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Every September, we proudly collaborate with seven other organizations- Arthritis Foundation, Foundation for Sarcoidosis Research, The Myositis Association, PF Warriors, Scleroderma Foundation, Scleroderma Research Foundation, and Wescoe Foundation for Pulmonary Fibrosis- to support the Pulmonary Fibrosis Foundation’s initiative to raise awareness about interstitial lung disease (ILD) and pulmonary fibrosis. 

The fourth annual ILD Day kicks off on September 18th, 2024 at 12 pm CDT (1 pm EST) with an educational webinar titled, “The journey to diagnosis: Process, evaluation, and your care team.” The presentation will address how doctors recognize ILD and find the right treatments for each individual. Important information about the roles of your care team and how to advocate for yourself will be provided. The webinar will be presented by Dr. Sonye Danoff, pulmonologist with John Hopkins Medicine and Senior Medical Advisor, PFF Care Center Network. 

Approximately 10-20% of patients with Sjögren’s are also diagnosed with ILD. If you would like to learn more about ILD in Sjögren’s, you can read our expert blog from this year entitled "Journey to Diagnosis: Interstitial Lung Disease in Sjögren’s" by Dr. Hassan Baig, MD, M.B.B.S. and last year's blog "Interstitial Lung Disease in Sjögren’s" by Dr. Nishant Gupta, MD.


ILD Day logo

ILD Day

For more information about ILD Day and how to register for the ILD Day educational webinar, please visit www.ILDDay.org

Click Here to Learn More or Register for ILD Day Webinar