Finding hope on my journey with ANCA-associated vasculitis

Finding hope on my journey with ANCA-associated vasculitis

Steven Chetham runs a 5K race in Boulder, Colorado, in September 2024. (Photos courtesy of Steven Chetham) This is Steven Chetham’s story: I was diagnosed with granulomatosis with polyangiitis (GPA) in September 2023. Everyone’s journey with ANCA-associated vasculitis (AAV) is different, but we do have many…

AAV combo therapy allows for early glucocorticoid withdrawal

Induction therapy with cyclophosphamide and rituximab allows for early discontinuation, without compromising efficacy, of an oral-only glucocorticoid regimen in people with severe ANCA-associated vasculitis (AAV), a study found. Patients on oral glucocorticoids for up to three months showed comparable remission and relapse rates, but tended to have fewer infections…

Becoming a caregiver is all about adjustments and problem solving

Lynette Matson, left, provides care for her wife, Laure Larkin, who has granulomatosis with polyangiitis and liver problems. (Photos courtesy of Lynette Matson) This is Lynette Matson’s story: Before my wife was diagnosed with granulomatosis with polyangiitis (GPA), I thought being a caregiver meant fluffing pillows, offering…

Immune protein is prognosis sign in ANCA-associated vasculitis

Blood levels of CCL23, an immune molecule that may be involved in blood vessel formation and repair, are significantly increased in people with ANCA-associated vasculitis (AAV) relative to healthy people, a study finds. High blood CCL23 levels accurately differentiate people with active AAV from those in remission and increase…

Finding resilience after a challenging vasculitis diagnosis

Laure Larkin, left, and her wife, Lynette Matson, celebrate their anniversary. (Photos courtesy of Laure Larkin) This is Laure Larkin’s story: It all started with what seemed like a stubborn sinus infection and a chest X-ray that raised some eyebrows. No big deal, right? Fast forward a couple of…

How I learned to thrive while living with vasculitis

John Stadler poses for a photo at his home. (Photos courtesy of John Stadler) This is John Stadler’s story: My journey with vasculitis has been both a challenge and a profound learning experience, filled with emotional ups and downs. I was diagnosed…

Awareness Month to focus on personal experiences, connections

Personal stories, community connections, and encouraging videos will be among the highlights as patients, doctors, researchers, and advocates recognize International Vasculitis Day on May 15 and the rest of Vasculitis Awareness Month. Vasculitis is a group of rare autoimmune diseases characterized by inflammation and damage to blood vessels. Most…

We all have different approaches to living with chronic illness

I’ve come to realize that there is no single way to live with a chronic illness like ANCA vasculitis. There are countless realities and processes people use to navigate such a life-altering diagnosis. Some dive into research, anchoring themselves in science, facts, and clinical studies, finding comfort in…