Here to Bring you Hope: Nikki Richard
February 27,2020
My story starts like most patients living with pulmonary arterial hypertension (PAH). One day I became short of breath without Read More...
A Rare Community: Letter from the Director
February 20,2020
February 29th is Rare Disease Day. It’s a day when we come together as a community to raise awareness, advocate, Read More...
Thriving with PH: Shannon Morrison
February 18,2020
My daughter Shannon is an eight year old identical twin with a vivacious passion for life and incredible strength. When Read More...
Years of Misdiagnosis: Tiffany Ray
February 13,2020
I was diagnosed with PH after years of misdiagnosis. When my symptoms started, I was sent to a psychologist for Read More...
Lifestyle Changes: Trace Cluck
February 11,2020
Living with complications from CTEPH has been difficult to say the least. In February of 2019 I had to step Read More...
30 Years of Dormancy: Linda Cantrell
February 04,2020
I was born with pulmonary hypertension. Unlike the majority of people with PH, mine didn’t develop over time. When I Read More...