welcome to DuchenneXchange- a positively charged Duchenne muscular dystrophy community.
- join today!
- log in
Little Hercules Foundation is a registered, non-profit organization based in Dublin, Ohio. It started on January 1, 2013 when three moms, two of whom had sons diagnosed with Duchenne muscular dystrophy (DMD), decided to host events to help fund research.
The Foundation works to identify meaningful, outside resources across the United States that can provide a life-line for some key needs one may face when living with DMD.
Little Hercules Foundation aims to improve the lives of those diagnosed with DMD, including their families, through four main pillars:
• Family Assistance
• Funding Research
25th World Congress Of Neurology – WCN 2021We warmly invite you to join us for the ...
DMD Pioneers.orgDMD Pioneers is for people with Duchenne...
Brothers with rare condition painting postcards to fund custom vehicleTwo brothers in Cambridge with a rare ge...
Action DuchenneAction Duchenne’s main aim has always ...
Duchenne Muscular Dystrophy Spinal Fusion Before and AfterThis group was formed to help those who ...
What are the TREAT-NMD Global Registries?New therapeutic strategies for neuromusc...
Ohio woman creates free coloring books featuring kids with disabilities in memory of her sonWhen Sue Nuenke remembers her son Chris ...