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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.

Lynn Bastian Transcript

Dec 29, 2016


Lynn Bastian is a long-term pulmonary hypertension survivor. Though she was diagnosed over ten years ago, Lynn discusses how she continues to learn all she can about this progressive, rare disease and why it’s import for patients to educate family, friends and medical professionals and make them #phaware. 

My name is...


Dec 29, 2016

Lynn Bastian is a long-term pulmonary hypertension survivor. Though she was diagnosed over ten years ago, Lynn discusses how she continues to learn all she can about this progressive, rare disease and why it’s import for patients to educate family, friends and medical professionals and make them #phaware. Learn more...


Kalena Sawyer Transcript

Dec 26, 2016


Pulmonary hypertension patient, Kalena Sawyer is always spreading the word about her rare, life-threatening illness. Because PH is an invisible disease, Kalena wants people everywhere – especially medical professionals to become #phaware.

My name is Kalena Sawyer and I'm from Okemos, Michigan.

It was May of 2013 and...


Dec 26, 2016

Pulmonary hypertension patient, Kalena Sawyer is always spreading the word about her rare, life-threatening illness. Because PH is an invisible disease, Kalena wants people everywhere – especially medical professionals to become #phaware.

Listen to “I’m Aware That I’m Rare: the phaware™ podcast” at


Lindsey and Josh Belt Transcript

Dec 22, 2016




In January of 2013, Lindsey and Josh Belt’s 5 year-old son Joel was diagnosed with a severe lung disease called idiopathic pulmonary hypertension (PH). Since Joel's diagnosis, the Belts have been on a mission to spread the message of HOPE! In 2013 & 2014, they hosted Color PHor A Cure 5K to raise awareness for...