Our final advent calendar gift is something we offer every day of the year. Thank you to all our members, fundraisers and supporters who make it all possible. Happy Christmas!
If you’ve ever wondered how a person with nystagmus sees or how the condition affects their sight, listen to Richard, Harriet and Will explain in our video. You can show our video to anyone or use it, completely free of charge, for training purposes. All we ask is that you let us know. Nystagmus, the … Continue reading Nystagmus, the way we see it
When you contact the Nystagmus Network, by phone, email or on social media, it will be one of our 3 staff members who responds. Introducing our staff team.
Without the dedication of just one woman, Vivien Jones, our Founder and Honorary President, the Nystagmus Network would not exist. Vivien is supported by a strong team of Trustees, all volunteers. Watch Vivien’s story here. Find out more about our trustees, here.
Nystagmus Network staff members will visit your clinic, school or group to deliver a talk about nystagmus and the work of the charity. If we can’t make it in person (there are only 3 of us) we will send you materials for your visitors to take away. Please contact us today to request a talk.
Normally our wristbands are 99p each, but today we’re offering you, as part of our advent calendar, 5 FREE wristbands. you just need to pay £1 to cover p+p. Order your wristbands here.
The Nystagmus Network distributes leaflets, postcards and charity business cards to anyone who needs them to signpost people for support. Contact us today to order your supply.
Find out all about the biggest nystagmus event in Europe, here.
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The Nystagmus Network provides much needed information for parents of newly diagnosed children and babies . We understand that this is a very difficult time and that there is sometimes not very much information available. Our free to download Parents Booklet provides a clear introduction to the condition and gives parents an idea of what … Continue reading Information for Parents