INFORMATION. SUPPORT. HOPE.

If you or a loved one is living with pulmonary hypertension, we offer information, support and the chance to become active in our community’s search for a cure. Family: Mom, dad, and daughter

The Pulmonary Hypertension Association was founded by patients, for patients -- and our community, now thousands strong, is here for you as a source of support, connection and hope. Our patients are a knowledgeable, inclusive and inspiring group who are eager to listen and share their experiences. Connect with other patients now!

We also offer a vast collection of top-notch resources and medically reviewed information to help you live a better life. Explore the resources below, or join us at one of our national, regional or international education programs to get information on the latest research, PH treatments and coping with PH. Attend a patient education event!

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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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NORD

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.