Claire and her young son smile for the camera

Thank you, Claire

Both Claire and her young son, Zac have nystagmus. In 2019 Claire decided she was going to do a sky dive for the Nystagmus Network. Postponements because of the weather and then again this year because of lockdown, meant Claire was waiting nervously nearly a whole year before she could make her leap. But she finally did it in 2020 and raised £420.

Thank you, Claire.

This year has been a difficult year for us all, but Giving makes us feel Good! #GiveBack2020 is your chance to take something positive from 2020 and make a difference at the same time!

Please volunteer, fundraise or make a donation to the Nystagmus Network for #GiveBack2020  

Contact us here to volunteer

Find fundraising ideas here

Please make a donation here

THANK YOU

A woman holds her head in her hands and appears o be in some discomfort.

Living with Acquired Nystagmus and Oscillopsia?

The Nystagmus Network runs a virtual support group where people living with Acquired Nystagmus and/or Oscillopsia chat together on email and on zoom to share their experiences and try to find answers together.

If you’re living with AN or oscillopsia and would like to join the group, you’d be most welcome. 

At our recent virtual Open Day we were lucky enough to be joined by Professor Chris Harris, a leading UK expert in AN and oscillopsia at the Royal Eye Infirmary, Plymouth. Chris recorded a presentation for us, which you can view here and then took part in a live Q+A session with our group on 3 October.

Since then we have continued to reach out to more people living with AN and Oscillopsia so that we can support Chris in his research endeavours. We are gathering a sizeable ‘patient’ group together and are collating meaningful data on causes, symptoms, treatments (conventional and alternative therapies, helpful or otherwise) and evidence of the effects of these conditions on general wellbeing, including mental health.

We are also writing up and recording your stories and drafting a questionnaire to help us collect even more information.

All of this will enable Chris to strengthen his applications for further funding for research into these debilitating and often life-changing conditions.

If you would like to be included in invitations to all future zoom get togethers for people living with Acquired Nystagmus and Oscillopsia, please contact us here.

At our most recent online meeting we were joined by people with experience of new drug and surgical treatments.

Our next call will be in January when we will share an update on the work we have done so far in our evidence gathering.

If you would like to join our virtual AN support group, please contact us here and we will be happy to introduce you.

Please do help us with this exciting new project. We look forward to having you with us.

The logo of Gene Vision

Gene Vision launches

Gene Vision launched to support those diagnosed with genetic eye diseases

London, 01 December 2020

A new website, Gene Vision, has launched today, developed by Professor Mariya Moosajee and Dr Alex Yeong, supported by Dr Peter Thomas (Director of Digital Innovation at Moorfields Eye Hospital). The new site is intended for adults, children and their families who are diagnosed with rare genetic eye diseases.

The site includes in-depth condition-specific information for patients and their families as well as current research and clinical trials. It will also act as a resource for clinicians and allied healthcare professionals who are diagnosing patients, as well as those in earlier career stages learning about the conditions themselves. In addition, it is anticipated that the site will be used by GPs and other referring specialists so that they can learn more about their patient’s condition quickly and easily, whilst understanding how to provide the best care plan.

Genetic disorders are rare, but together they affect 1 in 25 children in the UK1, and contribute to more than 60% of blindness among infants worldwide2. Inherited retinal diseases are the commonest cause of blindness among working-age adults generating a huge burden for those with the disease and their families.3

“It can be devastating for those receiving rare genetic diagnoses, and frequently patients are not provided with the accurate information they need. Unfortunately, there is also a lack of professional knowledge so patients are not always signposted to relevant resources for information and support, or offered the appropriate investigations, nor information on the latest research and trials, which could really benefit them in the short and long term,” says Professor Moosajee.

“Families deserve to know whether the condition could reoccur in future pregnancies or be passed on to the next generation, or if there are clinical trials they could access. Receiving a genetic diagnosis can cause a great deal of anxiety and worry, hence we needed to develop a trustworthy open-access knowledge resource that complements other credible and accurate information already out there, like the Retina UK website.”

