In 2017 Garfield Davies a Father, Husband, Grandpa and friend to so many was diagnosed with PSP, after many hospital appointments and perseverance. In the last 3/4 months Garfield has been declining in his general wellbeing, requiring more support with daily activities. It has been a emotional turmoil for not only Marian (Garfield's wife) but also his family and friends. Garfield has achieved so much throughout his life and has always given back to so many through his career and life choices to his family and friends.
Therefore myself and my family would like to give back to Garfield and the charity to not only raise money for funding, but also to raise awareness about the disease. 4,000 people in the UK are living with PSP which is small in comparison to many other diseases that are around. The charity relies solely on volunteers and fundraising to keep the research going.
PSP Association (PSPA) is a national charity providing support and information to people living with PSP and CBD, while funding research into treatments and ultimately a cure.
£50 of donations will fund laboratory equipment for a day's research
£20 could provide a carers information pack
£10 could provide a pair of specialist prism glasses
Please be generous in whatever you may be able to afford to donate to make a difference.