CF Foundation Carolinas Central/Eastern Chapter of the CF Foundation. Proudly serving Eastern and Coastal North Carolina. #CysticFibrosis#CureFound#FightCF
Positive clinical trends seen in the 2020 and 2021 CF Foundation Patient Registry were sustained in 2022, with continued improvement in lung function. Lung function is a primary indicator of health for people with cystic fibrosis. Read more highlights: https://t.co/IUt2p6riQE
You can make a difference for the CF community today. Join our Online Day of Action and tell your member of Congress to support the PASTEUR and HELP Copays Acts. #CFAdvocacy https://t.co/1vmhdNHOPf
An increasing number of health plans don’t count copay coupons or manufacturer assistance cards toward a patient’s out-of-pocket costs, leaving patients on the hook. Help elevate this issue and ask your legislators to support the HELP Copays Act. https://t.co/1vmhdNHOPf
Nicole Kohr, an adult with cystic fibrosis, realized she's always had the power to advocate. Using her strength of storytelling to advocate for the CF community showed Nicole that a good advocate is someone who is authentically themselves. #CFAdvocacy https://t.co/6ukta1f1mE
Teens from across the country are joining us for our 15th annual Teen Advocacy Day! Help to amplify their impact by urging your members of Congress to support the #PASTEUR Act and the HELP Copays Act. #CFAdvocacy https://t.co/1vmhdNHOPf
More than 2.8 million people get an antibiotic-resistant infection in the U.S. each year. People with #cysticfibrosis face an increased risk for difficult-to-treat infections. We need new antibiotics now, and we’re asking Congress to help. #CFAdvocacy
Add your voice to the thousands of volunteers who are urging their members of Congress to support legislation critical to the #cysticfibrosis community today.
Take action with us: https://t.co/5x1UZT97UV
What’s a sweat test? It’s considered the most reliable for diagnosing #cysticfibrosis. The test is painless and it measures the concentration of salt in your or your baby’s sweat. https://t.co/1qp1E0UwZH
Hear the perspective of four adult cystic fibrosis community members as they share their experiences with chronic illness and how life with CF is evolving.
This event will be hosted virtually.
Register now at https://t.co/LWKyGcQlJS
Hear the perspective of four adult cystic fibrosis community members as they share their experiences with chronic illness and how life with CF is evolving. This event will be hosted virtually.
Register now and the Zoom link will be emailed.
https://t.co/xJpDLVKe3h
“Knowing that everyone here has gone above and beyond to contribute to this dream of a cure inspires me to do more. Learning about the advancements in science tells me that we’re on the right path and that we’re going to get there.” – Ray Poole #CFFVLC
“We are not done – and will not be done – until every person with cystic fibrosis has a treatment and a cure so they can live their dream. To be able to say YES to the experiences they want to based on their heart — not what CF limits them to do.” – Julie Riedy #CFFVLC
We’re live from #CFFVLC 2022! At our 18th annual conference, we’re excited to hear from volunteers, such as event co-chairs Ray Poole and Julie Riedy, in addition to Foundation leadership including Michael Boyle, MD, Steven Rowe, MD, and more.
When your prescription isn’t covered by your insurance, be sure to ask if it can be covered under the medical portion of your plan benefits, or if there are any alternatives that your plan will cover.
When your prescription isn’t covered by your insurance, be sure to ask if it can be covered under the medical portion of your plan benefits, or if there are any alternatives that your plan will cover. https://t.co/TcfXGdFn11