People living with muscular dystrophy, ALS and other related neuromuscular diseases, are robbed of the strength that most of us take for granted every day – the strength to walk, talk, laugh, hug, even breathe.
I'm participating in the 2021 MDA Virtual Muscle Walk to give strength to MDA so that they can continue to fund breakthrough research and provide comprehensive, compassionate care to kids and adults.
Please donate and join me in being part of the movement and the MDA mission to transform the lives of people living with neuromuscular disease.
Thank you!
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