
The Children's Craniofacial Association empowers and gives hope to individuals and families affected by facial differences.
The Cleft Advocate educates and inspires families whose lives are touched by cleft lip and/or palate or other craniofacial anomalies.
FACES: The National Craniofacial Association assists children and adults who have craniofacial disorders resulting from disease, accident or birth.
AdoptCleft is a support group for parents wanting to adopt cleft children, parents that have cleft children (biological or adopted), and others that can contribute or learn from the conversations.
ACPA is an international nonprofit medical society of healthcare professionals who treat and/or perform research on birth defects of the head and face.
Changing Faces provides support and promotes respect for everyone with a visible difference. Helpful resources include advice for meeting new people when you have a visible difference.
The Foundation provides medical, educational, psychosocial and local support resources for people with the 22q11.2 deletion syndrome and their families.