His lungs were clear, but a chest X-ray revealed something his family never expected.
In this preview of Building The Noise, Steve Van Wormer of PHAWARE shares how a substitute pediatrician discovered an enlarged heart in his son Lucas, setting the family on a pulmonary hypertension journey.
Full episode drops August 31.
Watch & subscribe: https://t.co/g83h1aYwRQ
#PulmonaryHypertension #PHAware #PatientAdvocacy #BuildingTheNoise
Team PH is proud to welcome Eric “EB” Borstein as our new Board Chair! A PAH warrior, advocate, & walking 14,500+ miles of hope, EB brings unmatched passion to our mission. Join us in celebrating his commitment to the PH community. ⚡ https://t.co/TgByYCiSkb
#TeamPH#WhereIsEB
The countdown is on! Studio City PXL is all revved up for the new season of @IndyCaronNBC 🏁
Our creative and production team was proud to partner with @NBCSports to provide adrenaline-filled field production, filming and directing of the #IndyCar series class of 2023.
SHARE YOUR RARE on the @phaware podcast! Patients, Care Partners, Doctors, Nurses - Be part of the All-New Season 7 of” I'm Aware That I'm Rare.” We can record you anytime from anywhere on the planet! Be our guest. Write us @: [email protected]
PH Kiddos 7-17, @campdelcorazon is a summer camp on Catalina Island for kids living with heart & lung disease. Thanks to numerous donations generously made in Lucas Van Wormer's honor, 5-6 campers will be able to attend at NO COST every year for the next
https://t.co/vqGs3wk8De
Check out this fun #WorldCup spot for a new partnership project between @crayola@foxsports and @ussoccer to celebrate creativity, community, and the beautiful game!
Tune in to the #BlackFriday#WorldCup2022 game USA vs England on Fox. 11am PT! It is widely expected to be one of the most watched soccer games in U.S. TV history! Thanks to Gordon Ramsay for another F@$&#' Fun Shoot!
Sign up for our zoom event screenings of “Aware I’m Rare.” A breathtaking short film. NOV 5, 12 & 19 at 1pm PT | 4pm ET https://t.co/xrqpYB3Db8 It explores the lives of a group of young adults battling #pulmonaryhypertension and how they cope with their rare disease diagnosis.
Sign up for our zoom screenings of "Aware I’m Rare." A breathtaking short film. Nov 5, 12 & 19 at 1pm PT | 4pm ET https://t.co/xrqpYB3Db8 The film explores the lives of a group of young adults battling pulmonary hypertension and how they cope with their rare disease diagnosis.
I'm Aware That I'm Rare: The @phaware podcast launches Season 7 on 10/17/22 - In time for Pulmonary Hypertension Awareness Month! Subscribe now: https://t.co/GJPvrja4sf Listen on your favorite platform. Share your Rare Story: [email protected]
phaware presents: "Aware I'm Rare" A Breathtaking Short Film. Join us for an online screening to celebrate Pulmonary Hypertension Awareness Month. November 5th, 12th & 19th @ 1 pm - 2pm PT
Register now: https://t.co/xrqpYBlMpg Click to watch trailer 1: https://t.co/mpyqPTc8aj
Calling all Pulmonary Hypertension Patients, Care Partners, Nurses, Doctors... @phaware is enlisting PH Community Members from across the globe for an All-New Season of stories. Share Your Rare Story Today! https://t.co/WHTW5VdtFp
My condition is rare. I saw the top professionals in my area. I had no indication that I had heart trouble. Had I not made a Facebook post, I would be dead. That's literally what would've happened. CTEPH patient, Karri Reynolds phaware® interview 386 https://t.co/QBfNzJsICU