• Nerve, Muscle, and Bone Diseases

• 37.

Kurts Fund

The Kurt+Peter Foundation raises funds for research for a treatment and cure for limb-girdle muscular dystrophy, type 2c or "LGMD2C.

Michaels Cause Inc

www. michaelscause. org Michael's Cause raises awareness of Duchenne Muscular Dystrophy and directs funding to the best medical and scientific research to find better treatments and a future cure.

• Nerve, Muscle, and Bone Research

• 39.

FSHD Society

World’s largest research-focused patient organization for facioscapulohumeral muscular dystrophy (FSHD).

• Nerve, Muscle, and Bone Research

• 40.

Lgmd2L Foundation

We’re a nonprofit searching for a cure for LGMD2L, a rare disease that causes muscle weakness and atrophy, pain, and eventually leads to many sufferers being unable to walk.

• Fund Raising and/or Fund Distribution

• 41.

Coopers Cure

COOPER39S CURE HOME DONATE COOPERx27S STORIES COOPER FEST COOPERx27S TRIBE CONTACT More.

• Single Organization Support

• 42.

Beck S Helping Hands Inc

Helping Families of Kids with Duchenne Muscular Dystrophy DMD What is Duchenne.

• Fund Raising and/or Fund Distribution

• 43.

Collagen 6 Research Charity Inc

Raising money to cure Collagen VI-related dystrophy, a rare congenital muscular dystrophy.

• Nerve, Muscle, and Bone Diseases

• 44.

PIETROS FIGHT INC

Home Page 1 Our Mission The mission and vision of Pietros Fight is to increase worldwide awareness of Duchenne Muscular Dystrophy.

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.