Help make the 🌎 #phaware. Pulmonary hypertension (PH) is a rare, life-threatening disease of the lungs that can lead to right heart failure. 💜💙💚🧡❤️
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phaware® podcast ep 595: Jennifer Lombardi
After devastating loss, brutal pain, and a second shot at survival, this story lands with grit, grace, and pure perspective. A rare reminder that renewal can come after the unthinkable.
November is Pulmonary Hypertension Awareness Month. Everyone has something that makes them rare. #ShareYourRare, because one’s rare isn’t just a diagnosis. It’s what makes you uniquely you! Get your SHARE YOUR RARE kit today: phaware.global/ph-awareness-…
phaware® podcast ep 595: Jennifer Lombardi
A full-circle, fist-pump moment: one dance, one rush of adrenaline, and a reminder that surviving pulmonary hypertension means fighting for every beautiful second.
phaware® podcast ep 595: Jennifer Lombardi
At 21, she was brushed off as anxious and told it was allergies—until a second specialist spotted the life-threatening clue everyone else missed. A tense, infuriating reminder that persistence can save your life.
Share Your RARE: Join the Pulmonary Hypertension Awareness Movement. Celebrate #phawarenessmonth with heart, hope, and community. Share your RARE talents, stories, and spirit with @phaware because being RARE doesn’t mean being alone. Learn More: phaware.global/ph-awareness-…
More than a podcast. A Global Conversation about Pulmonary Hypertension. Season 11 is here in time for #phawarenessmonth. Like | Subscribe | Follow. 600+ Conversations. 1 Global PH Community. phaware.global/podcast 2026 Signal Award Winner: "Best Health and Wellness Podcast"
Twice Transplanted. Still Dancing. Most people never face one life-saving transplant. Jennifer Lombardi has survived two. Now, when the music hits and she steps onto a dance floor and she remembers why she fought so hard. @phaware podcast Ep 595 phaware.global/ph-stories/ph…
We’re thrilled to announce that the @phaware podcast has been honored with a 2026 Signal Award for Best Health and Wellness Podcast. We couldn’t be more grateful. To everyone who’s listened, shared, and been part of this RARE journey, thank you. #SignalAwards #phaware
November is Pulmonary Hypertension Awareness Month. Everyone has something that makes them rare. We invite you to #ShareYourRare all month long, because one’s rare isn’t just a diagnosis. It’s what makes you uniquely you! Download a SHARE YOUR RARE kit: phaware.global/ph-awareness-…
After two years of limitations, she’s finally doing things without losing her breath—and now she’s chasing one unforgettable goal: ditch the IV and dive back into the water. A resilient, feel-good moment that turns survival into joy.
After losing so much of her old social self, she shares the small comeback that means everything: work, normalcy, and holding on for the future. It’s raw, hopeful, and impossible not to root for.
November is Pulmonary Hypertension Awareness Month. Join the global #phawarenessmonth conversation to help raise awareness for pulmonary hypertension (PH). #ShareYourRare, because one’s rare isn’t just a diagnosis. It’s what makes you uniquely you! phaware.global/ph-awareness-…
Time is Running Out! Vote NOW for @phaware We are a finalist for Best Health and Wellness Podcast, 2026. Voting ends THURSDAY! TAKE :30 to vote. vote.signalaward.com/PublicV…
Help @phaware win a 2026 Listeners Choice Award for "Best Health and Wellness Podcast" VOTE Now: vote.signalaward.com/PublicV… VOTING ENDS Thursday! Take :30 to cast your ballot!
She Checked the Organ Donor Box at 16, Now She’s Waiting for Someone Else’s Lungs. Canadian pulmonary hypertension patient, Kirsty McGeown on reclaiming life’s normal moments and dreaming of becoming a grandmother. @phaware podcast ep 594 @phacanada phaware.medium.com/im-aware-…