Mum was diagnosed with PSP in July 2022. PSP has no cure and there is no medication. It is quite rare and often goes undiagnosed. The prognosis is 5-7 years. The symptoms are akin to advance Parkinsons. 

Looking back, Mum was displaying the early symptoms around 5 years ago. It made her everyday life very difficult, and during her rapid decline in the last couple of years, it impacted all our lives.

Donations will help research and families who are not as fortunate as ourselves.

Evie & Jonn x