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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Adam Buxton Comedy Night in aid of Nerve Tumours UK
Our charity comedy night was certainly nothing short of a success. Find out exactly what went down here:
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Meet Megan
Megan Crews is a 30 year-old special needs tutor in Salisbury. She recently spoke out in The Sun.
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How does your visible difference affect you?
Researchers would love to understand your experience of how a visible difference affects your daily life
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Gabriella’s Story
"I believe everyone should think the same and be kind to people however they look and whatever condition they have."
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One More Nurse Appeal Press Release
Have a read of our #OneMoreNurse appeal press release here:
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Recent Research from DR Shruti Garg
Find out more about some of the recent research carried out by DR Shruti Garag
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Advisory group of parents needed to help shape future research
Maia Thornton is a PhD student looking for an advisory group of parents who's child has an appearance altering condition
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Olivia’s Story
Olivia is an enthusiastic and determined young girl. Have a read of her inspiring story here!
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The Big Lottery Fund pays for 2 Patient Info Days
Nerve Tumours UK receives Lottery funding
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