Gene Vision provides in-depth information on conditions and specific genes in a searchable format. There is opportunity to find out about the latest research, external support including specific charities. In addition, an overview of the eye anatomy is provided to give context for those without prior insight.

Gene Vision has been jointly supported and funded by the The National Institute for Health Research (NIHR) Biomedical Research Centre (BRC) at Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology and Retina UK, a charity which works for people with inherited sight loss. Key medical charities including Microphthalmia, Anophthalmia, Coloboma Support, Aniridia Network, International WAGR Syndrome Association, Nystagmus Network and others have also inputted on content.

The website has been tested by patients with differing levels of sight loss, who use a range of digital accessibility software and magnification devices, together with parents of affected children and health care professionals. It has also had formal design input by digital accessibility consultants who suffer from genetic eye disease themselves. This website is also mobile friendly and so can be accessed anywhere.

Dr Yeong who led on the project said, “I am really proud of what has been achieved with Gene Vision and I am excited to hear from some of the patients and their families who will benefit from it now.” 

References

  1. Jeans for Genes; http://www.jeansforgenes.us.com accessed 17.11.20
  2. Cleveland Clinic; https://my.clevelandclinic.org/health/diseases/17130-eye-disease-inherited–genetic  accessed 17.11.20
  3. Liew G, Michaelides M, Bunce C. A comparison of the causes of blindness certifications in England and Wales in working age adults (16–64 years), 1999–2000 with 2009–2010 BMJ Open. 2014 Feb 12;4(2):e004015.

Notes to editors

Professor Mariya Moosajee

Professor Mariya Moosajee is a Consultant Ophthalmologist in Genetic Eye Disease at Moorfields Eye Hospital and Great Ormond Street Hospital for Children. She is a Professor of Molecular Ophthalmology at UCL Institute of Ophthalmology, and Group Leader of Ocular Genomics and Therapeutics at the Francis Crick Institute in London. Professor Moosajee’s current clinical focus is providing a genomic ophthalmology service for children and adults affected with pan-ocular genetic eye disease. She also leads an active research group and is focused on both clinical research, which involves detailed characterisation of patient’s clinical features and natural history studies to understand disease progression and define outcome metrics for clinical trials. In the laboratory, she is advancing our understanding of the molecular basis of ocular maldevelopment and inherited retinal dystrophies. Dr Moosajee is the joint President of the UK Eye Genetic Group, sits on the Education and Academic committees at the Royal College of Ophthalmologists, and is the President of Women in Vision UK.

Mr Peter Thomas

Peter is the Director of Digital Innovation and a Consultant Ophthalmologist at Moorfields Eye Hospital. Clinically, he specialises in paediatric ophthalmology and strabismus surgery. He has been involved in digital health for many years, and his main interest is in driving the digital transformation of eyecare in the UK. His work supports the creation of new models of care, for example the recent deployment of video consultations and home monitoring at Moorfields, that are more convenient and more available for patients. He sits on a number of national committees and boards to drive this process agenda across all of ophthalmology and in the NHS more generally. His current research with the Moorfields’ Digital/Clinical Lab involves the assessment of environmental impact of healthcare, and the creation and implementation of clinically helpful artificial intelligence solutions.

Dr Alex Yeong

Alex is a fifth-year ophthalmology specialist trainee based at the Royal Victoria Hospital in Belfast, Northern Ireland. He graduated from University of Dundee in 2013 and remained there for two years to complete his foundation training. He moved to Northern Ireland in 2015 to commence his ophthalmology training, but spent the past year at Moorfields Eye Hospital in London creating Gene.Vision. Alex has an interest in retinal diseases and has been involved in various research projects, including a Cochrane systematic review on a form of investigative treatment for age-related macular degeneration, he has contributed to the Textbook of Genomic Ophthalmology by writing the chapter on inherited retinal dystrophies under the supervision of Professors Mariya Moosajee and Andrew Webster. He also organised and run a research clinic in Belfast recruiting patients with nystagmus into the 100,000 Genomes Project, which subsequently piqued his interest in genetics and applied to help create the Gene.Vision website. Alex believes that patient care can be enhanced by bridging the gap between patients and healthcare professionals through sharing clinical information in a comprehensive and easily-understood manner. The Gene.Vision website is created around this core value.

