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Bardet-Biedl syndrome (BBS) is an inherited condition which impacts many parts of the body including the retina.

Achromatopsia is a rare hereditary vision disorder affecting approximately 1 in 30,000 newborn babies.

Face your fears and support Retina UK with a charity skydive this summer!

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Gyrate atrophy of the choroid and retina, shortened to gyrate atrophy, is an inherited disorder of protein metabolism characterised by progressive vision loss.

Are you ready to sign up for a spooky skydive and face your fears for Retina UK?

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Since we were founded in 1976, we have invested more than £18 million into some of the most pioneering medical research - because of amazing supporters like you.

Do you want to take part in the world-famous TCS London Marathon, from the comfort of your own city? Take part virtually on race day and join #TeamRetinaUK in 2026!

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Our new Retina UK online auction is now live! Get bidding to win fantastic prizes and support those living with inherited sight loss.

Charles Bonnet syndrome (CBS) causes people who have lost a lot of sight to see things that aren’t real (hallucinations).

X-linked retinoschisis (XLRS) is an inherited condition that causes early loss of mainly central vision in males.