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.
![](/images/common/THE_NEVIS_RANGE_LOOKING_TOWARDS_FORT_WILLIAM_SCOTTISH_HIGHLANDS_SEP_2013_(9682656691)_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...
![](/images/common/Celia_Baxter_Crafts_for_Nerve_Tumours_UK_Image_1024x768.jpg)
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
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The Royal Society - A Quest for the perfect Human…? A debate on the implications of human genome editing
Find out more about the debate recently undertaken at The Royal Society here:
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Appearance Matters: Prof Diana Harcourt and Maia Thornton
Find out both Diana's and Maia's views on their work and the importance of their work for people with NF:
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Jane Frances
Here Jane Frances tells us how findings from psychological research can help parents and teachers of children with NF
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Sarah’s Story
Sarah has NF1 and works full time for the NHS check out her intriguing story here
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Laura’s Story
Read about Laura's experience of undergoing surgery to remove a tumour from her spine here:
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Visible Difference Equality Law Research: summary of findings
Find out more about the results here:
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The Galloway Family and their “amazing” four year old Ruby
Have a read about the incredibly brave young Ruby Galloway (NF1) and check out their previous and future fundraiers.
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“Framing the face: History, Emotion, Transplantation” a blog from James Partridge
Find out more about the blog and what is concerns here:
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A Spooktacular Halloween day for NTUK
Find out more about the wonderful fundraising event here:
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