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Duchenne UK - Bringing an end to Duchenne muscular dystrophy
Duchenne UK is the leading UK charity for Duchenne muscular dystrophy. We're going further and faster than ever before to find effective treatments for DMD.
Michael's Cause – Fighting Duchenne Muscular Dystrophy
Fighting Duchenne Muscular Dystrophy
Jesse's Journey | Duchenne Muscular Dystrophy | Canada
Duchenne Muscular Dystrophy (DMD) is a progressive genetic muscular system disease that affects 1 in every 5,000 boys.
CARE-NMD: Improving care for Duchenne muscular dystrophy
Improving care for Duchenne muscular dystrophy
Parent Project Muscular Dystrophy (PPMD) | Fighting to End Duchenne
Parent Project Muscular Dystrophy fights to end Duchenne. We accelerate research, raise our voices to impact policy, demand optimal care for every single family, and strive to ensure access to approved therapies.
Alex's Wish | fundraising charity for Duchenne Muscular Dystrophy
Alex’s Wish is a charity set up to eradicate Duchenne Muscular Dystrophy, an aggressive form of Muscular Dystrophy that affects 1 in every 3,500 boys born and results in total paralysis. Established by Emma and Andy Hallam (parents to Alex) in late 2012, Alex's Wish helps raise vital funds to help bring about new treatments and ultimately a cure for this devastating condition.
Muscular Dystrophy Association
MDA is the nonprofit health agency dedicated to curing muscular dystrophy, ALS and related diseases by funding worldwide research.
VISION-DMD – Designed to ensure a timely & cost-effective **** development for Duchenne muscular dystrophy
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Sam's Night is an opportunity to help raise funds to benefit the research programs of Parent Project Muscular Dystrophy, and to fight to end Duchenne.
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The Zack Heger Foundation is an organization dedicated to raising money for finding a cure for Duchenne Muscular Dystrophy. We are part of the The Duchenne Alliance
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WE are so glad that you visit this site of DUCHENNE MUSCULAR DYSTROPHY. This is a registered Humanitarian FOUNDATION located in the country of SURINAME SOUTH AMERICA. WE are here to help you and your loved ones to have HOPE as you face the challenges in
Home Page 1 - Pietro's Fight
Help Pietro fight Duchenne Muscular Dystrophy (DMD). Join us in learning more about this disease that affects 300,000 children worldwide and donate to help fund the fight for a cure. This is our mission of love and our fight for a cure!
Home - Action Duchenne
Formed in 2001 Action Duchenne was the first national charity dedicated to supporting those living with Duchenne muscular dystrophy (‘DMD’). Our work to date has seen over £10m invested in ground-breaking research, educational programmes and campaigns.
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Little Hercules Foundation » Little Hercules Foundation
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Save Our Sons Duchenne Foundation: SOS
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Save Our Sons is the peak body for Duchenne muscular dystrophy in Australia. We have focused our energy and fundraising efforts toward finding a cure. Open Monday To Friday. Donate Online. Founded In 2008. Highlights: Founded In 2008, Donation Option Available.
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Candle in the Dark is a charitable organisation funding research into gene therapy for inherited eye disorders causing blindness in young children. Its aim is to help develop effective treatments, ultimately providing a cure for blindness and visual impairment. Visit our pages to find out more and see how you can help.
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