Our Mission

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.

Resources for Patients and Medical Professionals


Resources for PH Association Leaders


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Resources Available by Language

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International Faces of PH


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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.