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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

Pattern dystrophy is an umbrella term for a group of retinal conditions. It is characterized by various patterns of pigment deposition within the macula.

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.

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.

A new approach to treating inherited sight loss

• News

Chris McCausland is heading to Blackpool for week 10 of Strictly Come Dancing.

• Story
• Retinitis pigmentosa

Creating without limits: artistic expression and sight Loss

• Webinar

Join us for an inspiring webinar where four artists share their creative passions and journey with sight loss.

• Webinar
• Audio
• Video