In our third episode we talk about delayed diagnosis. Denise Hunt and Navin Sewak share their experiences of their mums receiving a delayed diagnosis, the impact this had on the family and the care they received. They also share why raising awareness is so important.

In our second PSPA Podcast we talk to Julia Tickridge. Julia shares details of caring for her husband Laurie who is living with a diagnosis of evolving PSP. Julia also talks about where she has found support in her role as a carer.

Find out more about Beth’s personal experience of PSP and how support from the Pavers Foundation for the podcast came about.