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!

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.

2024 sponsorship support was made possible from: Johnson & Johnson, Liquidia Technologies, Inc., Pulmovant, Gossamer Bio and Merck & Co, Inc.

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...

I'm Aware That I'm Rare: the phaware® podcast

Amanda Howard phaware® interview 369

Episode 369 - Amanda Howard

Categories

Archives