Become an NF Patient Representative
15 January 2021
As patients and caregivers of those with Neurofibromatosis Type 1, Neurofibromatosis Type 2, or Schwannomatosis, your voices and lived experiences play an important role in determining the direction that research should take!
The REiNS (Response Evaluation in Neurofibromatosis and Schwannomatosis) Collaboration is looking for patients and caregivers to help in the fight to cure all types of NF by helping to design clinical trials. This is a chance for you to make a real difference in finding treatments for these conditions. A scientific background is not necessary – lived experience with neurofibromatosis and schwannomatosis is. We are looking for people from all backgrounds, including people of all genders, races, ethnicities, education level, and health status.
For more information about REiNS, please watch this video at
If you are interested in joining the patient representative program, please click the link below.
Filter News
![](https://nervetumours.org.uk/images/made/images/common/jonnyPage-Preview-800-x-500-px_800_600_s_c1.png)
Jonny’s Story
Jonny has chosen to open up and share his incredibly brave battle with Cancer over the past year, find out more here:
Read More![](https://nervetumours.org.uk/images/made/images/common/james_2__800_600_s_c1.jpg)
James on Tour
James Wiggin is taking on the Tour de France on behalf of Nerve Tumours UK – or at least a part of it.
Read MoreNerve Tumours UK Specialist Neurofibromatosis Nurses attend the National NF1 Meeting in Manchester
Have a read what was talked about at this year's National NF1 Meeting in Manchester
Read More![](https://nervetumours.org.uk/images/made/images/common/lets-go-regional-coverPage-Preview-800-x-500-px_800_600_s_c1.png)
Let’s Go Regional/ Let’s Go Outside
Read about the website that offers new exciting opportunities to help you find a fundraiser/event that is most suited to you
Read More![](https://nervetumours.org.uk/images/made/images/common/Meet-harley-Mobile-600-x-800-px_800_600_s_c1.png)
Meet Harley
Have a read about the amazing 7 year old boy with NF1 and his fundraising family
Read More![](https://nervetumours.org.uk/images/made/images/common/PerculiarArtboard-1_800_600_s_c1.png)
Funny Peculiar
Peculiar Productions has chosen to donate all their proceedings to NTUK this year! Find out more:
Read More![](https://nervetumours.org.uk/images/made/images/common/christmas-card-website-2019Page-Preview-800-x-500-px_800_600_s_c1.png)
Christmas Card Competition 2019
Check out this year's Christmas Card Competition and how to enter
Read More![](https://nervetumours.org.uk/images/made/images/common/LanyardsPage-Preview-800-x-500-px_800_600_s_c1.png)
Sunflower lanyards to support patients and visitors with hidden disabilities
Read about the new lanyards being given out at Heathrow, Sainsbury's and Gatwick to help support those with disabilities
Read More![](https://nervetumours.org.uk/images/made/images/common/Small-Charity-NTUKPage-Preview-800-x-500-px_800_600_s_c1.png)
NTUK attends Small Charity Week
Nerve Tumours UK attended Small Charity Week, find out more about the week and why we attended here:
Read More