The South Carolina chapter of the @CF_Foundation raises funds through special events and other campaigns to advance the search for a cure for cystic fibrosis.
This is what #CysticFibrosis actually looks like. These are the real heroes, the real warriors fighting every single day. If you are inspired by them please consider donating to @clairewineland & or @CF_Foundation. Together we can raise enough awareness & funds & #curecf.
This week, volunteers from the #cysticfibrosis community will storm D.C. for March on the Hill! You can help make the voice of the CF community heard: Get involved and learn how you can participate in our Online Day of Action. #CFadvocacy https://t.co/Qa3dLBSE2f
Just wrapped a few days of sharing and brainstorming about our Finest events at the Bethesda office with colleagues from across the country! Can't wait to bring it all back to SC! #cff#untilitsdone
We had a great time kicking off #GreenvillesFinestCFF last night w/ Bird’s Fly South Ale Project and Woodside Bistro! We can't wait to see what this year’s group of emerging leaders do over the next few months as they take up the fight against CF!
#TeamMateTuesday...As a clinical trial volunteer, you can help us pave the way for new treatments. Learn more about what it means to be a trailblazer &
find a trial near you: https://t.co/xpK5Gj9NX0 #CFFtrailblazer
Did you know? In 2018, the Foundation enabled 64 multicenter clinical trials, more than doubling the number of trials from just six years ago. #CFresearch
Thanks for all of your help in making 2018 a year to remember! We look forward to continued success in 2019 towards our mission to cure cystic fibrosis and wish all of you a year filled with peace and happiness.
We’ll be sharing live updates 10/18 – 10/20 from the 32nd annual North American Cystic Fibrosis Conference! Follow #NACFC for all our coverage from the conference. #CFresearch
As a member of Community Voice, you can have an active say in programs and initiatives that affect everyone in the #cysticfibrosis community. Make your voice heard, and learn more about joining today! https://t.co/6e4GSSK0vT
Heading off to college? Check out 1️⃣0️⃣ tips from Ana Alford, an adult with #cysticfibroisis in her second year of law school, on finding balance while at school. https://t.co/RlctEnSOSg
Deciding to get a transplant can be one of the most difficult decisions for people living with #cysticfibrosis and their families. Register today to connect and learn from others who made the decision at CF MiniCon: Transplant. https://t.co/hQ3fgiZJJu