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We believe that open communication is the key to a better life and a cure for those whose lives are touched by pulmonary hypertension. We believe that associations of patients, caregivers and medical professionals are essential for a better future. Finally, we believe that global partnerships enhance best practices in PH, create new opportunities for the PH community and transform hope into reality.
- Learn About Pulmonary Hypertension- PH Treatments Available by Region- Join a Medical Membership Network
- Become an MOU partner- Apply for a Seed Grant- Watch the Leader Lessons from the 1st International Leaders' Summit
Find a PH Association Near You
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International Faces of PH
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There are thousands of pulmonary hypertension patients waiting to meet you!
Highlights from 2010 Conference
World PH DayMay 5, 2012www.WorldPHDay.org
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The information provided on the PHA website 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.
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The National Organization for Rare Disorders (NORD) awarded PHA the Abbey S. Meyers Leadership Award in 2012 for outstanding service to PHA members in advocacy, education and other key areas.