New website to unite cystic fibrosis patients and UK researchers

PEOPLE with cystic fibrosis (CF) will be able to access the latest research findings about their condition, volunteer for clinical trials and influence the direction of future scientific studies through a new website being launched later this week.

CF Unite.org is the brainchild of academics at The University of Nottingham who wanted to find a way of bringing patients together to discuss scientific and medical breakthroughs without risking the spread of infections that can be dangerous to those living with the condition.

Dr Matthew Hurley, leading the CF Unite project in the University’s School of Clinical Sciences, said: “There are a number of charities and groups that support CF patients with their condition but until now there has been nowhere that they can go to directly engage with the scientists and researchers who are studying the disease.

“Equally, patients with CF have a wealth of untapped experience because they live with the condition every day. This unique knowledge could be extremely useful in designing new clinical trials and in guiding experts on the type of research that is going to have the greatest impact.”

CF is the one of the UK’s commonest life-threatening inherited diseases. It is caused by a faulty gene that controls the movement of salt and water in and out of the cells in the body, which leads to the internal organs, especially the lungs and digestive system, becoming clogged with thick sticky mucus.

People with CF are affected by bacteria, which grow in the lungs.  These are harmless to healthy people but could be potentially dangerous to other people with CF. These infections can usually be eradicated or kept at bay with early antibiotic treatment but bugs often eventually become established or become antibiotic-resistant, leading to patients’ lungs becoming colonised.

The risk of cross-infection from such bacteria means that people with CF often have to avoid contact with others, which can lead to them becoming isolated.

The new website is a public engagement with science project which has been supported by a Wellcome Trust People Award. The site has been designed to work as a virtual ‘conference,’ where patients and their families will be able to access live webcasts of experts discussing the latest research findings and explaining the impact they could potentially have for people with CF. Patients will have the opportunity to ask the experts questions in real time.

As the disease affects just 9,000 people in the Air Max 1 Ultra Flyknit