VPPRN enrolling patients outside the US now
The V-PPRN is a research network with the ability to collect and securely store patients' disease experiences, known as patient-reported data to build robust data for vasculitis research.
We are enrolling patients with vasculitis, parents of a child with vasculitis, and caregivers of adult patients with vasculitis. The V-PPRN is studying the following forms of vasculitis: |
The V-PPRN is a whole new way of finding answers for the questions most important to YOU and other patients living with vasculitis.
We hope you will join us in creating a new vision for vasculitis research by becoming a vasculitis visionary and powering the V-PPRN!
Here is how to join:
- Follow this link: www.vpprn.org/webapp/views/consent
- After you register, answer questions about yourself to complete your MyV-PPRN patient profile.
- Check in regularly and make sure your information is up-to-date.
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