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Different inherited sight loss conditions present noticeable symptoms at different times.

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This edition marks the start of the charity's 50th anniversary year. It includes lots of ways to get involved over the next 12 months along with details of our Annual and Professionals' Conferences in September.

• Look Forward
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The following questions are often asked by people contacting Retina UK.

Be a souper-star and raise funds whilst having lunch for #TeamRetinaUK

Our monthly e-Newsletter featuring the latest updates from Retina UK.

• e-Newsletter
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Tickle everyone’s taste buds and help raise funds for Retina UK with our Great Bake fundraiser!

Including a gift to Retina UK in your Will is an incredibly special way to help our vital work continue into the future.

Luxturna, a gene therapy, is only for the treatment of Leber congenital amaurosis type 2 (LCA2) and severe early-onset RP caused by mutations in a specific gene called RPE65.

• FAQ
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We’re all still buzzing from our recent conferences. We do hope you enjoyed them as much as we did. If you weren’t able to join us, then you can watch or listen to the recordings on our website.

• Look Forward
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My name is Mark Baxter and from an early age I was diagnosed with a deteriorating retinal eye condition called retinitis pigmentosa or RP for short, which will slowly lead to blindness.

• Case study - community
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