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.

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.

Generously Supported in part by Actelion Pharmaceuticals US, Inc., Bayer, United Therapeutics Corporation, Acceleron, CVS Health & PhaseBio Pharmaceuticals.

Amanda Howard phaware® interview 369

Apr 5, 2022

Pulmonary hypertension caregiver, Amanda Howard, discusses her 17-year-old daughter Abby's lifelong battle with PH after being diagnosed in the PICU at 8 months old.

Amanda Howard:
My name's Amanda Howard. I'm connected to PH through my 17-year-old daughter, Abby. Abby was diagnosed with PH when she was eight months...

Episode 369 - Amanda Howard

Apr 4, 2022

In this episode, pulmonary hypertension caregiver, Amanda Howard, discusses her 17-year-old daughter Abby's lifelong battle with PH after being diagnosed in the PICU at 8 months old.

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

KC Yates - phaware® interview 368

Mar 29, 2022

Pulmonary hypertension patient, KC Yates, discusses battling COVID-19 twice during the pandemic and how she relies on her inner-strength to battle her rare disease.

KC Yates:
My name is KC Yates. I'm from Michigan. My PAH just came on randomly. I was pretty much having headaches, where you couldn't talk to me. You...

Episode 368 - KC Yates

Mar 28, 2022

In this episode, pulmonary hypertension patient, KC Yates, discusses battling COVID-19 twice during the pandemic and how she relies on her inner-strength to battle her rare disease.

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

Dawn Meador - phaware® interview 367

Mar 15, 2022

Long-term pulmonary hypertension patient, Dawn Meador, discusses navigating her PH during a pandemic as well as why she and her husband chose to adopt after her PH diagnosis.

Dawn Meador:
Hi, I'm Dawn Meador. I am from Springfield, Tennessee. I was diagnosed with PH in March of 1998, so I've been living with PH for 24...