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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.

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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.

2023 sponsorship support was made possible from: CVS Specialty, Enzyvant, Janssen, Liquidia Technologies, Inc., 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.

Rosemary Graham - phaware® interview 405

Feb 28, 2023

Pulmonary hypertension and lupus patient, Rosemary Graham details her 39 year history navigating multiple rare disorders and  the importance of her faith, self-care and never giving up.

My name is Rosemary Graham. I live in Atlanta, Georgia. I have been diagnosed with pulmonary hypertension since 2012. Before that, I...


Feb 27, 2023

Pulmonary hypertension and lupus patient, Rosemary Graham details her 39 year history navigating multiple rare disorders and  the importance of her faith, self-care and never giving up.

Learn more about pulmonary hypertension trials at www.phaware.global/clinicaltrials. Follow us on social @phaware Engage for a cure:


Macy Thames - phaware® interview 404

Feb 21, 2023

Pulmonary hypertension patient, Macy Thames, discusses her PH diagnosis, her fear of not being there to see her son grow up, and the power of having not only a supportive partner, but a strong support system.

My name is Macy Thames. I currently live in St. Paul, Minnesota, and I was diagnosed with pulmonary...


Feb 20, 2023

In this episode, pulmonary hypertension patient, Macy Thames discusses her PH diagnosis, her fear of not being there to see her son grow up, and the power of having not only a supportive partner, but a strong support system.

Learn more about pulmonary hypertension trials at www.phaware.global/clinicaltrials. Follow us...


Lindsay Thurman - phaware® interview 403

Feb 14, 2023


Pulmonary hypertension patient, Lindsay Thurman, shares her experience of long distance running while living with a chronic lung disease.

Follow Lindsay's Running with PAH blog page on facebook.

My name's Lindsay Thurman. I have been living with PAH since 2008. When I was first diagnosed, I was having a lot of...