Do you have a story about how antibiotics have made a difference in your lives or the lives of your loved ones? Your story and photo could be up in lights at #PiccadillyCircus in London during #WAAW25. Visit the Fleming Initiative to find out more. ➡️ www.fleminginitiative.org/thank-you-an...

Every time a #researcher applies to the Trust for money, or shares a report for a grant that is in progress, three or four other researchers working in a similar area review their applications or reports. It’s a process that is known as #peerreview. And it is all done on a voluntary basis. (1/3)

In 2017, we established the Clinical Trials Accelerator Platform to support the delivery of a wide range of CF clinical research studies across the UK. If you are curious to know more about how CTAP helps people to take part in research, check out our 2025 Impact Report. ➡️ ow.ly/yvZe50WU0Ox

Do you have questions about your career in research? Want tips and advice from others who work in this area? Why not sign up to attend the latest in our Coffee and Careers webinar series on Wednesday 10 September. ➡️ ow.ly/Zwze50WNHCp #cysticfibrosis #cftrust #researchwednesday #researcher

Our Coffee and Careers webinars are a chance to listen to conversations with researchers sharing tips, advice, and anecdotes about following a career in research. Join us on Wednesday 10 September for a conversation with Dr Guy Moss, Associate Professor in Neuroscience ➡️ ow.ly/b25w50WG1C8

Building effective research partnerships is vital to help us achieve a life unlimited for people with CF. This #ResearchWednesday we’re announcing a new partnership with The British Society for Research on Ageing @bsrageing.bsky.social

Want to find out what's new in #cysticfibrosis research? Join us and your peers at UK Cystic Fibrosis Conference in London on 1–2 October 2025. Our early bird rate ends soon, so make sure you book before 5pm on 31 July to secure your place! ➡️ www.cysticfibrosis.org.uk/about-us/con...

*Research opportunity* Are you an adult with cystic fibrosis who has had cancer? If so, please consider taking part in a research interview about your experiences of getting a cancer diagnosis and any cancer treatment that you had or are having. Thank you.

Over the next 5 years, our Translational Innovation Hub Network will address challenges around finding new lung infection treatment options, detecting and treating flare-ups, and developing new ways to diagnose infections. ➡️ cysticfibrosis.org.uk/innovation-hub-network #cysticfibrosis #cftrust

"I’m not thinking about where I could be limited by CF. For the first time, challenges are logistical, rather than health-based." We spoke to Declan about running an ultra-marathon, being a science teacher, and changes in his life since taking Kaftrio. ➡️ ow.ly/VshL50WfWf3 #cysticfibrosis #cftrust

Through our #worlkforwards programme, we want to empower everyone with #cysticfibrosis to live without limits by supporting the #CFcommunity with your career goals and aspirations. What do you wish your employer knew about CF? Drop your thoughts in the comments! ➡️ ow.ly/GscB50Wf5pw #cftrust

SAVE THE DATE: UK CF Conference 2025 is back this October! Join us for a two day hybrid event of cutting-edge updates on CF research, clinical trials, and insights from the UK CF Registry. Registration now open! ➡️ www.cysticfibrosis.org.uk/about-us/con...

Our project director Jo Fothergill, and co-investigator Philip Mitchelmore, will be taking part in the upcoming @cysticfibrosis.org.uk CF LIVE event about phage on Wednesday 25th June at 7pm. Find out more and register to attend here: www.cysticfibrosis.org.uk/about-us/con...

Today is wear yellow for CF (Cystic Fibrosis) day! Here we have some of our team ( and doggo's) wearing yellow in support of students who are in our schools at CCHS.  #CysticFibrosis #EduSky #disability #AcademicSky #EduSkyUK  @chelseacommunityhospitalschool @cftrustuk

Trailfinder-CF partner, Alder Hey Children's Hospital supporting Wear Yellow Day as part of Cystic Fibrosis week #alderhey #cysticfibrosistrust

🗣️ #cysticfibrosis AWARENESS WEEK 🗣️ Pls RT! 🔀 Happy Wear Yellow for Cystic Fibrosis Day! 💛 @cysticfibrosis.org.uk website: www.cysticfibrosis.org.uk #cfweek

And that's day 19 with a little helper today (Henry) who did keep correcting me on my dance moves 🤣 Wear Yellow Day tomorrow for #cysticfibrosis led by the @cysticfibrosis.org.uk Yes I have done my leg in, but determined to finish what I started! www.justgiving.com/crowdfunding...

Our team in Milan have been busy with symposiums, workshops, and plenty of conversations on day 1 of #ECFS Read on for some of the key takeaways #cysticfibrosis #cftrust

Our CTAP posters are catching attention! #ECFS #cysticfibrosis #cftrust

#ECFS has well and truly started with three 'Meet the Experts' sessions: 🔵 Lessons learned from real-world studies. 🔵 Menopause – understanding and supporting women. 🔵 Lung transplant – indications and management. Follow this thread for more #cysticfibrosis #cftrust #menopause #transplant

If you are an innovator, our support can accelerate the design and delivery of your clinical trials. We’ll be at European CF Society Conference this week, so please come and find us to talk about our research support offer. Follow us for our #ECFS daily updates! #cysticfibrosis #cftrust

Are you looking for a rewarding new role, where you can work hard, have fun and really see the impact of your work? We're recruiting for the following vacancies: ⭐ Head of Policy and Public Affairs ⭐ Senior Events Development Manager (Mat Cover) Find out more on our website! ow.ly/iNFM50W1vsg

Content warning: this story discusses the topics of loss and grief. “We are keeping his memory alive” We spoke to Mitchell about his brother Jordan, and about Team J, a charity football team keeping Jordan's memory alive and raising money for the Trust. Read their story 👉 bit.ly/43tHUfv

This year, at a @smclondon.bsky.social briefing, Dr @freddy-frost.bsky.social said "It’s great news that people with CF are living longer, but ageing is now a top priority” bit.ly/4jgRgkO You can now read about this in more detail in the latest European Respiratory Review bit.ly/4jcy47I

Hi! 👋🏻 We’re Cystic Fibrosis Trust, working to make sure everyone with CF can live a life unlimited. We're new to Bluesky but you can expect stories, updates and ways to get involved 💛 To find out more head to our website or feel free to say hi! ➡️ www.cysticfibrosis.org.uk