Monday, 29 April 2013

The patient perspective: Oli Rayner blogs about our new research strategy

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The CF Trust’s new research strategy is ambitious and exciting. I want to talk about three aspects which I think are particularly ...

Ed Owen live from our research and scientific conference

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Our science conference is underway It's an exciting moment for the Trust as we seek to exploit the extraordinary developm...
Friday, 26 April 2013

Sophie's Marathon story, are you inspired to run the VLM in 2014?

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Sophie Ormsby spoke about the emotion of running the London M arathon for her sister Emma, who has cystic fibrosis and raised ov...
3 comments:
Wednesday, 24 April 2013

Transforming research into cystic fibrosis, an exciting strategy

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Janet talks about exciting plans for research in cystic fibrosis. On April 29, the Cystic Fibrosis Trust will publish its ambiti...
Thursday, 28 March 2013

Berniece Phillips has cystic fibrosis and gives an insight into what cystic fibrosis means to her

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Berniece Phillips has cystic fibrosis and is one of the faces of Cystic Fibrosis Trust rebrand My name is Berniece Phillips, I...
6 comments:
Tuesday, 26 March 2013

Alex Stobbs explains why he supports the Cystic Fibrosis Trust and why he’s looking forward to the future.

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Hi, I'm Alex, I have cystic fibrosis and I turned 23 this year, you might remember me from the book about my life ‘A boy ...
Monday, 11 February 2013

Ed Nash-Steer's Marathon Challenge - blog three

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Ed Nash-Steer’s niece Hannah was diagnosed with cystic fibrosis four years ago, and seeing what people with CF go through everyday motivated...
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