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We’re highlighting how people with CF and their loved ones are shaping the direction of the CF Lung Health Network, co-funded by #CFTrust and LifeArc.

Rebecca shares her passion for ensuring the views of people with CF are incorporated into research studies.

➡️ https://ow.ly/YJJG50YtrqG

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This week we’re highlighting how people with CF and their loved ones are shaping the direction of the CF Lung Health Network, co-funded by #CFTrust and LifeArc.

➡️ https://ow.ly/NqBi50YseGq

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We are looking for someone to join our Trustee Board as our new Treasurer, overseeing the financial affairs of the charity and ensuring that they are conducted legally, transparently, and in line with the charity’s governing document.

➡️ https://ow.ly/qPLb50YrGe4

#cysticfibrosis #cftrust

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This week we’ve been visiting researchers within our Translational Innovation Hub Network for CF Lung Health and Infection funded by the Trust and LifeArc.

Find out more about our Trailfinder-CF and Pulse-CF Innovation hubs on our website.

➡️ https://ow.ly/iERe50Yp1g7

#cysticfibrosis #cftrust

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We’re currently recruiting for two roles in our Fundraising team!

⭐ Trusts Fundraising Manager

⭐ Senior Philanthropy Manager – Major Donors (12 months FTC)

🗓️ Closes midnight on 22 February.

➡️ https://ow.ly/32v750XSo7E

#cftrust #CharityJobs #cysticfibrosis

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Development Award: Investigating the cardiovascular health in people with CF (ITCH-CF) Dr Freddy Frost from University of Liverpool is leading a research programme to understand more about cardiovascular disease in people with CF as they get older.

Click on the link to find out more about research underway in this area.

➡️ ow.ly/Mr5S50Y8FKk

#cysticfibrosis #CVD #cftrust #cardiovasculardisease #heartdisease

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Upper Logo: Cystic Fibrosis Trust

Text: The Airtivity Study: investigating a new anti-inflammatory medicine in people with bronchiectasis.

Arrow: find out more on our Trials Tracker

Upper Logo: Cystic Fibrosis Trust Text: The Airtivity Study: investigating a new anti-inflammatory medicine in people with bronchiectasis. Arrow: find out more on our Trials Tracker

Head to our Trials Tracker to find out more. (4/4)

➡️ cysticfibrosis.org.uk/trialstracker

#cysticfibrosis #cftrust #clinicaltrials #researchwednesday

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UK Cystic Fibrosis Conference Find out more about Cystic Fibrosis Trust's UK Cystic Fibrosis Conference

All the recordings from the UK CF Conference are available now! Catch up on our website or YouTube channel. 2/2

www.cysticfibrosis.org.uk/about-us/con...

#cysticfibrosis #cftrust #ukcfc #researchwednesday

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This week we’re shining a spotlight on some of the additional symptoms and complications of CF outside of the lungs, from gut symptoms and diabetes to fertility and bone health.

➡️ ow.ly/HW7g50XlCJQ

#cysticfibrosis #cftrust #notjustlungs

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Trailfinder CF Director Professor Jo Fothergill, presented the work we are undertaking at the annual UK Cystic Fibrosis Trust meeting in London. Several of our ECRs are also in attendance. #cysticfibrosis #cftrust

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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.

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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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

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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

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Probably the greatest charity plant stall in the world #cftrust #cysticfibrosis

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"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

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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

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Dan wearing a yellow jumper.

Dan wearing a yellow jumper.

Dan’s poster and impact statement for his PhD research, developing a toolkit to support the communication of lung magnetic resonance imaging results in cystic fibrosis.

Dan’s poster and impact statement for his PhD research, developing a toolkit to support the communication of lung magnetic resonance imaging results in cystic fibrosis.

Dan’s certificate for winning the Judges Choice award for his presentation.

Dan’s certificate for winning the Judges Choice award for his presentation.

Very pleased to have won the Judges Choice award at the School of Medicine Research Impact Forum today for my presentation on my PhD research! Of course it’s also #WearYellowDay so I was dressed accordingly!

#CysticFibrosis #MRI #CFweek #CFTrust #PhD

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Great to catch up with colleagues from CF AMR syndicate at their poster at #ECFS today.

Colin from LifeArc and Lesley from Medicines Discovery Catapult were sharing information about a programme accelerating the development of new treatments for CF lung infections. #cysticfibrosis #cftrust

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Ellie Mindel, Lead for Children and Young People,
presented our new resource for children affected by #cysticfibrosis during one of the workshops.

"Cracking the CF Code" was written by young people in our Youth Advisory Group. Find out more on our website.

➡️ ow.ly/2g3a50W5ni7

#ECFS #CFTrust

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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

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Our CTAP posters are catching attention!

#ECFS #cysticfibrosis #cftrust

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#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

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It was a packed room for the opening plenary of #ECFS last night! The attendees were treated to some opera arias to kick off the conference. #cysticfibrosis #cftrust

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Light blue background with a yellow logo for Cystic Fibrosis Trust at the top left. At the bottom there are photos of four people on a dark blue circle background, their names are Claire, Sarah, Becca, and Deb. Above their photos, text says "Going to ECFS? Chat to us about our research offer!)

Light blue background with a yellow logo for Cystic Fibrosis Trust at the top left. At the bottom there are photos of four people on a dark blue circle background, their names are Claire, Sarah, Becca, and Deb. Above their photos, text says "Going to ECFS? Chat to us about our research offer!)

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

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Little brother helping raise money for our CF Trust skydive #cfaware #cftrust #skydive

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