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We asked teens at PHA on the Road: PH Patients and Families Education Forum in Chicago,Ill., and on PHA Teens, our teen social network, their thoughts on living with PH. Want to weigh in? Join the conversation at PHA Teens!
The information provided on the PHA website is provided for general information only. It is not intended as legal, medical or other professional advice, and should not be relied upon as a substitute for consultations with qualified professionals who are familiar with your individual needs.
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The National Organization for Rare Disorders (NORD) awarded PHA the Abbey S. Meyers Leadership Award in 2012 for outstanding service to PHA members in advocacy, education and other key areas.