Webinars

NEW DISEASE EDUCATION WEBINAR SERIES AND PFF WEBINAR LIBRARY

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.

New Disease Education Webinar Series

Join us for our recently launched 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

Wednesday, September 17, 2014
12:00 p.m. - 1:00 p.m. CDT

"Drug Development Process and the FDA"

Presented by
David J. Lederer, MD, PFF Senior Medical Advisor, Patient Communications
Harold Collard, MD, PFF Medical Advisory Board Member and PFF Summit 2015 Chairman
Eugene Sullivan, MD, Principal at EJS Consulting, LLC

A Q+A session follows the presentation. Participants can pose questions to the presenters.

Register and Submit Questions


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

WHAT IS PULMONARY FIBROSIS? - SPANISH VERSION

2013
Denver, Colorado
Evalución Diagnóstica de la Fibrosis Pulmonar Idiopática?
Evans Fernández, MD, MS
Recorded at National Jewish Health



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

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
Introduction


Daniel M. Rose, MD
Welcome


Gregory P. Cosgrove, MD
What is Pulmonary Fibrosis?


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


Panel
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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