Pulmonary hypertension (PH) is a rare, debilitating disease in which high blood pressure in the arteries of the lungs can lead to right heart failure.

From simple beginnings — four women who met around a kitchen table in Florida in 1991 — the Pulmonary Hypertension Association (PHA) has evolved into a community of over 16,000 PH patients, caregivers, family members and medical professionals. PHA's mission is to find ways to prevent and cure PH, and to provide hope to the community through support, education, research, advocacy and awareness.

Join our vibrant community, donate to support PHA's mission, or get involved in advancing the cause.

News & Events

Find more news & events on the PHA Daily Beat blog.

 

Featured Video: PHA on the Road, Atlanta, Ga.

 

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MEDICAL PROFESSIONALS

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Patient-to-Patient Support Line: 1-800-748-7274

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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.