Leighton Linslade Rotary Club hosts Brains of Leighton Buzzard Quiz
23 March 2020
Emily is one of the Trustees at Nerve Tumours UK and she recently hosted a dinner and NF presentation at the Rotary Club of Leighton, where 36 people attended the event to learn more about Neurofibromatosis. She suffers from Neurofibromatosis Type 2 herself.
People were very interested to learn more about Neurofibromatosis type 2 and the affect it has on people, with many people wanting to know more and asking lots of engaging questions from the floor after the presentation
![](/images/common/Rotary1024x768.png)
Nerve Tumours UK was the chosen charity for the annual Brains of Leighton Buzzard Quiz, held at the Cedars school in Leighton Buzzard on Monday 9th March 2020
![](/images/common/IMG_6718-1024x768.png)
Forty five teams and nearly two hundred competitors took part in the event, and through ticket sales, raffle, tombola and refreshments, the Club managed to raise a substantial sum for the charity.
![](/images/made/images/common/IMG_6698-edit_800_600_s_c1.png)
![](/images/made/images/common/IMG_6679_800_600_s_c1.jpg)
![](/images/made/images/common/IMG_6730-edit_800_600_s_c1.png)
![](/images/made/images/common/IMG_6710-edit2_800_600_s_c1.png)
The president of the Club Andrew White said “ I’m over the moon that we managed to raise this amount for my chosen charity, this was chosen by me as my son Jack is affected by NF2” , and for the tremendous support he has received and treatment over the past 12 years. I was keen to raise a large sum for the charity, and to make the participants of the quiz aware of this condition.
Despite the anxiety caused by the current Health Crisis the people of Leighton Buzzard turned out to support this worthy cause and to make the event a success, the amount they spent was incredible and I would like to thank each and every one of them.
Filter News
![](https://nervetumours.org.uk/images/made/images/common/robina-weermeijer-3KGF9R_0oHs-unsplash_370x280_800_600_s_c1.jpg)
NF1 stem cell research study
Julieta is carrying out stem cell research to understand brain development in those with NF1
Read More![](https://nervetumours.org.uk/images/made/images/common/FB_IMG_1646043328094_370x280_800_600_s_c1.jpg)
Ava-Lily’s NF1 story
Ava-Lily is thriving at school despite various NF1 related difficulties - read her story
Read More![](https://nervetumours.org.uk/images/made/images/common/image_(12)_370x280_800_600_s_c1.jpg)
Westminster Virtual Rare Disease Day 2022 Reception
NTUK joined the annual international event aimed at raising awareness & highlighting the needs of people with rare diseases
Read More![](https://nervetumours.org.uk/images/made/images/common/NTUK_supports_RDD_370x280_800_600_s_c1.jpg)
Rare Disease Day 2022
Nerve Tumours UK joins events showcasing Rare Disease Day, hosted by the Genetic Alliance, on 28 February 2022
Read More![](https://nervetumours.org.uk/images/made/images/common/IMG_7612_370x280_800_600_s_c1.jpg)
Runderpants Winchester 2022
The Runderpants fun run makes a successful return to Winchester
Read More![](https://nervetumours.org.uk/images/made/images/common/fruit_fly_370x280_800_600_s_c1.jpg)
NF1 Research study with fly model
How can studying the brain of a fruit fly help with understanding of NF1?
Read More![](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