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A community for Cystic Fibrosis by people with Cystic Fibrosis. Join our server: https://xitter.cf/t.co/mexqvRdQyI

Joined March 2017
Photo by CF Discord (@CFDiscord)Photo by CF Discord (@CFDiscord)Photo by CF Discord (@CFDiscord)Photo by CF Discord (@CFDiscord)Photo by CF Discord (@CFDiscord)Photo by CF Discord (@CFDiscord)Photo by CF Discord (@CFDiscord)Photo by CF Discord (@CFDiscord)Photo by CF Discord (@CFDiscord)
☀️Make sure you keep your Hypo treatment close! @CFAware @bda_cf @CF_physios #CF #CFRD #CFdiabetes
Love or hate the hot weather 🥵 for some it can lead to more hypos ⚠️ keep a close eye on your glucose levels, adjust insulin doses if needed, keep hypo treatment with you and act on hypo symptoms quickly. Oh and don't forget suncream 👍 @CUH_dietitians @CambsDiabetes @CUH_NHS
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On 13 July we're running an #AmongUs #GamesNight for young people with #cysticfibrosis ages 12-18 & siblings! Email cfyouth@cysticfibrosis.org.uk to find out more or to sign up! Big ups @NormalLife7 for your continued support! *LIMITED SPACES - FIRST COME FIRST SERVE!!*
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CF Discord retweeted
New rapid test can identify dangerous infections in cystic fibrosis patients in minutes £paywall telegraph.co.uk/news/2022/06…
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CF Discord retweeted
UK Based CFers wanted for a survey on Medication adherence and mental wellbeing! Fill the survey in now: blss.eu.qualtrics.com/jfe/fo…
An excellent review from the University of Torino on "CFTR Modulator Therapy for Rare CFTR Mutants" 📜mdpi.com/2673-527X/2/2/5 #cysticfibrosisnewstoday #cysticfibrosis #CFnews #CF #treatingCF #CFTRModulator @CFNewsToday @CFAware @CFAwareness @CFawarenesss @KnowCF @unito
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YOOO YOUNG PEEPS! Check out our Spring calendar of events for children and young people with #cysticfibrosis ages 6-16! Email cfyouth@cysticfibrosis.org.uk for more info or to sign up. Siblings welcome!
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Developing genetic therapies will take a long time and a lot of collaboration. Following plenary two of #NACFC, Art Brace, a scientist and adult with CF, shares the key moments that resonated with him from each of the presentations. on.cff.org/3mHG2M6
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Ready for #NACFC 2021? Follow our Twitter list to virtually connect with others in the cystic fibrosis community who are attending the conference. on.cff.org/3bvN2p3
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**DEADLINE TO APPLY SUNDAY 26TH SEPTEMBER!!!!** Applications are open for this year’s Helen Barrett Bright Ideas Awards, which support people with #cysticfibrosis ages 18+ to develop their business ideas and make self-employment a reality. cysticfibrosis.org.uk/the-wo…
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CREW MATES, LISTEN UP! On 23rd September from 6pm we're running #AmongUs #GamesNight for children with #cysticfibrosis ages 8-16 and their siblings! Email cfyouth@cysticfibrosis.org.uk to find out more or to sign up! ***LIMITED SPACES - FIRST COME FIRST SERVE!!***
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If you're a young person who lives with #cysticfibrosis, we would love to hear from you, whatever your idea! Get in touch at cfyouth@cysticfibrosis.org.uk, or just send a message to our Instagram! instagram.com/cftrustyouth/ Looking forward to seeing what you come up with 🤩😃💛💫
Wishing everyone in the #cysticfibrosis community a great week ahead!
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CF Discord retweeted
Make sure you join our forum using @discordapp ! Get the chance to talk directly with other people with Cystic Fibrosis! Click this link: join.cfdiscord.com/ to get started! #cysticfibrosis #cf
Are you an online shopper? For any of your online shopping, make sure you use Amazon Smile. You can help support us with your Amazon purchases and make a real difference to people with #cysticfibrosis. Just shop through smile.amazon.co.uk and choose Cystic Fibrosis Trust.
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"COVID-19 has brought so many changes for all of us, and physiotherapists are no exception to this". Tracey Daniels a York based CF physiotherapist spoke to us about how they have adapted to help people with #cysticfibrosis, like Oliver, from home: bit.ly/397z36L
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**THURSDAY 23rd JULY, 6PM** #MovieNight for young people with #cysticfibrosis is back! If you're ages 8-14, have #CF or are a #CF sibling, you can sign up to our #NetflixParty, by emailing cfyouth@cysticfibrosis.org.uk We're watching Hotel Transylvania youtube.com/watch?v=q4RK3jY7…
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We are incredibly proud to have worked alongside the #cysticfibrosis community in the long campaign for life-saving medicines. The four-year battle to secure access to Orkambi was a critical step and remains the only medicine suitable for many children. (1/2)
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Who's ready for @Charles_MDuke 24-hour stream on Sunday? Hear him chat about #cysticfibrosis, how #lockdown has been and what he's going to be up to this weekend! If you want to learn more about how you can get involved with #CFNextLevel click here: ow.ly/dMDG50AoM3q
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NHS patients with cystic fibrosis will be among the first in Europe to benefit from the new triple therapy for the condition following a landmark deal, NHS Chief Executive Simon Stevens has announced today.
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Meagan Tenyer, an adult with #cysticfibrosis, shares why she refuses to let her lung function stop her from having a completely full, happy life. on.cff.org/3dpl10X
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