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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.

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.

• 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.

Formal notice of the forthcoming Annual General Meeting in September 2024.

• News

Formal notice of the forthcoming Annual General Meeting in June 2023.

• News

This year the AGM will be held on Saturday, 9 July at 4.00pm:

• News