MSD Action Foundation
Working towards a cure for Multiple Sulfatase Deficiency
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Working towards a cure for Multiple Sulfatase Deficiency
Provides information about H-ABC to spread awareness about this degenerative disease, and raises funds for research on gene therapy treatments that could stop the degenerative effects of H-ABC.
It aims to exponentially accelerate the discovery of novel genetic variations responsible for childhood leukodystrophies and to translate these findings into clinical treatments.
Join the team committed to finding a cure for MSD
Raising funds and awareness to help find a cure for H-ABC.
The mission of the National Institute of Neurological Disorders and Stroke (NINDS) is to seek fundamental knowledge about the brain and nervous system and to use that knowledge to reduce the burden of neurological disease.
Their fundraising efforts helped establish the nation's first Leukodystrophy Center of Excellence at CHOP. Learn about their cupcake challenge and how to get involved, and find information about current and upcoming clinical trials.
Chloe’s Fight Rare Disease Foundation is dedicated to supporting the development of cures and treatments for childhood lysosomal storage diseases (LSDs) by funding research, advocating policy for patients, and raising awareness.
If you have a child with asthma, you know that daily life can sometimes be a real challenge. Knowing what triggers your child's asthma can help make things much easier for your child and your family.
A telephone is provided in your child's room for your convenience. Other courtesy phones can be found throughout the Hospital.