PSPA MARKS 30 YEARS OF PROVIDING SUPPORT
30 years ago, PSPA was registered with the charity commission by our founder Michael Koe.
The charity was established to support families as well as funding research into PSP & CBD, driven by personal experience after Michael’s wife, Sara, died from PSP in 1995.
Over the years, PSPA has grown from strength to strength becoming the UK’s leading centre of knowledge, information and support to people living with PSP or CBD, their families and Healthcare professionals. As well as cultivating a community of researchers and clinicians to lead the charge to better understand PSP & CBD, improve diagnosis and investigate possibilities of treatments.
To mark PSPA’s achievements since its conception in 1994, we will be hosting a year full of special activities.
From opportunities to learn more about our history, to events to connect with both professionals and other families affected by the conditions, and fun challenges to help raise vital funds. We have activities to suit all interests and abilities.
We would love for you to immerse yourselves in our 30-year journey and help us mark this important anniversary year.