Vivien Jones

Does size really matter? Making it as a small charity.

What Charity asked the Nystagmus Network for tips on how a small charity can make a big impact.

1.What encouraged you to start your charity? 

The Nystagmus Network was founded in the early 1980s, by Vivien Jones, a young mum with a baby boy called Sam who was diagnosed with nystagmus when he was 3 months old. Vivien found a complete lack of information available for parents of a child with nystagmus. Today, we all take advantage of having immediate answers to questions via the internet, but back in 1983 there was no Google. Although there were umbrella charities which supported the visually impaired, such as the RNIB, even they had little or no information on nystagmus. 

2. What difficulties did you encounter starting out?

Vivien had to undertake her own research and identified that the London Refraction Hospital, now the Institute of Optometry, was taking a lot of interest in nystagmus. She got an appointment. Meeting other families and adults with nystagmus, it became clear there was a need for a group which provided information to families, offered support and gave them the opportunity to meet. The Nystagmus Network was born. Its first meeting was held in 1984 and it quickly achieved media coverage which led to people from around the UK wanting to join. Letters began to pour in. Vivien remembers sitting up late into the night answering them and creeping out into the darkness to post the replies at the post box on the corner of her road. There was a huge unmet need for support, and membership rapidly grew. The group also started to produce leaflets, including a guide for adults with nystagmus and a school form for parents to give to teachers who had a child with nystagmus in their class. 

3. Why should people support your charity?  

The charity has achieved great things in the last thirty years. It hosts an annual Open Day which brings together the nystagmus community (both families and researchers) and this has grown from a few families to over 200 people attending the Open day in 2019. The Nystagmus Network also plays a prominent role in research into the condition and hosted the first International Research Meeting into nystagmus in 2005. Since then, there have been 3 subsequent meetings and an annual UK workshop, which have seen breakthroughs in understanding the condition and potential treatments for nystagmus. The charity also set up national and international Nystagmus Awareness Day in 2013. The day, celebrated on 20 June, has raised thousands of pounds and put the word nystagmus and the condition on the map.

4. What makes you unique? 

Nystagmus is not a rare condition, but until someone they know is born with it or they acquire it themselves, people have usually never heard of it before. The Nystagmus Network is the biggest European patient group for nystagmus. We are a small charity, supporting the 1 in 1,000 people at least living with nystagmus. We are a membership organisation and represent the voice of our members at every opportunity, working alongside teaching professionals, clinicians and research teams as well as supporting parents of newly diagnosed infants, who still need that same support Vivien was looking for, but could not find all those years ago.

5. Do you have any top tips for people starting their own charity? 

Starting a charity takes a lot of hard work and dedication. It is never going to be easy, but, if your heart is in it, you will succeed. As founder, Vivien is still very much involved with the work of the charity today. She serves as Honorary President and heads up the charity’s research sub-committee. Her son, Sam, is a charity trustee and in recent years has run the London Marathon to raise vital funding for more research. The charity is built on the dedication of one woman who inspires loyalty, respect, purpose and ambition in the charity’s volunteers and small staff team.

Nystagmus and driving by Sophie

Please download our guide to Nystagmus and Driving here

This guest post is from blogger, Sophie who shares her experience of living, laughing and loving with nystagmus in her blog ‘Nystagmus in a Nut Shell’.

Nystagmus and Driving – what’s the real deal?

Well, I’ve had experience in this matter, so let me share it with you…

Can people with Nystagmus drive? Without a doubt, that’s one of the most common questions for parents of or any person with nystagmus to have…

In my previous blog post “5 things to NEVER say to someone with Nystagmus” I mentioned that a lot of people with the condition can’t drive, which is true. HOWEVER, and this is a BIG however, it all depends on each individual case.

If any of you attended the Nystagmus Network’s open day in Birmingham a few years ago, you may have witnessed my appalling presentation where I rambled on aimlessly about my life, including being able to drive. Well, for starters, my nerves were level 500000, and when I’m nervous I babble on with no filter. Please let me set the story straight and explain from the beginning:

Here’s my experience of driving with nystagmus

(Sorry – it’s a long one!)

