The Pulmonary Hypertension Association (PHA) is a donor-based nonprofit that funds the nation’s largest PH patient and caregiver support group network, lifesaving early diagnosis awareness and education programs, specialty care resources, and research to find ways to prevent and cure PH.
It is a young organization that is changing the history of an illness. From simple beginnings — four women around a kitchen table in Florida in 1991 – PHA has evolved in size and complexity. While it has grown, PHA has stayed true to its roots and the vision and ingenuity of the founders. Today it’s a 501(c)(3) nonprofit organization, serving more than 16,000 members and supporters. It continues to work every day to end isolation, provide education, involve our constituents in everything they do to find a cure for pulmonary hypertension.
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