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/Mary-nurse-specialistPage-Preview-800-x-500-px_800_600_s_c1.png)
Mary Thomas wins Specialist Nurse of the Year 2019!
Have a read about the Guy's and St Thomas' Celebration of International Nurses Day here
Read More![](https://nervetumours.org.uk/images/made/images/common/Luke-and-his-NF-NinjasPage-Preview-800-x-500-px_800_600_s_c1.png)
Luke and his NF Ninjas
Have a read of Luke's story of growing up with NF and how he plans to bring his chidren up proud of their NF as well.
Read More![](https://nervetumours.org.uk/images/made/images/common/Stannington-park-Page-Preview-800-x-500-px_800_600_s_c1.png)
Stannington Community Association’s Easter Fête
Stannington Community Association's Easter Fête was a success! Read about this years superb event here:
Read More![](https://nervetumours.org.uk/images/made/images/common/Marathon-Page-Preview-800-x-500-px_800_600_s_c1.png)
London Marathon 2019: 26 hard miles for 26,500 people affected
Thank you so much to all our incredible Marathon runners for going the extra mile (or 26)!
Read More![](https://nervetumours.org.uk/images/made/images/common/youtubePage-Preview-800-x-500-px_1_800_600_s_c1.png)
Take a look at our new YouTube Channel
Take a look at our new YouTube channel and how to subscribe here
Read More![](https://nervetumours.org.uk/images/made/images/common/Pear-KellyPage-Preview-800-x-500-px_800_600_s_c1.png)
Meet Pearl
Pearl Kelly is 22, and has multiple complex problems caused by her NF1. Here she explains her outlook on life
Read More![](https://nervetumours.org.uk/images/made/images/common/JoannaPage-Preview-800-x-500-px_800_600_s_c1.png)
Meet Joanna
Joanna is a lecturer in Mitochondrial Genetics at Newcastle University, she recently ran the London Marathon. Meet her here
Read More![](https://nervetumours.org.uk/images/made/images/common/Maia-Thornton-ResearchPage-Preview-800-x-500-px_800_600_s_c1.png)
New Research Into Appearance Altering Conditions
Maia Thornton PhD is looking for both parents and professionals who care for someone with an appearence altering condition
Read More![](https://nervetumours.org.uk/images/made/images/common/AdamPage-Preview-800-x-500-px_800_600_s_c1.png)
Adam’s Story
Adam has NF1 yet is still one of the most active and athletic people in the UK. Read about his fascinating story here:
Read More