The PSP Association is committed to improving the support that the NHS and Local Authorities in the UK provide for people with PSP and CBD and those who care for them.
We do this by:
- Representing the views of the people with PSP and CBD direct to Government, mainly during the policy consultation phase.
- Taking an active part in groups of like-minded organsiations.
- Liaison with other Charities with similar interests to promote joint working, the exchange of best practice and a common response to Government.
The PSP Association is a member of:
For more information email