Funny Peculiar
01 July 2019
Funny Peculiar
UPDATE:
Thank you so much to Peculiar Productions for putting on such incredible shows in their rendition of Terry Pratchett’s classic comedy “Men At Arms”. We have been told that roughly 900 tickets were sold in total between the 21st-24th of August and we couldn't be more thankful as all proceeds are being donated towards our vital cause!
Thanks again and we are so glad to see that your show received such great reviews Find out more here






Peculiar Productions is an amateur theatre company which puts on very accomplished productions, principally of Terry Pratchett adaptations. This year’s show brings to life on stage Terry Pratchett’s classic comedy-fantasy thriller, Men at Arms. The company gives all the proceeds from their shows to charity, and this year has chosen Nerve Tumours UK as the beneficiary.
The director, Matthew Hitchman, explains the connection to the charity.
“We chose Nerve Tumours UK as this year’s charity because one of our members, Sarah Burrows, sadly lost a good friend this year, who passed away due to the condition. As a company, we aim to give our audiences a great time, and also make a contribution to a worthwhile cause, so we’re delighted to be able to support the important work of Nerve Tumours UK. We’ll also take the opportunity at the shows to raise awareness about nerve tumours, a condition I suspect people know very little about – I certainly didn’t.”


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