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/Nimo_NF1_Story_370x280_preview_800_600_s_c1.png)
Nimo’s NF1 Story
Read Nimo's incredible journey of coming to terms living with NF1 & how Nerve Tumours UK has changed her life for the better
Read More![](https://nervetumours.org.uk/images/made/images/common/Georgia_Schwannoma_Story_370x280_800_600_s_c1.png)
Georgia’s Schwannoma Story
Read Georgia's inspirational Schwannoma story and how she had to fight for her diagnosis
Read More![](https://nervetumours.org.uk/images/made/images/common/Screenshot_2020-09-30_Changing_Faces_»_New_research_on_experiences_of_men_with_visible_differences_370x280_800_600_s_c1.png)
Voices of Visible Difference #YoureNotAlone Men’s Campaign
Two-thirds of men with visible difference are affected in their day to day life. Read more
Read More![](https://nervetumours.org.uk/images/made/images/common/Childhood_Neurological_Conditions_Survey_Website_Header_370x280_800_600_s_c1.png)
Childhood Neurological Conditions Survey
Find out how you can help shape the future of treatment for Childhood Neurological Conditions such as Neurofibromatosis
Read More![](https://nervetumours.org.uk/images/made/images/common/Karen_Portrait_Colour_370x280_2_800_600_s_c1.jpg)
We’re Here for You, Our NF Community.
A big thank you from Karen our Charity Director - your support has been amazing!
Read More![](https://nervetumours.org.uk/images/made/images/common/Global_Genes_Virtual_event_370x280_800_600_s_c1.jpg)
Global Genes LIVE!
Join Global Genes September 15-25, 2020 at Global Genes LIVE! A RARE Patient Advocacy (un)Summit.
Read More![](https://nervetumours.org.uk/images/made/images/common/Disorder_channel_promotion_370x280_800_600_s_c1.jpg)
Shine A Light on Neurofibromatosis now streaming on The Disorder Channel
Find out how we are bringing NF Awareness to people's homes
Read More![](https://nervetumours.org.uk/images/made/images/common/Finalist_artwork370x2801_800_600_s_c1.jpg)
Best Film Nomination “Shine A Light on Neurofibromatosis” PM Society Digital Awards
Join the awards ceremony virtually this Wednesday 16th September
Read More