In 2013 my dad was diagnosed with Progressive Supranuclear Palsy.  At this time we already knew that he was having problems with his balance and had gone through a number of possible diagnoses as his condition got worse.  Over the next two years we saw my mum and dad battle on as dad's condition worsened, knowing that his condition was incurable.  During this time my dad never lost his fighting spirit or sense of humour, even in his last weeks when he could no longer speak.  As well as this my mum Lyn was amazing as she supported dad through his illness.  Both my parents are a source of pride and inspiration to me and my brother.

Over the last year I have grown my beard to the longest it's ever been, with the plan to shave it for charity.  None of the students or colleagues at my school have seen me clean shaven, so my class have had a lot of fun giving me various nicknames (especially around Christmas 2020!).

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. We aim to improve the lives of everyone affected by PSP and CBD. We rely entirely on voluntary donations, and that's why we need your support.