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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.

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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., Bellerophon Therapeutics & CVS Health.

Jan 23, 2017

Billy Keith is a mother on a mission. She discusses her daughter Brooke's road to a pulmonary hypertension diagnosis, why Dr. Robyn Barst is her angel and why advocating on behalf of children with PH is so important.

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


Scott Bonar
over a year ago

Billie, your daughter's diagnosis sounds very familiar to what our son Mike went through, i.e. went in for something totally non-PH related only to have them find the PH. The main difference is that Mike was 17 and turned 18 before we were able to see a PH specialist so we went directly to the adult docs. Hope your daughter is doing better and keep up the good PHight!