The CF Trust Blog
Tuesday, 16 February 2016

Wind, wind and more wind

›
Last week in Oxford, the Cystic Fibrosis Trust brought together  gastrointestinal  (GI) health experts from across Europe to look at the di...
145 comments:
Friday, 5 February 2016

Stopping the Clock - You Voice Matters

›
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

›
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

›
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

›
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?

›
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…

›
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:
›
Home
View web version

Contributors

  • CF Trust
  • Cystic Fibrosis Trust
Powered by Blogger.