
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
Contact Information
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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