Find out all about the biggest nystagmus event in Europe, here.
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 … Continue reading Information for Parents
Following the success of the Nystagmus Network photography competition in 2017 in honour of our former trustee, the late Steve McKay, we’ve decided to launch a Christmas 2018 photo competition. … Continue reading Our Christmas photo competition
Whether you’ve had nystagmus all your life or have acquired it more recently, the Nystagmus Network is here to support adults with the condition, with information, research updates, news, meetings, … Continue reading Support for adults with nystagmus
Great for inclusion and awareness raising, the Nystagmus Network has free to download materials for schools. Don’t see what you need – please ask us. Download your free resources here.
Our very first regional nystagmus network is already up and running in Manchester, hosted by our trustee, Marie. There are lots more local groups to come in 2019, giving more … Continue reading Our new local groups
Improving eye development for children with albinism and other sight disorders – hear from groundbreaking researcher Dr Helena Lee, Academic Clinical Lecturer in Ophthalmology at the University of Southampton. Watch … Continue reading Dr Helena Lee on treatment for albinism and childhood eye conditions
A Wandsworth student visited the House of Commons to lobby Parliament this week on behalf of Young Vision Alliance (YVA), according to an article in Your Local Guardian. Katie, who … Continue reading Katie lobbies MPs
Have you visited our online Education Resource HUB? You’ll find everything you need to know about supporting a child through education, as a parent, carer or teacher, from the early … Continue reading Education information for all