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/O2_Guildhall__Southampton_370x280_800_600_s_c1.jpg)
Shine a Light 2020 Success!
Check out some amazing blue buildings that took part in our Shine a Light On Neurofibromatosis 2020 campaign
Read More![](https://nervetumours.org.uk/images/made/images/common/Sarah_Shine_A_Light_on_Neurofibromatosis_-_370x280-preview_800_600_s_c1.jpg)
Sarah’s Story as told by her Father Clemence
Read more about Sarah's story and her Shining a Light on NF from home for World NF Awareness Day!
Read More![](https://nervetumours.org.uk/images/made/images/common/helen-tomkins_370x280_800_600_s_c1.png)
Statement by Helen Tomkins our Specialist Neurofibromatosis Nurse UK
A statement on coronavirus by Helen Tomkins specialist Neurofibromatosis nurse in Devon & Cornwall
Read More![](https://nervetumours.org.uk/images/made/images/common/Courtney_Deaken_Story-_370x280_800_600_s_c1.png)
Courtney’s Story
Read more about Courtney's NF Story and how she overcomes her difficulties
Read More![](https://nervetumours.org.uk/images/made/images/common/Toms_NF2_Story_-_No_Laughing_Matter_preview_website_370x280_800_600_s_c1.png)
No Laughing Matter
Tom is a former journalist, here he describes his journey from music journalism to comedy, & what his NF2 has to do with it
Read More![](https://nervetumours.org.uk/images/made/images/common/Shine-a-Light_1600x900px_1600_900_80_s_c1StaySafepreview_800_600_s_c1.png)
Shine A Light on Neurofibromatosis 2020
Find out what we're up to for our Shine A Light campaign this year!
Read More![](https://nervetumours.org.uk/images/made/images/common/Michael_Fry_Preview_Coronavirus_Statement_370x280_800_600_s_c1.png)
Statement by Michael Fry our Chair of the Board of Trustees
The impact of the corona virus on the charity sector and Nerve Tumours UK's continued support to those affected by NF
Read More![](https://nervetumours.org.uk/images/made/images/common/person-holding-blue-ballpoint-pen-on-white-notebook-669610nologopreview_800_600_s_c1.png)
NF1, Plexiform Neurofibromas Market Research Study
Find out more about an NF1, Plexiform Neurofibromas market research survey
Read More![](https://nervetumours.org.uk/images/made/images/common/Rebecca_Rennison__Rachel_Jonesa_800_600_s_c1.png)
Statement by Rachel Jones & Rebecca Rennison our Specialist Neurofibromatosis Nurses UK
A statement on coronavirus by Rachel Jones & Rebecca Rennison specialist Neurofibromatosis nurses in the North East & Cumbria
Read More