Tuesday 16 February 2016
Wind, wind and more wind
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Last week in Oxford, the Cystic Fibrosis Trust brought together gastrointestinal (GI) health experts from across Europe to look at the di...
141 comments:
Friday 5 February 2016
Stopping the Clock - You Voice Matters
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With the ongoing success of our Stopping the Clock petition on availability of precision medicines for cystic fibrosis , our Chief Execut...
41 comments:
Friday 29 January 2016
More Than Lungs - Digestion & CF
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On 8–9 February, the Trust will be hosting a research ‘sandpit’ exploring issues related to digestion in cystic fibrosis, a meeting bringin...
29 comments:
Monday 4 January 2016
A 2016 Unlimited
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The New Year is here! We're ready and raring to go in our fight for a life unlimited for everyone affected by cystic fibrosis! Our ...
196 comments:
Sunday 6 December 2015
Reaching Out From Parliament - Getting CF Heard
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The Cystic Fibrosis Trust has been working closely with the Outreach team in the UK Parliament to look at how we can continue to ensure cys...
16 comments:
Thursday 12 November 2015
Precision Medicines - Why?
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Precision medicine is the talk of today, with a cancer drugs fund for Wales in the news and our own 'Stopping The Clock' campaign ...
38 comments:
Monday 9 November 2015
Gene editing: a therapy with masses of potential, but not only in treating cancer…
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Last week gene editing hit the news with the story of young leukaemia patient Layla and a pioneering treatment at Great Ormond Street. Here ...
18 comments:
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