Patients Needed for International Childhood Takayasu Study My name is Katrina Bargender, and I was diagnosed with Takayasu arteritis when I was 14 years old.
His Grandmother’s Kidney Donation Helped Save His Life Nathan Rose, 17, plans to spend his spring break with his grandmother in Arkansas. The high schooler
Allison Long Keeps Moving Toward Her Goals: A Marathon and a Medical Career Allison Long had never run a marathon, but it was a goal.
Dr. Catherine Sims Leads Team Researching Pregnancy and Vasculitis Pregnancy can be complicated, even for healthy women. But for someone with a rare autoimmune disease,
Sharan Knoell Champions Doctor Who Diagnosed Her Sharan Knoell is one of those rare vasculitis patients who got a diagnosis quickly. She has two people
Rare Disease Day is All About Sharing Information Get ready to show your support for everyone who has been diagnosed with a rare disease. Rare
Annie Reynolds laughingly tells her mom she is her glitch child. She says she has been a monster – making her siblings walk on egg
Veterans Affairs is Working to Give Its Patients Greater Access to Vasculitis Care, No Matter Where They Live Dr. Paul Monach, chief of the rheumatology
Lack of Vasculitis Expertise Leads to Devastating End Karen Miller has joined her local hospital’s patient advisory board after her mother, Lynn Johnston, died from
Blog “It was the best of times, it was the worst of times, it was the season of Light, it was the season of Darkness,
