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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.

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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., Bellerophon Therapeutics & CVS Health.

May 10, 2018

Shari Caffrey is the founder of TaylorsWish.org. Taylor’s Wish was created in memory of Taylor Renee Caffrey, Shari and Michael’s daughter and twin sister to Brooke. Taylor lost her battle with Pulmonary Hypertension at the tender age of 4 1/2 years.  In this episode, Shari discusses how she honors Taylor’s memory by helping raise awareness and funds for more research in order to find a cure for this widely unknown terminal illness. The 9th Annual Saturday, RACE 2 CURE PH takes place on May 12th in Anaheim, CA.

Learn more about pulmonary hypertension at www.phaware365.global. Never miss an episode with the phaware® podcast app. Follow us @phaware on facebook, twitter, instagram, youtube & linkedin Engage for a cure: www.phaware.global/donate #phaware