Share Your Rare
Disease Expertise
Join the Conversation.
Make an Impact.
Pulmonary hypertension patients, caregivers, medical professionals, pulmonologists, cardiologists, nurses, and global thought leaders — your voice matters.
At phaware global association, we’re amplifying your insights on PAH through the “I’m Aware That I’m Rare” phaware® podcast series.
Whether you’re a patient or an expert, your story has the power to inspire and educate listeners in over 110+ countries.
Interviews are short, lasting just 20-30 minutes, and will be shared across all @phaware social platforms and major podcast networks.
Ready to share? Tap “Schedule Interview” and join us 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, care partner, 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.