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Supporting people living with nystagmus

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Category: Posts

Nystagmus Network staff under lockdown


Nystagmus Network staff team members, Sue, Sara and Debbie are all adjusting to the current pandemic and a slightly different way of doing things. Though they all usually work from … Continue reading Nystagmus Network staff under lockdown

Posted on April 17, 2020April 17, 2020Author Sue RickettsCategories PostsTags COVID-19, nystagmus network, our staff team
Nystagmus Network quiz night postcard.

Join our virtual quiz night


This Saturday at 7pm Thank you to everyone who took part in the very first Nystagmus Network virtual quiz night last week. There may have been a few technical hitches, … Continue reading Join our virtual quiz night

Posted on April 3, 2020April 3, 2020Author Sue RickettsCategories Fundraising, PostsTags family, fun, Virtual quiz night

Have you been on a bear hunt yet?


A great way to make your time outdoors fun with the children is to go on a bear hunt. Inspired by the lovely Michael Rosen’s fabulous book “We’re going on … Continue reading Have you been on a bear hunt yet?

Posted on April 1, 2020April 1, 2020Author Sue RickettsCategories PostsTags Bear Hunt, information for parents, mascots, Michael Rosen

East Sussex Parent Carer Forum – get involved


Parent carer voices are essential to help shape the services they need for their children and young people. The East Sussex Parent Carer Forum would like you to get involved.

Posted on February 21, 2020February 21, 2020Author Sue RickettsCategories Guest posts, Information and Support, PostsTags East Sussex Parent Carer Forum, parents and carers
Fight for Sight logo.

Fight for Sight survey on eye conditions and sight loss


Fight for Sight needs your help as part of a ground-breaking survey into the experience of living with sight loss or an eye condition. By taking part in the survey … Continue reading Fight for Sight survey on eye conditions and sight loss

Posted on January 22, 2020January 24, 2020Author Sue RickettsCategories Living with nystagmus, Posts, researchTags eye conditions, Fight for Sight, nystagmus, sight loss, survey

Happy New Year


from everyone at the Nystagmus Network Image by Free-Photos from Pixabay

Posted on December 31, 2019January 8, 2020Author Sue RickettsCategories Posts
Mike wears his Nystagmus Network T short and smiles for the camera

Trekking through Middle Earth for nystagmus research


Follow Mike’s wiggly progress on his Facebook page, here and donate to his Nystagmus Network fundraising page, here. A sight-impaired young Englishman, Mike Larcombe, is preparing to trek across New … Continue reading Trekking through Middle Earth for nystagmus research

Posted on November 27, 2019November 27, 2019Author Sue RickettsCategories Events, Fundraising, Posts, researchTags Mike Larcombe, New Zealand, Walk for Wiggly Eyes

Would your child like a German pen friend?


Thanks to our partnership with the German Nystagmus Network, we can now offer children and young people, who have nystagmus, living in the UK, the chance to make friends with … Continue reading Would your child like a German pen friend?

Posted on October 3, 2019October 3, 2019Author Sue RickettsCategories PostsTags German Nystagmus Network, pen friends

13% of MS patients have acquired nystagmus


In a report presented this summer, 15 of a sample of 116 patients with Multiple Sclerosis were found to have Acquired Nystagmus. Ocular manifestations often present first in multiple sclerosis … Continue reading 13% of MS patients have acquired nystagmus

Posted on September 9, 2019September 9, 2019Author Sue RickettsCategories Posts
Trustees smile at the camera.

Are you a digital champion?


Do you have the digital know how to take the Nystagmus Network up to the next level? The Nystagmus Network is keen to recruit a new trustee with the right skills set. … Continue reading Are you a digital champion?

Posted on August 9, 2019August 9, 2019Author Sue RickettsCategories PostsTags digital champion, Opportunities with us, trustees

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