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2024 Vasculitis Foundation Annual Appeal

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Living with a rare disease like vasculitis can be challenging, especially when family, friends, physicians, and others don't know what it is or understand your experience. In this video, people living with the disease and their care partners share what they wish others knew about vasculitis.

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Annaruth, who's living with Takayasu arteritis, a form of vasculitis, shares how participating in research has positively impacted her life and empowered her community.

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Annruth and John share how the Vasculitis Foundation resources such as support groups and webinars have helped them navigate Annaruth's vasculitis diagnosis.

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Victor James, who is living with vasculitis, shares why he supports the Vasculitis Foundation through monthly giving. www.vasculitisfoundation.org

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Jess Kanciruk received the life changing diagnosis of GPA in the summer of 2021. Because of donors like you, she was able to turn to the Vasculitis Foundation for support on her vasculitis journey. Thank you for standing with people living with vasculitis. Please consider investing in the VF’s mission today! Donate now: https://vasculitisfoundation.org/donate-to-the-vf/

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annual appeal teresa searls 1080p

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2022 Annual Appeal

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2024 Vasculitis Foundation Annual Appeal

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