Ryan's Quest
Fighting for an end for Duchenne muscular dystrophy! Ryan's Quest is primarily focused on supporting research for near-term, potential therapeutics and better testing platforms (tools) for development of DMD compounds. We are also interested in helping support families that are enrolled in clinical trials The mission of Ryan's Quest is to increase awareness of Duchenne muscular dystrophy with the purpose of allocating funds for research that has the greatest potential of finding a cure or treatment for this disease.
Founded
2008
3100
X (Twitter)
624
Address
Hamilton
Ryan's Quest – Ryan's Quest Hamilton NJ Raising AwarenessFunding ResearchHelping families impactedfinding a cure Hope In Action Join us in our fight for this generation of boys living with Duchene Muscular Dystrophy About US and Our Mission From raising awareness to helping families in need to funding research. together we are making a difference. The mission of Ryans Quest is to increase awareness of Duchenne muscular dystrophy with the purpose of allocating funds for research that can accelerate a treatment for this disease. We also grant financial assistance to help provide an independent lifestyle to those with Duchenne.
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On the 4th February 2016, our beautiful son Connor was diagnosed with Duchenne Muscular Dystrophy.
THE DUCHENNE RESEARCH FUND (uk)
The Duchenne Research Fund has raised more than Β£6m to fund research and treatments for DMD.
Duchenne UK has one clear aim β to end Duchenne, a devastating muscle-wasting disease.
The Gillin Boys Foundation Muscular Dystrophy Awareness Warrnambool Inc (au)
The Gillin Boys Foundation Muscular Dystrophy Awareness Warrnambool is FIGHTING to cure Duchenne.
Save Our Sons was founded in 2008 and is now the peak body for those living with Duchenne and Becker .
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