Parents Raise Money for Rare Disease Research Through the Million Dollar Bike Ride at PENN Orphan Di
Parents of children and young adults with the rare disease Congenital Muscular Dystrophy (CMD), Susan Lee-Miller, Andy Parks, and Diane...
Parents Raise Money for Rare Disease Research Through the Million Dollar Bike Ride at PENN Orphan Di
Mathea Manley Representing the CMD Community at Rare Disease Week on Capitol Hill
Megan Meyer Representing the CMD Community at Rare Disease Week on Capitol Hill
An Important Message About the Flu
Cure CMD hosts 380 attendees at its 2017 Scientific Family Conference
Cure CMD's 5-Year Research Goals
Team Cure CMD will be an official charity partner at the Los Angeles Marathon
Cure CMD welcomes three new board members
CMDIR Newsletter
2017 Kicks Off with New Treatments for Pediatric Neuromuscular Disorders
Adapted Vehicles and Driving
CMDIR Newsletter December 2016