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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!

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.

2024 sponsorship support was made possible from:  Johnson & Johnson, Liquidia Technologies, Inc., Pulmovant, Gossamer Bio and Merck & Co, Inc.

To learn more about PH visit www.phaware.global. phaware® is a 501(c)3 organization. © Copyright 2023. All Rights Reserved.

Contact

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, care partner, or medical professional, we are enlisting PH community members from across the globe. We can record anyone... from anywhere... anytime. Write us to share your story or if you have questions about the show.  Please tell us a little about yourself and your connection to PH.

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