We have just published a video to speak about our strategy for a better future for those with PSP and CBD. The video is quite moving and speaks about symptoms, diagnosis (and sadly misdiagnosis), lack of treatments, and lack of a cure. https://youtu.be/_zGjFfpLCIw

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.

This is the first time I have ran The London Marathon and for PSPA since 2010, but the first London Marathon with my daughter Ella, so it's gonna be a tough day out there, but Dad will be smiling, and I hope you can support me (again for many of you)  in my efforts to raise more money than I did 13 years ago! Check Ella's page out on https://www.justgiving.com/fundraising/ella-rogers9