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Please get in touch with us using the method which suits you best. You'll find details of all of the different ways you can contact us on this page.
The content on this site will have answered some of your queries about inherited sight loss and associated syndromes, but everyone’s circumstances are different and you may have further questions.
This edition of Look Forward includes the very latest news about an experimental therapy by Retina UK funded researchers, an article about one of our PhD students, a calendar of events in 2025, the usual research news round-up and lots more. Please take the time to complete our Sight Loss Survey, enclosed with this edition. You can find out more about the Survey.
Our Retina UK Peer Support Group network offers information and support via regular meetings both online or in-person.
Achromatopsia is a rare hereditary vision disorder affecting approximately 1 in 30,000 newborn babies.
Welcome to the winter edition of Look Forward. It’s packed full of news from our Conferences, the latest research news and an interview with Hassina Zeriri, one of our funded PhD students.
We have also included details of lots of ways you can get involved with Retina UK over the coming months, along with some suggested festive fundraising for the Christmas period.
Cataracts and macular oedema are both associated with inherited sight loss and may respond to treatment.
As well as many of the well-known races, we also have exclusive places available in hundreds of local runs. Wherever you live, you can run as part of #TeamRetinaUK this year!
Could you run the London Landmarks Half Marathon 2025 for #TeamRetinaUK?
RideLondon has been postponed for 2025, but if you would like to find out more information about future events, please get in touch to join our waiting list.