Bruce and Neda share their experience of living with CBD as part of the ITN Business programme – Inside Neurology: Our Unique Brain.
The couple talk about the symptoms Bruce experiences, his diagnosis journey and the impact on their family.
Watch the video below:
Gemma's story
“I hope in the future research studies will enable PSP to be diagnosed early and for a form of treatment to help improve quality of life.”
Tracy's story
“Dad can’t speak anymore but his infectious smile and sense of humour keeps us all laughing.”
PSPA is the only UK charity dedicated to creating a better future for people living with Progressive Supranuclear Palsy (PSP) and Corticobasal Degeneration (CBD). We work to ensure the 10,000 people living with PSP or CBD receive support and care that is co-ordinated, has continuity and is compassionate. We rely entirely on voluntary donations. PSPA is a registered charity in England and Wales (1037087) and in Scotland (SC041199).
© 2024 PSPA | All Rights Reserved | Website by Geek | Disclaimer | Terms and Conditions | Privacy Policy | Supporter Promise
