Kebabathon for Nerve Tumours UK
11 November 2020
Meet Derek Breakey. A 34-year-old Street photographer from Manchester whose ten-year-old little girl was born with Neurofibromatosis Type 1. He's taking on the unusual challenge of a ‘Kebabathon’ – eating 60 kebabs over 30 days, that’s 2 a day to fundraise for Nerve Tumours UK!
“I’ve been training for this since I was six-years-old. I know I can do it.”
![](/images/common/derek_2_1024x768.jpg)
Des realised that he had a hidden talent after inadvertently eating 39 kebabs over 28 days a few months ago, eating nine in one week and three in a day!
“After that, I thought, I might as well do it properly and do it for charity.”
He is a regular contributor to the Manchester Donner Connoisseurs Facebook review group and his friends encouraged him to take on this epic challenge.
“I’m not too worried. I have been doing this forever and I’m still standing. My last MOT was two years ago and my blood pressure and everything was fine. I’d better do it while I’m young and healthy. I’ve been eating kebabs since I was six-years-old and I’m 34 now. I’ve just always been good with spicy food. I’m a kebabhead. I’m addicted.”
He wants to raise as much money as possible to support people affected by Neurofibromatosis & Schwannomatosis. “It’s a charity close to my heart, so hopefully I can help them out,” he says. The Just giving page will be closed 7 days after the last day of eating. Let’s help Des reach his fundraising target and support him taking on this mammoth meat challenge!
Don't let Derek stand in the cold in lockdown in front of a kebab shop, support his fundraiser!
Source: Manchester Evening News
Filter News
![](https://nervetumours.org.uk/images/made/images/common/callumPage-Preview-800-x-500-px_800_600_s_c1.png)
Callum Axford’s Story
Vote for Callum's nomination for Positive Role Model (Disability) in this years National Diversity Awards!!
Read More![](https://nervetumours.org.uk/images/made/images/common/Film-festivalPage-Preview-800-x-500-px_800_600_s_c1.png)
The results are in for our Nerve Tumours UK film nominated at the Rare diseases film festival!
Check out our film & view the results from the film festival here:
Read More![](https://nervetumours.org.uk/images/made/images/common/Noah_Fundraising_Story_3-370x280_(preview_image)_800_600_s_c1.jpg)
Noah’s Inspirational Fundraising Story
Noah Herniman, 14, raises over 1,000 Easter eggs for charity
Read More![](https://nervetumours.org.uk/images/made/images/common/Janet_Holloway_2-370x280-preview_image_800_600_s_c1.jpg)
“Going dry in January” for NF
Janet Holloway and Val Goeghegan complete dry January for Nerve Tumours UK
Read More![](https://nervetumours.org.uk/images/made/images/common/Winchester_Runderpants_2020_-_370_x_280_-_news_tile_800_600_s_c1.jpg)
Runderpants Winchester 2020
Winchester Student Union RAG are taking on the Runderpants Mile, our unique fun run in your undies!
Read More![](https://nervetumours.org.uk/images/made/images/common/BMC_2020_preview_news_images_800_600_s_c1.jpg)
A Magical Weekend
Blackpool Magic Convention 2020 supports Nerve Tumours UK this year as it's chosen charity
Read More![](https://nervetumours.org.uk/images/made/images/common/BeckyPage-Preview-800-x-500-px_800_600_s_c1.png)
Becky’s Story
From dealing with her family's NF1 to improving her fitness and running marathons, have a read of Becky's amazing story here:
Read More