Cystic Fibrosis Trust
@cysticfibrosis.org.uk
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We're dedicated to uniting for a life unlimited for those living with cystic fibrosis. Our social & Helpline teams monitor our accounts between 9-5 weekdays. cysticfibrosis.org.uk
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cysticfibrosis.org.uk
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
Cystic Fibrosis Trust Homepage | CF Trust
www.cysticfibrosis.org.uk
cysticfibrosis.org.uk
Last week saw scientists and clinicians come together for #UKCFC, the UK's biggest conference dedicated to CF research, from biomedical science to improving clinical care. 🔬

It was inspiring to see the research community uniting to bring us closer to a life unlimited for everyone with CF. 💛
cysticfibrosis.org.uk
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 currently recruiting for a new vacancy on a part time basis:

⭐ Information Officer

➡️ https://ow.ly/iNFM50W1vsg
cysticfibrosis.org.uk
"Even with the huge advancements in recent decades with Kaftrio, it is reassuring to know that researchers are not stopping; if anything, they're pushing on faster and with more determination."

Lucy Baxter shares some of her key takeaways from day 1 of #UKCFC.

➡️ https://ow.ly/xRGI50X5KLS
cysticfibrosis.org.uk
Thank you for joining us at UKCFC Peter!
cysticfibrosis.org.uk
Dr Jamie Duckers shares his insights from day 1 of #UKCFC! We’ll be back here and over on our Instagram stories tomorrow to cover day 2! 🔬
#cysticfibrosis
cysticfibrosis.org.uk
An insight from Professor Daniel Peckham on conference highlights so far! #UKCFC #cysticfibrosis
cysticfibrosis.org.uk
"There's a clear call for CF-specific pregnancy guidance."

Dr Imogen Felton delivers a powerful presentation on the Matriarch study, which is answering questions on pregnancy, maternal and infant health for people with CF.

You can hear more in our CForYourself podcast episode on pregnancy and CF
cysticfibrosis.org.uk
PhD student Jonathan, a researcher at our MAGNIFY Strategic Research Centre with his poster at #UKCFC, exploring the use of lung MRI in the management and monitoring of CF
cysticfibrosis.org.uk
This morning we caught up with Lorna Allen, our Community Involvement and Engagement Manager, to find out about some of the research she’s most excited to hear about at #UKCFC this year!
Reposted by Cystic Fibrosis Trust
alexhorsley.bsky.social
Great opening talk by Prof Gwyneth Davies of GOSH at #UKCFC highlighting the research goals and challenges for CF
cysticfibrosis.org.uk
Welcome to day 1 of UKCFC 2025! 🔬

We have kicked off this year's conference with a Welcome an Introduction from conference chair, Dr Gwyneth Davies.

If you're attending in person or online, we'd love to hear from you!

Tag us in your stories on Instagram or here on Bluesky!

cysticfibrosis.org.uk
Today marks the one year anniversary of our CF Lung Health Network 🎉

Find out more about this area of research on our website now!

➡️ https://ow.ly/zlz250X4nka
cysticfibrosis.org.uk
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...
cysticfibrosis.org.uk
Together we’re moving closer to achieving a life unlimited for people with CF. 💛

Click the link to find out more about our research funding process.

➡️ www.cysticfibrosis.org.uk/research/sup...

#peerreviewweek #prw2025 #cftrust #cysticfibrosis

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Our funding process and governance - Cystic Fibrosis Trust
Information on our funding process and governance for applications for research funding from the Cystic Fibrosis Trust.
www.cysticfibrosis.org.uk
cysticfibrosis.org.uk
This week is #peerreviewweek – a good time to say a HUGE thank you to all of the #researchers who have kindly given up their time and shared their expertise with us. There were over 50 in the last year alone!

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Our funding process and governance - Cystic Fibrosis Trust
Information on our funding process and governance for applications for research funding from the Cystic Fibrosis Trust.
www.cysticfibrosis.org.uk
cysticfibrosis.org.uk
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.

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cysticfibrosis.org.uk
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
cysticfibrosis.org.uk
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
cysticfibrosis.org.uk
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
cysticfibrosis.org.uk
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
A quote from Claire Walter, Patient and Public Involvement and Engagement Partnership Manager at Cystic Fibrosis Trust: "We’re delighted to have formed a new partnership with The British Society for Research on Ageing. Research into growing older and ageing with CF is a top research priority for people living with CF and we’re keen to work with other organisations to help us address it."
cysticfibrosis.org.uk
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...
Reposted by Cystic Fibrosis Trust
rebecca-spencer.bsky.social
*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.
cysticfibrosis.org.uk
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
cysticfibrosis.org.uk
"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