Student Voice Prize 2021
23 September 2021
![](/images/made/images/common/Student_Voice_Prize_logo_2000x700_800_300_s_c1.jpg)
The Student Voice Prize returns for 2021 on the 6th October! The Student Voice Prize is an annual, international essay competition hosted by Findacure and Medics4RareDiseases.
The competition aims to raise the profile of rare disease within the medical field, particularly with medical students, nurses and scientists who may have never come across rare diseases in their training.
Every year, as part of the competition there is a Patient Group Pairing Scheme. The scheme gives students the chance to be paired with a rare disease patient group to learn first-hand about their condition and patient experience. It involves the student and patient group representative having a conversation over the phone or zoom for up to one hour so that the student can gather better insights into the experience of living with a rare condition. It's a great way for patient group advocates to raise awareness of their rare condition amongst the clinicians of the future, share insights and build connections!
Filter News
![](https://nervetumours.org.uk/images/made/images/common/Changing_Faces_Logo_370x280_800_600_s_c1.jpg)
Counselling support from Changing Faces
Changing Faces - Counselling support: confidential one to one support sessions for people with a visible difference
Read More![Nerve Tumours UK Community Survey](https://nervetumours.org.uk/images/made/images/templates/placeholder_800_600_s_c1.png)
Nerve Tumours UK Community Survey
This consultation provided direct feedback to the strategy group, to look at how we can continue to provide our services
Read More![](https://nervetumours.org.uk/images/made/images/common/IMG_7819_-_Suzi_NF2_-_edit_370x280_800_600_s_c1.jpg)
Suzi’s NF2 story
Suzi used her own NF2 diagnosis to inspire her research into how identity is experienced by people with NF2
Read More![](https://nervetumours.org.uk/images/made/images/common/Emma_Hartley_Liverpool_Fundraiser_Image_5_370x280_800_600_s_c1.jpg)
Emma’s Story
Emma shares her journey with NF after finding out her daughter, Poppy, has been diagnosed with NF Type 1.
Read More![](https://nervetumours.org.uk/images/made/images/common/tegan-mierle-fDostElVhN8-unsplash_preview_800_600_s_c1.jpg)
Tim’s Story: Living With Neurofibromatosis – it’s a family thing
Tim tells us how Nerve Tumours UK proved to be an invaluable resource and support to him and his family as he was growing up
Read More![](https://nervetumours.org.uk/images/made/images/common/Out_Walking_370x280_800_600_s_c1.jpg)
Dalvinder’s 100km Ultra Challenge for NF
Dalvinder on the 100km Ultra Challenge Thames Path walk to raise money for NF
Read More![](https://nervetumours.org.uk/images/made/images/common/Diana_Edwards_Nerve_Tumours_UK_Fundraiser_image_5_800_600_s_c1.png)
Diana’s One Month of Rowing for Neurofibromatosis
Diana is taking on an epic 150k rowing challenge - 5k per day to support her daughter Ellie & our NF community
Read More![](https://nervetumours.org.uk/images/made/images/common/Autistica_Research_Festival_Branded_Header_preview_800_600_s_c1.png)
Autistica Research Festival 2021
See how this year's event went and find out how you can watch the best bits if you couldn't make the conference.
Read More![](https://nervetumours.org.uk/images/made/images/common/IMG_1837_Carol_Irving_Nurse_Portrait_preview_800_600_s_c1.jpg)
OneMoreNurse joins the NTUK team in Leeds
We're delighted to announce our new Specialist NF Nurse for Leeds, find out more
Read More