#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
NF2 & Identity Research Study
If you have NF2, Suzi want's to hear from you! Find out more about her research study relating identity & NF2
Read MoreChallenge 100 – Everyone’s invited
Take on 100 of anything you can think of and fundraise to support our NF community!
Read MoreA very “Happy Easter” to you all!
A message from Karen, our Charity Director, wishing you all a very Happy Easter!
Read MoreStuart & William’s Story: Turning blue for World NF Month
Check out Stuart & William's creative fundraiser for World Neurofibromatosis Awareness Month
Read MoreCoordinated Care of Rare Diseases Study at UCL
Find out the results to the Coordinated Care of Rare Diseases Study at UCL
Read MoreWho is exempt from wearing a face mask? UK exemptions rules explained - and how to get a hidden disabilities exemption
Find out the up to date information on face mask rules in your area
Read MoreCarers Rights Day. Diane’s Story
Find out more about Diane's life as a carer and how more should be done for unpaid carers in the UK
Read MoreNF1 PN Impact on Patients’ and Caregivers’ Lives
If you have NF1 with plexiform neurofibromas or you care for someone with NF1 PN help shape future healthcare support
Read More