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cysticfibrosis.org.uk
@cysticfibrosis.org.ukThe #cysticfibrosis EYIM is a unique opportunity to network with CF researchers across Europe, hear from mentors, share your work and make career-long new connections.
Apply by submitting an abstract by 11pm GMT on Sunday 25 October.
Click the link to find out more.
@cysticfibrosis.org.ukWe’re funding early career researcher James Charlick to study how the CF protein works at a microscopic level. Understanding tiny details about faults in this protein can help researchers design more effective medicines for CF and make them available to a wider group.
@cysticfibrosis.org.ukOver the past two years, the Translational Innovation Hub Network for CF Lung Health and Infection has brought together researchers, clinicians, people with #cysticfibrosis and partners across the UK and beyond to make real progress against CF lung infections.
➡️ www.cysticfibrosis.org.uk/network
@cysticfibrosis.org.ukA new study is looking at an alternative pancreatic enzyme replacement therapy.
ANG003 is a new enzyme therapy being studied that is made using highly purified enzymes produced by microorganisms.
@cysticfibrosis.org.ukTo mark Organ Donation week, we’re pleased to share the UK CFMA and ALTP care recommendations for people with cystic fibrosis following a lung transplant, developed with involvement from people with CF who have had a transplant.
@cysticfibrosis.org.ukSince launching our Clinical Trials Accelerator Platform, we’ve now supported more than 10,000 screenings onto a CF study.
With more people being screened, we’ve been able to support a huge range of research to take place in the UK.
Click the link to find out more.
@cysticfibrosis.org.ukThank you to all those researchers, doctors, statisticians and members of the CF community who have helped us ensure that our research studies are of the highest standard.
Thank you all so much for helping us on our way towards achieving a life without limits for everyone with #cysticfibrosis
@lifearc.bsky.socialReposted by @cysticfibrosis.org.ukWhy choose a career in cystic fibrosis research?
4 researchers from across the CF Lung Health Network share what motivates them and the difference they hope to make for people living with CF.
@lukeallsopp.bsky.socialReposted by @cysticfibrosis.org.ukDiscussing my passion and career in #STEM + #infection in the #ScientistsMakingaDifference book. I work on the bacterium #pseudomonas that’s particularly common in people with #CF #Youngscientists
@cysticfibrosis.org.uk @lifearc.bsky.social @imperialnhli.bsky.social @imperialcollegeldn.bsky.social
@cysticfibrosis.org.ukDarren Sills, a CF dietitian and researcher, is leading the GRAMPUS-CF study, part of a wider, Trust-funded research programme of the same name. Find out more about the GRAMPUS-CF study on our Trials Tracker.
@cysticfibrosis.org.ukWe are working in partnership with #RNID, to ensure that people with serious infections – including those living with #cysticfibrosis – can receive life-saving treatment without losing their hearing.
