"I don’t worry about him getting scared away because of my disability," Tina Fegley tells PEOPLE of boyfriend Tyler Waldman Tina Fegley Couple Tina Fegley and Tyler Waldman met on Dateability, a ...

Nila Morton, a graduate student at Howard University, was excited to be traveling back to South Carolina for Thanksgiving after almost a year of being away from home. Morton, 25, was born with a rare ...

Friends and family of Sophie Hutchison, who was diagnosed with limb girdle muscular dystrophy at 13, will take part in this year's Kiltwalk to raise money for Muscular Dystrophy UK.

Omaha Fire Department's annual steak fry aims to raise funds for families affected by muscular disease through their Fill the Boot program.

"In many countries, health insurance changes when DMD men are no longer seen in a specialized pediatric center. This impacts massively on the quality of care they receive. For this reason, many DMD ...

Long-term data from DEVOTE/ONWARD studies show benefits of high dose nusinersen in people living with spinal muscular atrophy (SMA)New Phase 1b ...

Genethon, a pioneer and leader in gene therapy for rare diseases, unveiled results at the MDA Conference in Orlando confirming the long-term efficacy of its GNT0004 gene therapy in Duchenne muscular ...

SAN DIEGO, March 17, 2025 /PRNewswire/ -- Avidity Biosciences, Inc. (RNA), a biopharmaceutical company committed to delivering a new class of RNA therapeutics called Antibody Oligonucleotide ...

Add Yahoo as a preferred source to see more of our stories on Google. "I don’t worry about him getting scared away because of my disability," Tina Fegley tells PEOPLE of boyfriend Tyler Waldman Tina ...