The CMDIR has launched on a new and improved platform! Your Data Has Power Large amounts of data about affected individuals allow...

Learn what successful family fundraising looks like from veteran CMD Community Members, the Knutsons In 2012, my husband, Tim, and I...

This week, we’ve put a spotlight on families and individuals who share how Cure CMD and our community have made a difference in their...

High school senior brings light to SEPN1 muscular dystrophy on TikTok Wrapping her fingers around her wrist so they touch, folding her...

Find the Cure CMD app in both the App Store and Google Play by searching “Cure CMD” It feels like several lifetimes ago at this point...

Cure CMD would simply not be what it is today without the dedication, hard work, and commitment of our volunteers. They are the reason we...

How did Rachel Alvarez become part of Cure CMD? I was born with congenital muscular dystrophy, but I didn't learn the details of my...

Meet Molly Wagner, high school student from Florida with CMD. Molly was tasked with creating a research project that not only...

Check out Part 2 of Paul's 2-part series From a young age, I have always had an undying love for sports. My earliest sports memories are...

Funding Continues in a Challenging Year

The COVID-19 pandemic has been brutal, especially in the United States. Both the actual impact of the virus itself and the mental strain...

If you are a parent of a child with special needs, a disability, or a rare disease, you’ve probably heard the poem Welcome to Holland. By...