Making the most of education – Rory Cobb

The Nystagmus Network was delighted to have Rory Cobb with us at Open Day 2017 to lead off the parents’ conference with an informative and inspiring presentation. Rory has a life time’s experience of working in the field of education and supporting children with low vision. Rory was ably assisted by his RNIB colleague, Sue Keil.

Here is their presentation: Rory Cobb presentation

 

 

Nystagmus research update from Southampton

The Nystagmus Network was privileged and proud to be joined at Open Day 2017 on 30 September by representatives from the 6 UK centres of excellence in nystagmus research.

Each team presented news of the latest developments over the past year and highlighted work in progress for the future.

Mr Jay Self BM, FRCOphth, PhDAssociate Professor at Southampton University and Consultant Ophthalmologist at Southampton General Hospital, joined by his colleague, Dr Helena Lee, NIHR Academic Clinical Lecturer in Ophthalmology at the University of Southampton, delivered this presentation.

Jay Self
Helena Lee

 

Nystagmus research update from Sheffield

The Nystagmus Network was privileged and proud to be joined at Open Day 2017 on 30 September by representatives from the 6 UK centres of excellence in nystagmus research.

Each team presented news of the latest developments over the past year and highlighted work in progress for the future.

Dr Helen Griffiths, Senior Lecturer in Orthoptics at Sheffield University, delivered the following presentation:

Nystagmus research update from Plymouth

The Nystagmus Network was privileged and proud to be joined at Open Day 2017 on 30 September by representatives from the 6 UK centres of excellence in nystagmus research.

Each team presented news of the latest developments over the past year and highlighted work in progress for the future.

We were delighted to have John Sanders with us again at Open Day, this time representing the work of Professor Chris Harris, Professor of Neuroscience at Plymouth University. John has been involved with Chris’s work on the Nystagmus Care Pathway project.

 

Here is John’s report:

Thank you for the opportunity to say a few words about the Nystagmus Care Pathway. I’m standing in for Professor Chris Harris who has done most of the work along with his orthoptist colleagues in Plymouth.

I’d like to explain three things:

1) what the pathway is

2) why it’s a good idea

3) what stage it’s at now.

  1. Firstly – what is it?

The Care Pathway is a set of suggestions for hospital staff and other professionals about what to do when a patient has nystagmus. For instance:

  • The pathway recommends which diagnostic tests to carry out (these may differ from case to case).
  • The information to give to the family and/or patient.
  • How to minimise the impact of nystagmus and treat any associated conditions.

The professionals involved will include ophthalmologists, orthoptists and optometrists. An individual pathway may also bring in neurologists, paediatricians, imaging teams, genetic specialists, vision scientists, VI teachers, counsellors, rehab workers and others.

Basically, the Pathway is a set of minimum standards.

  1. Secondly, why do we need a Care Pathway?

The evidence gathered by the Nystagmus Network over decades suggests that, in some cases at least, what happens in eye hospitals isn’t what patients expect, especially in terms of diagnosis, support and information.

That said, we know that some hospitals provide a very good diagnostic and information service. So one aim of the Pathway is to make sure that what the best hospitals do already happens in all hospitals.

This should lead to better outcomes for everyone with nystagmus. By better outcomes we mean things like confidence, happiness, school work and ultimately life chances – as well as treatment where that may help.

So, the Pathway is a good idea because it’s what many of you want.

  1. Where are we now?

At the moment, the Care Pathway is only a proposal. We expect that BIOS, the professional body for orthoptists, will publish the proposed Pathway on its website shortly. That should get people in the medical world talking about the Pathway. And hopefully, before long, hospitals will start using it.

In the meantime an early version of the Pathway is available. Please note that the Pathway has been updated and amended since this version was published in 2015.

Conclusion

To sum up, the Pathway should ensure that everyone diagnosed with nystagmus has a minimum standard of care.

Or, to put it another way, we can already do a lot to help people with nystagmus. The Pathway should make sure that everyone gets that help.

Maria Theodorou speaks at a Nystagmus Network event.

