On 29 April 2013, we launched an ambitious research strategy,“Investing in research to change lives”, in which we set out a roadmap for the Trust to deliver high quality research that will make a difference to people with cystic fibrosis.
One of the critical components of this new strategy is the formation of Strategic Research Centres/Virtual Centres of Excellence. Through these centres, researchers are encouraged to work together to tackle major research questions in cystic fibrosis. Scientists were asked to bring together the best team of scientific experts, wherever they are based, to form a cohesive group intent on using research to solve problems for cystic fibrosis. Members of these teams form the virtual centre, which can be truly international because, although led from the UK, team members can be recruited to the virtual centre from anywhere in the world. For the first time the Trust will be funding scientists in other countries. These Strategic Research Centres were deliberately set up to provide funding for five–six young career scientists who will work alongside these experts. Our aim is to attract the brightest and best young scientists into problem-solving research within the best teams; helping to shape the next generation of leading researchers for cystic fibrosis. Experience shows that investment in these individuals at this stage of their careers results in a long-lasting interest.
I am delighted to say that the first round of Strategic
Research Centres has now been completed.
Although this may seem slow, it has in fact been achieved in record time!
Following the strategy publication, we invited applications from the research
community and then established an independent peer-review process to select
those that best fit the overall aims of the Trust for Strategic Research
Centres. A number of very high quality applications were received at all stages
of the process. In the end, there were three outstanding applications but funds
were only available to support two. It was very difficult to select which would
be funded but after long, detailed and careful consideration, the two have been selected. Both consortia are led by
international experts based in the UK but have created teams that bring
together international experts to work together to find solutions for people
with cystic fibrosis. This is the first time the Cystic Fibrosis Trust has led
such an initiative and has funded research beyond the UK.
As a sign of gratitude for how my son was saved from cystic fibrosis , i decided to reach out to those still suffering from this.
ReplyDeleteMy son suffered cystic fibrosis in the year 2013 and it was really tough and heartbreaking for me because he was my all and the symptoms were terrible, he always have shortness of breath , and he always complain of burning in the chest . we tried various therapies prescribed by our neurologist but none could cure him. I searched for a cure and i saw a testimony by someone who was cured and so many other with similar body problem, and he left the contact of the doctor who had the cure to cystic fibrosis. I never imagined cystic fibrosis has a natural cure not until i contacted him and he assured me my son will be fine. I got the herbal medication he recommended and my son used it and in one months time he was fully okay even up till this moment he is so full of life.cystic fibrosis has a cure and it is a herbal cure contact the doctor for more info on drwilliams098675@gmail.com on how to get the medication. Thanks for reading my testimony.