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.
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.
It was the summer of my senior year of high school. I remember the doctor coming into the room and diagnosing my mother with pulmonary hypertension (PH).
After diagnosed with PH, I felt many mixed emotions. But, as unbelievable as it can sound, my main emotion was that of HAPPINESS.
Bobby Hall is a social media influencer and activist who lends his voice to raising awareness for pulmonary hypertension.
Darby Hetrick was diagnosed with pulmonary hypertension (PH) when she was only 2 years old. She needed to be on a life-sustaining, I.V. infused medication 24/7, and eventually was able to move to a subcutaneous pump.
Both mother and daughter were diagnosed with PAH. This is how their lives have changed.
