Research
One of the aims of The Lee Spark Necrotising Fasciitis (NF) Foundation is to help the medical profession gain a better understanding of how NF develops, how it can be identified early, and how it can be treated. We so this through our Necrotising Fasciitis Research.
Our necrotising fasciitis research
INFECT EU Programme Results
Watch a short video outlining the results of the INFECT EU programme.
Lee Spark NF Foundation to participate in EU research programme
We were selected to be part of a five year EU programme working with seven European countries. The name of the project INFECT.
Related information
Useful links
Dedications to those lost to Necrotising Fasciitis
Real life experiences
Support for parents and carers of children with Necrotising Fasciitis
Caring for a child who has suffered from Necrotising Fasciitis can be tough, but you’re not alone. In this section Lucy, a mother, shares her experiences.
Our blog
Buying a T-shirt can bring HOPE
Summer seems to be making a resurgence in the UK! After a slightly grey and miserable July, things seem to be brightening up again! We at The Lee Spark NF Foundation HQ are so happy! The sun makes such a difference to our health and mood, is the same true for you? To...
Luke Abrahams memorial football day raises over £3,000 for Lee Spark NF Foundation
On Saturday the 24th June 2023 a football Memorial Day was organised in respect of a wonderful young man Luke Abrahams who passed away on the 23rd January 2023. He passed away suddenly of necrotising fasciitis, which had started from strepA throat. Luke left...
‘Tis the season – Charity giving at Christmas
It’s December! which means it’s officially Christmas (that’s what we think anyway) and what better way to spread some Christmas cheer, save the planet and do some good for an important cause than to send a charity e-card. We’ve teamed up with the lovely people at...