The Nystagmus Network supports the 1 in 1,000 adults and children living with nystagmus, raises awareness and funds research. Thank you for supporting the Nystagmus Network 19-21 challenge. The charity and the nystagmus community need your help now more than ever.

When Harper was diagnosed with Nystagmus, we had so many questions. Luckily for us, there is an amazing charity called the Nystagmus Network that provides all the answers and more. There are support groups, information booklets for all agencies and anything we could ever need. We don’t know how much this will affect our girl but we know we have the right support and information available to us thanks to the Nystagmus Network charity. 

Nystagmus is a form of visual impairment, characterised by wobbling or flickering of the eyes, from side to side, up and down or round and round. This affects the ability to focus, judge speed and depth and recognise faces.

The Nystagmus Network is a registered charity in England and Wales. The charity provides advice, support and information to everyone living with nystagmus and their families, an educational advocacy service and benefits advice, training for teaching staff and eye care professionals.