Jaclyn Prystupa was always interested in science. In school, biology was her favorite subject, and the Saskatchewan Science Centre was...

CMD has given me many things throughout my life: A wonderful community and the ability to play wheelchair hockey are at the top of the...

Registration open now World Premiere + Live Q&A on December 27, 2020 Many people affected by neuromuscular disorders may not know that...

I was born in 1976 and my parents always knew some things were different, but my physical anomalies were always blamed on a birth...

We wind our way up the parking ramp at Children’s of Wisconsin every six months. After parking, we make the long trek on foot through the...

It is that time of the century, about twenty years in, for our regularly scheduled once-in-a-lifetime global pandemic. A pandemic is a...

Check out Part 1 of Paul's 2-part series There are some days that leave a lasting mark on your life. Years later you’re able to look back...

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...