Roger stands in his garden.

#YouMadeItHappen – Roger

This year on #YouMadeItHappen Day we’re celebrating the nystagmus heroes of 2019 who’ve really helped make a difference for the nystagmus community.

Roger inspired us to write a brand new guide to nystagmus – for adults. He generously shared his own thoughts on the subject to start us off and members of our community chipped in with their own thoughts.

The result? A brand new guide to nystagmus, which will be published in the New Year.

Thank you, Roger

Read Roger’s description of nystagmus here.

Nadine smiles for the camera

#YouMadeItHappen – Nadine

This year on #YouMadeItHappen Day we’re celebrating the nystagmus heroes of 2019 who’ve really helped make a difference for the nystagmus community.

Nadine decided she didn’t want her little daughter to grow up in a world where people didn’t know about nystagmus, so she wrote her book ‘Can I tell you about Nystagmus?’ which explains nystagmus so simply that even a child can understand it.

Thank you, Nadine

You can order your copy of Nadine’s book, here.

Mike explains nystagmus and benefits at Open Day.

#YouMadeItHappen – Mike

This year on #YouMadeItHappen Day we’re celebrating the nystagmus heroes of 2019 who’ve really helped make a difference for the nystagmus community.

Mike is a professional benefits expert who also happens to have nystagmus. He is always ready with advice and guidance which he offers freely to Nystagmus Network members. He also writes our guide to nystagmus and benefits.

A regular at our annual Open Day, Mike lends his time, support and expertise to Nystagmus Network members every day of the year.

Thank you, Mike

Download the latest version of Mike’s guide: DLA, PIP and Nystagmus, here.

Patsy

#YouMadeItHappen – Patsy

This year on #YouMadeItHappen Day we’re celebrating the nystagmus heroes of 2019 who’ve really helped make a difference for the nystagmus community.

Patsy is one of our newest volunteers. It’s thanks to her that we were able to start up our virtual support group for people diagnosed with Acquired Nystagmus.

Living with AN herself, Patsy is well aware of the frustrations of getting a diagnosis and any advice or treatment for the condition. She is championing the cause of AN, asking the researchers all your most searching questions, supporting others and giving them a voice.

Thank you, Patsy

If you or someone you know would like to join our virtual Acquired Nystagmus support group, please contact us today.

Open Day 2019 – the highlights

Over 200 people gathered together on Saturday 28 September at the spectacular Principality Stadium, Cardiff for the Nystagmus Network Open Day 2019.

To the strains of Sospan Fach, by Cerys Matthews, Chairman of the Nystagmus Network, Richard Wilson OBE took to the stage to welcome everyone.

Up next, Nystagmus Network Founder and Honorary President, Vivien Jones, introduced lead researchers from Cardiff, Leicester, London, Plymouth, Sheffield and Southampton.

Elsewhere in the stadium, the children were enjoying the first drama workshop of the day, courtesy of UCAN Productions.

Next to take to the stage was Daniel Williams, Founder of Visualise Training and Consultancy and our keynote speaker for the day. Daniel shared his own sight loss story and reinforced the message that, with the right support in place, children and young people with impaired vision can achieve their goals.

There was a strong emphasis on education and, in particular, SEN support for children with nystagmus today in Cardiff.

Next to the stage were Nystagmus Network trustees and volunteer education advocates, Frances Lilley and Claire Brinn.

Following close on their heels was Michael Charles from Sinclairs Law, Cardiff. Mike and his colleague, Kevin, were there to provide information and advice for those families whose children attend schools in Wales, where SEN legislation is slightly different from that which applies to English schools.

Later, parents and carers had the opportunity to attend surgeries, drop ins and Q+A sessions with our legal experts.

Gwyn McCormack is the Founder of Positive Eye, an award winning teacher training provider, working to support children with special educational needs and impaired vision.

Gwyn introduced us to her character, Marvin and showed parents how to support their children’s learning and development using simple, everyday objects and tasks.

Elsewhere, Hannah-Elisabeth Ricketts ran a workshop on nystagmus in the workplace.

At lunch time Dr Gareth Rees from DVLA answered delegates’ questions about nystagmus and driving.

Researchers and clinicians were inundated with visitors to the Research HUB.

Our visitors also enjoyed the exhibition, which included suppliers of assistive technology, VI charities, the colleges and a beautiful selection of paintings by Neill Mison the ‘visually impaired artist’ who was there to chat with families about his art.

Parents were networking and getting down to their most burning questions in our Parents’ Forum with mother and daughter team, Jules and Hannah.

Meanwhile, Sara was busy in the Nystagmus Network charity shop selling T-shirts, mascots, raffle tickets and Christmas cards.

Nadine Neckles, author of this year’s fabulous new book “Can I tell you about Nystagmus?” joined us next. Nadine told us all about her book and her experiences of parenting a young child with nystagmus.

At tea time she signed copies of her book.

You can buy your copy, here.

We heard from our speakers in the afternoon about all the services available across the UK for people living with impaired vision and those supporting someone who has a vision impairment.

Representatives of all of these services were part of our exhibition.

Meanwhile, the children are enjoying a second drama workshop or taking part in a team-building exercise with VI rugby ace, Wil Maudsley. Wil was joined by surprise guest and total rugby fan, Adam Hills.

