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
Milton Keynes NF1 Medical Information Day 2026
Our Milton Keynes NF1 Medical Information Day was on 9 May 2026.
Read More
Beyond Diagnosis: Manchester Community Festival 2026
NF1 and Noonan Syndrome Community Festival. A Day connected to community, learning and curiosity.
Read More
Evie’s NF1 story
Evie's mam Emily & brother Riley are doing 5k/day during May, after Evie was diagnosed with NF1 at the age of three.
Read More
Sacred Heart Chorus and Orchestra Summer Concert
Sacred Heart Chorus and Orchestra are supporting the charity with a concert at Sacred Heart Church Wimbledon
Read More
Team NTUK London Marathon 2026
Congratulations and thank you to Team NTUK for their epic efforts!
Read More
Living with Neurofibromatosis Type 1: A Journey of Resilience, Transformation, and Impact
Our charity ambassador, Amit Ghose, shares his inspirational story.
Read More
London Marathon Motivation 2026
Find out why our Team NTUK runners are taking on the 2026 London Marathon.
Read More
Rare Disease Day 2026: Equity for Rare
A look back on Rare Disease Day: Equity for Rare, 28 February 2026.
Read More