Pulmonary Fibrosis Foundation

PFF Board of Directors member and lung transplant recipient, Laurie Chandler, wrote a letter for the New Hampshire Union Leader to urge lawmakers to pass the SOAR act.

Read it below:

📰 unionleader.com/opinion/letter… #SOARActO2

PFF Summit 2023 sessions are now rolling out on YouTube! In our first Summit premier, join a panel of experts to learn how federal agencies play a crucial role in research for pulmonary fibrosis. Watch now! youtu.be/bOB-sL8a3Ds?si…

Chronic cough has a significant impact on pulmonary fibrosis patients’ physically and mentally. Learn more about the causes, treatments and impact on quality of life by registering for EU-PFF’s webinar this Thursday, May 9th.

Sign up at us06web.zoom.us/webinar/regist…

Have you ordered your Shop PFF merch yet? Raise awareness of PF everywhere you go at goshoppff.com

Join the 18th annual FREE in-person patient/family education day event hosted by The American Thoracic Society’s Public Advisory Roundtable (PAR) in sunny San Diego!

Date: May 18, 2024
Location: San Diego, CA
RSVP: Email par@thoracic.org by MAY 10, 2024

See flyer for details!