In May 2018 my dad was diagnosed with PSP (Progressive supranuclear palsy) before this I had never heard of PSP. Following the unexpected death of my mum in December 2018 I became a carer for my dad. I want to raise awareness of this terminal and untreatable condition.

PSPA is a national charity providing support and information to people living with PSP and CBD, while funding research into treatments and ultimately a cure. They aim to improve the lives of everyone affected by PSP and CBD and rely entirely on voluntary donations.