Billy & Logan’s Story
02 July 2020
This is me Billy and my son Logan.

We both have NF1 but we don't let it stop us!
Logan is a squad member for the England Karate squad, as well as being a member of the kickboxing & Brazilian Jiu-Jitsu squads. He is also an avid runner. Logan only suffers midly with NF1 but does have mild hypermobility associated with it.
I myself was diagnosed with NF1 at 7 years old. I have undergone many surgeries, around 15-20 surgeries in total of the head, neck and left ear area to remove plexiform fibromas and associated problems that go with them. I try not to let it stop me too much and last year I was able to run both Brighton and London marathons in the space of 2 weeks.
The hardest part was the fundraising for sure!
Filter News

The Big Lottery Fund pays for 2 Patient Info Days
Nerve Tumours UK receives Lottery funding
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New research into non-discrimination law
Durham University is looking for participants who look different due to their health complications. such as NF.
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A letter detailing the vision of our new chair, and the future of the charity.
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Following a major strategic review, the Neuro Foundation charity is now known as Nerve Tumours UK.
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Dr Shruti Garg is the first non-US resident to receive NF1 $555,000 research award.
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EDEN Study Progress Report
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Have a read of Ella's story here. An uphill battle which we know she will turn around!
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Have a read of Grace's story and she overcame her insecurites surrounding her NF
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