Getting a referral
If you have a diagnosis of an inherited retinal condition, or you are a close relative of somebody living with one of these conditions, you are entitled to access testing and genetic counselling.
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If you have a diagnosis of an inherited retinal condition, or you are a close relative of somebody living with one of these conditions, you are entitled to access testing and genetic counselling.
If you could use the long bank holiday weekend to fundraise for Retina UK, we would love to hear from you!
The latest research news from Retina UK.
Ocugen’s gene therapy candidate, OCU410ST, is an experimental treatment designed to slow vision loss in Stargardt disease, an inherited retinal disease (IRD) with no approved therapies currently.
Beacon Therapeutics announced positive results from their phase 2 gene therapy trial for X-linked retinitis pigmentosa (XLRP) caused by mutations in the RPGR gene.
Join #TeamRetinaUK at the Chester Marathon 2026 and proudly run in support of our vital work.
Celebrate the life of your loved one, by donating in their memory and help us fund more research and support, now.
Find out how you can mark your special day while fundraising for people with inherited sight loss.
Caryn talks about her experience taking part in the 2021 Virtual London Marathon.
The collective partnership of eight of the leading charities in the sight loss sector, known for the last three years as the VI Charity Sector Partnership, has re-launched under a new identity of the ‘Vision Partnership’ with a re-invigorated purpose and new strategic focus.