Webinars enable the PF community to easily learn about the disease from the leading pulmonary fibrosis specialists. They are a great tool for support groups to utilize at meetings or other events.

Explore webinars from our popular PFF Summit sessions, Global Pulmonary Fibrosis Awareness Day, and others, in our library below.

Disease Education Webinar Series

Join us for our Disease Education Webinar series! This program allows the pulmonary fibrosis (PF) community to virtually learn from, connect with, and pose questions to leading pulmonary fibrosis specialists.

Upcoming Schedule

Caregiving and Pulmonary Fibrosis
April 19, 2017
12:00 p.m. - 1:00 p.m. CT

Presented by
Robyn L. Mowery, Ph.D., LMFT, Piedmont Hospital Ethics Committee Co-Chair, Director of Healthcare Integration for Mercer Medical Family Therapy-Atlanta, Mercer University School of Medicine

Piedmont Healthcare is part of the PFF's Care Center Network.

Register and Submit Questions

To view previous webinars in this series, click on "Disease Education Webinar Series Archive" below.

Disease education webinar series archive


Hypersensitivity Pneumonitis - February 15, 2017


Pulmonary Fibrosis Progression and What to Expect - October 12, 2016

What is Pulmonary Fibrosis? - September 7, 2016

Ask a Doc: "GERD and Sleep Apnea" - March 16, 2016

"Update on PF Research and the PFF Patient Registry and the PFF Care Center Network" - April 13, 2016

"Oxygen Equipment Overview" - May 11, 2016

"Pulmonary Rehabilitation" - July 13, 2016


"Lung Transplantation" - January 14, 2015

“Occupational and Environmental PF” - February 4, 2015

"Pulmonary Hypertension and Pulmonary Fibrosis" - March 11, 2015

"Ask A Doc" - March 18, 2015

"Palliative Care" - April 15, 2015

"Ask A Doc" - June 10, 2015

"Ask a Doc: IPF Treatment Guideline" - August 19, 2015

"Pulmonary Fibrosis Advocacy" - September 2, 2015

"Familial Pulmonary Fibrosis" - October 28, 2015

“Understanding Pulmonary Function Tests (PFTs)” - December 16, 2015


"What is Pulmonary Fibrosis?" - May 14, 2014

"Ask A Doc Clinical Trial Update" - May 28, 2014

Health Care Professional Focused Webinar - "Making An Accurate Diagnosis: How to Use IPF Consensus Guidelines" - July 16, 2014

Tools for Living Better with PF - "Pulmonary Rehabilitation and Support Groups" - July 23, 2014

Patient and Caregiver Focused Webinar - "Caregiving 101: Supporting Others While Supporting Yourself" - August 20, 2014

Tools for Living Better with PF - "Supplemental Oxygen" - September 3, 2014

"Drug Development Process and the FDA" - September 17, 2014

"Talking with PF Patients: Truth-Telling While Maintaining Hope" - October 22, 2014

"Autoimmune-Related Pulmonary Fibrosis" - November 12, 2014

"Coping with Pulmonary Fibrosis: What About My Mental Health?" - December 10, 2014

PFF Summit 2015: From Bench to Bedside

PFF Summit 2013: From Bench to Bedside

December 5-7, 2013
La Jolla, California

Presented by the Pulmonary Fibrosis Foundation and certified by National Jewish Health

Patient and Caregiver Sessions 

Scientific and Clinical Sessions for Physicians, Researchers, Registered Nurses, and Allied Health Professionals 

Pulmonary Fibrosis Patient Support Day

July 13, 2013
Nottingham, England
Sponsored by the Pulmonary Fibrosis Foundation and the British Association for Lung Research

The Pulmonary Fibrosis Foundation and the British Association for Lung Research (BALR) sponsored a special "Pulmonary Fibrosis Patient Support Day" following the BALR Summer Meeting 2013 in Nottingham, England. The patient education event focused on living with pulmonary fibrosis and included reviews of clinical trials, treatment options, disease management, and an update on the NICE guidelines. The event was supported by Boehringer Ingelheim and the Friends of the Center for ILDs at University of Washington Medical Center.

Dr. Ben Hope-Gill – Cardiff
Interstitial Lung Disease: Why It is So Difficult

Dr. Gisli Jenkins – Nottingham
IPF: What is It? Why it Occurs?

Geraldine Burge/Professor Sherwood Burge – Birmingham
IPF Guidelines Update – National Institute for Health and Care Excellence (NICE) Update on the Recommended Guidelines

Manjiry Tamhane
Caring for an IPF Patient

Annette Duck – Manchester
Hoping for the Best, Planning for the Worst

Dr. Michael Gibbons – Exeter
Update on Therapeutic Options

Dr. Helen Parfrey – Cambridge
Review and Update on Clinical Trials in IPF

Malcolm Weallans
Pulmonary Fibrosis Trust

Dr. Sara Booth – Cambridge
Self Management of Breathlessness

Mike Bray – Cambridge
Launch of Action for Pulmonary Fibrosis

Dr. Gauri Saini – Nottingham
Management of Cough

Dr. Nazia Chaudhuri – Sheffield
Lung Transplantation for IPF


Denver, Colorado
Evalución Diagnóstica de la Fibrosis Pulmonar Idiopática?
Evans Fernández, MD, MS
Recorded at National Jewish Health

Global Pulmonary Fibrosis Awareness Day 2012 “Living with Pulmonary Fibrosis Webinars

September 22, 2012
Denver, Colorado
Presented by the Pulmonary Fibrosis Foundation in partnership with National Jewish Health.

The Pulmonary Fibrosis Foundation wishes to thank platinum sponsor Boehringer Ingelheim, silver sponsor The Culliton-Metzger Family, and bronze sponsor InterMune for their generous support of Global Pulmonary Fibrosis Awareness Day.

Gregory P. Cosgrove, MD

Daniel M. Rose, MD

Gregory P. Cosgrove, MD
What is Pulmonary Fibrosis?

Tristan J. Huie, MD
Tools for Living Better with Pulmonary Fibrosis

Open Forum Discussion

IPF Summit 2011: From Bench to Bedside

December 1-3, 2011
Marriott Magnificent Mile, Chicago, Illinois

Presented by the Pulmonary Fibrosis Foundation, in partnership with National Jewish Health and The France Foundation, and endorsed by the American Thoracic Society.

Patient and Caregiver Sessions

Scientific and Clinical Sessions for Physicians, Researchers, Registered Nurses, and Allied Health Professionals

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