TODAY is the last day to submit investigator applications for the #PHA2026 Research Room.
Apply to conduct your #pulmonaryhypertension study during PHA's conference, June 11-14, in Dallas. View submission criteria and submit your application today.
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#PHixintoFindaCure
This week PHA joins National Sleep Foundation for Sleep Awareness Week.
Did you know that between 17-53% of people with sleep apnea also have #pulmonaryhypertension?
Learn more in our free brochure: buff.ly/KHomsOW
Join us tomorrow, March 11, at 8 p.m. EDT for our monthly virtual Parent Support Group.
Connect with other parents and learn strategies and tips on how to best manage your child’s #PH.
Register now: buff.ly/UyTIfhn
Did you hear the news? Scholarship applications for #PHA2026 are open!
Applications are open through May 11, or until funds run out. Your #PHA membership must be valid through June 14 to be eligible.
View submission criteria and submit your application today: buff.ly/rnb16b4
#PHixintoFindaCure
¡Aún estás a tiempo de inscribirte en el almuerzo del #GrupoDeApoyo de Puerto Rico de la #PHA, que se celebrará el sábado 28 de marzo!
Únete a nosotros para disfrutar de sesiones con expertos, expositores, networking y un almuerzo gratuito. Inscríbete ahora.
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Happy International Women’s Day!
Today we celebrate our four founders, Pat Paton, Judy Simpson, Teresa Knazik and Dorothy Olson, who met around a kitchen table in 1991 and laid the groundwork for PHA.
Visit our website to learn more about our history: buff.ly/8pFqZ7t
The 2026 Tampa O2breathe Walk and 5K is two weeks away.
Join the local #PH community for a morning of celebration, connection and movement towards a cure.
The walk is free to attend, and registration for the 5K is $40. Register now: buff.ly/9r7P7tJ
The Women’s PHorum, sponsored by @gossamerbio.bsky.social with support from PHA, recently launched PHORWARD, a series of webcasts designed to elevate leadership and resilience across the PH provider community.
The second webinar recording is available on our website.
Watch now: buff.ly/vwT7czp
Join the Orlando PH community on Saturday, March 21, at Lake Eola Park for a morning of movement, celebration and hope.
The walk is free to attend and is open to everyone affected by PH.
Register now: buff.ly/DxpZm0g
The Women’s PHorum, sponsored by @gossamerbio.bsky.social with support from PHA, recently launched PHORWARD, a series of webcasts designed to elevate leadership and resilience across the PH provider community.
The first webinar recording is available on our website.
Watch now: buff.ly/6TTVfc9
Know someone that goes above and beyond for the #PH community?
Nominate them for the PHA Outstanding Member Awards!
Nominations are open through April 20, and awards will be presented at #PHA2026, June 11-14, in Dallas.
View award categories and submit your nomination: buff.ly/mFu9d5l
Your next job opportunity starts with the PHA Career Center.
Whether you're a physician, nurse, respiratory therapist or allied health professional, explore the PHA Career Center for job opportunities in pulmonary hypertension.
Start your search now: buff.ly/5g3dzrS
As a licensed professional counselor, Michele Freeman has developed strategies to cope with caregiving as she cares for her husband, Les, who lives with #PAH.
PHA has caregiver resources to help support your physical and mental health while you care for a loved one.
Learn more: buff.ly/wTTwh8G
In the past 35 years, PHA has achieved many wins in fulfilling our mission to improve and extend the lives of people affected by #PH.
This year, we’re looking forward to PHA 2026 and much more.
Learn more: buff.ly/qd1La9x
A recent study found non-adherence to some #PAH medications increases the risk of death and poor clinical outcomes.
Additionally, non-adherence to PDE5 inhibitors was associated with more than double the risk of death for patients with #PAH.
Learn more: buff.ly/YQcEDmo
Registration is open for #PHA 2026! 🎉
Join the #PHcommunity June 11–14, in Dallas for education, connection and onsite surprises from #PHA. View the agenda, apply for a scholarship and register now.
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#PHixinToFindACure
In a recent opinion piece, Diana Derbas shares her support for the #SOARAct as someone who relied on supplemental oxygen before receiving a double lung transplant.
Learn more about her story: buff.ly/n9tE7UW
Today is Rare Disease Day!
PH is a rare and frequently misunderstood condition that’s easy to overlook or misdiagnose.
Raising awareness and ensuring access to care can save lives.
Learn more: buff.ly/WnynsW2
Up to 60% of patients with left heart disease also have #PH.
This is caused by high pressure in the left side of the heart, which increases the pressures inside the lungs.
Visit the PHA website to learn more about symptoms, diagnostic tests and treatments.
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Maurita Andrews was diagnosed with #PAH in 2019 and has dedicated her time to raising #PH awareness.
In 2025, she attended PHA’s Hill Day to share her story with members of Congress and get support for patients with PH.
Learn more about her experience: buff.ly/0oshcba
Join us tomorrow, Feb. 26, at 8 p.m. EST for our monthly virtual Patient Support Group meeting.
Connect with others with #PH to foster community and share experiences about how to best manage your PH.
Register now: buff.ly/0gZxSIf
On the latest episode of PH Insights, Meghan Cirulis and Katherine Clapham discuss methamphetamine-associated #PAH.
They explore the increasing prevalence of methamphetamine use and its severe health implications.
Listen now: buff.ly/6qBw6W5
Únete a nosotros mañana, 25 de febrero, a las 8 p.m. (hora del este) para participar de la reunión mensual del grupo de apoyo telefónico en español.
Conéctese con otros pacientes con HP que hablen español.
Inscríbase ahora: buff.ly/88pH6Lh
¡Solo queda un mes para el #GrupoDeApoyo de la #PHA en Puerto Rico!
Acompáñenos el sábado 28 de marzo para disfrutar de una tarde de educación, exposiciones, empoderamiento y conexión. Este evento gratuito incluye almuerzo. Inscríbase para reservar su lugar.
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A pulmonary hypertension diagnosis can be scary at first, but connecting with others who share similar experiences can help you move forward with confidence.
Join PHA’s “Newly Diagnosed with PH” Facebook group to gain support, knowledge and empowerment.
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🎉#PHA2026 scholarship applications are now open.
Apply for financial assistance for registration, hotel, and/or travel costs before you register. PHA membership must be valid through June 14, 2026.
Learn more and apply: buff.ly/1iBMTuW
Registration opens Monday, March 2. #PHixintoFindaCure
Rare Disease Day is February 28.
#PH is often associated with other rare diseases such as #scleroderma, #HHT, idiopathic #pulmonaryfibrosis, #sicklecell disease and #lupus.
Raising awareness, improving diagnosis and ensuring access to care can save lives. Learn more: buff.ly/8TU8sC5
Thank you to everyone who attended the 2026 Houston #O2breatheWalk! We appreciate your support and commitment to the #pulmonaryhypertension community. The next two walks are March 21 in Orlando and March 22 in Tampa. Learn more and register. phassociation.org/pha-fundrais...
The American Thoracic Society-Pulmonary Hypertension Association Early Career Award is a $50,000 grant to foster the development of junior investigators with the potential to make strong, sustained contributions to #PH research.
Learn more and apply today: buff.ly/q8bQKtf
The 2026 Tampa #O2breathe Walk and 5K is just one month away!
Join the local #PH community on Sunday, March 22, at Al Lopez Park for a morning of celebration, connection and movement towards a cure. 👟
The walk is free to attend, and registration for the 5K is $40.
Register now: buff.ly/hbbYadT
