My Daughter, Diagnosed at Eight Months Old: Amanda Howard
January 28,2020
My name is Amanda Howard. I first learned about pulmonary arterial hypertension (PAH) when my daughter Abby was eight months Read More...
Letter from the Director: Join us in 2020
January 24,2020
Happy New Year! 2020 is the start of Team PHenomenal Hope’s second decade serving the PH community. We have been Read More...
Iceman Race Report: Julie Tracy
January 21,2020
Iceman! I was a little nervous (sort of, not really?) for this race, mostly just because I have little to Read More...
My PAH Diagnosis: Suzanne Miller
January 16,2020
When I was 16 I discovered the "Diet Doctor." I lived in an affluent community where vanity was more important Read More...
Breathing Life with CTEPH: Kristin McCoy
January 14,2020
The first part of my life was awesome, for the most part. I joined the rescue squad and became an Read More...
My PAH Diagnosis: Kevin Green
January 09,2020
My name is Kevin Green. I’m 49 years old and diabetic. In March, 2019 my doctor started me on a Read More...
Diagnosis, Blood Thinners, and PTE: Tamara Moffett
January 07,2020
My name is Tamara, I’m 33 years old. On Christmas Eve of 2016, I attempted to walk my dog, but Read More...
Being Well-Informed About our Diagnosis: Kirsten Braley
January 03,2020
When you have a chronic lung condition, catching a respiratory illness is a challenge. Pulmonary hypertension patients are faced with Read More...