Tomorrow is #WorldPHDay2026! Join us throughout the month as we share stories of those affected by #PH and raise awareness about the importance of clinical trials. Visit our toolkit to learn more about this year’s theme. buff.ly/CsvOaJ3

Join PHA on Tuesday, June 2, at 3 p.m. EDT for a webinar outlining the transplant evaluation process. Experts will share insights to help patients better understand the transplant referral process and feel confident talking with their care teams. Register now: buff.ly/QLIetFv

Thank you to everyone who attended the SoCal O2breathe Walk! The PHorce was strong at Don Knabe Park, raising $21,000 for the #pulmonaryhypertension community. Our next O2breathe Walk is in Boston on Saturday, June 6. Register now: buff.ly/OQnmiMu buff.ly/IbTVCWT

Living with #pulmonaryhypertension as a teen comes with unique challenges, but you don’t have to face them alone. Join PHA’s “PH Teens” Facebook group to connect with fellow patients ages 13-19 and gain support, knowledge and empowerment. buff.ly/ZmZP3Fe

In 2003, Carson Smith was diagnosed with #PH and #PVOD as a sophomore in high school. Twenty years later, she began volunteering with PHA as a peer mentor to help others navigate life with PH. Learn more about her story: buff.ly/uSfA7cv

Each year on May 5, PHA observes World #PH Day by sharing patient stories and valuable resources. This year’s theme, “Hope in Every Trial,” focuses on the importance of #clinicaltrials and how #research findings can improve care for people with PH. Learn more: buff.ly/814LzOQ

April is Sarcoidosis Awareness Month. #Sarcoidosis is an inflammatory disease that can affect many different organs. In sarcoidosis-associated PH, increased pressure in the lungs can weaken the right side of the heart and cause it to fail. Learn more in our free brochure: buff.ly/Jw50eHH

New research suggests that #PAH could drive cognitive decline. Animals with induced PAH showed signs of disease progression as well as signs of early cognitive dysfunction. These findings support growing evidence that PAH impacts more than the heart and lungs. Read the report: buff.ly/i0mStbw

Matt Granato is halfway through his journey to #PHA2026! His last stop was Seattle; did you guess correctly? Now he’s traveling south to a city full of stars and home to five PHA support groups. Know the city? Drop your guess for a chance to win #PHA swag!

Struggling with chronic health stress? You’re not alone. Join us for the #PHA2026 closing session, “Empower Your Mind,” where experts will break down how the brain responds to chronic illness and offer tools to help you cope. Register now: buff.ly/JJ7yz46

April is Donate Life Month, a time to honor organ donors and celebrate the lives of pulmonary hypertension patients who benefit from their generosity. Learn more about the power of organ donation: buff.ly/eVtrEGr

On the latest episode of PH Insights, host Jolie Lizana gives us a behind-the-scenes look at PHA’s Capitol Hill Day. Tune in to hear from individuals who traveled to the Capitol to speak on behalf of the #PH community and learn how their voices are shaping policy. Listen now: buff.ly/ea1suZl

After a quick stop in Chicago, Matt Granato, #PHA’s president and CEO, is heading to the West Coast! Location of the 2025 PHPN Symposium, this city has two #PHCCs and a world-famous coffeehouse. Know where Matt is? Comment your guess below. Stay tuned to follow his journey to Dallas for #PHA2026!

PHA’s new quarterly impact report illustrates how the organization fulfills its mission through patient and caregiver services. The first report for 2026 highlights support group leader and PH advocate Sophia Esteves and her journey with pulmonary hypertension. Read the report: buff.ly/cnO3wxJ

Last year, PHA support line volunteers answered 793 calls, lending a sympathetic ear and guiding callers toward #resources. No experience is necessary, and the only skills you’ll need are compassion and a desire to help others with #PH. Learn more: buff.ly/i50RPJP

Join us tonight, April 23, 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: buff.ly/eaS2XCQ

As a support group leader, Michelle Reller enjoys sharing words of encouragement, smiles and laughs with fellow patients. “I enjoy being there for others with the same battle as me,” Michelle said. Learn more about becoming a support group leader: buff.ly/KaLjZso

