Community member, Daniella Slon wrote this article about accessibility in her hometown. We hope this inspires you to investigate your...

Dear parent of a newly diagnosed child, When our oldest son was 5 years old, we attended a Muscular Dystrophy Association (MDA)...

The second weekend of March brought the CMD community together in a brand-new way this year with the Los Angeles Marathon, when more than...

Susan is an "OG" mom who has a son with COL6-CMD. Susan has supported Cure CMD's mission from Day 1. Her ongoing engagement in...

Diane is mother to two wonderful young men, one of whom has COL6-CMD. Diane is one of our "OG" moms - a Cure CMD supporter even before...

Robin's two grandsons were diagnosed with SEPN1-RM in late 2014 after a terrible diagnostic odyssey that led them through three states...

Char has been a mainstay of Cure CMD almost since inception. Mom, wife, sister-in-law and daughter-in-law to four (and counting)...

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

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