In March this year we had the devastating diagnosis for Mum. PSP is rare neurological disease that affects one in a million, with no known cause and no treatment.

Mum has shown formidable strength and positivity but the condition is cruel and we have a bumpy road ahead.

We’re not the kind of family who give up easily and Mum would definitely not want anyone to fuss or feel sorry for her. Instead we want to take action - making new memories, reminiscing over old ones and making plans to make life comfortable.

This year’s soulful charity yoga event will be raising money for PSPA - the only UK charity dedicated to creating a better future for everyone affected by Progressive Supranuclear Palsy and Corticobasal Degeneration.

We will do this by: Providing information and support to enable families living with PSP & CBD to live their best possible lives; Improving the quality of life for people living with the condition via research and awareness raising; Putting the voice of the PSP & CBD community at the heart of what we do.