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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!

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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.

May 18, 2017

Pulmonary hypertension patient Christine Liles lives on oxygen 24/7.  She was born with serious heart and breathing problems along with scoliosis. While Christine is dependent on O2, she is quick to assert that this doesn't mean her life is over.  Christine is also a blogger who shares her experience on Living on O2 for Life.

Learn more about pulmonary hypertension at phaware365.global. Never miss an episode with the phaware® podcast app. Follow us on facebook, twitterinstagram, youtube & linkedin @phaware #phaware