Take part in nystagmus research

The Nystagmus Network works closely with the UK nystagmus research and clinical centres to bring you opportunities to take part in research.

How much do you know about nystagmus?

Everyone can take part in this 5 minute survey. Then share the link with your friends, family, colleagues, whoever you can think of, especially with people who may never have heard of nystagmus before.

The more people who take the survey, especially people who don’t know about nystagmus already, the better information we will gather.

The survey is about people’s perceptions of nystagmus. The results will help shape further nystagmus research and awareness raising strategies, contributing to better understanding of the condition and improved quality of life as a result.

Take part in the survey here


Albinism researchers in Southampton (Jay Self and Helena Lee) would love to hear from anyone with any form of albinism who is over the age of 60. If you or anyone you know fits the bill, please complete the form.


Do you have recently diagnosed Acquired Nystagmus. Do you suffer from oscillopsia some or all of the time? Would you like to take part in a trial involving virtual reality glasses to see if they can alleviate the worst of your symptoms? If so, please contact us and we will put you in touch with the Sheffield team.


Parents and carers of 0-6 year olds with nystagmus are invited to take part in an online questionnaire about their children’s vision use. The study is being carried out at the Australian Catholic University.

Find out more and take part here