Stitched up by Celia
28 January 2021
Celia, from the Scottish Highlands, continued to support Nerve Tumours UK throughout lockdown with her unique handicrafts, selling her products online.
Follow her example and get creative with your online fundraising ideas – who knows what incredible ideas you may come up with!
In her own words "My 10-year-old granddaughter was diagnosed with NF1 as a 14-month-old and the family became aware of Nerve Tumours UK from the beginning. When I retired in 2015, I realised I had more time to indulge my passion for sewing and knitting, but would soon have kitted out all the family with things they probably didn't really need, so I decided to make things for charity, and Nerve Tumours UK seemed the obvious choice.
I just make what I feel like as I sew and knit for pleasure...
I do not sew and knit to order as I don't want to put myself under that pressure. Selling is not easy up here in the Scottish Highlands and I have, in the past, had stalls at community markets and Christmas fairs. This was not possible in 2020, so I decided to try to sell through my Facebook page which proved more successful, though not so much fun!
I am hoping to sustain my output so, hopefully, there will be another donation for 2021!"
If you have any fundraising ideas, please contact us info@nervetumours.uk or have a look at the following.
Filter News
Disclosing and explaining visible differences - CAR Workshop
Read more about the workshop, featuring additional guidance from Specialist NF Nurse Rebecca Rennison
Read MoreJo Ward’s Avastin Blog
Jo Ward, CEO of NF2 BioSolutions UK, shares a blog about her son Oscar's Avastin journey
Read MoreNigel’s story - Normal is as normal does
Nigel lived a normal life until age 47. The next 20 years took him from NF1 to NF2 to Schwannomatosis to mosaic NF2
Read MoreWorld Mental Health Day 2023
NTUK (as part of the Neurological Alliance) has signed a joint letter aimed at improving access to mental health services
Read MoreCAR Research visible difference experiences during recruitment
Research participants required, find out more and take part
Read MoreNF Academy 2023 - Ella’s Blog
Ella, who has NF1, attended the week-long 2023 NF Academy in Portugal, meeting young adults with NF from all over Europe
Read MoreUniversity of Manchester Research
Read about the latest PHD research, involving Nerve Tumours UK, at the University of Manchester
Read MoreNew Research Study for Children and Young People with NF1
Find out more about the study and how you can participate here
Read MoreNeurofibromatosis Type 2 name change
The new name for Neurofibromatosis Type 2 is NF2-related-Schwannomatosis (NF2)
Read More