The Foundation has awarded nearly $4M for research to improve the success of lung transplants. The research will be focused on Chronic Lung Allograft Dysfunction (CLAD), a widespread post-transplant complication about which little is known. #CFresearch on.cff.org/2TqyEqo

Make sure to check out our #Facebook Page to keep update on our local events: facebook.com/CFFGreaterILPe…

This #GivingTuesday, help us reach our goal of 650 gifts and add tomorrows for people living with #cysticfibrosis. Give today: on.cff.org/650gifts

Waiting for a #lungtransplant? Talk to someone w/CF who's been through the transplant process with CF Peer Connect: on.cff.org/2j5c57l

Thinking about having kids? Talk to someone w/ #cysticfibrosis who's been there. Sign up for CF Peer Connect: on.cff.org/2ANL8N5

Applying for college next year? Talk to someone w/ #cysticfibrosis who's been there. Sign up for CF Peer Connect: on.cff.org/2liyZsn

2017 is nearly over, but there's still time left to add tomorrows for people living with #cysticfibrosis. Make your tax-deductible gift today: on.cff.org/2lskGSO

Help us blaze our path to a cure for #cysticfibrosis. Join people like Marcus who are becoming a #CFtrailblazer, and find an enrolling clinical trial near you. on.cff.org/trailblazer

Facing a challenging life transition? You're not alone. Connect with someone w/CF through CF Peer Connect: on.cff.org/2rjZALE

Want to connect with others in the #cysticfibrosis community? Join us at our next CF MiniCon on self-care and relationships on 2/27. Register today: cff.org/minicon

How do you balance advocating for you or your loved one with #cysticfibrosis and find time for self-care? Connect with other adults with CF and CF family members about this and more at our next CF MiniCon! cff.org/minicon

Our Annual Chapter Meeting & Awards Night is coming up on March 8th! A night to say Thank YOU and show you the advances the Cystic Fibrosis Foundation has made in the last year! #CureCF

Streaming Live! Join us! #CFFVLC

Lung Transplant initiative being discussed right now live at #CFFVLC

So proud of @cherizkunkel !! Sharing your story and participating in the Living with CF Panel on the big screen at VLC! #CFFVLC

ILLINOIS legislators hard at work! Amazed at the beauty of the House assembly building! Advocating for CF patients and families! #CFAdvocacy Cystic Fibrosis Foundation CFF_Peoria

some of our IL advocates after being recognized on the floor of the House for their amazing #cfadvocacy! thank you for advocating for access to affordable & adequate health care for people with CF!

Wrapped up the day with a great meeting with Senator Dave Koehler and his staff! Thank you for your support of policies that preserve access to adequate affordable healthcare for cf patients! ILLINOIS state advocacy day 2018 in the books! #CFadvocacy