Me and my daughter Paige will be walking 20 miles around the edale skyline to raise awareness and money for psp. This year our mum/gran was finally recognized as having psp after originally being diagnosed with Parkinson's in 2017. PSP is a devastating rare progressive brain disease that many people have never heard of including drs, paramedics and carers and is commonly misdiagnosed. PSP affects movement, control of walking (gait) and balance, speech, swallowing, eye movements and vision, mood and behavior, and thinking. Up to yet there is limited medication to help the symptoms and no cure.

Funds raised will go to support the psp  Helpline Services, Education, Outreach Groups, and Research into more effective treatments and ultimately a cure.

Thankyou xx

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