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Retinitis pigmentosa (RP) is an inherited eye condition that affects the photoreceptor cells responsible for capturing images from the visual field.

Cone-rod dystrophies are a group of inherited diseases that affect the photoreceptor (light sensing) cells that are responsible for capturing images from the visual field.

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

This Easter bank holiday weekend, join Retina UK at various airfields around the UK and face your fears by taking on a skydive for us!

• Extreme challenges
• Various

As part of Retina UK's birthday celebrations, we would love for you to face your fears by taking on a skydive for us!

• Extreme challenges
• Various

At the scariest time of the year, do you dare to face your fears by taking on a thrilling skydive for Retina UK? Join us at various airfields around the UK.

• Extreme challenges
• Various

We are currently funding a range of exciting projects and programmes, all of which aim to enhance our understanding of inherited sight loss, and inform the development of treatments for the estimated two million people affected worldwide.

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

• Annual Report
• Written

Refsum syndrome is an inherited metabolic condition, associated with elevated phytanic acid plasma levels, which impacts many body systems.

These very rare syndromes (NARP, Bassen-Kornweig, PXE, Norrie) affect the eyes as well as other parts of the body.