Spastic Paraplegia Foundation, Inc.

Hereditary Spastic Paraplegia #hsp & Primary Lateral Sclerosis #pls together we are #HSPandPLS The Spastic Paraplegia Foundation is committed to promoting research to find cures for Hereditary Spastic Paraplegia and Primary Lateral Sclerosis, to educating people and their families affected by these conditions to help them live full and productive lives and to creating opportunities for mutual support and sharing.

• Nerve, Muscle, and Bone Diseases

• 29.

CureDuchenne

We are committed to improving the lives of those affected by Duchenne through accelerating research, improving care and empowering the community.

• Specifically Named Diseases Research

• 30.

Muscular Dystrophy Association

MDA is the #1 voluntary health organization in the United States for people living with #MuscularDystrophy, #ALS, and related #neuromuscular diseases.

THE PARENT PROJECT FOR MUSCULAR DYSTROPHY RESEARCH INC

Let's advance the research evolution. #EndDuchenne Our mission is to end Duchenne.

• Community Health Systems

• 32.

Delaware Health Sciences Alliance LLC

Collaborating across the health sciences for research, education, and service in Delaware.

• Nerve, Muscle, and Bone Research

• 33.

Alex Rezkalla Foundation

A non-profit organization raising funds to support research for Duchenne Muscular Dystrophy Our primary purpose is to increase public awareness of Duchenne muscular dystrophy through advocacy and fund scientific research aimed at treating those living with Duchenne muscular dystrophy.

• Fund Raising and/or Fund Distribution

• 34.

Chloe Strong Foundation

The Chloe Strong Foundation The Chloe Strong Foundation is a 501c3 nonprofit organization that exists to improve the quality of life for those that struggle with the rare neurological disorder Rett Syndrome by providing financial assistance support and prayers.

• Services to Promote the Independence of Specific Populations

• 35.

Friends Foundation of the Carolinas

Our mission is to create and maintain a community support system to help enhance the life experience of those living with neuromuscular disease.

• Fund Raising and/or Fund Distribution

• 36.

Family Strong Foundation Inc

FAMILY STRONG FOUNDATON 550000Raised for Researchsince 2014 Raising awareness while supporting the reasearch for a CURE for ALS.