Welcome The mission of the Society for Progressive Supranuclear Palsy is to promote and fund research into finding the cause and cure for progressive supranuclear palsy (PSP). The Society for Progressive Supranuclear Palsy (Society for PSP) provides information, education, support, and advocacy to persons diagnosed with PSP, their families, and caregivers. The Society for PSP educates physicians ...

The PSP Association was set up as an advocacy and support organisation and registered as a Charity and Company Limited by Guarantee in April 1994 by Sara and Brigadier Michael Koe, after Sara was diagnosed as having PSP.