“I thought my life was over, but through the PHA and friends and family and doctors, I found the help I needed.” In recognition of Rare Disease Day and American Heart Month in February, the Pulmonary Hypertension Association’s (PHA’s) The Right Heart blog brings you a video featuring Quinland Folkestad. Quinland has pulmonary arterial
Holly Szmutko is a passionate volunteer and advocate on behalf of the pulmonary hypertension (PH) community. She became involved after she was diagnosed with pulmonary hypertension in January 2019 after several misdiagnoses. Then she had to try multiple therapy options before finding a combination that made her feel better instead of worse. She was
I was diagnosed with idiopathic pulmonary arterial hypertension (IPAH) a little more than seven years ago. I’ve participated in studies. I have a care team that allows me to ask questions and be a part of my treatment journey. I’ve used SubQ pump therapy and recently transitioned to IV therapy. I participate in the
Nominations are now open for the Pulmonary Hypertension Association (PHA) Outstanding Member Awards. The Outstanding Member Awards honor people who raise awareness and give a voice and face to the pulmonary hypertension (PH) community. The awards recognize their advocacy, fundraising, promotion of quality patient care, and efforts to advance PH research. The Outstanding Member
As I’ve gotten older, my heart seems to be getting stronger. I am on medications for my heart and two medications for my PH. Each test comes back better than the last. I am kicking PH’s butt. If I can do it, so can you!
A new issue of Advances in Pulmonary Hypertension is available at AdvancesinPH.org. The issue, Volume 18, No. 4, “Pulmonary Hypertension: Every Picture Tells a Story,” was edited by Jeffrey D. Edelman, M.D., and Harrison W. Farber, M.D. Drs. Edelman and Farber are members of the Advances in Pulmonary Hypertension Editorial Board. Radiology, echocardiography, cardiology
In celebration of Valentine’s Day, The Right Heart blog brings you a love story about Georgette and Dean Bridger, who have been married for nearly 27 years. Dean was diagnosed with scleroderma in 1996 and with pulmonary arterial hypertension (PAH) in 2016. Along the way, Georgette has been by his side through “this remarkable
This spring, the Pulmonary Hypertension Association (PHA) is bringing together the pulmonary hypertension (PH) community for a common goal: raising funds to help support those affected by PH and ultimately find a cure. PHA will host O2breathe events throughout the country to raise money to fund PHA’s support, education and research initiatives. Register for
Learn, connect and share our common “Vision for a Cure” at PHA 2020 International PH Conference and Scientific Sessions. Set for June 12-14 in Anaheim, California, the event is expected to bring together more than 1,400 individuals with pulmonary hypertension (PH), caregivers and health care professionals from all over the world. PHA 2020 is
