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The Maddi Foundation

The Maddi Foundation was originally started as ‘Save Our Maddi Appeal’ in 2016 when teenager ‘Madeleine Thurgood’ was diagnosed with a life limiting genetic disease called Hereditary Spastic Paraplegia 15 (SPG15). Maddi’s mum and Co-Founder, Carina Thurgood began pushing the necessity of raising awareness of SPG15, to advance research and developement of a Gene Therapy for this rare disease.
About Us
Conditions We Support

Central Nervous System

    Other Rare Disease

      If you've been diagnosed with any of these conditions, we're here to help.

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