DEADLINE UPDATE: Letters of intent for PHA’s Pediatric PH Research Award are now due April 24 at 5 p.m. EDT. The grant provides up to $65,000 to support #research projects to advance the #diagnosis and treatment of #pediatric #PH. Submit now: buff.ly/1xrDx9F

Thank you to everyone who attended the AnMed O2breathe Walk, held in memory of Tina Lisenby. The event was a big success, raising over $10,000 for the #PH community. Want to be a part of the O2breathe magic? Check out our list of upcoming events: buff.ly/IbTVCWT

In 2025, more than 5,300 people attended a PHA support group. Participants say the connections they build in support groups reduce their stress and anxiety and help them build advocacy skills. Find a support group near you: buff.ly/RgNfcdF

Contribute to the future of #PH research by participating in the #PHA2026 Research Room. Sign up when you register for PHA 2026 to help medical professionals better understand PH and improve care. Visit the conference website to learn more and register. buff.ly/M31naMW

Rachel Roberts felt alone when she was first diagnosed with #pulmonaryhypertension. As a support group leader, she strives to be the person she needed when she was diagnosed. During #VolunteerAppreciationWeek, learn more about making a difference in the PH community: buff.ly/KaLjZso

Join us tomorrow, April 21, at 8 p.m. EDT for our monthly virtual CTEPH Support Group meeting. Connect with others to discuss challenges and coping strategies to best manage life with #CTEPH. Register now: buff.ly/qEr3Fot

Today is your last chance to submit a nomination for PHA’s Outstanding Member Awards. Submit your nomination by 11:59 p.m. EDT tonight, April 20, to recognize someone for their service to the #PH community. Visit the #PHA2026 website to submit your nomination now. buff.ly/wAIoKm5

In 2025, PHA’s Facebook support groups grew to more than 6,700 members. Interacting with fellow patients and caregivers can alleviate feelings of isolation. Find a PHA Facebook group that’s right for you: buff.ly/MHzmvoR

Dawn Grandell volunteers as a support group leader to raise awareness for #pulmonaryhypertension and help others feel less alone. This #VolunteerAppreciationWeek, learn more about the benefits of PHA support groups and how you can get involved: buff.ly/KaLjZso

PHA recently hosted a workshop in Puerto Rico to increase #PH awareness. More than 125 people were in attendance, including #patients and #caregivers, Puerto Rican care health officials and PH specialists. Learn more about the event: buff.ly/0tmA8iN

April is Sjögren’s Awareness Month. About 16% of Sjögren’s patients have pulmonary complications. Common signs of Sjögren’s-related PH include cough, shortness of breath, leg swelling, chest pains and fainting. Learn more: buff.ly/DNOV0Hu

In the latest issue of Pathlight, PHA celebrates its 35th anniversary! In the cover story, founders Judy and Ed Simpson reflect on the founders’ goals and the organization’s history. The new issue also explores the evolution of patient education. Learn more: buff.ly/FgZM9mZ

Cheryl Dehoney was diagnosed with #PAH in 2021. Since then, she has spent thousands of dollars on airfare, traveling from Hawaii to California in search of the right care team and treatment. Learn more about her story: buff.ly/qG3eE8C

Join us tonight at 8 p.m. EDT for our monthly virtual Young Adult Support Group. Connect with other young adults with #pulmonaryhypertension and share experiences, support and tips to thrive with #PH. Register now: buff.ly/kRh9hWY

During Capitol Hill Day, one of PHA’s goals was securing additional co-sponsors for the Safe Step Act. As a result of these efforts, the bill gained three new co-sponsors: U.S. Reps. John Rutherford, Shomari Figures and Joe Wilson. Learn more about the bill: buff.ly/V429vT3

Join us tomorrow, April 15, at 7 p.m. EDT for our monthly virtual Caregiver Support Group meeting. Connect with others who understand what it’s like caring for someone with #PH and share caregiving strategies and advice. Register now: buff.ly/WjuCCrx

Looking for a way to get involved at #PHA2026? Become a conference volunteer! Volunteers are needed to provide translation support in the Research Room, assist with wheelchair services and pass out t-shirts at registration. Register now to sign up as a volunteer. buff.ly/O5Epwgp

