Farewell Richard and thank you

On Saturday 28 September the Nystagmus Network bid a very fond farewell to its Chairman of 8 years, Richard Wilson OBE

Richard joined the charity as a trustee in 2008 and rose to Chairman in June 2011.

At the Annual General Meeting Nystagmus Network Founder and Honorary President, Vivien Jones gave a heartfelt speech in tribute to Richard. There followed a presentation including the highlights of Richard’s time as chair.

As Richard steps down the charity welcomes a newly elected Chair of Trustees, Tim Cuddeford. Tim has served as a trustee since 2017 and has held the chair of the charity’s finance team since then.

Tim Cuddeford, Chair of Trustees, Nystagmus Network

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!

Jeans for nystagmus genes

Children with nystagmus receive a grant from Jeans For Genes Day 2019

In July 2019, the Nystagmus Network is celebrating after hearing the news they will receive a grant from Genetic Disorders UK, the national charity which organises the annual fundraising day, Jeans for Genes Day. This grant, from funds raised on the Day, will be used to fund the Nystagmus Network Big Adventure.

Nystagmus Network chairman, Richard Wilson OBE said: “This grant is wonderful news. It means we can fund an exciting event for our nystagmus children and their families.”

Genetic Disorders UK’s Jeans for Genes Day is an annual fundraising event when school children and office workers wear their jeans in exchange for a donation to the charity. Although, individually, genetic disorders are rare, together they affect 1 in 25 children. This means that more than 30,000 babies each year are born in the UK with a genetic condition. Sadly, genetic disorders and their associated health problems mean that they are the biggest cause of death of children aged 14 years and under. Funds from Jeans for Genes Day are granted to specialised charities to provide care and support for children affected by genetic disorders. This year the charity is encouraging supporters to pick a day that is best for them to hold their Jeans for Genes Day between Monday 16 and Friday 20 September.

The Nystagmus Network has chosen Wednesday 18 September as our Jeans for Genes Day.

Laura Pattison, Campaign Director at Jeans for Genes Day said: “We are delighted to be helping the Nystagmus Network support children with nystagmus. Our grant programme is open to all UK support groups and registered charities who work to improve the lives of children and families affected by genetic disorders. In 2019, 22 charities will benefit from the funds raised by the public on Jeans for Genes Day.”

Notes for Editors

  • Jeans for Genes Day raises money for Genetic Disorders UK, a charity that provides much needed advice and support for individuals and families affected by genetic disorders. www.jeansforgenes.org
  • Jeans for Genes Day is an annual fundraising event, held from Monday 16 – Friday 20 September 2019. School children and office workers are encouraged to wear their jeans for the day in exchange for donations. www.jeansforgenesday.org

  • Genetic disorders are caused by an alteration in DNA. This may mean that either a gene or several genes are missing, repeated or in the wrong order. Altered genes can affect a child’s senses, movement, ability to learn or appearance.

  • The Nystagmus Network is a Jeans for Genes Day 2019 grant charity. They will receive a grant towards the Nystagmus Network Big Adventure.

We will post more news about the Nystagmus Network Big Adventure and how to take part in Jeans for Genes Day soon.

The Nystagmus Network eye logo and the words Nystagmus Awareness Day 20 June

Thank you – you are amazing

As ‘wobbly week’ draws to a close for another year we just wanted to thank everyone for making Nystagmus Awareness day 2019 such a success.

Thank you to our fundraisers, event organisers and all the parkrunners. Thank you for your amazing nystagmus success stories, your videos, photos, your donations, presentations, displays and quizzes and thank you, too, for baking all those cakes!

We couldn’t do any of this without you. You truly are amazing!

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.

Mike wears his Nystagmus Network T short and smiles for the camera

Mike’s wiggly walk

On Nystagmus Awareness Day we are proud and delighted to announce that our newest supporter, Mike plans to walk the length of New Zealand to help find a cure for nystagmus.

The route he’s following is the Te Araroa pathway, taking in both the north and south islands, on foot and sometimes in a kayak, to raise funding for two charities close to his heart: Nystagmus Network and Gift of Sight.

Mike will set off on his walk in December this year. He thinks it will take him around 131 days to complete. We are in awe of his dedication and will be with him in spirit every step of the way.

Read about Mike’s inspiration and follow his progress on his Walk for Wiggly Eyes website.

Our wobbly week competition

It’s wobbly week! And it’s Nystagmus Awareness Day this Thursday, 20 June.

We want to raise as much awareness of nystagmus as possible and make sure that everyone has a chance to take part, so today we’re launching our wobbly week competition:

Nystagmus is

Following on from Roger’s amazing description of his nystagmus, we want you to tell us what it’s like to have nystagmus – for you. So whether you’re young or a little older, whether you have congenital or acquired nystagmus and wherever you are in the world we want to hear from you.

PRIZES

There will be 1 adult winner and 1 child winner of our competition, with a choice of fabulous prizes on offer, including free membership of the Nystagmus Network for one year, a free place at Open Day 2019 in Cardiff, a T-shirt in your size and a knitted Nystagmus Network mascot.

All entries will be compiled into a brand new digital publication which will be free to download from our online shop at the end of the year, helping us continue to raise awareness of nystagmus well beyond wobbly week.

How to enter

Please complete the form below to enter our wobbly week competition.

Closing date: Sunday 23 June.

Good luck!

Community Fund logo

Parent Power – our new project, funded by the Community Fund

The Nystagmus Network is delighted to announce that we have been awarded funding by the Community Fund for a brand new project, called Parent Power.

The aim of the project is to empower parents and carers to advocate for their children with nystagmus to ensure they access appropriate educational support in school or early years settings.

Parents will be recruited from our membership and the wider nystagmus community to receive information on the rights of their children under the SEND Code of Practice, advice on how to access the full range of services available to visually impaired children and an explanation of the EHC plan application process.

At each of 5 regionally based training sessions in the academic year 2019/20 local parents and carers will come together to build a mutually supportive network so that they are able to provide and enjoy peer to peer support whilst working to support their own child.

As a result of parental empowerment, children and young people with nystagmus will receive appropriate, timely support in education to enable them to achieve their expected potential, were they not visually impaired, to follow their chosen career path and make a valid contribution to their local communities.

There will be more news about the dates and locations of our first Parent Power workshops very soon.