September 15, 2020

Polycythemia Vera patient advocate on living with MPN, Diane’s story

September Blood Cancer Awareness Month Spotlight

by David Wallace

David Wallace, your host with PV Reporter, talks to fellow PV patient advocate Diane Rose about living with Polycythemia Vera. Diane shares her patient story as we talk about how she was diagnosed, treatment, ET shifting to PV, being your own advocate, fear of needles and much more. As September is Blood Cancer Awareness month, we highlight the importance of getting a blood test. If you would like to share your patient or caregiver story please drop us a note. With your help, we are planning to conduct more video interviews.

About David Wallace

Founder of PV Reporter, a resource for Myeloproliferative Neoplasm (MPN) patients and caregivers. After being diagnosed with Polycythemia Vera (PV) in 2009, I utilized social media to connect with "informed patients" and develop a better understanding of emerging treatment options. My philosophy on patient care is straight forward - "educating the patient is essential, so the patient can guide their physician to meet his or her needs." PV Reporter is a comprehensive resource hub giving visitors vital tools to become "empowered patients."