#DareToThinkRare
21 October 2020
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!
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
Worshipful Company of Horners and Wingwalk fundraiser
NTUK was chosen as the Worshipful Company of Horners' Charity of the Year, and their Deputy Master is doing a wing walk.
Read More
Oliver’s Blog
Oliver Bromley shares some personal experiences of visible difference, and how education and kindness can reduce stigma.
Read More
Laura’s fundraising for Shine A Light 2026
Laura and her mum fundraised for World NF Day on Sunday 17 May.
Read More
Ralph’s NF1 Story
Three year old Ralph has NF1 and has been undergoing treatment to preserve his eyesight, read his story.
Read More
Mel’s Swimming Challenge
Specialist NF Nurse/ Advisor Mel Murrell is going to great lengths with her swimming challenge!
Read More
Reflecting on World NF Awareness Month 2026
Looking back on World NF Awareness Month 2026.
Read More
Nerve Tumours UK Virtual Coffee Mornings
Chat and connect in our Virtual Coffee Mornings. NF2 Coffee Morning on 1st July 2026
Read More
Raising Awareness: Georgia’s Blog
My name is Georgia Baum, I’m 25 years old and an Ambassador for Nerve Tumours UK. Read my Blog and follow my journey!
Read More