7Runs4Hay: Nicole Phillips
April 06,2022
To know Haylee, is to love Haylee. She had two rules: 1. Have Fun 2. Be Yourself! And she certainly Read More...
You're in Our Crew Van: Letter from the Director
March 23,2022
Last month we amplified the voices of pulmonary hypertension on Rare Disease Day. Our founder and president Dr. Patricia George Read More...
Kim Downey: Telehealth vs. in-person and what worked for me
March 10,2022
My name is Kim, and I am from Kenmore, NY, a suburb of Buffalo (yes, that Buffalo of the snowy Read More...
What Does it Mean to Celebrate Rare Disease Day?
February 28,2022
Every year on February 28 we celebrate Rare Disease Day. Team PHenomenal Hope (Team PH) celebrates Rare Disease Day because Read More...
Rare Disease Day
February 28,2022
February 28 is Rare Disease Day. Today (and every day) we celebrate the rare disease community and and push for Read More...
Join the Team Today!
February 17,2022
This year is our 10th anniversary year with Team PHenomenal Hope, and we are excited about the relaunch of our Read More...
Celebrating a Decade of Serving the Community
February 11,2022
We have begun the new year with much gratitude for our community, who made 2021 a widely successful year. For Read More...
Telehealth or In-Person Medical Care for PH Patients--What's Right for You?
February 01,2022
In the third video from our Living Well Now and Beyond campaign, Dr. Tim Lahm and Dr. Jeff Robinson weigh Read More...
Don't Ignore Your Symptoms or Delay Your Care
January 18,2022
In our latest informational video in the Living Well Now and Beyond series, Dr. Natasha Pradhan and Dr. Matt Lammi Read More...
Team PH January Support Group Meeting
January 05,2022
We'd love to see you at this month's support group meeting on Saturday, January 29 at 1 p.m. CT (2 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...