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The latest news and research from the world of cystic fibrosis, keeping you up-to-date and in the know.

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“We just want Oliver to know he's not the only one living with the condition”: Mum Zoe shares Oliver’s story

With your support this festive period, we can continue to fund research into life-changing treatments that work for everyone with cystic fibrosis (CF). Together, we can ensure children with CF like five-year-old Oliver can look forward to a brighter future.

“My mother petitioned for a menorah in Southend – and this year, we will be taking Baker to see it!” Mum Caroline shares Baker’s story and their festive plans

We spoke with Caroline, mum to 18-month-old Baker, who has CF, about his diagnosis, their plans for Hanukkah and Christmas, and her hopes for Baker’s future

New initiative to accelerate antimicrobial innovation

Innovate UK, LifeArc, and Medicines Discovery Catapult have come together to create Pathways to Antimicrobial Clinical Efficacy (PACE), a £30M initiative supporting early-stage innovation against antimicrobial resistance (AMR)

What’s happening in clinical trials: Kaftrio in children

We talk a lot about the difference Kaftrio has made to the lives of people with CF, but there is still a lot to understand about it as a treatment for younger age groups. Here we take a look at the latest results from clinical trials looking at Kaftrio in children, including new studies in children as young as 12 months.

Adam's story: "Kaftrio has been the most significant change of my life"

We sat down with Adam, a graphic designer who has CF, who spoke to us all about his fitness journey, the impact Kaftrio has had on his physical and mental health, and his plans for the future.

Cystic Fibrosis Trust help fund ENHANCE study to understand CF in young children

Cystic Fibrosis Trust is delighted to be contributing to the study in various ways, including, research funding through a Venture and Innovation Award and helping with the study design though our Involvement activities. When the study begins, it will also be listed on our Trials Tracker and be supported by UK CF Registry.

“I just want Orlaith and Elijah to know that they're here because of how much we loved them even before they were here” - mum Michaela shares her family’s journey with CF.

We spoke with Michaela, mum to twins Orlaith and Elijah who have CF, about her husband Chris’s diagnosis, the twins’ health, and her hopes for their future.

Inside the lab with CF researcher Laura

Every month, we’ll be chatting to some of the amazing people working in cystic fibrosis research. Today, we’d like to introduce Laura, who is based in Leeds. In this blog, Laura talked to us about her research into gut bacteria, diet and the gastrointestinal symptoms of CF.

Life with CF test 1

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