About NIHR Biomedical Research Centre at Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology

The NIHR Moorfields Biomedical Research Centre was established in April 2007 and awarded a third five-year term by the NIHR from April 2017. Its purpose is to conduct translational research that is designed to take advances in basic medical research from the laboratory to the clinic, enabling patients to benefit more quickly from new scientific breakthroughs. The Centre is currently one of 20 Biomedical Research Centres that were awarded to NHS/university partnerships with an outstanding international reputation for medical research and expertise, and experience of translating that research into the clinical setting. For further information, please visit www.moorfieldsbrc.nihr.ac.uk/

About Retina UK

Retina UK is a Retina UK is a CIO, Registered Charity Number: 1153851, working for people with inherited sight loss. They fund medical research to understand these complex conditions and speed up the search for treatments and provide information and support services to help more people lead fulfilling lives. Retina UK has funded more than £16.5 million of research into inherited sight loss conditions in its 43-year history. For further information, please visit www.RetinaUK.org.uk.

About Moorfields Eye Hospital NHS Foundation Trust

Moorfields Eye Hospital NHS Foundation Trust is one of the leading providers of eye health services in the UK and a world class centre of excellence for ophthalmic research and education. Our main focus is the treatment and care of NHS patients with a wide range of eye problems, from common complaints to rare conditions that require treatment not available elsewhere in the UK. Our unique patient case-mix and the number of people we treat mean that our clinicians have expertise in discrete ophthalmic sub-specialties.

We treat people in 32 locations in and around London, the south east and Bedford, enabling us to provide expert treatment closer to patients’ homes. We also operate commercial divisions that provide care to private patients in both London and the Middle East.  

With our academic partners at the UCL Institute of Ophthalmology, Moorfields is recognised as a leading centre of excellence in eye and vision research. Together we form one of the largest ophthalmic research sites in the world, with the largest patient population in Europe or the USA. We publish more scientific papers than any other eye and vision research site and have an extensive joint research portfolio.

About UCL Institute of Ophthalmology

The UCL Institute of Ophthalmology (UCL IoO) delivers innovative ophthalmic research and education in partnership with Moorfields Eye Hospital. UCL is ranked eighth in the QS 2020 World University Rankings and rated as the top UK University by research strength. According to the 2017 Centre for World University Rankings, UCL IoO is the best place in the world to study ophthalmology. Part of the Faculty of Brain Sciences, UCL IoO attracts researchers and academics of the highest international calibre. The institute works with education institutions and hospitals around the world to help raise teaching standards and train the next generation of eye and vision health experts. For further information go to: https://www.ucl.ac.uk/ioo/  

About UCL
Founded in 1826, UCL was the first English university established after Oxford and Cambridge, the first to admit students regardless of race, class, religion or gender, and the first to provide systematic teaching of law, architecture and medicine. It is among the world’s top universities, as reflected by performance in a range of international rankings and tables. UCL currently has almost 29,000 students from 150 countries and in the region of 10,000 employees. For further information, please visit: www.ucl.ac.uk.

Helen Khan

Communications Manager

NIHR Biomedical Research Centre at Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology

A close up of a man's eyes.

New nystagmus research

We are excited to announce the start of a new research study into nystagmus

The aim of the study is to gather evidence about people’s perceptions of nystagmus. The results will help shape further nystagmus research and awareness raising strategies, eventually contributing to better understanding of the condition and improved quality of life as a result.

Anyone can take part in this research, whether they have nystagmus or not, know someone who has the condition or, even more importantly, have never heard of nystagmus before and don’t know what it is.

Participants just need to take a survey which will collect responses anonymously. Members of the nystagmus community helped devise some of the questions.

The survey takes 5 minutes to complete. Please take part today and then share the link with your friends, family, colleagues, whoever you can think of, especially with people who may have never heard of nystagmus before.

The more people who take the survey, especially people who don’t know about nystagmus already, the better information we will gather.

Take part in the survey here

Thank you.

Chris Harris sits behind a microphone and prepares to speak.

Do you have Acquired Nystagmus or Oscillopsia?

