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The Pulmonary Hypertension Association (PHA) is the largest and oldest pulmonary hypertension association in the world, celebrating its 25th anniversary in 2016. PHA provides support for patients and caregivers, advocacy and awareness, medical education, and research to find ways to prevent and cure PH.

Our mission is to extend and improve the lives of those affected by PH.

Our vision is a world without PH, empowered by hope.

PHA Conference attendeesPHA Conference Scholarships Open

PHA’s International PH Conference and Scientific Sessions will take place in Dallas, Texas, on June 17-19, 2016. Through the Conference Scholarship Program, PHA assists as many patients as possible in attending Conference. Apply today!

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PHANews.org screenshotPHA Launches PHANews.org, a New Website for PH Health News and Public Awareness

PHA is pleased to launch PHANews.org, a new source of PH health news, PHA events listings and public awareness information for the pulmonary hypertension community and our supporters. The website and weekly e-newsletter are designed to be mobile-friendly and to make it easy to share materials on social media.

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Pathlight Cover Fall 2015Are you in?

There is no better time to become a PHA member. Join now and enjoy a subscription and online access to Pathlight, PHA's quarterly magazine, in its beautifully-redesigned format.

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Visit our other websites:
PHANews logo 2015 PHA Classroom icon myPHA icon PHA Online University icon
The latest PH and PHA news and community events, on the web and delivered to your inbox each week.
Free educational resources for PH patients and families.
An online community for those living with PH to connect and share.
Earn CME/CE credits at PHA's educational website for healthcare professionals.

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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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.