We may not be celebrating the 25th anniversary of our friendship quite yet, but, to the tune of “I’ll be there for you” by the Rembrandts we welcomed to the lectern two of the Nystagmus Network’s very best friends, Joanne Green, Head of Events and Fundraising at Moorfields Eye Charity and Rubina Ahmed, Head of Research at Fight for Sight.

Jo celebrated the amazing achievements of our abseilers and eye to eye walkers who have together raised very nearly £20,000 towards nystagmus research at Moorfields Eye Hospital and University College, London.

Rubina told delegates about our joint funding, to the tune of £250,000 over the next 3 years, of a brand new post-doctoral research project in nystagmus and other joint investment projects to come.

Young Oliver Mitchell welcomed us back into the Millennium Lounge with his rendition of “Danny Boy” in a respectful nod to our charity patron, Sir James Galway. Well done, Oliver!

And finally, we welcomed to the stage singer/songwriter, Ben Haynes. Ben knows only too well what it’s like growing up with nystagmus and albinism, but it hasn’t stopped him from pursuing a career in music. He generously shared his story and some of his music. You can hear Ben’s latest single, here.

Thank you to everyone who made the Nystagmus Network Open Day 2019 such a success and thank you to each and everyone who said yes to Cardiff.

We’ll be doing it all again next year on Saturday 3 October. The location and venue are still to be decided but you can put the date in your diary NOW!

Roger stands in his garden.

Nystagmus is …

In the run up to Nystagmus Awareness Day on 20 June, we published lots of your nystagmus success stories in our campaign “How amazing are you?”

One of the most popular stories was Roger’s.

When Roger first contacted us he began by saying “I have enjoyed Nystagmus for nearly 80 years.” He went on to describe how nystagmus affects him and that he’d really like others to do the same so that everyone knows what it’s like.

We thought: What better way to raise awareness of nystagmus? So we launched our competition ‘Nystagmus is …’

We received loads of entries which will feature in our new publication later this year. Meanwhile, we’d like your help in choosing the winning competition entry. Please vote in our Facebook poll, here or on Twitter, here.

We are hugely indebted to Roger for his inspiration. You can read his description of his nystagmus here.

Trustees discuss Parent Power with Marsha

On Thursday 20 June, Nystagmus Awareness Day a group of Nystagmus Network trustees met with Marsha de Cordova MP in Parliament.

Earlier that morning, Marsha had tweeted her own Nystagmus Awareness Day video message in which she asked us all to celebrate the amazing achievements of people with nystagmus and support and encourage our children and young people with nystagmus to achieve their potential.

Watch Marsha’s video message here.

Among the many topics discussed at the meeting, trustees were able to tell Marsha about the charity’s brand new National Lottery funded project ‘Parent Power’ designed to provide parents and carers with the knowledge and skills they need to ensure that their children with nystagmus access the special educational support they need in school.

The picture shows Marsha with Nystagmus Network trustees, left to right, Vicky Pitman, Claire Brinn and Tim Cuddeford.

How amazing is Claire?

In the run up to Nystagmus Awareness Day on 20 June, we’re celebrating all your success stories in our campaign “How amazing are you?”

Claire is doing a fundraising tandem sky dive for the Nystagmus Network this summer, because she and her son both have nystagmus.

This is going to make her son even more proud of his Mum!

If you’d like to share your amazing nystagmus story, please contact us today. To help the Nystagmus Network support even more people to reach their amazing potential, please consider making a donation. Thank you.

Mike explains nystagmus and benefits at Open Day.

How amazing is Mike?

In the run up to Nystagmus Awareness Day on 20 June, we’re celebrating all your success stories in our campaign “How amazing are you?”

For those of you who don’t know Mike, he’s a hugely valued member of the Nystagmus Network team. He’s our volunteer benefits adviser and the fount of all knowledge when it comes to nystagmus, DLA and PIP.

Mike has helped 100s, if not 1000s of people apply for benefits, whether they’ve sought his advice on applications or appeals, attended his enormously popular Open Day workshops or simply downloaded our free guide to nystagmus and benefits, which Mike writes and updates for us each year.

Mike has nystagmus himself, but doesn’t let it stop him from pursuing his career as a professional benefits adviser, volunteering and just being a Dad.

So Happy Father’s Day, Mike and thank you for all you do.

If you’d like to share your amazing nystagmus story, please contact us today. To help the Nystagmus Network support even more people to reach their amazing potential, please consider making a donation. Thank you.

How amazing is Hanna?

In the run up to Nystagmus Awareness Day on 20 June, we’re celebrating all your success stories in our campaign “How amazing are you?”

Today we introduce our friend, Hanna

Have you met Hanna? Hanna has congenital nystagmus and lives in Germany. She has been coming to the UK Nystagmus Network Open Day for a number of years and recently achieved her goal of setting up a German Nystagmus Network, too. It was incredibly hard work, but Hanna achieved it and now her own group is growing from strength to strength. Find out more about the German Nystagmus Network, here.

Hanna – we think you’re amazing!

If you’d like to share your amazing nystagmus story, please contact us today. To help the Nystagmus Network support even more people to reach their amazing potential, please consider making a donation. Thank you.