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Helping patients with pulmonary arterial hypertension live life to the fullest.

A diagnosis of pulmonary arterial hypertension (PAH) can be life-changing. This rare, complex disease can bring shortness of breath, fatigue, chest pain, dizziness, and swelling. Patients might wonder if they can still live an active life.

Even though PAH has no cure, coordinated care management can relieve symptoms and slow disease progression. Treatment focuses on relaxing blood vessels in the lungs to reduce blood pressure.

No matter the treatment method—pills, inhaler, subcutaneous therapy, or IV line— our expert staff checks in regularly to help patients with side effects and maximize adherence. We support the entire healthcare team, including consulting pulmonologists and cardiologists, so patients can do more of what they love.

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