Rare disease research
Hope for children with Congenital Muscular Dystrophy
Advancing research and support for children living with Congenital Muscular Dystrophy. A portion of every Galaxy Fund donation goes directly to Cure CMD to fund research, care, and community support.
Rare disease research
Supporting Cure CMD
A portion of the donations the Galaxy Fund collects goes directly to Cure CMD, an organization dedicated to advancing research and support for those affected by Congenital Muscular Dystrophy (CMD). Founded in 2008 by three parents of children with CMD, the organization is committed to finding treatments and improving the lives of those living with this rare genetic disorder.
What is CMD?
Congenital Muscular Dystrophy is a group of rare genetic disorders characterized by muscle weakness present at or shortly after birth. Mutations in more than 30 known genes cause muscle tissue to break down faster than the body can repair it, leading to progressive physical challenges. Individuals with CMD may experience:
- Limited or lost ability to walk
- Respiratory weakness
- Scoliosis and joint contractures
- Feeding difficulties and cardiac complications
- In some cases, significant cognitive impairments
By supporting Cure CMD, we are helping to fund vital research, medical advancements, and community support programs that bring hope to affected children and families. Together, we can work toward a future with better treatments and improved quality of life.
Together, we can bring better treatments within reach
Every gift helps fund vital research and brings hope to children and families living with CMD.