The Lee Spark NF Foundation

The mission of The Lee Spark Necrotising Fasciitis (NF) Foundation is to help those whose lives have been affected by necrotising fasciitis and other severe streptococcal infections and medical staff who are involved with investigating, diagnosing and treating NF.

Our aims are to:

  • support the families and of those affected,
  • educate the medical profession and the general public,
  • promote recognition of the early signs and symptoms of necrotising fasciitis and severe streptococcal infection,
  • highlight the causes, effects, treatment and management of this horrific disease and
  • promote research into prevention and treatment.

Our charity was established in January 2000 by Doreen Marsden following the loss of her son to this dreadful disease. Doreen realised the need to give support to those people forced to deal with NF both personally and professionally.

If you can't find what you're looking for, please contact us.

Fundraising is a vital part towards the running of our charity and every penny raised is gratefully received.

The Lee Spark NF Foundation is the United Kingdom's only support group for people who have been affected by severe streptococcal infections or necrotising fasciitis has helped thousands of sufferers, relatives and medical staff from organisations around the world.

Training module DVD

To aid understanding of severe streptococcal infections, we have produced a Training Module DVD.

The DVD explains how severe streptococcal infections can develop into necrotising fasciitis. You can find out more on our DVD page.

Help our research

As part of our work in trying to improve the understanding of NF we're gathering personal experiences of the onset and treatment of necrotising fasciitis and severe streptococcal infection.

If you have been affected by NF either as a patient or relative, please do contact us with your details and story.