Patients 2018-01-24T18:42:33+00:00

INFORMATION. SUPPORT. HOPE.

FamilyIf you or a loved one is living with pulmonary hypertension, we offer information, support and the chance to become active in our community’s search for a cure.

The Pulmonary Hypertension Association was founded by patients, for patients — and our community, now thousands strong, is here for you as a source of support, connection and hope. Our patients are a knowledgeable, inclusive and inspiring group who are eager to listen and share their experiences. Connect with other patients now!

We also offer a vast collection of top-notch resources and medically reviewed information to help you live a better life. Explore the resources below, or join us at one of our national, regional or international education programs to get information on the latest research, PH treatments and coping with PH. Attend a patient education event!

I’m looking for resources to help me: