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

Another effort to repeal and replace the Affordable Care Act (Obamacare) is underway. The amended replacement bill, still called the American Health Care Act, would remove protections for individuals with pre-existing health conditions. It would also eliminate federal quality standards for health insurance policies. Congress must insist on health policy with strong protections for individuals with costly, complex health conditions. Email your Representative today!.

Telephone iconMake a Phone Call

Did you know you can "meet" your Members of Congress from the comfort of your home? A scheduled phone conversation with legislative staff can be a highly effective way to engage them in fighting PH. PHA will manage the scheduling and provide materials to help your conversation run smoothly. Request a phone meeting now.

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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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.