Nystagmus research update from London

The Nystagmus Network was privileged and proud to be joined at Open Day 2017 on 30 September by representatives from the 6 UK centres of excellence in nystagmus research.

Each team presented news of the latest developments over the past year and highlighted work in progress for the future.

Maria Theodorou, Consultant Ophthalmologist at Moorfield’s Eye Hospital, London gave the following presentation:

London – Maria Theodorou

Delegates at Open Day were also able to sign up for Maria’s latest research study into nystagmus in young children.

 

rebecca presents at the Nystagmus Network Open Day

Nystagmus research update from Leicester

The Nystagmus Network was privileged and proud to be joined at Open Day 2017 on 30 September by representatives from the 6 UK centres of excellence in nystagmus research.

Each team presented news of the latest developments over the past year and highlighted work in progress for the future.

Dr Rebecca McLean (PhD), Research Associate, Department of Neuroscience, Psychology and Behaviour, The University of Leicester gave the following presentation alongside her colleague, Frank Proudfoot.

Leicester – Rebecca McLean

 

Jon Erichsen speaks with delegates at a Nystagmus Network Open Day event.

Nystagmus research update from Cardiff

The Nystagmus Network was privileged and proud to be joined at Open Day 2017 on 30 September by representatives from the 6 UK centres of excellence in nystagmus research.

Each team presented news of the latest developments over the past year and highlighted work in progress for the future.

Professor Jonathan T. Erichsen, DPhil, Professor of Visual Neuroscience, School of Optometry and Vision Sciences at Cardiff University gave the following presentation:
Meanwhile, Jon’s colleague, Asma Zahidi, a researcher with the School of Optometry and Vision Sciences at Cardiff University, was recruiting to her latest study into Characteristics and Impact in Children with and without Down’s Syndrome. This is a joint project between the Research Unit for Nystagmus (RUN) and  the Down’s Syndrome Vision Research Unit.
Delegates at Open Day were able to sign up to take part in the study and also try the eye-tracker machine which Asma had kindly brought along.

World Film Première – Through my Lenses

The Nystagmus Network was proud to be granted permission to hold the first public screening anywhere in the world of a brand new short film about nystagmus at our 2017 Open Day in Birmingham on 30 September. Almost 200 members of the nystagmus community were present to watch the film. The film’s creator is a member of the Nystagmus Network.

Internationally acclaimed photographer David Katz shares his story in the film Through My Lenses which describes his journey from being diagnosed as blind at three months old to becoming one of the top sports photographers in the British national press by the time he was 20.

Through the film, David shows how he excelled in his chosen career of over 30 years, working as a highly respected and accomplished photographer for national and international newspapers and media, while keeping the fact that he is legally blind from almost everyone who knew him.

Remarkably, this career at the highest level of international media encompassed not only press photography, notably capturing shots of the British Royal Family including the Queen, and intimate images of celebrities such as Elton John and Amy Winehouse, but two long-term photographic documentaries, three political campaigns, and being chosen to be the personal photographer to a Prime Minister.

David created Through My Lenses in order to show what is possible with the right encouragement, persistence, dedication and commitment, and the spirit that anything is possible. His belief, based on his personal experience, is that there is no such word as ‘can’t’, and for anyone with a disability or impairment who is told that something is not possible, to know that it is.

“I was given my first camera when I was seven years old and have been in love with photography ever since,” he says. “I see things in a different way to other people. As a child I found it difficult to express what I saw through drawing or painting – a camera was the next best thing.”

Until now David hasn’t spoken about his condition as he didn’t want to be treated any differently to anyone else but feels the time has now come to share his story in the hope of helping others.

“There is some fantastic work being done out there, by organisations including the #valuable campaign, headed by Caroline Casey, which calls on businesses to recognise the value of one billion people with disability, and the Nystagmus Network. My hope is that I can add to that work and use my experience, knowledge and understanding to show children and their parents that they can achieve anything they want to. I hope my story proves that.” David Katz, September 2017