Pulmonary Fibrosis Foundation Free Webinar, April 11, to Focus on ‘Non-Genetic Causes of PF’

Pulmonary Fibrosis Foundation banner - "just breathe"The Pulmonary Fibrosis Foundation (PFF) offers a free webinar Wednesday, April 11, of interest to specialists in pulmonary and critical care medicine. It begins at 10 a.m. Arizona/Pacific Daylight Time.

The speaker is David J. Lederer, MD, PFF senior medical advisor for Education and Awareness, and faculty physician with Columbia University/New York Presbyterian Hospital.

In February 2015, PFF recognized Banner – University Medical Center Tucson as a member site in its PFF Care Center Network.

This event is part of PFF’s Disease Education Webinar Series. The program allows the pulmonary fibrosis community to learn from, connect with and pose questions to leading pulmonary fibrosis specialists.

Dr. David J. LedererPRESENTER: David J. Lederer, MD, MS
Co-Director, New York Presbyterian/Columbia University Interstitial Lung Disease Program;
Pulmonary Director , Pulmonary & Intensive Care Translational Outcomes (PICTOR) Group, Columbia University, New York City

TOPIC: “PFF Webinar: Non-Genetic Causes of Pulmonary Fibrosis”
WHEN: April 11, 2018
    1:00 p.m. - 2:00 p.m. ET
   12:00 p.m. - 1:00 p.m. CT
   11:00 a.m. - 12:00 p.m. MT
   10:00 a.m. - 11:00 a.m. PT (Current Arizona time)
WHERE: Online

REGISTER HERE

DID YOU MISS A WEBINAR?
VISIT THE PFF ARCHIVE AND WATCH ONLINE

All presentations in the PFF Disease Education Webinar Series are recorded at the time of broadcast and are available to watch online soon after their air date.

Be sure to visit the PFF website often for topics and details about how to register for upcoming webinars.

VIEW WEBINARS

The PFF Patient Communication Center (PCC) is a comprehensive resource for the pulmonary fibrosis community. The PCC staff:

  • Provide the most up-to-date medical information
  • Offer information on how to find support services, obtain available treatments, and participate in clinical trials
  • Distribute the Foundation's educational materials

THE PFF DISEASE WEBINAR SERIES IS MADE POSSIBLE BY THE GENEROUS SUPPORT OF:

   Genentech logo

About the Pulmonary Fibrosis Foundation
The Pulmonary Fibrosis Foundation mobilizes people and resources to provide access to high quality care and leads research for a cure so people with pulmonary fibrosis will live longer, healthier lives. The PFF collaborates with physicians, organizations, patients, and caregivers worldwide. For more information, visit pulmonaryfibrosis.org or call 844-TalkPFF (844-825-5733).

ALSO SEE:
"Pulmonary Fibrosis Foundation Sponsors UA Lecture on Interstitial Lung Disease, Dec. 8" | Posted Nov. 30, 2017
"Pulmonary Fibrosis Foundation Free Webinar to Spotlight ‘Nutrition and ILD’ – Aug. 16" | Posted Aug. 9, 2017
“Free Webinars on Pulmonary Fibrosis Care, Feb. 15-16” | Posted Feb. 2, 2017

Release Date: 
04/04/2018 - 3:15pm