Headquartered in Silver Spring, MD, the Pulmonary Hypertension Association (PHA) is the country’s oldest and largest nonprofit patient association dedicated to the pulmonary hypertension (PH) community. Pulmonary hypertension is a rare, chronic and life-threatening disease of the lungs for which no cure currently exists. PHA’s mission is to extend and improve the lives of those affected by PH. To achieve this mission, PHA engages people with PH and their families, caregivers, health care providers, and researchers worldwide who work together to advocate for the PH community, provide support offer up-to-date education and information on PH, improve quality patient care, and fund and promote research.
PHA seeks mission-driven, talented professionals to join our team of dedicated employees working to advance our mission and improve the quality of life of those who live with this deadly lung disease.
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51-200 employees
View all Pulmonary Hypertension Association employees
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Non-profit Organization Management
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301-565-3004
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1629 K Street, Suite 300, Washington D.C., US
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1991
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Nonprofit, Medical Education, Outreach, Ph, Accreditation, Patients, Pah, Rare Disease, Pulmonary Hypertension, Cteph, Chronic Thromboembolic Pulmonary Hypertension, Pulmonary Arterial Hypertension, Pulmonary Hypertension Due To Lung Disease, Pulmonary Hypertension Due To Unknown Causes, Pulmonary Hypertension Due To Left Heart Disease
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Matt J Granato is the CEO of Pulmonary Hypertension Association. To contact Matt J Granato email at [email protected] or [email protected].
The decision makers in Pulmonary Hypertension Association are Courtney Durham, Elizabeth Joseloff, James Wetherill, etc. Click to Find Pulmonary Hypertension Association decision makers emails.
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