Sign up now to be one of the first to be notified when the
PFF Community Registry is open for enrollment.

The PFF Community Registry will launch in early 2022. Patients with PF, including those who have received a lung transplant, as well as their caregivers and family members, are encouraged to join to help accelerate PF research and hopefully improve lives of patients living with the disease. Participants must be 18 years or older, reside in the United States, and have access to the Internet.

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Please note, CAPTCA codes are case-sensitive.

Your Privacy Matters

The Pulmonary Fibrosis Foundation Registry considers the protection of your privacy to be one of our most important responsibilities. We have set up strict protocols to protect your personal information. To review our policy, click here.