K-Star Wrestling in aid of NTUK
23 September 2019
K-Star Wrestling in aid of NTUK
Thank you so much to Carl Brooks and his K-Star Wrestlers for putting on such an exciting and wonderful event in memory of Carl's incredibly brave sister, Tanya Brooks, who sadly passed away in 2014 as a result of her NF2.
The event took place at the OLD OSCOT WMC Birmingham and was thoroughly enjoyed by the many who turned up to support Carl and his K-Stars. It is certainly one of the more unique fundraisers we have ever had in aid of Nerve Tumours UK and we are so glad to see it was such a success 😊
The fundraiser was set up in memory of Carl's sister Tanya
![](/images/common/Wrestling-done-3Artboard-1.png)
![](/images/common/Wrestling-done-2Page-Preview-800-x-500-px.png)
![](/images/common/Wrestling-done-2Page-Preview-800-x-500-px-copy.png)
Thanks again Carl 😊
Filter News
![](https://nervetumours.org.uk/images/made/images/common/2021-10-27_15-11-36_324_370x280_800_600_s_c1.jpg)
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![](https://nervetumours.org.uk/images/made/images/common/IMG_4619_370x280_800_600_s_c1.jpg)
Sian & Connor’s story
Sian & Connor describe the invaluable support from NTUK during her pregnancy with baby Reuben
Read More![](https://nervetumours.org.uk/images/made/images/common/17397DC99F38479194C0E2ADD6B8CDA8_370x280_800_600_s_c1.jpg)
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![](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