Rare Disease Day is All About Sharing Information
January 24, 2025
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
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
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,
Eliza Johnstone’s Vasculitis Diagnosis Came Late, She Now Champions Early Diagnosis for Others Eliza Johnstone, a 19-year-old living in the United Kingdom, feels like she
Late Vasculitis Diagnosis Steals Nearly One Decade Christine Gerchow was in her final semester at Villanova University in 2002 and planning for a promising career,
Raising Money for the VF Can Be Fun and Easy Suzanne DePaolis, a Vasculitis Foundation board member, believes in supporting the foundation’s mission and its
When vasculitis has you feeling down, turn UP the beat! We asked our community what their go-to pick-me-up songs are. This playlist, created from their
Leaving a Legacy Matters When Scott Gongaware was diagnosed with Vasculitis more than 20 years ago after a year of being sick and with kidney
Meet VF Young Investigator Cecilia Barnini, MD “The problem with rare diseases like vasculitis,” Cecilia Barnini, MD, said, “is there are not enough doctors and