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You can download the last three years’ Trustees’ Annual Report & Accounts. They are also available on the Charity Commission website.

• Annual Report
• Written

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

Since we were founded in 1976, we have invested more than £17 million into some of the most pioneering medical research - because of amazing supporters like you.

James, who lives with retinitis pigmentosa, is running the TCS London Marathon in April 2025 to raise vital funds for Retina UK.

• Case study - community
• Written

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.

• Look Forward
• Audio
• Written

Leber Congenital Amaurosis (LCA) is a rare genetic eye disease that appears at birth or in the first few months of life.

Is 2024 the year that you join #TeamRetinaUK & take on the Easter 50 Ultra Challenge?

• Walks & Treks
• United Kingdom

Is 2024 the year that you join #TeamRetinaUK & take on the National Three Peaks Challenge?

• Walks & Treks
• United Kingdom

Is 2024 the year that you join #TeamRetinaUK & take on the Snowdon For Sunrise Challenge?

• Walks & Treks
• United Kingdom

Is 2024 the year that you join #TeamRetinaUK & take on the Isle Of Wight Ultra Challenge?

• Walks & Treks
• United Kingdom