CFF_Peoria

[CFF_Peoria @CFF_Peoria]

Make sure to check out our #Facebook Page to keep update on our local events:

https://t.co/nrQjyHUbho

[Cystic Fibrosis Foundation @CF_Foundation]

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 https://t.co/CAgAm521GO

[CFF_Peoria @CFF_Peoria]

Wrapped up the day with a great meeting with @SenatorKoehler 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

[Molly @mollyvoigt]

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!

[CFF_Peoria @CFF_Peoria]

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

[CFF_Peoria @CFF_Peoria]

@SenChapinRose @smithbolton talking policy in our hallway meeting! See you in - district!

[CFF_Peoria @CFF_Peoria]

@SenChapinRose Thank you for stopping to chat with @CFF_Peoria @SmithBoltonLab advocating for affordable access to healthcare! #CFadvocacy

[CFF_Peoria @CFF_Peoria]

@ThomasMBennett Thank you for listening to our story! Until it’s done! @CFF_Peoria #CFadvocacy

[CFF_Peoria @CFF_Peoria]

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

[CFF_Peoria @CFF_Peoria]

Lung Transplant initiative being discussed right now live at #CFFVLC

[Pamela Mertz @PamMertz]

when patients can say 'I used to have CF'....THEN, we will be DONE! Dr. Preston Campbell. #CFFVLC #CFF

[CFF_Peoria @CFF_Peoria]

Streaming Live! Join us! #CFFVLC

[CFF_Peoria @CFF_Peoria]

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

[CFF_Peoria @CFF_Peoria]

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! https://t.co/2JSdNffgD3

[CFF_Peoria @CFF_Peoria]

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: https://t.co/2JSdNffgD3

[CFF_Peoria @CFF_Peoria]

Facing a challenging life transition? You're not alone. Connect with someone w/CF through CF Peer Connect: https://t.co/Bn7RJOxJyP

[CFF_Peoria @CFF_Peoria]

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. https://t.co/eMu2XixEXX

[CFF_Peoria @CFF_Peoria]

2017 is nearly over, but there's still time left to add tomorrows for people living with #cysticfibrosis. Make your tax-deductible gift today: https://t.co/uy4zjD5cdO

[CFF_Peoria @CFF_Peoria]

Applying for college next year? Talk to someone w/ #cysticfibrosis who's been there. Sign up for CF Peer Connect: https://t.co/6bNXP38IMP