• Private Grantmaking Foundations

• 1.

Jain Foundation Inc

The Jain Foundation's mission is to identify treatments for Dysferlinopathy also known as LGMD2B/R2 or Miyoshi Myopathy ORCHESTRATING A CURE FOR DYSFERLINOPATHY The Jain Foundation is singularly focused on finding a cure for dysferlinopathy also referred to as LGMD2B LGMDR2 Miyoshi Myopathy 1 ORCHESTRATINGA CURE FORDYSFERLINOPATHY The Jain Foundation is singularly focused on finding a cure for dysferlinopathy also referred to as LGMD2B LGMDR2 Miyoshi Myopathy 1 WHAT IS DYSFERLINOPATHY.

• Birth Defects, Genetic Diseases Research

• 2.

Cure CMD

Cure CMD’s mission is to advance research toward treatments for congenital muscular dystrophies and empower those living with CMD.

• Fund Raising and/or Fund Distribution

• 3.

Cure Lgmd 2T Inc

🧬 Genetic Testing Access 🗒️ Patient Registry 🔬 Advancing and Funding Research 📚 Educating & Raising Awareness Help Us Cure LGMD 2T Limb Girdle Muscular Dystrophy Our mission is dedicated to raising awareness for Limb Girdle Muscular Dystrophy 2T and providing critical funding for research into effective treatments.

• Nerve, Muscle, and Bone Research

• 4.

FSHD Society

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

• Nerve, Muscle, and Bone Research

• 5.

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.

CureLGMD2i Foundation

The CureLGMD2i Foundation strives to raise awareness and to support scientific research that is geared directly toward finding a treatment or cure for Limb Girdle Muscular Dystrophy type 2i (LGMD2i).

• Medical Specialty Research

• 7.

FIBROMUSCULAR DYSPLASIA SOCIETY OF

The recognized leader in the support of Fibromuscular Dysplasia (FMD) awareness, education and research.

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.

• Specifically Named Diseases Research

• 9.

Dion Foundation for Children with Rare Diseases Inc

Support research. Find a cure. Help children and families fight rare diseases.