Laura’s NF1 Awareness Story
13 May 2025
My name is Laura and I have Neurofibromatosis type 1.
I wanted to tell you a little bit about myself. I was diagnosed with NF1 at 8 years old.
The tumours grow all over my body and I now have many on my face. Some of the fibromas have turned out to be cancerous and I have had them surgically removed .
Over the years, I’ve had to have numerous surgeries to remove the ones causing problems: clumps of fibromas on the balls of my feet and other areas of my body where they have grown. Some of the non-cancerous fibromas grow back again but I am now finding that the older I get, the NF1 is getting worse and will continue to do so for the rest of my life.
I have joined the Nerve Tumours UK Community Group on Facebook.
I have raised awareness through Facebook and created an information booklet that I sent to my friends and colleagues at church. A church in my community, Rosyth Parish Church, are lighting up blue on 17 May for World NF Awareness Day and the minister will wear turquoise for the Sunday service.
My local church, Dalgety, are hosting a soup and pudding lunch on Sunday 18 May to raise awareness and funds.
Mum made cupcakes and we both wore blue for an awareness event at church

It's not too late for you to get involved - we need the NF Community to help us make NF visible.
Download and display the Shine A Light 2025 poster
Take on one of our Shine A Light 2025 Challenges
Check the list of buildings lighting up for us - If there's a building or landmark lighting up in your area, please send us a photo: info@nervetumours.org.uk