I’ve always had it drummed into me from a young age that I’d never be able to drive, and I didn’t really have a choice but to accept that.  When I went to uni (three weeks after my 18th birthday) the only form of ID I owned was my passport and of course, giving the infamous university culture, I was ‘out out’ every night. After a while I was growing tired of all the near-misses of losing my most valuable form of documentation.

It must have been during my first semester of my second year when I went for a check-up at Moorfields Eye Hospital, when the optician asked me if I was driving yet. Of course, my immediate reaction was to give her the dirtiest of looks because surely, she of all people should know that people with Nystagmus can’t drive. However, she assured me this wasn’t the case and that I meet all the driving requirements.

Absolutely flabbergasted, I went online and applied for my provisional driver’s license as soon as I got home. My little brother had applied for his a few weeks before me and he received it in the post after ten or so days, so I thought that it’d be the same experience for me – WRONG.

When filling in the online form, you must declare whether you have any medical conditions etc. Not going to lie, I was tempted to put no, because Moorfields had said I was okay to drive, and they’re the best eye hospital in the world so they know their stuff, right? Luckily my mum (who was also shocked that I’d been given the all clear) said that I needed to declare it for insurance purposes; like if I had an accident I may not be able to claim make a claim if I hadn’t declared my eyesight problem and it came out that I have Nystagmus.

A few week or so later, the DVLA got in contact with me saying that they need more information about my eyesight before they could process my application further, which is fair enough. I can’t recall exactly what I said to them (we’re talking over five years ago now – I’m getting old), but they eventually got back to me and said they had rejected my application. Of course, me being the stubborn lass that I am, wouldn’t take no for an answer, so I asked Moorfields to compile a letter for me explaining exactly what they told me.

Fast forward to what must have been two month or so later and I final got another letter from the DVLA, saying that they were going to have to conduct some tests on me to confirm that it was okay for me to sit behind the wheel. For the first test, I had to go to my local Specsavers to have a sight and peripheral vision test. The sight test was pretty much basic – reading numbers descending in size off a chart (something I’ve had to do at least once a year since I was too young to remember). The peripheral one on the other-hand, I’d never had done before; it consisted of positioning my head in this white fish bowl-type container, keeping my head still, staring straight ahead and clicking every time I saw a a light pop up. The guy who was monitoring my responses gave me about five or six attempts to pass the test because he was fascinated by my eyes and how there was no reoccurring pattern to which ones I’d miss because of my eye movement. Normally, he said, people would either miss the lights appearing to the right or left, or up above, but there was no correlation with me. I think I finally managed to pass on the sixth attempt, however when the guy did say that he would never want to be in a car with me. The cheek.

A few months later I received another letter from the DVLA saying that the final stage was to go and do the classic number plate reading test. Leading up to it, my mum and I were measuring out the distance (around 67 feet) and getting me to practice reading the plates, which I was just about doing. So when the day came for my official number plate test, I felt semi confident. My boyfriend, who had just passed his test at the time, took me to my local test centre where, this is no word of a lie, I spent 45 minutes trying to make out the letters/numbers on the designated plate. FORTY FIVE MINUTES. But I still passed, and I received my provisional license. The whole process probably took over a year.

I honestly thought that getting my provisional would be the hardest part of the driving experience for me – how wrong was I? First, I had lessons in a manual car, and to be honest, I wasn’t progressing as fast as I should have been. 20 lessons and around £600 in, I couldn’t even drive on the main road, we were just driving around my estate or a car park. I was still misjudging the distance between the vehicle and the curb as well as constantly stalling and turning either too early or too late. My instructor suggested that perhaps learning in a manual was giving me too much to focus on, so maybe I was better taking lessons in an automatic.

I had a break for about a year, in the meantime I switched so taking a break from the stress of driving did me the world of good. I then found an automatic instructor around the corner from work, so he collected me at 17:30 every Tuesday. The first time I drove an automatic, I found it so much easier than a manual (as everyone does). It enabled me to focus more on the other aspects of driving, such as if I was going to hit anyone or mount the curb, rather than spending the entire time worrying if I still had the ‘bite’. (some manual term). Without a doubt, I progressed further than I had previously and even drove home from work multiple times (the instructor did have to take over at the roundabouts because I kept freaking out).

