The story of Margaret

My son Josh is diagnosed with a rare form of muscular dystrophy , Myontonic Dystrophy type 1. There is no cure at this moment. He just got a g button put in July 2017 for failure to thrive. We are praying that a cure is found one day. My son is the strongest person I know. He faces many challenges and he always pushes through no matter how scared he is. 

 

*Find others with Myotonic Dystrophy on RareConnect, the online platform for people affected by rare diseases.

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