Xmas Party Superheroes
17 December 2020
Has covid cancelled your Christmas Party
Join many other businesses in making a BIG difference to a LOT of people’s lives this Xmas. Donate the unused cost of your Xmas party to Nerve Tumours UK. You and all your staff can become instant #XmasPartyHeroes and support the 26,500 that have Neurofibromatosis in the UK alone.
1) Choose your pledge amount (add a zero on for luck)
2) Choose Nerve Tumours UK on our charities page and click their logo.
3) Here you will be able to donate directly to Nerve Tumours UK.
4) You can also pay your donation via our mobile app donation partner Thinking of You the place where charities benefit more. Download the app here
5) Notify us of the pledge amount via the contact us (see below)
6) Share the news of becoming Xmas Party Heroes on your social channels, making sure you use the hashtag #XmasPartyHeroes and share the amount.
7) Let us know and for any questions please contact us at info@nervetumours.org.uk
Any donation you give will make a great difference to a person's life if they are provided with support. Here are some examples how your donations will help.
£10 – Funds a school pack
£20 – Enables us to raise awareness
£60 – Supports the Helpline plus a follow up initial call
£127 – Pays for a school visit
£155 – Funds a home visit
Filter News
![](https://nervetumours.org.uk/images/made/images/common/durham-researchPage-Preview-800-x-500-px_800_600_s_c1.png)
New research into non-discrimination law
Durham University is looking for participants who look different due to their health complications. such as NF.
Read More![](https://nervetumours.org.uk/images/made/images/common/MichaelFry2_800_600_s_c1.png)
Letter from our new Chair
A letter detailing the vision of our new chair, and the future of the charity.
Read More![](https://nervetumours.org.uk/images/made/images/common/NTUK-logo_800x500px_800_600_s_c1.gif)
Launch of Nerve Tumours UK
Following a major strategic review, the Neuro Foundation charity is now known as Nerve Tumours UK.
Read More![](https://nervetumours.org.uk/images/made/images/common/shruti-garg_800_600_s_c1.jpg)
NF1 research award first for UK consultant
Dr Shruti Garg is the first non-US resident to receive NF1 $555,000 research award.
Read More![](https://nervetumours.org.uk/images/made/images/common/PoppyPage-Preview-800-x-500-px_800_600_s_c1.png)
Polly’s Story (as told by Mum Emily)
"Despite being on weekly chemotherapy she is a happy child and never fails to inspire us all"
Read More![](https://nervetumours.org.uk/images/made/images/common/eden-baby_800_600_s_c1.jpg)
EDEN Study Progress Report
The EDEN study has enrolled 30 babies and toddlers to understand how infants with NF1 develop.
Read More![](https://nervetumours.org.uk/images/made/images/common/EllaPage-Preview-800-x-500-px_800_600_s_c1.png)
Ella’s story
Have a read of Ella's story here. An uphill battle which we know she will turn around!
Read More![](https://nervetumours.org.uk/images/made/images/common/Grace-colourPage-Preview-800-x-500-px_800_600_s_c1.png)
Grace’s Story
Have a read of Grace's story and she overcame her insecurites surrounding her NF
Read More![](https://nervetumours.org.uk/images/made/images/common/Helpful_Charities_800x500_preview_800_600_s_c1.jpg)
Helpful Charities
Find some of the other helpful charities that may be able to support you here
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