Last year, my mum was diagnosed with Multiple System Atrophy (MSA), a rare and life-limiting condition that has completely changed our lives. Watching someone you love face something like this is heartbreaking, and it’s made me realise just how important support, awareness, and research really are. That’s why I want to do my bit and raise money for the MSA Trust — to help families like ours, and to support the incredible work they do for people living with MSA and those who care for them.