We need you!

The Nystagmus Network is supporting Professor Chris Harris and his team at the Royal Eye Hospital, Plymouth to investigate further Acquired Nystagmus and Oscillopsia.

If you have either or both, we’d love to hear from you. You can help us develop a further research study into these complex, life changing conditions.

We can also offer you support.

Please contact us today

Watch a video message from Chris here

Join our AN Facebook group here

An image shwoing the Nystagmus Network eye logo and the words Nystagmus Network Acquired Nystagmus and Oscillopsia Facebook Group, call 01427 718093, www.nystagmusnet.org
Nystagmus Network trustees stand together and smile at the camera.

Could you be a Nystagmus Network trustee?

Trustees play an essential role in the running of the Nystagmus Network. Whilst it is not a role to be taken on lightly and may be demanding of time and skills, especially within a small organisation like ours, it can be rewarding for many reasons. Meet our trustees here.

The charity’s trustees share ultimate responsibility for making sure the charity is fulfilling its charitable objectives, and that all decisions put the needs of the nystagmus community first.

Becoming a trustee is a great opportunity to make a contribution. As a trustee you can guide the direction of the charity’s growth and have the opportunity to make a significant impact on an issue of value to you personally. It undoubtedly also offers professional development and the opportunity to work within a diverse team in support of the same cause.

If you would like to become a trustee of the Nystagmus Network and have skills in

  • Fundraising
  • Volunteer Management/Networking
  • Corporate Law
  • Clinical Practice
  • IT and Web Design

please email [email protected]

A screenshot of the Nystagmus Network UK research workshop on zoom, showing thumbnail images of 20 delegates.

Nystagmus Network hosts UK research workshop

On Friday 2 October, the Nystagmus Network once again hosted the annual UK nystagmus research workshop.

This is an opportunity for researchers, clinicians and academics to get together to share their work and plan greater collaboration. They are, after all, all working towards the same goal. The workshop took place via zoom.

Nystagmus Network trustees and staff were delighted to be joined by nystagmus experts from

  • The School of Optometry and Vision Sciences, Cardiff University
  • The Ulverscroft Eye Unit, University of Leicester
  • Moorfields Eye Hospital, London
  • Royal Eye Infirmary, Plymouth
  • Academic Unit of Ophthalmology and Orthoptics, University of Sheffield
  • University of Southampton and Southampton General Hospital

Barry Smith head shot

How your eyes help with balance

People living with nystagmus often experience dizziness and problems with balance. In his radio programme ‘The Uncommon Senses’, Barry Smith explores the senses involved in balance and why our vision is so important.

A journey into the human multi-sensory experience, with philosopher Barry Smith and sound artist Nick Ryan. In this episode, we look at the intricacies involved in standing up. For thousands of years people thought we had 5 senses, now it’s believed we have up to 33. In this new series, philosopher Barry Smith and sound artist Nick Ryan take us into the extraordinary world of sensory perception. Barry Smith explores how ballet dancers can whirl around like spinning tops, and why the classic ‘drunk driver’ test works. And we examine the strange workings of the 3 senses involved in the simple task of getting to our feet: vision, vestibular, and proprioception, and ask what happens when they go wrong.

Listen to the programme on BBC Sounds here

Libby smiles at the camera.

Can you help Libby with her research?

Introducing Libby

I am a geography student studying in my final year at Loughborough University. 

I am seeking participants for my dissertation study which aims to explore the experiences of young adults (18-25) in their local space / environment & the impacts on identity formation.

This study is inspired by my two younger sisters, who both have nystagmus. 

I am seeking individuals who would be able to offer me an hour of their time to chat and discuss their experiences of entering the ‘adult world’ with a visual impairment. I am open to hear about experiences of people who use visual aids and those who choose not to.

The aim is to increase awareness of the daily experience individuals with VI have, be that positive or negative.

I am currently seeking around 5-6 participants aged 18 to 25.

Due to COVID-19, I am unable to meet individuals in person.

To find out more or to take part, please email Libby at [email protected]

Disclaimer: This study has full ethical clearance and is fully insured by Loughborough University.