Local man shares what it's like living with Duchenne muscular dystrophy
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Local man shares what it's like living with Duchenne muscular dy…
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There are 250,000 people living with Duchenne muscular dystrophy around the world, including 2,500 in the UK. Today on World Duchenne Awareness Day support families affected by Duchenne muscular dystrophy by sharing red balloons across social media. Find out more about Duchenne musuclar dystrophy >> http://qoo.ly/hkkdc. | Muscular Dystrophy UK
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Adults living with Duchenne muscular dystrophy - Action Duchenne
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actionduchenne.org
One of the most powerful tools for people living with Duchenne muscular dystrophy is something many people have never heard of: switch access. As muscle weakness progresses, pressing small buttons, pulling triggers, or gripping objects becomes harder. But that doesn’t mean the activity has to stop - it just means we adapt how it’s done. Take a Nerf gun, for example. By modifying it to work with a large external switch button, the trigger no longer needs hand strength. A light press of a switch,
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New treatment options are now available and continue to emerge for people living with Duchenne muscular dystrophy (DMD). This is an exciting time for individuals and their families, who have long held out hope for stopping or slowing down the progression of their disease. #aptavirginia #fallsummit20025 #physicaltherapy #pediatricphysicaltherapy #dmd #duchennemusculardystrophy | APTA Virginia - formerly VPTA
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