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 or Instagram using the hashtag #ANCASpotlight.
Christine MacFadyen’s symptoms appeared 15 years ago, and she was diagnosed five years ago. (Photos courtesy of Christine MacFadyen) This is Christine MacFadyen’s story: I was a fun-loving, always smiling, energetic, adventurous woman. I was only 24 and…
Read moreSarah Wellings, left, smiles with Isla Bell before her ANCA vasculitis diagnosis. (Photos courtesy of Sarah Wellings) This is Sarah Wellings’ story: Last night I dreamed I was running again. It seems my running days are over. Don’t…
Jennifer Feinson Destours is an American with ANCA vasculitis living in Paris. This photo was taken two years post-diagnosis. (Photos courtesy of Jennifer Feinson Destours) This is Jennifer Feinson Destours’ story: My life has often been fantasized, the…
Rob Nelson explores Peggy’s Cove in Nova Scotia, Canada, in fall 2021. (Photos courtesy of Rob Nelson) This is Rob Nelson’s story: Receiving a vasculitis diagnosis has a dramatic effect physically, emotionally, and socially on both…
This is Pam Squires’ story: Pam Squires says her life with her wife, Sarah Jones, who has eosinophilic granulomatosis with polyangiitis (EGPA), is like having EGPA by proxy. (Courtesy of Sarah Jones) My wife, Sarah, and I attended…
Sarah Jones smiles for the camera. (Photos courtesy of Sarah Jones) This is Sarah Jones’ story: I thought on the day of my EGPA diagnosis — fully, eosinophilic granulomatosis with polyangiitis — that I was finally going…
Karna Karlsrud, left, poses for a photo with her daughter, Clea, who has vasculitis. (Photos courtesy of Karna Karlsrud) This is Karna Karlsrud’s story: When I adopted my beautiful daughter, Clea, 23 years ago, the social worker told…
Kathy Olevsky prepares to record a Vasculitis Foundation medical webinar in her office. (Photos courtesy of Kathy Olevsky) This is Kathy Olevsky’s story: In late 2008, I was diagnosed with microscopic polyangiitis or MPA. It plunged me…
Ioana Miclea has eosinophilic granulomatosis with polyangiitis. (Photos courtesy of Ioana Miclea) This is Ioana Miclea’s story. So, picture this: I’m Ioana, your quintessential 20-something girl, living it up with nights out, camping escapades, and a newfound love…
Janice Barnett poses with a textile piece in the making. (Photos courtesy of Janice Barnett) This is Janice Barnett’s story: My diagnosis of eosinophilic granulomatosis with polyangiitis, formerly known as Churg-Strauss syndrome, in December 2021 plunged…
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