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/Workplace_resources_preview_370x280_800_600_s_c1.jpg)
Equality, Diversity and Inclusion in the Workplace
Nerve Tumours are here to support you in the workplace: iNForm; workplace equality research & creating an inclusive workplace
Read More![](https://nervetumours.org.uk/images/made/images/common/Wayne_Littlewood_2_370x280_800_600_s_c1.jpg)
Wayne’s World of Marathons
Read about Wayne's world: marathons, running a wedding fayre business with wife Leanne and their son Harley who has NF1
Read More![](https://nervetumours.org.uk/images/made/images/common/London_Marathon_2023_preview_370x280_800_600_s_c1.jpg)
Team NTUK London Marathon 2023
Meet some of our runners and read their inspiring marathon motivation stories
Read More![](https://nervetumours.org.uk/images/made/images/common/Pip_Vilday_running_vest_370x280_800_600_s_c1.jpg)
Pip’s London Marathon
Pip describes life with NF1 & limited vision and his motivation to run the London Marathon
Read More![](https://nervetumours.org.uk/images/made/images/common/image_(48)_370x280_800_600_s_c1.jpg)
The Scottish Parliament Rare Disease Day Online Reception 15/03/2023
NTUK attended the Scottish Parliament Rare Disease Day online reception
Read More![](https://nervetumours.org.uk/images/made/images/common/Screenshot_2023-03-03_at_11.20.57_370x280_800_600_s_c1.jpg)
Support Derry’s and Dan’s Marathon Run for NTUK
Dan and Derry will be taking on the London Marathon in support of Nerve Tumours UK
Read More![](https://nervetumours.org.uk/images/made/images/common/0BCDA8DF-DF60-47D5-A705-BB6EE3A5BBEF_370x280_800_600_s_c1.jpg)
Ragbir’s London Marathon
Ragbir is the Paediatric Lead for NF1 in Leeds and is running the London Marathon
Read More![](https://nervetumours.org.uk/images/made/images/common/IMG_8289_370x280_800_600_s_c1.jpg)
Rare Disease Day 2023
NTUK joined in with Rare Disease Day 2023, helping raise awareness of how better coordination of care can improve lives.
Read More