Bringing Awareness to Duchenne Muscular Dystrophy
February 20, 2021
Helping those dealing with DMD
Duchenne Muscular Dystrophy (DMD) is the leading fatal genetic disorder for young boys. Back in November of 2010, Michael Capolongo was diagnosed with DMD and his family has been helping others dealing with the disorder ever since.
From yearly volunteer possibilities to donating money to the best research, Michael’s Cause is changing the future of DMD.
The National Organization for Rare Disorders (NORD®) is celebrating Rare Disease Day 2021 with The Balancing Act.
Travis Flores is a 29-year-old cystic fibrosis survivor and a recipient of a very rare third double-lung transplant in May 2020.
The Balancing Act has partnered with the National Organization for Rare Disorders (NORD) and WEGO Health to shine a light on rare diseases and the impact they have on patients.