09/10/2025
Today is ILD Day! Learn how you can get involved and spread awareness about this challenging condition. 🫁
Interstitial lung disease (ILD) is one of the most serious complications of scleroderma, affecting how people breathe and live each day. That's why the Scleroderma Research Foundation (SRF) is partnering with ten organizations to host the 5th Annual ILD Day, to spread awareness about this condition and help people learn how to recognize the signs of ILD.
There’s still time to join the Pulmonary Fibrosis Foundation for a special ILD Day Webinar TODAY at 10AM PT / 1PM ET. Learn about the causes, treatments, and strategies for living well with ILD—including the role of genetics. Register now: https://bit.ly/3IfLtPW
Then mark your calendars, extending the awareness of ILD Day, the SRF is hosting a special webinar on September 16, 9AM PT / 12PM ET to spotlight ILD and how it affects people living with scleroderma. This webinar will cover how symptom management and share the latest research aimed at improving patient outcomes. Register now: https://bit.ly/4mvGJUR
If you’re living with scleroderma, it’s important to be aware of the signs of interstitial lung disease (ILD). Shortness of breath may be an early symptom. Other signs can include a dry, persistent cough, fatigue or weakness, chest discomfort, thickening of the tissue beneath the nails (“clubbing”), loss of appetite, or unexplained weight loss.
Get involved this ILD Day by spreading the word—share your experiences with ILD or what you've learned about the condition with people in your community, both online and in person. By raising awareness, we can help ensure earlier diagnosis, better treatment, and stronger support for those impacted.
Thanks to Boehringer Ingelheim for sponsoring SRF’s ILD awareness education initiatives.