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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., Bayer, United Therapeutics Corporation, Acceleron, CVS Health & PhaseBio Pharmaceuticals.

Melanie Brown - phaware® interview 334

Jul 21, 2020

Pulmonary Hypertension Patient, Melanie Brown discusses her complicated road to a proper PH diagnosis, counseling to cope with not being able to get pregnant and the power of giving back to the community by participating in PH trials & studies.

My name is Melanie Brown and I live in Portland, Oregon, where I was...


Jul 20, 2020

Pulmonary Hypertension Patient, Melanie Brown discusses her complicated road to a proper PH diagnosis, counseling to cope with not being able to get pregnant and the power of giving back to the community by participating in PH trials & studies.

Learn more about pulmonary hypertension trials at 


Kathleen Grady - phaware® interview 333

Jul 14, 2020

Pulmonary Hypertension Patient, Kathleen Grady discusses her road to diagnosis, her optimistic view on her rare disease and how she navigates the impact of #covid19. 

My name's Kathleen Grady, and I live in Cleveland, Ohio, and I have pulmonary hypertension for the last 11 years. My older brother, David Grady, has...


Jul 13, 2020

Pulmonary Hypertension Patient, Kathleen Grady discusses her road to diagnosis, her optimistic view on her rare disease and how she navigates the impact of #covid19. 

Learn more about pulmonary hypertension trials at www.phaware.global/clinicaltrials. Never miss an episode with the phaware® podcast app. Follow us 


Allison Wells - phaware® interview 332

Jul 7, 2020

Pulmonary Hypertension Patient Allison Wells is a substitute teacher from Gander Newfoundland. In this episode, Allison discusses self-diagnosing her PH and her decision to adopt.

My name is Allison Wells, I'm currently living in Gander, Newfoundland. I am a substitute teacher and I have a two-year-old daughter and I...