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Ashley has completed the London Marathon numerous times. He was part of #TeamRetinaUK in 2021 and talks here about his experience.

• Case study - supporter
• Written

Stickler syndrome is a genetic connective tissue disorder.

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

May is National Walking Month! Are you ready to join #TeamRetinaUK in May for our brand new daily 5K challenge? Your support will allow us to continue supporting those who are living with inherited sight loss.

• Walks and treks
• United Kingdom

Could you take part in RideLondon 2025 for #TeamRetinaUK?

• Cycle
• London

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

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.

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

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

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