
Annual Report and accounts
You can download the last three years’ Trustees’ Annual Report & Accounts. They are also available on the Charity Commission website.
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You can download the last three years’ Trustees’ Annual Report & Accounts. They are also available on the Charity Commission website.
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 £18 million into some of the most pioneering medical research - because of amazing supporters like you.
The Retina UK Annual Conference will be held on Saturday 20 September. You can join the Conference in-person or online.
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.
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 July 2025.
Formal notice of the forthcoming Annual General Meeting in September 2024.
This year the AGM will be held on Saturday, 9 July at 4.00pm:
Formal notice of the forthcoming Annual General Meeting in June 2023.