phaware: Aware That I’m Rare

phaware®

About this app

Become #phaware with the most convenient way to access I'm Aware That I'm Rare: the phaware podcast.

Join the global #phaware conversation in an engaging podcast series of impactful, insightful and, most importantly, hopeful stories from members of the global pulmonary hypertension community.

phaware™ brings you dynamic stories from PH patients, caregivers and medical professionals from around the world. New Episodes every Monday & Thursday!

With this app you are always connected to the latest episodes and the show. You can also star your favorite episodes and save them to a list so you can easily enjoy them over and over! This app is complete access to I'm Aware That I'm Rare: the phaware podcast and if you're a fan of the show you won't want to be without it!

This app contains the following additional features:

* Streaming access to play episodes from anywhere
* Always updated with the latest episodes- and an archived back catalog
* Playback resume (when interrupted by a call or other distraction)
* Access to exclusive extras like PDFs, wallpapers, and bonus content
* Quick access to all the contact methods for the show like call, email, web, Facebook, and Twitter

Thank you for downloading this app and supporting our mission!

Please note, not all episodes may have exclusive extras.

Are You #phaware?
Pulmonary hypertension (PH) is a rare, life-threatening disease of the pulmonary arteries that can lead to right heart failure.

phaware creates global PH awareness engagement on behalf of families, caregivers and medical professionals and supports PH research efforts to find a cure for this deadly disease.

Follow @phaware on facebook, twitter & instagram. Get our phaware™ and phaware365™ apps. Available on the App Store™and on Google Play™.

phaware global association is a 501(c)3 nonprofit organization. ©2016 All Rights Reserved. To learn more about pulmonary hypertension visit www.phaware.global

Ratings and reviews

I love listening to all the other stories and information. It helps to remember I'm not alone in this PHight.

Good app

I am so impressed! Dr Jeremy Feldman is my pulminologist and absolutely amazing. I am so lucky to have ended up in his care. I do have to say that i didnt really know that PAH is so rare. I lost my sister to it in 2006 and she was on flolan. She didnt quit smoking or change eating habits, or exercise. I was diagnosed in 2008 and made sure i followed Dr. Orders. Im doing better ans better. Thank you Dr. Feldman, i owe you my extended life. B. STOKLEY