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, ...

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 ...

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 ...

We were unable to process your request. Please try again later. If you continue to have this issue please contact [email protected]. Diacerein 1% did not outperform vehicle in study ...

The Kansas City Fire Department is asking the community for help in putting together a parade for boy battling a rare genetic ...

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

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

Tripp Roth, 2 and dying, is covered in painful blisters inside and out. Dec. 19, 2011— -- The pain never ends for Tripp Roth, a 2-year-old boy who has outlived all medical predictions with a ...

The "Plunge for Elodie" raises awareness and funds for critical research to treat and cure Epidermolysis Bullosa (EB) Born with Recessive Dystrophic Epidermolysis Bullosa (EB), 6-year-old Elodie Kubik ...

Epidermolysis bullosa is a skin condition where blisters appear following minor injuries. Epidermolysis bullosa (EB) is a group of inherited disorders in which the skin is extremely fragile. Skin ...

We were unable to process your request. Please try again later. If you continue to have this issue please contact [email protected]. Back to Healio Researchers will analyze the safety and ...

Born with a rare skin condition that leaves her skin blistered and peeling, this baby is turning one and needs your support to find a cure. As Makenzie Cadmus nears her first birthday, her parents are ...