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.

Mary Jan Hicks - phaware® interview 277

Aug 30, 2019

Mary Jan Hicks discusses her daughter Meaghan's PH diagnosis and road to double-lung & heart transplant.

My name is Mary Jan Hicks. I live in Gig Harbor, Washington. My connection to pulmonary hypertension is as a caregiver for my daughter, Meaghan Hicks.

We were stationed in Heidelberg, Germany. Meaghan went in for...

Episode 277 - Mary Jan Hicks

Aug 29, 2019

Mary Jan Hicks discusses her daughter Meaghan's PH diagnosis and road to double-lung & heart transplant.

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, Twitter, Instagram, YouTube & Linkedin Engage...

Stephanie Bachelder - phaware® interview 276

Aug 27, 2019

Pulmonary Hypertension patient Stephanie Bachelder on being diagnosed with a terminal illness, the power of combination therapy and why she feels she is no longer dying of her disease, but living with it.

My name is Stephanie Bachelder and I am a pulmonary arterial hypertension patient.

For probably about 15 years,...

Episode 276 - Stephanie Bachelder

Aug 26, 2019

Learn more about pulmonary hypertension trials at www.phaware.global/clinicaltrials. Never miss an episode with...

Cathy Downard - phaware® interview 275

Aug 23, 2019

Lupus and Pulmonary Hypertension patient Cathy Downard discusses her rare disease diagnosis and how she battles depression by helping kids in her the community become citizens.

My name is Cathy Downward, and I am a pulmonary hypertension patient.

I was diagnosed with lupus when I was 17. Like most teenagers, I was...