Share Your Rare
Disease Expertise
Pulmonary Hypertension Medical Professionals, Pulmonologists, Cardiologists, Investigators, Nurses and Global Thought Leaders
phaware global association wants to highlight your PAH expertise on the “I'm Aware That I'm Rare: the phaware® podcast” series with interviews taking place during ATS 2024.
Interviews will last between 20-30 minutes and be shared across our @phaware social sites, on your favorite podcast platform and heard in over 110+ countries!
Visit us in the ATS Exhibit Hall: Booth 3209.
Won’t be in San Diego on May 19-21 but would love to participate? Email us to be interviewed remotely.
“Voted Top 3 of the ‘10 Best Pulmonary Hypertension Podcasts You Must Follow in 2024’ from thousands of podcasts on the web ranked by traffic, social media followers, expertise, credibility & freshness.”
New Episodes
Every Monday
Topics range from the importance of early diagnosis and global PH awareness, to the impact of clinical trials to how patient support and advocacy are paramount to battling this disease.
Everybody has a Story. What’s Yours?
Whether you are a patient, caregiver, or medical professional, we are enlisting PH community members from across the globe.
We can record anyone... from anywhere... anytime.
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About the phaware global association
phaware® is a 501(c)3 organization dedicated to raising global awareness and creating innovative technology for research. Our goal is to use technology to create a global footprint and address PH patients’ needs around the world.