Story
My mum, Mary Ann Gazeley, passed away from Multiple System Atrophy in December 2025. It’s a rare and often misdiagnosed neurological condition. In her memory we will be raising awareness and fundraising for the MSA Trust.
The MSA Trust provides vital support, information, and advocacy for people and families affected across the UK.
Thank you for honouring Mum with us and helping make MSA impossible to ignore.
I’ve started a UK Parliament petition asking the government to increase awareness, training, and funding for MSA — so doctors can recognise it earlier, and families don’t have to fight for answers while watching someone they love decline.
This petition is in memory of my mum, Mary — and for every family affected by MSA. Please sign, share, and help make sure this disease is no longer overlooked.