• Scholarships, Student Financial Aid, Awards

• 100.

John Kerr Foundation

The John Kerr foundation is a 501(c)3 nonprofit dedicated to enhancing the lives of those living with Muscular Dystrophy.

The LAM Foundation

Delivering facts about #LAM #RareDisease and The LAM Foundation.

• Fund Raising and/or Fund Distribution

• 102.

Ellie White Foundation for Rare Genetic Disorders Inc

We will not give up until a cure for Wolfram syndrome is found for Ellie and the children suffering from this disorder.

• Brain Disorders

• 103.

DYSTONIA MEDICAL RESEARCH FOUNDATION

Our mission is to advance research for improved dystonia treatments and a cure, promote awareness, and support the well being of affected individuals.

• Services to Promote the Independence of Specific Populations

• 104.

Project Strong Inc

Strong missioN Our mission at Project Strong is to empower children and young adults living with neuromuscular diseases discover and express their unique strengths by providing educational programs activities events that meet their needs.

Dlg4 Research Fund

DLG4-related Synaptopathy / SHINE Syndrome *Managed by the board of the DLG4 SHINE Foundation A page for people interested in learning more about DLG4-related Synaptopathy / SHINE Syndrome *Managed by the board of the DLG4 SHINE Foundation Mission To find specific treatment options and a cure for DLG4 patients by building a collaborative network of patients, families, clinicians and scientists that will work together to raise awareness and accelerate the understanding, diagnosis and treatment of DLG4 related synaptopathy.

• Health - General & Rehabilitative N.E.C.

• 106.

LS Classic Foundation

The Lone Star Paralysis Foundation's mission is to cure spinal cord paralysis through funding research, recovery & recreation.

• Birth Defects, Genetic Diseases

• 107.

LEO'S LIGHTHOUSE FOUNDATION INC

Leo’s Lighthouse is a non-profit making a difference in the lives of children affected by Bainbridge-Ropers Syndrome.

MUSCULAR DYSTROPHY FAMILY

The Muscular Dystrophy Family Foundation uses the power of giving to increase the quality of life and independence of people with muscular dystrophy—and empower their families—through advocacy, education, and financial assistance Living with a neuromuscular disease means facing new challenges every day.