Throughout May, ANCA Vasculitis News is recognizing Vasculitis Awareness Month with a variety of stories that represent different perspectives on life with vasculitis that we hope help to inspire and empower our readers. These stories highlight some of the unique challenges of living with vasculitis, as well as stories of hope, inspiration, and other topics that help to generate awareness among the ANCA vasculitis community. Follow along with the series here or visit us on Facebook, Instagram, or X using the hashtag #ANCASpotlight.
Heather Fish takes in the fresh air of the coast after seeing improvements following treatment for her EGPA. (Photos courtesy of Heather Fish) This is Heather Fish’s story: It was a terrible time…
Read moreJanessa Kaneaster’s 7-year-old daughter, Kaylee, who has ANCA vasculitis, takes a break for a picnic lunch. (Courtesy of Janessa Kaneaster) This is Janessa Kaneaster’s story: When your 7-year-old gets diagnosed with something as…
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…
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…
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…
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…
Jordyn, left, and Cody Blagg, five months before Jordyn’s diagnosis. (Photos courtesy of Cody Blagg) This is Cody Blagg’s story: It’s complicated. As I sit here in the emergency room with my wife,…
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