I used to date someone who lived a ten-minute drive from the office, so rather than driving back to my village which took around half an hour, we used to go to the industrial estate near his to drive around. I remember once, I thought I was doing well with my turning and my instructor made me pull over. I pulled the car to the side of the curb (with his help because I either got too far up the curb or not close enough), and he asked me how many parked cars I thought I nearly hit. Even though I said none, the correct answer was every single parked car I less than 1 mm away from hitting.

Him saying that was a massive realisation for me – what if those cars had been people? What if those cars were moving and had people in them? I started crying and we called it a day for that lesson.

I resumed the next week, feeling more optimistic, but by the end of the lesson I was in tears again. This happened for at least three more weeks, then my instructor said to me that he personally didn’t feel that I should continue driving, but it was up to me. It was then that I decided he was right and that actually I should have pre-empted this considering how long it took me to pass the DVLA’s tests. The amount of time and money I had spent on lessons, someone could have passed their test at least two times and there I was having a breakdown at a roundabout. In hindsight, it took me that split second longer to focus, but that split second can be the difference between life and death on the road, not just for me but for others too.

I’m not going to lie to you, it was really hard for me to come to terms with the fact that I can’t drive and never will be able to, especially as I went from thinking I couldn’t to being told I’d be able to by Moorfields, which really got my hopes up. It was very bittersweet when my friends, little brother, cousins and stepsister passed their tests. Don’t get me wrong, I’m very happy for them, but it’s a constant reminder that I can’t drive through no fault of my own.

But, does that matter? No, it really doesn’t! I live a 20 min walk from a train station with a direct line into London, a 30 min walk from the local shops, so I’m having to exercise to get a pint of milk rather than jumping in my car, but so what? I’m keeping fit! In fact, 48% of adults in the UK don’t drive!

There are so many benefits of not being able to drive:

  • Keeping fitness levels up
  • Helping to save the environment – think about it, your carbon footprint will be smaller because you’re not producing as many emissions
  • Saving money – no lesson or test fees, insurance, finance, or petrol costs. Paying for public transport is far less in the long-term
  • You never have to be the designated driver on a night out – for me, this is the most important one!!!!

However, just because this is my experience doesn’t mean that all people with Nystagmus can’t drive. Someone else I know with the same eyesight problem has been driving for years, which continues my point from previous blog posts; Nystagmus effects people in different ways. What may be true for me may not necessarily be the case for you.

What would my advice be for driving with Nystagmus? Give it a shot if you get the option – you don’t know until you try. But if you’ve already been told by your optician that driving isn’t on the table, then it really isn’t a big deal. So many people have said to me “how do you cope not driving?” and to be honest I just look at them and laugh. It’s actually funny how people are so dependent on driving and couldn’t imagine life without their car – how sad is that? If you replaced a car with another materialistic object such as Ray Ban sunglasses, they’re saying how they can’t live without their Ray Bans. Yeah, how silly does that sound. At the end of the day, no car? So what? There are other ways of transportation. If you can drive, then brilliant! Some people can, some people can’t, it’s no big deal and people will think no less of you no matter what. If they do, are they worth having in your life?

So, I’ve shared my experience of driving with Nystagmus with you – what’s yours?

Bye for now,

Sophie xx

For information on nystagmus, driving and the DVLA requirements, please see our free to download booklet ‘Nystagmus and Driving’.

Design our Christmas card

At Open Day we announced our competition for children to design the Nystagmus Network 2018 Christmas card. Cards will be available to purchase from early November and will help us raise much needed funding for the charity.

Ben and Charlotte, Lilly, Jack and Rowan are our current front runners, but there’s still time for you to enter your design.

Entrants must be aged 5 to 15 years and have nystagmus. Please scan and email your design to [email protected] or post your drawing to:

Nystagmus Network, 15 Robinia Green, Southampton SO16 8EQ

Closing date: Friday 12 October

Sign up to the Nystagmus Network lottery

Did you know that for just £1 per week you could be in with a chance to win £25,000? You could, if you signed up to the Nystagmus Network lottery.

