The Jeffrey Young Research Programme for Progressive Supranuclear Palsy Research has been established at the University of Edinburgh thanks to a generous donation by a family member, whose much loved uncle was affected by the devastating effects of Progressive Supranuclear Palsy (PSP).

PSP is a destructive, progressive and incurable neurodegenerative movement disorder, broadly similar to motor neuron disease. It can present with a range of symptoms including problems with balance, swallowing and speaking, as well as general slowness of movement which means it is often mistaken for Parkinson's disease.

Sadly, there are no disease slowing treatments at this time and typically people with PSP lose independence within 2-3 short years, with a life expectancy of only 6-8 years from diagnosis. With such a bleak outlook, there is an urgent need for research.

The Jeffrey Young Research Programme for Progressive Supranuclear Palsy Research aims to support research to discover new drugs that may slow, stop or even reverse the devastating symptoms of PSP.

Your donation today is very much appreciated and will directly support vital PSP research at the University of Edinburgh. Together we can bring hope to those affected by PSP.