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. 

Subscribe to this series of impactful, insightful and most importantly, hopeful conversations with members of the global PH community. 

Click to get our all new custom smartphone app (for iPhone™, Android™, Microsoft Windows™ and Amazon™ devices). It's the most convenient way to access the phaware™ podcast. New Episodes every Monday & Thursday!

Click Play on the phaware™ podcast player below to Listen & Share episodes with your friends.  Be sure to fill out the form at the bottom of this page to submit your story for a future episode!

phaware™ podcast player

Click "More Episodes" to explore additional content.  The most recent episodes are at the top.

Everybody has a story.  What's yours?

phaware wants to share your pulmonary hypertension story with our engaged global audience.  Whether you are a patient, caregiver, or medical professional, we are enlisting PH community members from across the globe for a series of video and audio interviews. 

Name *
Phone *
NOTE: In most cases you need a laptop or desktop with a microphone and the lasted Chrome or Firefox browser. If so, we can record anyone, from anywhere at anytime!

Get an official “I’m Aware That I’m Rare” FREE T-shirt. when you donate $25  at www.represent.com/phaware.

Get an official “I’m Aware That I’m Rare” FREE T-shirt. when you donate $25  at www.represent.com/phaware.

The views and opinions expressed in the phaware™ podcast do not necessarily reflect the official policy or position of phaware global association. Information on www.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.