WASHINGTON, D.C. (Dec. 3, 2025) — The Pulmonary Hypertension Association has launched a redesigned website that makes it easier for people with pulmonary hypertension, their caregivers and health care providers to find accurate, medically reviewed information about this rare, life-threatening condition. The new site improves navigation, accessibility and readability, and expands PHA’s library of educational resources.
Pulmonary hypertension is complex, often difficult to diagnose and requires ongoing management. Many people turn to PHA first for information about symptoms, diagnosis, treatment, clinical research and support. The redesigned site was built to deliver clear, reliable guidance at every stage of one’s PH journey.
The updated website includes:
- Streamlined navigation and improved search to help visitors find information faster.
- Fully updated and medically reviewed content on all PH classifications, associated conditions and approved treatment options.
- A resource center with financial assistance and insurance information.
- PHA Classroom educational video content.
- Access to PH Insights, PHA’s podcast that features expert interviews and community stories.
- Digital copies of Pathlight, PHA’s quarterly print magazine.
- Patient and caregiver stories in PHA’s award-winning Right Heart Blog.
To ensure accuracy and relevance, PHA reviewed and rewrote every page over the past year. Content was evaluated by PH-treating professionals from PHA’s Scientific Leadership Council, and members of the transplant and CTEPH taskforces. Patients and caregivers on the Patient and Caregiver Education Committee also reviewed core sections for clarity and relevance.
Explore the redesigned site
About the Pulmonary Hypertension Association
Headquartered in Washington, D.C., the Pulmonary Hypertension Association is the oldest and largest nonprofit patient association dedicated to the pulmonary hypertension community. Pulmonary hypertension is a rare, chronic and life-threatening lung condition for which no cure currently exists. PHA’s mission is to extend and improve the lives of those affected by PH. To achieve this mission, PHA engages people with PH and their families, caregivers, health care providers and researchers worldwide who work together to advocate for the PH community, support patients, caregivers and families, offer up-to-date education and information on PH, improve quality patient care, and fund and promote research. For more information, visit www.PHAssociation.org and connect with PHA on Bluesky, Instagram, Facebook and LinkedIn.