The PHA community is a network of people with diverse backgrounds and experiences living their best lives. PHA highlights those experiences through inspiring first-person stories in our Right Heart Blog.
Ruth Greenspan, a widow for 54 years, lost her battle with PH after being diagnosed with the disease just five weeks before.
A love letter to Shanta Duncan from her beloved husband.
Nicole Lowe aunt's journey was amazing. She was braver than she truly knew and meant so much to so many.
Kathleen Sheffe and her sister took the trip of a lifetime after her heart-lung transplant.
Amanda Harvey-McKee balances a busy career and leadership in PHA’s St. Louis Support Group after overcoming CTEPH and major surgery.
Support group leader Stephanie Bachelder recently reached out as a PH advocate to Congressman Jim McGovern of the U.S.
Raele Robison was a student in a demanding PhD program when she was diagnosed with scleroderma and pulmonary hypertension. Now armed with answers about what was causing her mysterious symptoms, she is living her best life with PH.
Noah Wall is a singer, songwriter, and fiddler in the award winning acoustic band “The Barefoot Movement.” Her nephew Jackson Wall was diagnosed with pulmonary hypertension (PH) at one year old.
Born in 1976 and raised on the beautiful island of Puerto Rico, Luis Cortés had to endure the challenge of living with PH through a devastating hurricane.
