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

Centre for Appearance Research - Parent Support Materials Study
The Centre for Appearance Research is doing a study on parent support materials - can you help?
Read More
Centre for Appearance Research - YP Face IT
YP Face IT offers online support for young people with conditions or injuries affecting their appearance
Read More
Counselling support from Changing Faces
Changing Faces - Counselling support: confidential one to one support sessions for people with a visible difference
Read More
Nerve Tumours UK Community Survey
This consultation provided direct feedback to the strategy group, to look at how we can continue to provide our services
Read More
Suzi’s NF2 story
Suzi used her own NF2 diagnosis to inspire her research into how identity is experienced by people with NF2
Read More
Emma’s Story
Emma shares her journey with NF after finding out her daughter, Poppy, has been diagnosed with NF Type 1.
Read More
Tim’s Story: Living With Neurofibromatosis – it’s a family thing
Tim tells us how Nerve Tumours UK proved to be an invaluable resource and support to him and his family as he was growing up
Read More
Dalvinder’s 100km Ultra Challenge for NF
Dalvinder on the 100km Ultra Challenge Thames Path walk to raise money for NF
Read More
Diana’s One Month of Rowing for Neurofibromatosis
Diana is taking on an epic 150k rowing challenge - 5k per day to support her daughter Ellie & our NF community
Read More