I'M AWARE THAT I'M RARE: THE PHAWARE® PODCAST
This podcast series is devoted to raising global pulmonary hypertension awareness with dynamic stories from PH patients, caregivers and medical professionals from around the world.
Subscribe to this series of impactful, educational and most importantly, hopeful conversations with members of the global PH and rare disease community.
Click to get our all new custom smartphone app (for iPhone™, Android™ and Amazon™ devices). It's the most convenient way to access the phaware™ podcast. New Episodes every Monday!
Click Play on the phaware® podcast player below to Listen & Share episodes with your friends. You can also listen wherever you get your favorite podcasts. Be sure to fill out the form at the bottom of this page to submit your story for a future episode!
PHAWARE® PODCAST PLAYER
The most recent episode is at the top. Scroll to listen to additional episodes. Click the “Info” bubble on the right to read episode description.
EVERYBODY HAS A STORY. WHAT'S YOURS?
phaware wants to share your pulmonary hypertension story with our engaged global audience. Whether you are a patient, caregiver, or medical professional, we are enlisting PH community members from across the globe for a series of video and audio interviews.
The views and opinions expressed in the phaware® podcast do not necessarily reflect the official policy or position of phaware global association. Information on www.phaware.global and phaware social media sites is provided for general information only. It is not intended as legal, medical or other professional advice, and should not be relied upon as a substitute for consultations with qualified professionals who are familiar with your individual needs.