#DareToThinkRare
21 October 2020
![](/images/made/images/common/Student_voice_prize_website_header_1200X450_800_300_s_c1.png)
The Student Voice Prize
is now OPEN!
To those in our community that are medical students, trainee nurses, or know someone amongst your family and friends. Enter #DareToThinkRare for the 7th annual Student Voice Prize essay competition!
![](/images/common/GettyImages-478223964_1024x768.jpg)
What is The Student Voice Prize?
The Student Voice Prize is an annual, international essay competition that focuses on raising 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.
Findacure and Medics4RareDiseases host the competition together and the winner gets published in The Orphanet Journal of Rare Diseases!
Why Rare Disease?
Rare diseases affect approximately 350 million people worldwide and are some of the most difficult conditions to diagnose. Despite the large number of people affected around the world, little time is dedicated to rare disease training in medical school. It is why The Student Voice Prize challenges the doctors, nurses, and scientists of tomorrow to think about rare disease today. After all with a lifetime risk of 1 in 17 in the UK, it’s not rare to come across them!
Prizes
The 2020 Prizes include:
- Publication in one of the world’s most widely read scientific journals
- Speaking engagements
- Free trip to scientific conferences with all travel expenses paid*
- Become an advocate for rare disease
- Money
Who Can Enter?
If you fall under any of the following categories, you can enter The Student Voice Prize essay competition!
- Medical students
- Trainee nurses
- Undergraduate and masters students enrolled in biological sciences studies (pharmacy, biology, genetics, biomedical science, pharmacology etc.)
Deadline for Entry is 9:00 am GMT on 16th November 2020
Filter News
![](https://nervetumours.org.uk/images/made/images/common/image0_(11)_370x280_800_600_s_c1.jpg)
Tate’s Shine A Light Marathons
Support Tate with his 2023 Shine A Light 100 mile Challenge
Read More![](https://nervetumours.org.uk/images/made/images/common/IMG_20230214_094714_370x280_800_600_s_c1.jpg)
Beth’s NF1 story
"I had no idea what NF was until I got diagnosed with it." Beth shares her NF1 journey to help raise awareness
Read More![](https://nervetumours.org.uk/images/made/images/common/WhatsApp_Image_2023-05-18_at_00.36.57_Front_370x280_800_600_s_c1.jpg)
Shine A Light 2023
The Shine A Light 2023 campaign had 162 buildings around the UK & the Republic of Ireland lit up in blue!
Read More![](https://nervetumours.org.uk/images/made/images/common/Christine_Grant__Margaret__Sheila__Maureen_370x280_800_600_s_c1.jpg)
Christine’s Coronation fundraising
Christine has been fundraising for NTUK for 10 years, since her grandson was diagnosed with NF1.
Read More![](https://nervetumours.org.uk/images/made/images/common/PXL_20220930_101710232_370x280_800_600_s_c1.jpg)
Megan’s NF1 story
Megan has NF1 & other complications: "I will always live my life to the fullest and not let my diagnosis stand in my way"
Read More![](https://nervetumours.org.uk/images/made/images/common/NTUK_Shine_A_Light_2023_website_banner_V2_370x280_800_600_s_c1.jpg)
Shine a Light May 2023
Shine A Light Activities during World NF Month May 2023 - Get Involved!
Read More![](https://nervetumours.org.uk/images/made/images/common/image1_(11)_370x280_800_600_s_c1.jpg)
Charlotte’s NF1 story
Charlotte and her brother & dad have NF1. She is running the Shine a Light Marathon during May to raise awareness
Read More![](https://nervetumours.org.uk/images/made/images/common/Screenshot_2023-05-10_174650_370x280_800_600_s_c1.jpg)
Be seen, be counted: #PicsForThe1in6
Be part of the Neurological Alliance's photo collage, representing people with neurological conditions
Read More