As part of our 60th anniversary awards, we would love for you to put a nomination in to celebrate our wonderful researchers – it might be an inspirational student, mentor, peer or team-mate.

The categories are Clinical Research and Basic Science.

➡️ cysticfibrosis.org.uk/get-involved/s…

Loads of fun online events are happening over at CF Trust Youth this summer! 🎮

Check out our calendar of one-off workshops for children aged 6-14 with #cysticfibrosis (siblings are also welcome to sign-up!)

Email [email protected] to find out more.

Heading into further or higher education this year? Apply now for the Joseph Levy Education Fund, providing grants to support people with CF in their studies. 🎓
Apply by 31 May.

➡️ ow.ly/gEpl50Rv0i5

Our free body image booklet explores body image issues people with CF have told us they can struggle with, and provides support and advice for dealing with these issues. It also explores some of the positive aspects of body image and cystic fibrosis.

ow.ly/5RcH50RuPEW

Join us for this online session to develop your business planning skills and get access to helpful advice, tips and resources (and a head-start in planning your Helen Barrett Bright Ideas Award application!)

➡️ ow.ly/9Xm850RuthN

#cysticfibrosis #cfnews #workforwards

In our latest ‘inside the lab’ researcher profile, we caught up with PhD student Charlotte about her CF research and her recent experiences at a CF research conference.

➡️ ow.ly/ZQs650Rto9Z

#ResearchWednesday #CFNews #InsideTheLab #PhDStudent

Today our Head of Policy and Public Affairs, Ben Kind, has responded to reported PIP changes with the following statement.

Congratulations Joshua! It was a pleasure to supervise this project supported by funding from Cystic Fibrosis Trust. A well deserved award from @RoyalSocBio

London Marathon 2024 ⭐

Thank you to the runners, the supporters, the cheerers, to everyone who united with us for a life unlimited at this year's London Marathon! You have so far raised over £400,000 for #TeamCF ! 💛🏅✨

If you're a young person with CF you may have talked about moving from paediatric to adult care. 'Transition' is the medical term for this move and we want you to feel listened to and empowered.

Visit our website to download the resources.

🔗 ow.ly/2Zzf50RnEhj

Has your partner taken part in a clinical trial? We want to understand the positives and challenges of supporting a partner during a trial so we can help others to know what to expect.

If you’d be happy to share your experiences, please email [email protected].

Great to be working alongside Lucy Allen Cystic Fibrosis Trust and LifeArc at #LATSS2024 to promote cross sector collaboration and partnership. Very inspirational.

London Marathon was only the start for Sophie, today she is running her 3rd of 36 marathons in 36 days! 💛

Find out more ➡️ bit.ly/44eaVfb

Did you know we have set up a dedicated area for people in or about to go through the transplant journey?

Our online community is a safe, welcoming space to ask questions, share experiences and support each other. Join today by visiting our website.

➡️ forum.cysticfibrosis.org.uk

Absolutely incredible! Well done to everyone involved and thank you for your support! 💛

On Thursday this week, our research team have a stand at the ABPI conference.

Please come along and say hello to find out how we can support your research and move your projects closer to the clinic #ABPIconf24

Good luck for tomorrow to all of our London Marathon runners!! Our staff teams are excited to cheer you on today! #TeamCF

🏃‍♀️ If you're itching to get your running shoes on for next year's marathon, the 2025 London Marathon ballot is now open!

➡️ ow.ly/nCxW50Rh1By

Thank you Peter for looking after us this morning on our CrossCountry Trains train to Manchester. We start our 54 mile walk for Cystic Fibrosis Trust at 12!

Yabadabadoooooo! 🦕

justgiving.com/page/stephsfoo…

Good to see an article about the Right To Breathe campaign with Vertex Save Us co-founder Gayle Pledger in Cystic Fibrosis Trust magazine #CFLife

Fascinating read about how a grass roots organisation is making change happen for CF patients around the world

Read here:
cysticfibrosis.org.uk/the-work-we-do…

Ahead of the London Marathon this weekend, we chatted to #TeamCF runner Tom to hear all about his reasons for running, inspiring others, and what a life unlimited means to him.

🏃 Go Tom!

➡️ cysticfibrosis.org.uk/news/i-want-to…

#LondonMarathon2024 #CysticFibrosis #CFNews #MentalHealth