April is Sjögren’s Awareness Month
Learn about the link between PH and Sjögren’s. Download or order a brochure.
Empowering the pulmonary hypertension community.
As the world’s largest pulmonary hypertension organization, PHA provides support and resources to extend and improve the lives of those affected by PH. Together, we end isolation, deliver education and offer hope for the future.
Only two months to PHA 2026 in Dallas! Register now and start planning your trip.
Register now
This week at PHA
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How does sarcoidosis affect PH?Learn how this inflammatory disease affects the lungs and other organs for National Sarcoidosis Awareness Month.
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Looking to make new PH friends?Attend the PHA 2026 networking breakfast June 13 to meet patients, caregivers, family members and health care professionals.
About Pulmonary Hypertension
Learn about PH, tests to diagnose, available treatment and common risk factors.
- Types of PH
- Related conditions
- Pediatric PH
- Diagnosis and treatment
- Find a specialist or care center near you
Living with PH
Live your best life with PH, whether you’re newly diagnosed, a long-time thriver or taking care of someone you love.
- Medication management
- Emergencies
- Nutrition and exercise
- Coping and support
- Working and traveling
- Insurance and financial assistance
Patient and caregiver support
Patient and caregiver support is one of PHA’s founding principles. Our support groups, peer mentors and Patient and Caregiver Support Line foster connections, knowledge and empowerment.
- Join an in-person, online or Facebook group
- Connect with a peer mentor
- Call our support line
Events and Resources
Discover in-person events and patient education materials
- Order or download materials
- Watch videos in PHA Classroom
- Register for PHA Live webinar series
- Listen to PH Insights podcast
- PHA International PH Conference & Scientific Sessions
- Fundraising events
Get Involved
Become part of the PHA community.
- Become a member
- Volunteer
- Ways to give & fundraise
- Advocate
- Participate in research
- Advertising & sponsorships
Help us improve and extend the lives of people affected by PH
Help make life better for people with pulmonary hypertension and their families by supporting PHA.
- Join or organize a fundraising event
- Make PHA part of your estate plan
- Ensure consistent support through monthly giving or workplace programs
For PH Professionals
Connect, learn, share and discover.
- Professional member portal
- Become an accredited care center
- PHA Registry research
- Professional leadership opportunities
- Continuing education
- Apply for a grant
- PH Practice Library
News
Explore news from the Pulmonary Hypertension Association.
- Recent news
- News releases
- Advisories & policy statements
- Newsletters
- Right Heart Blog
- Pathlight magazine
- Advances in PH
News
‘My ultimate goal was to not give up on life’
Ron Ancrum was 25 when learned he had sarcoidosis, cell clusters that infiltrate the lungs and other organs Forty-one years later he was diagnosed with PH related to sarcoidosis.
Ron’s story
Recent News
Visit our News section for the latest stories from PHA News, including association news and PH in the News.
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Moms Advocate for Kids’ Oxygen Access
Two Cincinnati women work with their children’s PH care teams to promote better access to portable oxygen. The story originally appeared in the March 2026 issue of Pathlight magazine.
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6 Reasons to Attend PHA 2026
If you haven’t made up your mind to register for PHA 2026 International PH Conference and Scientific Sessions, discover these six must-attend general sessions.
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PHA Brings Patient Education to Puerto Rico
A March 28 workshop in Puerto Rico is PHA’s latest effort to increase PH awareness. The workshop about 125 patients, caregivers, Puerto Rican health officials and PH specialists.
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