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Polycythemia Vera (PV)

Voices BlogPolycythemia Vera
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New Diagnosis
Real Patient Stories
Health and Wellness
Events & Advocacy

Making a Meaningful MPN Connection: Matt and Josh

Author: Voices of MPN

Tracking My PV: Karen's Story

Author: Voices of MPN

Finding an MPN Specialist: Aimee's Story

Author: Voices of MPN

Turning Up the Volume on MPN Education

Author: Voices of MPN

What Every Patient With an MPN Should Know About the Spleen

Author: Voices of MPN

Rare Reflections: MPNs Unmasked

Author: Voices of MPN

My Experience With Polycythemia Vera and Cardiovascular Risk

Author: Matt W.

"Something So Rare" Documentary Sheds Light on Life With an MPN

Author: Voices of MPN

Taja Connects With the MPN Community for the First Time

Author: Voices of MPN

Nick Grapples With His MPN Diagnosis

Author: Voices of MPN

A Facebook Live Chat Follow-up: Unanswered Questions

Author: Paul Larson, MSN-NP, AOCNP®

Dave Accepts the Challenge of Polycythemia Vera

Author: Voices of MPN

Barbara Reveals Hidden Struggles in a Film About the Impact of MPNs

Author: Voices of MPN

Be Your Own Advocate

Author: Alisa R.

Recognizing PV Symptoms

Author: Voices of MPN

The PV Tracker Tool: Taking Charge of Your Polycythemia Vera

Author: Voices of MPN

When Polycythemia Vera Becomes Myelofibrosis

Author: Voices of MPN

What Is Polycythemia Vera? A Beginner's Guide

Author: Voices of MPN

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