Following her grandson Jace’s cystic fibrosis (CF) diagnosis earlier this year, our supporter Charlotte, who works in recruitment, has been motivated to raise awareness of the condition and the importance of supportive employment for the CF community. Here she shares her family’s CF story.
Tes Hodson, who has worked in CF specialist services since 2003, is finally getting some well-deserved R&R – so we sat down with her to talk about the highlights and changes she’s seen over two decades of CF care
Today we’re launching a revised grants programme, to help make sure everyone with cystic fibrosis (CF) has the support they need to deal with the financial pressures that living with the condition can bring. Becky Kilgariff, Head of Information and Support at the Trust, writes about some of the changes we’ve made and how the programme will meet the needs of those who need our support the most in these challenging times.
The Trust’s Clinical Trials Accelerator Platform (CTAP) has received £5.2 million of funding from the USA’s Cystic Fibrosis Foundation to expand access to clinical trials and accelerate the development of new treatments as we unite for a life unlimited, for everyone with cystic fibrosis.
We work hard to ensure that everything we do makes the biggest difference possible to people with cystic fibrosis (CF) and their families. Find out more about the work of Cystic Fibrosis Trust today.
