Welcome to Living PAH

Pulmonary arterial hypertension (PAH) is a rare form of pulmonary hypertension that is estimated to affect about 15 people per million worldwide.¹ Although it was once a diagnosis that offered little hope, the understanding of this disease and the number of treatment options has grown rapidly over the past two decades. PAH specific treatment has advanced from one treatment in 1996, to nine FDA-approved treatment options available today, with many more in clinical development.² Each day brings advancements in treatment, better diagnostic tools and new hope for people living with PAH.^2,3

Learn All You Can

Living PAH is dedicated to empowering patients — and their loved ones — who are living with PAH by providing the most up-to-date information on the disease and treatment, along with a variety of support services. You'll get information on PAH and treatment types, have the opportunity to gain perspective from someone who has walked the same path, learn how to be proactive in your care and get practical tips for living with PAH. And, you'll also find information on where to go for financial assistance.

There's a wealth of information available through Living PAH. Why not get started by browsing the PAH Kitchen for easy, delicious low-sodium recipes? Or, perhaps you'd like to learn more about the support available through the PAH community? When you're finished exploring, don't forget to enroll in Living PAH to get more information and resources not available through the website.

Have questions about the Living PAH program? Call the Living PAH call center at 1-877-948-9137 to get answers. Operators are available from
8 a.m. to 5 p.m. Central Standard Time (CST). At all other times, please leave a message. You will receive a call back during regular business hours.