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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!

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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.

May 29, 2017

Pulmonary Hypertension patient, Thekla McGinley shares her story. Thekla discusses her frustration in getting a proper PH diagnosis and the importance of PH awareness when it comes to the doctors and nurses treating her rare disease.

Listen to “I’m Aware That I’m Rare: the phaware™ podcast” at www.phaware.global/podcast. Learn more about pulmonary hypertension at www.phaware.global. #phaware