The pulmonary hypertension community is made up of thousands of people across the country and around the world. Each of us has a story to tell and that story is a powerful awareness raising tool.

Contact PHA for support the resources to make awareness raising easy. Here are a few ideas to get you started.


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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.