Progressive Supranuclear Palsy (PSP) is a rare & debilitating neurological disease that impacts balance, movement, vision & speech. It is often confused with Parkinson's disease. Currently, there is no effective treatment or cure.

The PSP Association (PSPA) is 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.

To find out more, please visit our website at: