Kindness Over Muscular Dystrophy Inc
Help us save our son Conner's life by raising money to cure Duchenne Muscular Dystrophy! Conner is 14 years old. He was diagnosed with DMD April 21 2015. We believe his diagnosis is not written in stone. With your Love and Hope we can beat DMD! THE MISSION OF THE ORGANIZATION IS TO PROVIDE CHARITABLE GIVING TO SUPPORT MUSCULAR DYSTROPHY RESEARCH AS WELL AS BENEVOLENT ASSISTANCE AND ADVOCACY TO THOSE IN NEED.
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Ridgefield
Home | Kindness Over Muscular Dystrophy Meet Conner Be Curious Get Inspired Take Action More Our dream our hope and our prayer is a cure for Conner and the thousands of boys with Duchenne Muscular Dystrophy. Annual Event Thank you for attending this year39s Annual Benefit. The event was an incredible success and that39s all thanks to you. We couldn39t do any of this without your support and we are forever grateful for the relentless kindness of all of our attendees sponsors vendors volunteers and donors.
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On the 4th February 2016, our beautiful son Connor was diagnosed with Duchenne Muscular Dystrophy.
Action Duchenne has a simple vision: a world where lives are no longer limited by Duchenne muscular dystrophy.
Promoting and funding research into the study and cure of Duchenne Muscular Dystrophy.
THE DUCHENNE RESEARCH FUND (uk)
The Duchenne Research Fund has raised more than £6m to fund research and treatments for DMD.
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Louise
2025-10-24
🌍🙌 Exciting news! A Kenyan app that translates speech into sign language in real-time just won Africa's top engineering innovation award! This inspiring invention bridges communication gaps and promotes inclusivity. Let’s celebrate innovation for a better world! ✨👩🦽 #Inspiration #InclusiveTech #Eduo
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