Wear Yellow Day is happening tomorrow (17 June) – and we’re so grateful to everybody who is getting involved. However you choose to fundraise, all the money raised will help make a big difference to those living with CF in the UK. Here’s how…
We know that the rising cost of living and the financial burden of living with a life-long condition is a worry for many people in the CF community. This CF Week, we're #liftingthelimits, so everyone can access the support they need.
Here, Sangeeta and Nicky from our Welfare team share their top tips to help the community cope with the increased cost of living. If you would like to talk things through, please get in touch with our Helpline, seek advice locally or speak to your CF team.
A new YouGov poll shows that the majority of people (84%) don’t know that those with cystic fibrosis (CF) are advised not to meet in person, in case they pass on deadly bugs to one another.
Over the course of this year’s CF Week - taking place from 13 to 19 June - we will be sharing stories from across the CF community about life with CF. Gillian, 36, from Glasgow had made the decision not to have children – until a ‘super response’ to Kaftrio changed everything.
Nearly half (47%) of children, and 11% of adults with cystic fibrosis have reported being unable to access a social worker. Cystic Fibrosis Trust calls on the Government to ensure everyone with CF has access to a CF social worker in light of the ‘concerning’ NHS staff shortages.