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.
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.
Kerry Babylon is living her best life with PH. In this video post from PHA's The Right Heart blog series, she talks about traveling with PH and the importance of family.
Temi and Lance Jones welcomed a beautiful baby boy named Jaxon into their lives in July of 2016. He was healthy, and they never had any cause for concern until the pediatrician heard a heart murmur during Jaxon's 4 month check-up.
Darby Hetrick of Pennsylvania has lived with pulmonary hypertension since she was 2 years old, but that hasn't stopped her. She traveled through Europe, played tennis in school and went on to college.
Shavini Fernando, 35, talks about her pulmonary arterial hypertension (PAH) diagnosis two years ago and her journey to the United States from Sri Lanka in search of better care and treatments.
