Holly Helm’s life changed forever. “It was like life changed within a blink of an eye,” she explained. “I was completely ...

The 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, ...

In a symbolic gesture of solidarity, the Rare Disease Ghana Initiative (RDGI) illuminated the Ministry of Health (MoH) building on February 28, 2025, to mark Rare Disease Day.

President Donald Trump is expected to sign an executive order designating English as the official language of the United ...

MADISON, Wis. (WIFR) - For 14 years, Treyson Wallace’s family searched for answers. Born in 2009, Treyson failed a newborn ...

Rare Disease Day, observed on Feb. 28, brings attention to uncommon diseases affecting populations of 200,000 or fewer. In ...

Every year since 2008, Rare Disease Day has been held on the last day of February to raise awareness about the research that goes into rare diseases like spinal muscular atrophy (SMA).

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 ...

Cheryl and Vera, two sisters bound by love and resilience, have not only faced these challenges head-on but raised awareness on rare disease.

At just 26 months old, Grace Visser was diagnosed with Rett Syndrome, a rare genetic disorder that affects brain development.