Pulmonary Hypertension Association
Serves Atlanta by phone or online (based in Washington, DC).
(800) 748-7274 · more numbers below
The Pulmonary Hypertension Association is a national group for people with pulmonary hypertension (PH), their families and caregivers. It offers support groups, peer mentors, a support line, free guides, videos, webinars and a podcast. It also points people to PH specialists and care centers.
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What they offer 16
- Info refreshed from their website· Oct 13
Educational MaterialsService
PHA has guides and brochures about PH that you can download or order in print. They include a guide for people newly diagnosed, brochures on related conditions, and toolkits.
- Info refreshed from their website· Oct 13
Insurance, Financial Assistance, and Treatment Access ResourcesService
PHA shares information on health insurance and help paying for PH care. Topics include Medicare, Medicaid, SSI and open enrollment, through videos, webinars and news.
- Info refreshed from their website· Oct 13
PH Insights PodcastService
A podcast with talks among patients, health care workers and others in the PH community. New episodes come out twice a month.
- Info refreshed from their website· Oct 13
PH Specialist and PH Care Center InformationService
PHA points people to PH specialists and care centers near them. Its site also has an interactive map of accredited PH Care Centers that take part in its patient registry.
- Info refreshed from their website· Oct 13
PHA ClassroomService
An online library of videos and resources about medical and daily-life topics for people with PH and their families. You can watch any time. It lists 171 items on topics like treatment, insurance, caregiving and children.
- Info refreshed from their website· Oct 13
PHA Community MembershipProgram
PHA offers free membership for patients, families and caregivers. Health care professionals can join through separate memberships.
- Info refreshed from their website· Oct 13
PHA Facebook GroupsProgram
PHA has Facebook groups where people affected by PH can connect with each other.
- Info refreshed from their website· Oct 13
PHA Peer MentorsProgram
PHA can connect you with a peer mentor. This is part of how the group helps people with PH and caregivers feel connected.
Events 5
- Info refreshed from their website· Oct 13
PHA International PH Conference and Scientific Sessions
Aug 3 – Aug 6, 2028
A large gathering for people with PH, caregivers, families and health care professionals, with separate tracks for patients and for professionals. The next one listed is Aug. 3-6, 2028, in Columbus, Ohio.
- Info refreshed from their website· Oct 13
Pulmonary Hypertension Wellness Expo
Date shown: Saturday, Oct
A free in-person expo with exhibits, talks with PH experts and activities for children. The date shown on the page is Saturday, Oct. 10, in South San Francisco, which has already passed.
- Info refreshed from their website· Jun 30
PHA Connects: PH Community Workshops
Date not announced
PHA Connects workshops are free in-person education events for people affected by pulmonary hypertension, including patients, families, supporters, and health care professionals.
- Info refreshed from their website· Jun 30
PHA Live Webinars
Date not announcedOnline
PHA hosts webinars during the year on health, wellness, science, and research topics for people affected by PH and related conditions.
- Info refreshed from their website· Oct 13
PHA Live: Hosted Webinars
Date not announcedOnline
PHA hosts online webinars during the year on health, wellness, science and research topics for people affected by PH. A Day of Action advocacy webinar is listed for Nov. 4.
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