Bright Futures: Empowering young adults with inherited sight loss
Join us for an inspiring webinar where young adults living with sight loss share their extraordinary stories and insights
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Join us for an inspiring webinar where young adults living with sight loss share their extraordinary stories and insights
Genetic testing and counselling services are usually coordinated through a main hospital where the eye clinic or clinical service is based; some also have clinics in local hospitals across the service’s area.
Alex Pitts from British Blind Sport talks about the benefits of sport and physical activity and the BBS Have a Go Days and Active at Home programme.
Luxturna, a gene therapy, is only for the treatment of Leber congenital amaurosis type 2 (LCA2) and severe early-onset RP caused by mutations in a specific gene called RPE65.
My name is Mark Baxter and from an early age I was diagnosed with a deteriorating retinal eye condition called retinitis pigmentosa or RP for short, which will slowly lead to blindness.
Organising your own fundraising is great fun and a brilliant way to involve your friends, family and local community.
In April 2022 we joined with another seven leading sight loss organisations to make a public commitment to increasing the number of blind and partially sighted people employed within our sector, including at senior management level.
Join Colin & Linda McArthur for their annual Isle of Wight walk in support of Retina UK. Last year's event raised a record-breaking £6,000+!
Come along to our Open Day at our headquarters and hear all about our upcoming 50th anniversary and our vital work.
The following projects were being funded by Retina UK and have recently come to an end.