MADISON, Wis. (WIFR) - For 14 years, Treyson Wallace’s family searched for answers. Born in 2009, Treyson failed a newborn ...
Holly Helm’s life changed forever. “It was like life changed within a blink of an eye,” she explained. “I was completely ...
WSPA Spartanburg on MSN3h
Union Co. group raises awareness for rare diseasesThe last day of February is Rare Disease Day, and one Union County group wanted to shine a light on those living with rare ...
On the very day Noa was diagnosed, an experimental gene therapy and clinical trial were posted to treat Canavan disease. Noa was only the third patient in the world to be dosed with the gene therapy, ...
President Donald Trump is expected to sign an executive order designating English as the official language of the United ...
Rare Disease Day, observed on Feb. 28, brings attention to uncommon diseases affecting populations of 200,000 or fewer. In ...
Williams, who has performed the National Anthem at baseball stadiums as part of Boehringer Ingelheim’s Breathless campaign, ...
A Lancaster County mother and father are sharing their story in hopes of raising awareness of the uncommon genetic disorder their child is facing. There's no treatment and no cure, but the family is ...
In honor of Rare Disease Day, the Celtics are teaming with Takeda Pharmaceuticals to raise awareness and support for the rare disease community.
At just 26 months old, Grace Visser was diagnosed with Rett Syndrome, a rare genetic disorder that affects brain development.
“So Ataxia-Telangiectasia is similar in ways to muscular dystrophy, meaning it’s a neuromuscular progressive disorder. So ...
Roanoke's Wells Fargo Tower is lit up Friday night to bring attention to illnesses that impact one in every ten Americans.
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