#CFTrust
Our CTAP posters are catching attention!

#ECFS #cysticfibrosis #cftrust
June 5, 2025 at 2:57 PM
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
July 9, 2025 at 12:13 PM
“Wearing Yellow on my way to work. Then into the habit” … it’s Wear Yellow Day raising awareness & research funds for @cftrust !

www.cysticfibrosis.org.uk/get-involved...
June 13, 2025 at 7:27 AM
Today is #WorldMicrobiomeDay!

We spoke to early career researchers Heritage and Lillie to find out more about the LUNG microbiome and why they’re studying it to improve treatments for CF lung infections.

➡️ https://ow.ly/nBox50ZhuyN

#PrecisionCF LifeArc #cysticfibrosis #cftrust
June 27, 2026 at 12:00 PM
We visited researchers from the Precision-CF team – part of our Translational Innovation Hub Network for CF Lung Health and Infection funded by the Trust and LifeArc.

Visit our website to find out more.

➡️ https://ow.ly/L1nX50Zja84

#cysticfibrosis #cftrust #researchwednesday
July 1, 2026 at 10:30 AM
Ellie Mindel & Tilly Green from @cftrust showed how their Youth Advisory Group (YAG) empowers young people with CF to shape research, create resources & balance fun with meaningful involvement.
How have you seen youth voice make a difference?
#CysticFibrosis #YouthVoice #MPWPractitionersCoP
November 19, 2025 at 12:17 PM
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
March 4, 2026 at 4:02 PM
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
June 6, 2025 at 10:39 AM
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
March 11, 2026 at 11:01 AM
Prof James Chalmers talks about bronchiectasis and a clinical trial he is leading called AIRTIVITY® that is looking at a new treatment, for people with or without CF.

Read our blog to find out more.

➡️ https://ow.ly/iqcP50YFwrw

#ResearchWednesday #CFTrust #CysticFibrosis #Bronchiectasis
April 8, 2026 at 10:01 AM
Rob entered the raffle last year because his three-year-old granddaughter, Sienna, lives with cystic fibrosis. He wanted to help fund the research and support that’s transforming the lives of families like his.

Buy your ticket today!

➡️ cysticfibrosis.org.uk/summerraffle

#cysticfibrosis #cftrust
July 23, 2026 at 8:00 AM
Today, the Government announced that health assessments for disability and sickness benefits will be audio recorded as standard to improve transparency in the benefit system.

Click the link to read the full statement.

➡️ https://ow.ly/xI1T50ZijSX

#cysticfibrosis #DisabilityBenefits #cftrust #PIP
June 29, 2026 at 5:20 PM
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
June 6, 2025 at 3:47 PM
#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
June 5, 2025 at 10:55 AM
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
September 3, 2025 at 6:51 AM
At the beginning of June, around 2,000 people working in CF gathered at the European CF Conference to hear updates, exchange ideas and make new partnerships.

Read our blog of some of our highlights from the meeting.

➡️ https://ow.ly/XMpZ50Zg9Vw

#ResearchWednesday #cysticfibrosis #cftrust #ECFS
June 24, 2026 at 1:01 PM
Delighted to see my friend Aram Kadoom win the Best Poster Award #ECFS2026 for his work on rapid saliva-based detection of P. aeruginosa using LAMP. A promising step towards faster, less invasive infection monitoring in CF. Congratulations to Aram and the team! #QUB #PULSE-CF #CFTrust #LifeArc
June 12, 2026 at 9:28 PM
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
October 2, 2025 at 1:44 PM
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
June 5, 2025 at 10:03 AM
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
February 16, 2026 at 12:55 PM
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
June 6, 2025 at 10:06 AM
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
March 10, 2026 at 11:01 AM
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
UK Cystic Fibrosis Conference
Find out more about Cystic Fibrosis Trust's UK Cystic Fibrosis Conference
www.cysticfibrosis.org.uk
December 3, 2025 at 10:42 AM
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
March 14, 2026 at 12:00 PM
Would love to hear how other people with #cysticfibrosisag/cysticfibrosis" class="hover:underline text-blue-600 dark:text-sky-400 no-card-link">#cysticfibrosis or parents of children with the condition are feeling about #COVID19 #coronavirus

Anyone else work in the health profession like me? @CFAware @cftrust @CF_Foundation #cfaware #cysticfibrosis #CF
December 1, 2024 at 12:02 PM