The even better news is that, once all the prizes are paid for, all profits come directly to the Nystagmus Network as a donation.

If you’d like to find out more and sign up, please click the link.

James and Thomas’s Summer Challenge

James and his little brother, Thomas, are taking on a very special challenge this summer to raise money for two charities very close to the family’s heart.

James (8) and Thomas (5) have decided to challenge themselves to walk 118 miles throughout August to raise money for Chromosome 18 Registry and Research Society Europe and the Nystagmus Network. This means an average of 3.8 miles per day consciously walked to get to their target.

Why these charities?

When James was 10 months old he was diagnosed with Nystagmus. He is registered visually impaired as a result.

James was later diagnosed with a very rare genetic disorder called Chromosome 18q-23 distal deletion syndrome.

At least 1 in 1,000 babies are born with nystagmus.

Chromosome 18q- effects 1 in 55,000 births.

Having both is super rare!

So that Chromosome 18 Registry and Research Society Europe and the Nystagmus Network, two tiny charities, can continue to offer support to families just like James’s, please sponsor the boys today.

CLICK THIS LINK TO SPONSOR JAMES. Thank you!

Sponsors sought for Open Day 2018

The biggest nystagmus event of the year takes place on Saturday, 29 September in Birmingham. This is our annual Open Day, where 200 nystagmus families get together to talk about research, education, support, assistive technology, mobility, education and general day to day living with a visual impairment. The Nystagmus Network is seeking sponsorship from commercial organisations. If you’re interested and would like to find out more, please contact us today.

Priority booking for free tickets to charity members opens at 12:00 on Thursday, 28 June, with any remaining tickets going on general sale from 26 July.

Nystagmus Awareness Day – for sports clubs

Calling all sports and athletics clubs – we want you to join us for ‘nystagmus in the open‘ on national and international Nystagmus Awareness Day on Wednesday 20 June. We need you to help us prove that children and adults with nystagmus can take part in sport and fitness, despite their visual impairment. So please organise a fun sports day or a try out session at your local club or recreation ground and invite everyone to come along. We have free flyers to help you publicise your event. There is even a free bunting template. But if you would like some balloons, you will need to contact us, please.

Last year, with the ‘nystagmus big swim’, we proved that people with nystagmus can be amazing swimmers. Our nystagmus water babies also helped us raise a lot of money through sponsorship. You can help us achieve the same success this year.

Thank you for your support.

To make a donation for Nystagmus Awareness Day, please visit our Justgiving page. Thank you.

Nystagmus Awareness Day – for snow men!

Whilst we are all looking forward to the very first Nystagmus Awareness Day in the summer – on Wednesday 20 June – for those of you who miss the old days, when Nystagmus Awareness Day was celebrated in November, you can get this year’s ‘Wobbly Week’ off to a great start by coming sledging or skiing with us at the Snow Dome, Milton Keynes.

Jamie Fuller, from the Outspan Rebels VI ski team, is organising the first of two amazing Nystagmus Network Snow Camps. It takes place on Sunday 17 June.

There will be skiing and sledging for adults and children with nystagmus, their fully sighted parents, siblings and friends. Everyone is welcome to come along. Each session costs just £10 per person.

Charlotte Evans MBE will be there on the day along with Jamie and the Outspan Rebels, themselves. There might even be a few very special visitors!

It is sure to be a great day. So please join us if you can. To register your interest, please contact us.

To make a donation for Nystagmus Awareness Day, please visit our Justgiving page. Thank you.

Steve McKay announcement

It is with great sadness that we announce the sudden and unexpected death of Trustee Steve McKay from Newton Abbot in Devon.  Steve suffered a tragic road accident on Thursday 1 December which rendered him unconscious and he never recovered, passing away on Sunday 4 December.  Steve has been a highly-valued Trustee with the Nystagmus Network since 2009 and was responsible for our public relations and social media engagement.

He has made a huge contribution to the charity with his commitment and dedication and his seemingly boundless enthusiasm. At many of our Open Days Steve would astound everyone with his stories of daring escapades in the west country, including driving tractors and having a good go at a range of sports. He was a role model in never letting nystagmus hold him back.  Most importantly for the nystagmus community, it was Steve who came up with the notion of “Wobbly Wednesday” and who saw the potential of an annual awareness day for nystagmus that mixed serious messaging with a strong element of fun and celebration.  He recently shared a video blog with everyone about his love of photography – another of his many talents.

