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I'm Aware That I'm Rare: the phaware® podcast

A new podcast series devoted to raising global pulmonary hypertension awareness with dynamic stories from PH patients, caregivers and medical professionals from around the world. New Episodes every Monday & Thursday!

Use the search bar above to search episodes by topic. Search "phawareMD" to discover podcasts with medical professionals.

Get our custom smartphone app (for iPhone™, Android™, and Amazon™ devices). It's the most convenient way to access the phaware™ podcast.

The views and opinions expressed in the phaware® podcast do not necessarily reflect the official policy or position of phaware global association. Information on 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.

To learn more about PH visit www.phaware.global. phaware® is a 501(c)3 organization. © Copyright 2015. All Rights Reserved.

Generously Supported in part by Actelion Pharmaceuticals US, Inc., Bayer Healthcare & Reata Pharmaceuticals.

Sep 7, 2016

A new podcast series from phaware global association devoted to raising global pulmonary hypertension and rare disease awareness with dynamic stories from patients, caregivers and medical professionals from around the world.

New 3-15 minute episodes of this series of impactful, insightful and most importantly, hopeful conversations with members of the global PH community are released every Monday and Thursday.

Learn more about pulmonary hypertension at phaware365.global. #phaware

Never miss an episode with the phaware® podcast app.

Follow us on facebook, twitterinstragram, youtube & linkedin @phaware

 


Karen sawyer
almost twelve months ago

I was diagnosed may 11th 2013 could not breathe.. Then had cardiac arrest reason was from pulmonary arterial hypertension
🙏🏻☮💜💜💜cure