Learn about dermatomyositis and the remarkable journey of Audrey Gouskos. Discover how St. Michael's Hospital has provided lifesaving support for her rare disease.
Jeremiah Marshall, 33, has epidermolysis bullosa, a rare genetic disorder that makes his skin tear or blister at the ...
Jeremiah Marshall has lived with epidermolysis bullosa since the day he was born and has had to endure teasing at school, ...
This case study explores a rare overlap of hidradenitis suppurativa and porokeratosis, as well as highlights the unique ...
An 84-year-old man left clinicians at a Hong Kong hospital utterly perplexed after arriving at the hospital to be treated […] ...
An editor in his early 40s thought the tiny numb spot on his nose was innocuous. A year and six doctors later, he learned it ...
LAS VEGAS, NV / ACCESS Newswire / January 23, 2025 / Skinvisible Pharmaceuticals, Inc. ("Skinvisible" or "the Company"), (OTCQB:SKVI), an innovative topical and transdermal pharmaceutical research and ...
Managing the unpredictable symptoms of indolent systemic mastocytosis prompted a search for answers and community.
Epidermolysis Bullosa (EB), or butterfly disease, affects 1 in 50,000 people, causing fragile skin that blisters easily, ...
Researchers find that allergy medicine could help patients with a rare genetic disease avoid liver transplants.