Talking about Neurofibromatosis A Guide for Teens
07 August 2019
Talking about Neurofibromatosis A Guide for Teens
A new incredibly informative and useful brochure, aimed at helping teens, provided through the generosity of the Doris and Donald Schnuck Fund for Children in Need and the St. Louis Children’s Hospital Foundation has been released and you can find it by clicking on the button below.
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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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Nicks Triathlon in Support of his daughter Eilidh
Find out more about Nick's Triathlon and his daughter's experiences with NF1 here:
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Tom GK- Hearing Loss: The Musical
Find out more about the musical and how you can secure your ticket here
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Nerve Tumours UK joins the “Embracing Complexity” Coalition
Find out more about the coalition we have decided to join
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Researching NF1
Rory Deasy has conducted research into the treatment of children with NF1. Here he talks about his research journey.
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