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The Pulmonary Hypertension Association Profile
The Pulmonary Hypertension Association

@PHAssociation

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Our mission is to extend and improve the lives of those affected by pulmonary hypertension.

Washington, D.C.
Joined September 2009
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@PHAssociation
The Pulmonary Hypertension Association
6 months
We’ve moved! We are no longer sharing updates about #PHA and #pulmonaryhypertension on this platform. Thank you for your support. We hope you’ll stay connected with us on BlueSky. https://t.co/b4r53yhMFo
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@PHAssociation
The Pulmonary Hypertension Association
6 months
Join the PHA community of health care professional members and gain access to patient-centered education and clinical resources. Sign up by June 30, 2025, to take advantage of a special 20% discount off your first year of membership. https://t.co/fe2Wq582tv
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@PHAssociation
The Pulmonary Hypertension Association
6 months
Carole Doody, a PHA Support Line volunteer, believes playing the bagpipes saved her life. After experiencing chest pain and difficulty breathing during band practice, Carole was diagnosed with #PAH in 2010. Learn more about Carole’s journey: https://t.co/dMofRiAA6b
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@PHAssociation
The Pulmonary Hypertension Association
6 months
Health care professionals: Find your next job opportunity at the PHA Career Center. Connect with top employers seeking your experience and expertise. Create an account and upload your CV by April 30, for a chance to win a $250 Amazon gift card. https://t.co/x04l6MgBUm
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@PHAssociation
The Pulmonary Hypertension Association
6 months
April is #SarcoidosisAwarenessMonth. #Sarcoidosis can lead to #PH when weakened lungs cause failure of the right side of the heart. Learn more about the link between PH and sarcoidosis in our free brochure: https://t.co/m6eUGCJ95K @StopSarcoidosis #MakeItVisible
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@PHAssociation
The Pulmonary Hypertension Association
6 months
The Health Disparities in PH Research Award deadline is quickly approaching. Don't miss your chance to receive $50,000 in funding to improve outcomes and treatments for #PH patients affected by health inequities. Apply by April 30, 11:59 p.m. EDT. https://t.co/nUc0HMrM3q
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@PHAssociation
The Pulmonary Hypertension Association
6 months
The SOAR Act has been reintroduced in Congress. Join PHA and our partner organizations tomorrow, April 29, at 3 p.m. EDT via Zoom for updates on the #SOARActO2 and how to urge lawmakers to support #supplementaloxygen reform. Register today: https://t.co/5OVgX70RSg
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@PHAssociation
The Pulmonary Hypertension Association
6 months
Thank you to everyone who attended the 2025 AnMed #O2breathe Walk! We appreciate your commitment and support of the #PH community. Our next two walks are on May 3 in Alexandria, Virginia and Cerritos, California. Learn more. https://t.co/xKk2b4Y56n
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@PHAssociation
The Pulmonary Hypertension Association
6 months
After receiving her #PAH diagnosis, Carole Doody connected with peer mentors through a support group. Now, Carole #volunteers as a telephone Support Line volunteer to help others in the #PH community. Learn more about volunteer opportunities with PHA: https://t.co/Nq4uvxVX0H
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@PHAssociation
The Pulmonary Hypertension Association
6 months
During #VolunteerApperciationWeek, hear from Mitzi McIver-LaBarge, a parent and caregiver who connected with #PHA following her daughter’s #pulmonary hypertension diagnosis. Listen now on the latest episode of PH Insights: https://t.co/HP1hQwhXyp
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@PHAssociation
The Pulmonary Hypertension Association
6 months
For #VolunteerAppreciationWeek, we thank our awesome Support Group Leaders who plan and run support groups across the country. In 2024, more than 5,000 people attended a support group meeting thanks to their efforts. Learn more about PHA support groups: https://t.co/F5UrNvTeC8
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@PHAssociation
The Pulmonary Hypertension Association
6 months
Kathryn Buffington has been living with #PH for 19 years and volunteers as a peer mentor to help other patients manage their PH. Learn more about how you can get involved with the PH community: https://t.co/P34ePUNA0t
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@PHAssociation
The Pulmonary Hypertension Association
6 months
Atención! El grupo de apoyo virtual en español se cancela esta noche. La reunión se reprogramará para este viernes, abril 25, a las 8 p.m. EDT. Esperamos verte allí! https://t.co/Jt5ZNjO2Yg
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@PHAssociation
The Pulmonary Hypertension Association
6 months
Join us tomorrow, April 24, at 8 p.m. EDT 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: https://t.co/hzOSP4eCPC
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@PHAssociation
The Pulmonary Hypertension Association
6 months
Thanks to the dedication of volunteers who oversee #PHA’s Facebook support groups, nearly 6,5000 people found support and built lasting connections in 2024. Join a Facebook support group and connect with others in the #PH community. https://t.co/a2mUFWkdi2
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@PHAssociation
The Pulmonary Hypertension Association
6 months
Únase a nosotros mañana en abril de 23 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. https://t.co/STSS9Hzgai
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@PHAssociation
The Pulmonary Hypertension Association
6 months
As a lung transplant pulmonologist, Sheila Krishnan gives back to people with #PH in her community by co-leading a #PHA support group. This #VolunteerAppreciationWeek, learn more about PHA support groups and how you can start one in your area: https://t.co/UwzV4TU6iE
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@PHAssociation
The Pulmonary Hypertension Association
6 months
Do you have important #pulmonaryhypertension research or clinical projects to share? Submit a poster abstract proposal(s) for the 2025 #PHPN Symposium, Sept. 18-20, in Seattle. Proposals are due Monday, June 2.  https://t.co/DeQA7fECbg #PHPN2025
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@PHAssociation
The Pulmonary Hypertension Association
6 months
This #VolunteerAppreciationWeek, join us in celebrating our incredible Support Line volunteers! In 2024, they answered more than 1,100 calls offering information and support to the #PH community. Learn more about becoming a Support Line volunteer: https://t.co/Om13F2C9eE
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@PHAssociation
The Pulmonary Hypertension Association
6 months
Lila Jaimes, a registered nurse at Austin Heart, has co-led the Austin Support Group for 8 years. She volunteers to help patients connect with others in the #PH community. This #VolunteerAppreciationWeek, learn more about #PHA support groups:  https://t.co/aSjCfMfYYk
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