Runderpants Winchester 2020
21 February 2020
Winchester Student Union RAG are taking on the Runderpants Mile as part of its 2020 RAG week campaign!
![](/images/common/RAG_Winchester_logo_1024_x_768.jpg)
On 31st of January 11 students ran just in their runderpants at the Bar End Stadium Winchester.
Winchester Student Union supported Nerve Tumours UK as part of its raising and giving week campaign! 11 Members of the RAG and Futsal Societies ran fearlessly in stormy ice cold rain to raise awarness for Nerve Tumours UK and raised a fair amount for the charity.
Why not join the challenge and help raise awareness for Nerve Tumours UK whilst doing a super fun run in your underpants alongside your fellow students.
Any funds raised will help our work to provide crucial medical and non-medical support to those living with Neurofibromatosis so we can empower them to live the best life they can.
Sign up today and receive your free unique pair of Runderpants!
![](/images/common/RAG_Winchester_runderpants_1024_x_768.jpg)
- Choose a date
- Get all your mates involved
- Create a page at our own Fundraising Hub
- Register for the event by paying £5, and get sent your own pair of Runderpants
- Raise as much sponsorship money for Nerve Tumours UK as possible!
- Run in your Runderpants on the day of the run! Feel the breeze!
- Have a celebratory drink afterwards
Filter News
![](https://nervetumours.org.uk/images/made/images/common/Rosalie_Ferner_370x280_800_600_s_c1.jpg)
Neurofibromatosis 1 in the 21st Century
Professor Rosalie Ferner delivers key speech “Neurofibromatosis 1 in the 21st Century” to the BPNA 2022 Annual Conference
Read More![](https://nervetumours.org.uk/images/made/images/common/image_(4)_370x280_800_600_s_c1.jpg)
The International Rare Disease Showcase 1st – 3rd February 2022
The International Showcase is a unique & important event, with interactive sessions taking place from 1st-3rd February 2022
Read More![](https://nervetumours.org.uk/images/made/images/common/Grace_Picture2_370x280_800_600_s_c1.jpg)
Grace’s NF1 story - Nothing stops me
Grace tells us how her NF1 hasn't stopped her from being active and achieving her goals
Read More![](https://nervetumours.org.uk/images/made/images/common/Mia_family_370x280_800_600_s_c1.jpg)
Mia’s NF1 story
Bridie & Warren describe their 17 month old daughter Mia's diagnosis with NF1
Read More![](https://nervetumours.org.uk/images/made/images/common/Ellie_on_rowing_machine_370x280_800_600_s_c1.jpg)
Richard & Diana’s 1,000,000 metre new rowing challenge
Diana & Richard have taken on a 1,000,000 metre rowing challenge in 100 days to raise funds & awareness
Read More![](https://nervetumours.org.uk/images/made/images/common/BZQO9932_370x280_800_600_s_c1.jpg)
A Message from our Charity Director
A message from Karen, our Charity Director, on looking forward to a special 2022
Read More![](https://nervetumours.org.uk/images/made/images/common/Childhood_Neurological_Conditions_Survey_Website_Header_370x280_800_600_s_c1.png)
Childhood Neurological Conditions Survey Part 2
Find out how you can help shape the future of treatment for Childhood Neurological Conditions such as Neurofibromatosis
Read More![](https://nervetumours.org.uk/images/made/images/common/HCTN0411_370x280_800_600_s_c1.jpg)
Graham’s Super Nine Shines A Light on NF
Graham's 7 year old great-nephew Nathan is his inspiration for his epic challenges to fundraise for NTUK
Read More