My father in law recently died as a result of PSP it went undiagnosed for nearly 4 years! It's a relatively rare condition, we lost more of Alan year on year without an understanding of what was wrong with him, it all made sense once we understood his condition I am hoping that our small contribution assist in the promotion of this condition so that it's better understood and treatments can be developed. PSP Association (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. But, we rely entirely on voluntary donations, that's why we need your support.