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Advocate

This year, Congress will debate and create laws that impact the every-day lives of individuals with pulmonary hypertension. Laws about healthcare services, insurance coverage, copay assistance programs and more. The Pulmonary Hypertension Association makes it easy for you to educate your elected officials about the needs of the PH community. Be heard. Be a PH advocate.

Take Action

Email iconSend an Email

Congress is currently debating significant changes to the healthcare system. PHA supports healthcare policies aimed at protecting and strengthening patient protections. Call or email your Members of Congress to educate them about pulmonary hypertension and the healthcare needs of those with PH.


Telephone iconMake a Phone Call

Congress is currently debating significant changes to the healthcare system. PHA supports healthcare policies aimed at protecting and strengthening patient protections. Call or email your Members of Congress to educate them about pulmonary hypertension and the healthcare needs of those with PH.


Corporate iconSchedule an In-Person Visit

Your elected officials work for you. Meeting with them to share your story is an effective way to gain their support of legislation affecting PH patients. There are several ways to meet with your Members of Congress, including visiting their local office, attending a town hall or inviting your senator or representative to your support group meeting.

PHA can set up an in-person meeting for you and provide all the information and materials you need. Email us to get started! Or, to set up a visit yourself, start with our search tool to find contact information for your Members of Congress.


435 Campaign logoStay Involved

When you join PHA’s grassroots advocacy network, we send you the resources you need to stay in touch with your Members of Congress a few times a year about the issues that impact your life. Be heard. Be a PH advocate.


Learn More

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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. PHA does not endorse or recommend any commercial products or services.

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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.