VPPRN Talk | ANCA Vasculitis in New Zealand

vasculitisfoundation

vasculitisfoundation

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Learn how the Vasculitis Patient-Powered Research Network (VPPRN) is bringing patients, caregivers, clinicians, and researchers together to advance vasculitis research around the world.

In this presentation, Dr. Peter Merkel and Dr. Jennifer Gordon explain how the VPPRN works, how patients can participate in research from home, and how patient-reported experiences are helping researchers better understand vasculitis, treatment, quality of life, and more. They also highlight current and upcoming VPPRN studies and answer questions about getting involved.

Discover how sharing your experience can help shape the future of vasculitis research.