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Stickler syndrome is a genetic connective tissue disorder.

Choroideremia is a genetic condition that causes progressive vision loss, mostly in males.

As well as many of the well known races, we also have places available in hundreds of local runs. Wherever you live, you can run as part of #TeamRetinaUK!

• Run
• Close to home

Many research studies could not take place without the participation of people living with inherited sight loss.

Gyrate atrophy of the choroid and retina, shortened to gyrate atrophy, is an inherited disorder of protein metabolism characterised by progressive vision loss.

Best disease, also known as Best vitelliform macular dystrophy (BVMD), is is an inherited eye condition associated with progressive degeneration of the macula and is a form of juvenile macular dystrophy.

Usher syndrome is an inherited condition that affects both hearing and vision.

Our Retina UK Peer Support Group network offers information and support via regular meetings both online or in-person.

X-linked retinoschisis (XLRS) is an inherited condition that causes early loss of mainly central vision in males.

Could you take on a thrilling skydive for Retina UK this summer? Join us at various airfields around the UK this July.

• Extreme challenges
• Various