When it comes to Duchenne Muscular Dystrophy, what a parent sees is more than just the diagnosis, it’s the quiet courage behind every struggle. She sees her child endure long stretches when he’d rather be playing. She watches lose a little physical strength every day and try to find solutions to find other ways to continue with his favourite activities, if possible, or invest time into other or new interests. Parents help their child get ready for therapies when he’d rather just stay home and be
When it comes to Duchenne Muscular Dystrophy, what a paren…
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Duchenne makes my muscles weaker every single day. I use to walk. Now my wheelchair gets me where I need to go. #wheelchair #duchenne #dmd #muscleloss #wheelchairlife #duchennemusculardystrophy #muscleweakness #independence #duchenneawareness | Harrison & Duchenne - Raising Awareness of Duchenne Muscular Dystrophy
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Duchenne makes my muscles weaker every single day. I use to …
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91 reactions · 9 comments | We thought we had more for him to walk. Just four years of independent walking. He stopped at 6yrs old. Duchenne isn’t fair. #duchennemusculardystrophy #dmd #duchenne #wheelchair #muscleloss #disabilityawareness #makingmemories #thelittlethingsinlife #duchenneawareness | Harrison & Duchenne - Raising Awareness of Duchenne Muscular Dystrophy | Facebook
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