Live Wrestling in aid of Nerve Tumours UK!
07 August 2019
Live Wrestling in aid of Nerve Tumours UK!
Carl Brooks is hosting one of the most unique and sure to be fun and exciting fundraisers in aid of NTUK. He is putting on his very own live Wrestling show where you can come and see the K-Stars "in some high-flying, body-slamming, death-defying action!"
The event is set to take place at the OLD OSCOT WMC Birmingham on the 20th Sept 2019, where you can buy tickets on the door
It is an event that we would encourage everyone within the Birmingham area to go and support, as it is sure to be one of the most exhillarating fundraisers in aid of our shared vital cause yet.
We would also like to thank Carl for his incredible effort and to also wish him the best of luck with his upcoming show 😊
If you would like to find out more about Carl's event you can do so by clicking on the link below:
Filter News

Runderpants Winchester 2022
The Runderpants fun run makes a successful return to Winchester
Read More
NF1 Research study with fly model
How can studying the brain of a fruit fly help with understanding of NF1?
Read More
Stuart’s Schwannoma Story Part Two
Stuart's update takes us through the operation to remove the Schwannoma, recovery and getting back to marathon training.
Read More
Sian & Connor’s story
Sian & Connor describe the invaluable support from NTUK during her pregnancy with baby Reuben
Read More
Anita, aka Fat Lady Slim, is running the London Marathon for NTUK
Anita is fundraising on behalf of niece Sophie & great-niece Lexie who have NF2 by running the London Marathon
Read More
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_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
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
Mia’s NF1 story
Bridie & Warren describe their 17 month old daughter Mia's diagnosis with NF1
Read More