Lee’s Santa Dash
09 December 2020
Between the 1st and 25th of December Lee’s aim is to run 100k dressed as Santa on the Isle of Mull! She also has a few elves out and about throughout Mull helping her raise awareness by donning their festive outfits and braving the weather to show their support. As well as raising funds Lee would also like to raise awareness. Mia her daughter was born with Neurofibromatosis Type 1.
![](/images/common/lee_Paterson_Virtual_Santa_Dash_for_NF_image_11_800x600.jpg)
![](/images/common/lee_Paterson_Virtual_Santa_Dash_for_NF_image_8_800x600.jpg)
![](/images/common/lee_Paterson_Virtual_Santa_Dash_for_NF_image_3_800x600.jpg)
![](/images/common/lee_Paterson_Virtual_Santa_Dash_for_NF_image_16_800x600.jpg)
– Lee"Yup, I hadn’t heard of it either until Mia was diagnosed a few years ago. Mia just gets on with it but there’s no denying it has a massive effect on her life, it can sometimes be really difficult. Very little is known about NF1, even by most health professionals. Nerve Tumours UK provide crucial support to families living with NF1. Without their support, life with NF1 would be even harder. Nerve Tumours UK are campaigning at the moment to raise funds for one more specialist nurse in the UK. I hope to raise funds to help this campaign #OneMoreNurse."
If you want to support and sponsor Lee:
Donate![](/images/common/lee_Paterson_Virtual_Santa_Dash_for_NF_image_1024x768.jpg)
Why not join Lee, grab your Santa/Elf suit and go for a run this December! You can organise yourself as Lee did and set up your own fundraiser or you can sign up to our Virtual Santa Dash which takes place throughout the month of December.
Everyone is welcome! Gather all your friends and family to take on this year’s Christmas challenge, spread joy and happiness to the 26,500 people affected with Neurofibromatosis in the UK.
Filter News
![](https://nervetumours.org.uk/images/made/images/common/comedians_cover_photo_370x280_800_600_s_c1.jpg)
RAISING THE ROOF COMEDY NIGHT
First night on the NTUK 40 years Comedy Circuit 2022 at London's Backyard Comedy Club
Read More![](https://nervetumours.org.uk/images/made/images/common/Chloe_1_370x280_800_600_s_c1.jpg)
Chloe’s NF1 story
Chloe gives an honest assessment about coming to terms with having NF1 and how it has made her determined & strong
Read More![](https://nervetumours.org.uk/images/made/images/common/KarennArtboard-1_500_572_s_c1_370x280_800_600_s_c1.jpg)
“Happy Easter”
A message from Karen, our Charity Director, wishing you a very Happy Easter!
Read More![](https://nervetumours.org.uk/images/made/images/common/image0_(2)370x280_800_600_s_c1.jpg)
Lisa helps Shine a Light on Neurofibromatosis in Belfast
Lisa has NF1, & lobbied the Belfast Lord Mayor to get Belfast City Hall lit up blue on Neurofibromatosis Day, 17th May
Read More![](https://nervetumours.org.uk/images/made/images/common/20170430_104321_370x280_800_600_s_c1.jpg)
Alex’s NF1 story
Alex describes her life with NF1, growing up in care, doing adaptive boxing & gym classes & getting NCFE Care qualifications
Read More![](https://nervetumours.org.uk/images/made/images/common/874A4A6E-C1C4-4F33-88A7-7BBF8ABBF870_370x280_800_600_s_c1.jpg)
Sumeeth’s Schwannoma story
Sumeeth, thought nothing of a muscle twitch after a hangover - it was the first symptom that led to a Schwannoma diagnosis
Read More![](https://nervetumours.org.uk/images/made/images/common/quino-al-rK_nz3DswX4-unsplash_370x280_800_600_s_c1.jpg)
Laura’s NF1 story
Laura is doing a skydive fundraiser to raise awareness & funds for NTUK, after her daughter was diagnosed with NF1
Read More![](https://nervetumours.org.uk/images/made/images/common/queen-mary-logo_370x280_800_600_s_c1.jpg)
Disfigurement equality at work - research
This research study by Queen Mary University, London, aims to improve workplace equality for people with disfigurements
Read More![](https://nervetumours.org.uk/images/made/images/common/Comedy_night_370x280_800_600_s_c1.jpg)
RAISING THE ROOF: CHARITY COMEDY NIGHT IN AID OF NERVE TUMOURS UK
Join us in London on our first comedy night to celebrate 40 years of Nerve Tumours UK
Read More