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Connect with Patients

Bringing patients and providers together

Are you looking for ways to better communicate with your pulmonary fibrosis patients? The Pulmonary Fibrosis Foundation provides educational and event planning materials to assist both you and your patients.

Do you have an idea for an important resource not currently available? Email the PFF Patient Communication Center at pcc@pulmonaryfibrosis.org to share your thoughts.

 

Patient Education Materials

The Pulmonary Fibrosis Foundation offers a variety of printed materials to facilitate conversations with patients that further enhance their understanding of PF. READ MORE

 

Host an Event

An educational event is an ideal way to provide pulmonary fibrosis patients, caregivers, family members and healthcare providers with accurate and up-to-date information about PF. READ MORE

 

Support Groups

A support group may improve your emotional well-being and have a positive impact on your health by offering you an opportunity to connect with others who are facing similar experiences, obtain practical information, and to receive support. READ MORE

 

PFF Ambassador Program

The PFF Ambassador Program empowers patients and health care professionals to become PF spokepersons.  Ambassadors take part in training to prepare them to speak and advocate on behalf of the PFF and the idiopathic pulmonary fibrosis community. READ MORE

 
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