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.

Friday is Rare Disease Day, which raises awareness for rare diseases and aims to improve access to treatment and medical representation for individuals with rare diseases and their families.

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

An estimated 60,000 people in Cyprus suffer from rare diseases, Health Minister Michael Damianos said on Friday. He pledged that the ministry would move methodically to establish a comprehensive ...

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

Growth hormone therapy was initiated for 20 children-14 diagnosed with Turner syndrome and six with GH deficiency-under the ...

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

A Million Acts of Love (AMAOL) has found their first grantee in Ella Gauthier, a student in Kamloops honouring her brother ...

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).