#ShareYourRare

Community Blog Initiative: The First Post

When this decade began, Cure CMD was a fledgling organization, less than two years old. For 14-year-old me, the highlight of those early...

Attention Content Creators: Introducing Cure CMD’s Community Blog Initiative: For You, by You

As you know, 2019 has been a big year for the CMD community. As 2019 SciFam recedes from view, we’re gathering the lessons we’ve learned...

Mathea Manley Representing the CMD Community at Rare Disease Week on Capitol Hill

At the end of next month, Matty will travel to Washington D.C. to represent the CMD community and advocate for congenital muscular...

Megan Meyer Representing the CMD Community at Rare Disease Week on Capitol Hill

At the end of next month, Megan will travel to Washington D.C. to represent the CMD community and advocate for congenital muscular...