• Professional Societies & Associations

• 19.

Suneel Research Foundation

Our mission is to spread awareness about Duchenne Muscular Dystrophy (DMD), raise funds to support treatments and find a cure for DMD.

• Specifically Named Diseases Research

• 20.

Coalition Duchenne

We're on a mission to do everything FUN to raise global awareness for Duchenne muscular dystrophy, to fund research for a cure.

• Neurology, Neuroscience

• 21.

JB'S KEYS TO DMD INC

Giving boys affected by DMD the opportunity of a lifetime.

• Birth Defects, Genetic Diseases Research

• 22.

Ryan's Quest

Fighting for an end for Duchenne muscular dystrophy.

• Private Grantmaking Foundations

• 23.

Colins Dream LLC

Raise awareness and funding for research to find a cure for Duchenne Muscular Dystrophy.

• Nerve, Muscle, and Bone Research

• 24.

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.

• Specifically Named Diseases Research

• 25.

Foundation To Eradicate Duchenne Inc

Dining Away Duchenne, a premiere charity event with DC chefs is on September 25, 2018.

My DMD Hero Inc

We meet Duchenne families where they are, give them hope, and meet the practical needs of children with Duchenne Muscular Dystrophy.

• Fund Raising and/or Fund Distribution

• 27.

Hope For Javier Inc

MISSION Dedicated to changing the predicted outcome for all boys with Duchenne muscular dystrophy Transforming Care Studies have proven that access to multidisciplinary care adds on average TEN YEARS to DMD boys life expectancy.