Today is the last chance to save on #PHA2026 registration. Register by 11:59 p.m. EDT to join the #pulmonaryhypertension community in Dallas, June 11-14. We’re PHixin’ to make PHA 2026 the best conference yet. Register now. buff.ly/O5Epwgp #PHixinToFindaCure

PHA Board of Trustees member Nicole Creech leads PHA’s Lexington, Kentucky, Support Group with Evelyn Mitchell. Each year, they dedicate one meeting to caregivers who share their time and love with support group members. Learn more about the importance of caregivers: buff.ly/F1ySLHC

Clinical trials play an important role in advancing #PH care. Anna Hemnes, chair of the Department of Medicine at Vanderbilt Health, says without clinical trials, there would be no FDA-approved therapies for #PAH, #CTEPH and ILD-associated PH. Learn more: buff.ly/R2yL5Wp

On the latest episode of PH Insights, host Jolie Lizana speaks with Mary Jo Farmer, a pulmonary, critical care and sleep medicine specialist, to discuss how #sleep can dramatically impact #pulmonaryhypertension. Listen now: buff.ly/XwYGPAj

Researchers can now submit letters of intent to apply for the PFF-PHA ILD-PH Joint Research Award. This grant supports research focused on #PH related to interstitial #lung disease, offering $100,000 of funding for two years. Letters of intent are due May 29. Submit now: buff.ly/M6qO2Jk

After leaving New York City, Matt’s on his next adventure on route to #PHA2026 in Dallas this June. His next stop is a windy city, home to two #PHCCs, a #PHA support group and #O2breatheWalk. Can you guess where he is? Drop your guess in the comments below.

Sawanda Cornett was 22 years old when she received her #PH diagnosis. Twenty years later, she’s not just surviving; she’s thriving. Your gift today ensures that PHA can continue to provide #resources, #community and #hope for every person affected by PH. Donate now: buff.ly/JFzri3f

PHA is now accepting letters of intent for the Health Access & Outcomes Award. This award supports research addressing health inequities in #PH, including early #diagnosis, #treatment outcomes and access to #care. Letters of intent are due May 27. Submit now: buff.ly/M6qO2Jk

Are you PHixn’ to save on registration for #PHA2026? Register by Monday, April 13, to score the best prices for PHA 2026, June 11-14, in Dallas. Make sure your #PHA membership is valid through June 14 to receive member-only register rates. buff.ly/ETJgR8c #PHixintoFindaCure

A new research study found that the number of patients with methamphetamine-related pulmonary arterial hypertension nearly doubled from 2018 to 2022. This finding is disproportionate to the rise in the estimated number of adults with past-year methamphetamine use. Learn more: buff.ly/lTpOuEs

There is still time to submit your nomination for #PHA’s Outstanding Member Awards. Recognize a fellow #PHcommunity member by nominating them for one of PHA’s nine awards. Visit the #PHA2026 website to view award descriptions and submit your nomination by April 20. buff.ly/b6xQZR0

The Greater Washington, D.C. O2breathe Walk is one month away! Join the local PH community on Saturday, May 2, at Franconia Park in Alexandria, Virginia for a morning of celebration, connection and movement towards a cure. Register now: buff.ly/aRRdntV

The SoCal O2breathe Walk is one month away! Join us at Don Knabe Park in Cerritos for a Star Wars themed O2breathe Walk on Saturday, May 2, at 10 a.m. PST. The PHorce is strong when we walk together. Register now: buff.ly/XxODBaN

The AnMed O2breathe Walk in Anderson, South Carolina is two weeks away! Join us to celebrate the #pulmonaryhypertension community and to spread #PH awareness. The event is held in memory of Tina Lisenby, founder of the Anderson #PH Support Group. Register now: buff.ly/S4gCF3w

In early March, 43 advocates attended PHA’s Capitol Hill Day to advocate for supplemental oxygen access for people with PH. Three days after the event, Rep. Shomari Figures cosponsored the SOAR Act as a direct result of our efforts. Learn more: buff.ly/Pmr3EID

Sawanda Cornett struggled to cope with her #PH diagnosis but found community and connection through PHA’s Houston Support Group. Your gift today helps PHA provide support groups, educational resources and connections that transform isolation into community. Give today: buff.ly/JFzri3f