Coping with Necrotising Fasciitis
We started The Lee Spark NF Foundation in order to support those affected by Necrotising Fasciitis. This section of the website is an area to share and educate in order to help those that need it.
How we support you

Useful links
A section of the website dedicated to providing links to useful resources and help for those affected by Necrotising Fasciitis, including links for professionals.
Research
Our research aims to help the medical profession gain a better understanding of how Necrotising Fasciitis develops, how it can be identified early, and treated effectively.
Dedications
A place to remember loved ones.
Personal experiences
A section dedicated to sharing the personal experiences and stories of people affected by necrotising fasciitis.
Coping with Necrotising Fasciitis:
Aftercare and support

We have a wonderful survivor who has experienced so much through her necrotising fasciitis journey and is going to be able to listen to you and understand your experiences and feelings.
Becky has survived necrotising fasciitis and knows how you may be feeling. She’s had those bad days, she’s struggled with the same emotions and is here to help.
We know that many people affected by necrotizing fasciitis have experienced issues around mental health, including but not limited to, PTSD and OCD. Anyone that has come close to, or been affected by necrotising fasciitis, knows that the time spent in hospital is just the start of the journey.
There is a tremendous amount of aftercare needed, particularly around mental health, and the aftermath isn’t always easy to clear up. Some people need a little extra support or guidance. It has been apparent that many countries have a lack of mental health aftercare sometimes due to a lack of funds. This is where The Lee Spark NF Foundation can help.
We have supported many survivors, bereaved, families and friends who have all been horrified by the sudden onset of necrotising fasciitis. The treatment if misdiagnosed can lead to irreparable damage to the skin and possible amputation to save lives. The whole necrotizing fasciitis experience often leaves the patient and family members extremely traumatised.
Some of your concerns may be what creams are or are not working for your scars, good days and bad days mentally and physically. You may also be worried about whether you’re being a burden to your friends and family. These are just a few of the commons concerns we hear from hear from survivors.
If you’d like to reach out and just have a chat, please drop Becky an email – info@nfsuk.org.uk
Our blog
Discover Adventure: Turn Your Next Adventure Into a Lifeline
Have you ever dreamt of trekking the Yorkshire Three Peaks, walking the Great Wall of China, or cycling from London to Paris? We are thrilled to announce that The Lee Spark NF Foundation has officially partnered with Discover Adventure: one of the UK’s leading...
Introducing Counselling Support for the NF Community
At The Lee Spark NF Foundation, we know that surviving Necrotising Fasciitis—or supporting a loved one through it—is only part of the journey. The physical recovery is often followed by a complex emotional road, where trauma, PTSD, and grief can feel overwhelming to...
Look Good, Do Good: Why Supporting Us Through Merchandise Matters
At The Lee Spark NF Foundation, we are often asked: "How can I help if I don't have time to volunteer or the stamina for a marathon?" The answer is simple, stylish, and sitting right in our shop! Choosing to buy our merchandise is one of the easiest ways to make a...
