Today, we are talking about how people with cystic fibrosis (CF) and their families have been balancing their condition during the coronavirus pandemic (COVID-19). In this blog, Sophie tells us about the lifestyle that she and her husband have adopted to support their son’s health, and the challenges they’ve faced while shielding as a family.
Each day during CF Week, we’ll be sharing stories from the cystic fibrosis (CF) community about how they balance the challenges of CF with everyday life. In the first of these, Derek talks about getting a CF diagnosis at 30, acceptance and living life your way.
Over the past few days we have heard the ups and downs of balancing cystic fibrosis (CF) and, in each, a strength and determination has shone through. Today, 23-year old Demi from Worcestershire shares how she went from growing up hiding her invisible illness to embracing it whole-heartedly.
In this blog in our CF Week series about how our community balances the challenges of cystic fibrosis (CF) with everyday life, Andrew shares his experiences and gives his tips for finding balance in treatment, exercise and relationships.
The Cystic Fibrosis Trust and Medicines Discovery Catapult (MDC) announced a joint partnership to form the ‘CF Syndicate in Antimicrobial Resistance (AMR)’ at the UK CF Conference today
In the March issue of CF Life magazine you met Marie, a paediatric CF social worker who works for Barnardo's. Here, Eileen, an adult CF social worker at Kings College Hospital who has specialised in CF care for nine years, explains her role and how she helps to support people with CF and their families.
The Cystic Fibrosis Trust is once again bringing you the latest in cystic fibrosis (CF) research, straight from the scientists funded by your donations and fantastic fundraising.
