Cure CMD and the impact of the new tax law As many of you know, there is something about living with a rare condition that gives affected...

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

Please see the end of this article for Frequently Asked Questions - CALLISTO Phase 1 Clinical Trial Pratteln, Switzerland, April 5, 2018...

Parents of children and young adults with the rare disease Congenital Muscular Dystrophy (CMD), Susan Lee-Miller, Andy Parks, and Diane...

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...

Flu Vaccinations and Proactive Respiratory Care are Critical for People with CMD Pulmonologist and CMD Advocate, Dr. Oscar H. Mayer,...

Cure CMD In May 2016, the Patient-Centered Outcomes Research Institute(PCORI) awarded funds to Cure CMD, a nonprofit, patient advocacy...

Cure CMD has achieved significant impact in its first nine years as the only nonprofit organization in the U.S. dedicated specifically to...

Dear California CMD Community! Cure CMD has been accepted as a charity partner for the 2018 Los Angeles Marathon on March 18th. The...

Cure CMD welcomed three new members to the Board of Directors in July 2017. With the addition of Dr. Carla Grossman, Dr. Oscar H. Mayer,...

CMD Tissue Repository Serving families and researchers in the quest to find treatment solutions. Click here for the latest news from...