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Information
Easy to understand information on all aspects of congenital nystagmus.
![Jay Self presents from a lectern. The Nystagmus Network logo appears on the screen behind him.](https://nystagmusnetwork.org/wp-content/uploads/2017/10/Jay-e1638201991509.jpeg)
Diagnosis
Our clinical adviser, Jay Self talks you through diagnosis of Congenital Nystagmus.
Watch the video here
![Helena Lee presents at a Nystagmus Network Open Day](https://nystagmusnetwork.org/wp-content/uploads/2021/03/Helena-e1638783636819.jpeg)
Treatment
Our clinical adviser, Helena Lee, explains the optical, medical and surgical options.
Watch the video here
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One man’s story
Living with Congenital Nystagmus through a global pandemic. One man’s experience.
Continue reading “One man’s story”![A family at Open Day.](https://nystagmusnetwork.org/wp-content/uploads/2018/12/family-at-open-day-scaled.jpg)
Facebook Groups
Find the nystagmus community online by joining a Nystagmus Network Facebook group.
Continue reading “Facebook Groups”![A hand holds a pen over a document with graphs and charts.](https://nystagmusnetwork.org/wp-content/uploads/2021/11/qtq80-7jz7hh.jpeg)
Research
The Nystagmus Network has been funding research since the 1990s.
Continue reading “Research”![A woman embraces a small child](https://nystagmusnetwork.org/wp-content/uploads/2021/01/IMAGE-267-scaled.jpg)
A guide to nystagmus
If you really want to know what it’s like to have nystagmus, read our guide written by people who have the condition.
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Come along to a get together
The Nystagmus Network hosts monthly online get togethers giving you the opportunity to share your experiences and learn more about nystagmus.
Continue reading “Come along to a get together”