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

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.

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

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.

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

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

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

Are you looking for a thrill with a view? Could you take on a skydive for Retina UK this summer? Join us at various airfields around the UK this July.

• Extreme Challenges
• Various