Parent Project Muscular Dystrophy
PPMD provides information about Duchenne muscular dystrophy, the most common fatal genetic disorder diagnosed in childhood, affecting approximately 1 in every 3,500 live male births.
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PPMD provides information about Duchenne muscular dystrophy, the most common fatal genetic disorder diagnosed in childhood, affecting approximately 1 in every 3,500 live male births.
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 Cleft Advocate educates and inspires families whose lives are touched by cleft lip and/or palate or other craniofacial anomalies.
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.
The Foundation provides medical, educational, psychosocial and local support resources for people with the 22q11.2 deletion syndrome and their families.
CHASA provides information and support to families of children who have hemiplegia, hemiparesis, or hemiplegic cerebral palsy.
CMS provides health coverage for millions of people through Medicare, Medicaid, and the children's health insurance program.