T-shirts are being made after thousands of people attended a parade for a boy with a rare genetic disorder. A 3-year-old boy, ...

Courageous Emma Fogarty, 41, is the longest living Irish person with Epidermolysis Bullosa (EB), a rare and painful condition ...

For Ms Miria Mukiibi Kibirige, that struggle is a daily reality. She cares for two children living with epidermolysis bullosa (EB), a rare genetic skin disorder causing painful, life-threatening ...

A local family thought they were planning a simple parade for their 3-year-old son, but what happened next was something no ...

Thousands gathered in Kansas City to honor 3-year-old Tucker Langford, a boy battling a rare skin condition, with a heartfelt ...

Abeona Therapeutics Inc. (Nasdaq: ABEO) and Children's Hospital Colorado today announced activation of Children's Colorado as ...

What started as a simple idea turned into a moment Kansas City will never forget. Thousands spent their Saturday at “Tucker’s Parade,” waving signs and cheering for a brave 3-year-old who was recently ...

Amryt Pharma said Filsuvez, a topical therapeutic gel, had demonstrated a significant increase in speed of wound healing in the rare disease Epidermolysis Bullosa (EB) in a late-stage trial, the first ...

Abeona Therapeutics Inc. (Nasdaq: ABEO), a commercial-stage biopharmaceutical company developing cell and gene therapies for ...

Dozens of trucks, motorcycles and even camels lined up Saturday to honor 3-year-old Tucker Langford, who is battling a rare ...

In the current U.S. market landscape, recent volatility has been marked by sharp declines in stock indexes following geopolitical tensions and trade policy announcements, even as the Nasdaq reached ...

Quoin Pharmaceuticals Ltd. (NASDAQ: QNRX) (the “Company” or “Quoin”), a late clinical-stage specialty pharmaceutical company focused on rare and orphan diseases, today announced that it has entered ...