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.

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

Cynthia Neilson - phaware® interview 497

Dec 3, 2024

Cynthia Neilson shares her journey as a mother raising her daughter Claire, who was diagnosed with pulmonary arterial hypertension (PAH) at a young age. Cynthia recounts the challenges she faced navigating the medical system, the emotional toll of dealing with an unexpected diagnosis, and the difficulties of balancing...

Episode 497 - Cynthia Neilson

Dec 2, 2024

Natalie Roy - phaware® interview 496

Nov 26, 2024

Natalie Roy is a double lung transplant survivor living in Canada. She was diagnosed with pulmonary arterial hypertension (PAH) in 2005 and received her transplant in 2017. .

After her successful transplant seven years ago, Natalie experienced a difficult initial recovery but felt amazing once she started healing. The...

Episode 496 - Natalie Roy

Nov 25, 2024

Natalie Roy is a double lung transplant survivor living in Canada. She was diagnosed with pulmonary arterial hypertension (PAH) in 2005 and received her transplant in 2017. .

After her successful transplant seven years ago, Natalie experienced a difficult initial recovery but felt amazing once she started healing. The...

Maureen Harper - phaware® interview 495

Nov 19, 2024

Maureen Harper, a CTEPH patient from Canada, shares her journey with this rare condition. She initially thought she had an infection in her leg, but further tests revealed enlarged pulmonary arteries and multiple blood clots in her lungs. After being diagnosed with pulmonary hypertension, she underwent a complex...