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. This can only help those who may befall this terrible disease in the future. These rare dieases only truly surface when you are personally involved and really want to raise awareness of all neurological diseases. I will be creating a blog to follow my training exploits, a 48 year old with very little long distance running in the legs. Raising awareness of SOCIAL WELFARE FOR ALL FOR WHEN WE NEED IT AT OUR MOST VULNERABLE.