Preview Mode Links will not work in preview mode

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.

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.

2023 sponsorship support was made possible from: CVS Specialty, Enzyvant, Johnson & Johnson, 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.

Natalie Roy - phaware® interview 202

Oct 30, 2018

Canadian Natalie Roy is a former pulmonary hypertension patient who received a double-lung transplant in September 2017. She discusses having an identity crisis post PH.

My name is Natalie Roy. I live in Vancouver, British Columbia, Canada. I was diagnosed with, what was called at the time, primary pulmonary...


Oct 29, 2018

Canadian Natalie Roy is a former pulmonary hypertension patient who received a double-lung transplant in September 2017. She discusses having an identity crisis post PH.

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


Brooke Paulin - phaware® interview 201

Oct 26, 2018

Canadian Pulmonary Hypertension Patient, Brooke Paulin discusses her road to PH Diagnosis.

My name's Brooke Paulin. I am from Mississauga, Ontario, just outside of Toronto. I was diagnosed in February of 2014, so I guess four and a half years ago, just shy of five.

I was a competitive athlete growing up. I represented...


Oct 25, 2018

Canadian Pulmonary Hypertension Patient, Brooke Paulin discusses her road to PH Diagnosis.

Learn more about pulmonary hypertension trials a www.phaware.global/clinicaltrials. Never miss an episode with the phaware® podcast app. Follow us @phaware on Facebook, Twitter, Instagram, YouTube & Linkedin Engage for a cure:


Iain Armstrong - phaware® interview 200

Oct 23, 2018

Chairman of PHA UK, Iain Armstrong talks about PHawareness Week 2018 (October 22-28), EmPHasis10 and the power of collaboration within the PH Community.

My name is Iain Armstrong. I'm chair of PHA UK. I do two jobs, I do that part-time. I'm also consultant nurse in one of the large PH centers in the UK.

I've been...