Eric Borstein to Walk from Los Angeles to San Diego for PH
August 07,2024
My name is Eric "EB" Borstein. On September 21st, 2020, while at home, I collapsed from massive right heart failure and Read More...
Where is EB?
July 24,2024
Eric Borstein, who lives with pulmonary arterial hypertension, is walking from Los Angeles to San Diego to raise funds and Read More...
2024 PHenomenal Hope: Research, Knowledge, & Advocacy in PH
June 12,2024
Join renowned experts as well as rising young investigators and allied healthcare providers as they share original research at the Read More...
New PH Therapies in 2024 Pre-recorded Webinar
May 14,2024
In March, we received news that two new therapies for the treatment of pulmonary hypertension, Opsynvi and Winrevair, were approved Read More...
128th Boston Marathon
March 20,2024
Vasili has been running his entire life. Upon joining Aerovate Therapeutics it became apparent that both his personal drive for Read More...
PHenomenal Hope 2023: Knowledge, Research & Advocacy in PH
May 19,2023
Team PHenomenal Hope is proud to announce the inaugural PHenomenal Hope 2023: Knowledge, Research & Advocacy in PH symposium. Join Read More...
PHenomenal Hope 2023: Knowledge, Research & Advocacy in PH
May 19,2023
Join renowned experts as well as rising young investigators and allied healthcare providers as they share original research at Team Read More...
Learn Live Breathe PH
February 28,2023
This Rare Disease Day, Team PHenomenal Hope is celebrating the pulmonary hypertension (PH) community with the launch of its new educational Read More...
PHenomenal Impact Fund Reopens for 2023
January 06,2023
Team PHenomenal Hope's research program, the PHenomenal Impact Fund for Global PH Research, is reopening for the fifth year on Read More...
PHenomenal Impact Fund for Global PH Research Application Window Open
January 03,2022
The PHenomenal Impact Fund for Global PH Research is now open and accepting letters of intent (LOIs) for the fourth Read More...
Tackling PAH With Inspiration From My Mom: Stefanie Leonard
March 16,2021
My name is Stefanie, I’m 46, and I’ve been living with symptoms of pulmonary arterial hypertension (PAH) as far back Read More...
My Genetic PAH: Brenda Vang
September 03,2020
My name is Brenda Vang. I am the oldest of seven. My father was a teacher in a Thailand camp Read More...
Rayetta Johnson: Controlling What is in my Control
September 03,2020
When I was diagnosed with pulmonary arterial hypertension in the beginning of 2018, I had to make a lot of Read More...
Receiving Care During a Pandemic: Quinlan Folkestad
September 03,2020
The COVID-19 pandemic has affected so many people in so many ways. It is hard to think about how it Read More...
A Support System is Essential: Tracy Martinez
August 31,2020
Hello, my name is Tracy Martinez, I’m 46 years old and I have pulmonary arterial hypertension. I live in Inkster, Read More...