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/Hannah_1_370x280_800_600_s_c1.jpg)
Hannah’s NF1 story
9 year old Hannah is running the Junior Great North Run, so other children with NF can also have access to doctors & nurses
Read More![](https://nervetumours.org.uk/images/made/images/common/Sam_Gaden_marathon_2_370x280_800_600_s_c1.jpg)
Sam’s Marathon
Sam, our Specialist NF Nurse for Merseyside & the North West, is running the London Marathon - her very first Marathon!
Read More![](https://nervetumours.org.uk/images/made/images/common/2022_Manchester_370x280_800_600_s_c1.jpg)
NF Patients Community Day
The NF Patients Community Day is on Sunday 9th October 2022 - register to attend virtually
Read More![](https://nervetumours.org.uk/images/made/images/common/Naomi_Marshall_Prof_Heather_Widdows_Susan_Ross__Chrissie_from_CF_370x280_800_600_s_c1.jpg)
Appearance, Identity & Law workshop
Appearance, identity & law workshop at Queen Mary University London School of Law
Read More![](https://nervetumours.org.uk/images/made/images/common/image8_370x280_800_600_s_c1.jpg)
Alfred the Pirate
Seven year old Alfred the Pirate takes NF1 in his stride, and is supported by Specialist NF Nurse Mel
Read More![](https://nervetumours.org.uk/images/made/images/common/Nicole_370x280_800_600_s_c1.jpg)
Nicole’s NF1 story & skydive
Nicole shares her NF1 journey and her motivation to inspire children with disabilities to achieve whatever they want to do
Read More![](https://nervetumours.org.uk/images/made/images/common/photo_collage_370x280_800_600_s_c1.jpg)
Sarah’s NF1 story & Langmead fundraising
Sarah describes her daughter Hannah's NF1 journey and organising a corporate charity day fundraiser at Langmead Herbs
Read More![](https://nervetumours.org.uk/images/made/images/common/Molly__Alfie_370x280_800_600_s_c1.jpg)
Molly & Alfie
Mollie has NF1 - her big brother Alfie & friend Kaelan are running to raise awareness & funds for NTUK
Read More