Pulmonary Fibrosis Week

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Information for Patients



Lung Information for Patients

The Pulmonary Fibrosis Foundation’s (PFF) Patient Communication Center is a hub for information and resources for patients, families, and healthcare professionals. Call 844.TalkPFF (844.825.5733) or email pcc@pulmonaryfibrosis.org.

Patient Educational Materials

The PFF has educational resources including our Information Guide, Brochures on Supplemental Oxygen, video series, and more.

Find Medical Care

The PFF’s Care Center Network is comprised of 60 medical centers nationwide offering comprehensive and individualized care to those living with PF.

Support Groups

There are over 150 volunteer groups around the country providing a safe environment for those affected by PF to share their experiences. PFF Voices is a national call-in support group.

Treatment Options

Learn about different treatment options and ways to manage symptoms. 

ATS Breathing in America Book

The Breathing in America: Diseases, Progress, and Hope compilationbriefly describes respiratory diseases and the progress that is being made in the quest to find their cures.

ATS Patient Information Series

The ATS Patient Information Series is a public service of the American Thoracic Society and its journal the AJRCCM (www.atsjournals.org). The information appearing in this series is for educational purposes only and should not be used as a substitute for the medical advice of one's personal health care provider.

Idiopathic Pulmonary Fibrosis (IPF)
Mechanical Ventilation
Oxygen Therapy