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.
_1024x768.jpg)
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

Olivia’s Story
Olivia is an enthusiastic and determined young girl. Have a read of her inspiring story here!
Read More
The Big Lottery Fund pays for 2 Patient Info Days
Nerve Tumours UK receives Lottery funding
Read More
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
Letter from our new Chair
A letter detailing the vision of our new chair, and the future of the charity.
Read More
Launch of Nerve Tumours UK
Following a major strategic review, the Neuro Foundation charity is now known as Nerve Tumours UK.
Read More
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
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
EDEN Study Progress Report
The EDEN study has enrolled 30 babies and toddlers to understand how infants with NF1 develop.
Read More
Ella’s story
Have a read of Ella's story here. An uphill battle which we know she will turn around!
Read More