The Trustees and staff of the Nystagmus Network and everyone in the wider nystagmus community will miss Steve very much and our thoughts are with his family at this time.  His inspiration and zest for life and his determination not to let his visual impairment get in his way will live on, especially as Wobbly Wednesday continues to grow year-on-year. Below is a short tribute video to Steve.

Steve’s funeral will be held on Wednesday 21st December at 11.15 at All Saints Church, Highweek, Newton Abbot, followed by refreshments at the Highweek Inn. Family flowers only with donations going to the Nystagmus Network, either by sending a cheque payable to “The Nystagmus Network” to Zealleys, Funeral Directors of 17 Devon Square, Newton Abbot, Devon. TQ12 2HR, or direct via our Just Giving page here.

A mum with nystagmus shares her story

I made my first contribution to the Nystagmus Network Focus newsletter after much parental cajoling and days, weeks, months, if not years, of adolescent procrastination, in the mid-1990s. To save readers from searching the archive, I’ve got what I consider to be mild nystagmus and bad short sight and astigmatism.

Contact lenses are better than glasses but even with them I can’t see the numbers of buses until they’ve whizzed past the stop. All right, there are a few other inconveniences, like not being able to drive, but you get the picture. Well, here we are a couple of decades later and I am a parent.

“ My parents were brilliant about my nystagmus. I have to say that, they’re reading this!” – Julia

My daughter is 18 months old and it was clear from early on that her eyesight was better than mine; a smile from her father across the living room that I would not have seen without glasses brought a response from our few-week-old girl. So far, so no myopia. Nor have we seen any signs of nystagmus, so we congratulate ourselves on the random allocation of genes. (My father has nystagmus, hence the fear of passing it on.) That didn’t stop me from wondering about what sort of parent I would have been if she had had similar eye problems.

But how to help her understand my eyesight? As she gets to grips with the world around her, I realise it won’t be long before she’s pointing to the sky and saying, “Mummy, what’s that up there?” and I’ll have to go through the checklist. “Is it a bird? Is it a plane? Is it a figment of your imagination or mine?” How do I convince her that she doesn’t need to sit as close to the television as I do or hold books as close? Parenting: a catalogue of unknowns.

As she grows older, she is becoming more interested in story books, rather than picture books with one or two large-print words per page. I’m already having problems reading the text while allowing her to look at the book too. It’s just like that you’ll-have-to-share problem I had throughout primary school; I could never get close enough without hogging the textbook. Fortunately, I know most of the books we’ve got by heart by now, and no one is able to complain when I get a turn of phrase wrong — yet.

My nephew, aged three and a half, has recently issued the rude reminder that I’m pretty ropey at ball sports. I could tell that he was getting frustrated with my lack of volleying skills playing badminton in Grandma and Grandpa’s garden. I shan’t take it personally but will make a note to try to improve myself before my daughter gets to that stage.

My parents were brilliant about my nystagmus. I have to say that, they’re reading this. They were, though – in all areas but one, and that is that I learned to play the flute when really I wanted to play the cello. As I remember it, I was coerced into choosing the flute. My mother remembers it differently, but I think the arguments were as follows: the flute is smaller and easier to carry and, crucially, it goes sideways so you can get as close to the music as you need. Plus, James Galway has got nystagmus and he plays the flute. Valid arguments, yes, but I still believe that the cello is basically better than the flute and I’m sorry I didn’t get to learn it when I was young.

I have a number of experiences as a musician, albeit an amateur, related to my eyesight that I may share in another piece. I might not wait twenty years to file that copy. The moral of this story, though, is that if my child, nystagmus or no nystagmus, chooses to learn an instrument, she has free choice. But if she picks something large like the drums, the harp or the double bass, she’ll have to negotiate that with her father, the driver.

“If my child, nystagmus or no nystagmus, chooses to learn an instrument, she has free choice.” – Julia

If you have a story you would like to share with the nystagmus community through our newsletter please get in touch with us here.