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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, United Therapeutics Corporation & CVS Health.

Patti Flanagan - phaware® interview 291

Oct 18, 2019

PH and Scleroderma patient, Patricia Flanagan discusses the bumpy roller coaster ride that led to her diagnosis and life with left heart disease.

My name is Patti Flanagan. I'm from Virginia, and I have pulmonary hypertension, due to diastolic heart failure.

I do remember hearing the word pulmonary hypertension for...


Oct 17, 2019

PH and Scleroderma patient, Patricia Flanagan discusses the bumpy roller coaster ride that led to her diagnosis and life with left heart disease.

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


Taryn Petry - phaware® interview 290

Oct 15, 2019

Pediatric pulmonary Hypertension patient, Taryn Petry talks about her passion for Irish dancing and how she grapples with restricting herself in certain activities.

I'm Taryn Petry and I'm a pulmonary hypertension patient.

I don't remember a lot, but I know I was diagnosed when I was five and since then I haven't...


Oct 14, 2019

Pediatric pulmonary Hypertension patient, Taryn Petry talks about her passion for Irish dancing and how she grapples with restricting herself in certain activities.

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


Josh Lampa - phaware® interview 289

Oct 11, 2019

Pulmonary Hypertension patient, Josh Lampa talks about the importance of online and in-person support groups and why disease awareness is so important for physicians.

Hi, I'm Josh Lampa and I have pulmonary hypertension.

I was diagnosed in 2010. I think I've always had PH, because I was always a little bit short of...