Advocacy Action Center

Fight PH through Legislative Advocacy

PH Professional Network (formerly PH Resource Network) at the Capitol

Pulmonary hypertension may not be as common as other well-known conditions, but when each member of the PH community speaks out, we have a powerful voice that gets powerful results.

Contacting your senators and representative is as easy as sending an email, and your contact makes Members of Congress many times more likely to support the Pulmonary Hypertension Research and Diagnosis Act and related legislation. Working together, PH advocates across the country have secured significant federal funding for PH research and awareness initiatives, but there is more to do!

Connect with experienced advocates and PHA staff. Learn more about the issues that need your voice. Take action and make a difference!

Lobby Locally!

Educate your elected officials about PH and build their support for our bill in Congress. Get started by watching the recording of our webinar

Sign up for Alerts

If you plan to take action at least three times a year, join the 435 Campaign.

Not ready to join? Receive updates through the Advocacy Action Alert List instead.

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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.