Taylor family fundraiser for The PSP Association

katie taylor is raising money for PSPA
In memory of Peter Taylor
PSPAVerified by JustGiving
RCN England and Wales 1037087 / Scotland SC041199
PSPA is the only UK charity creating a better future for everyone affected by Progressive Supranuclear Palsy and Corticobasal Degeneration. If you need support, please contact the PSPA Helpline on 0300 0110 122 helpline@pspassociation.org.uk

Story

After years spent fighting against a cruel neurological condition, Pete finally passed away peacefully on August 2nd, 2024.

Pete was diagnosed with a combination of 2 similar conditions- Progressive Supranuclear Palsy (PSP) and Corticobasal Degeneration (CBD). Both conditions are extremely rare, affecting approximately 5 out of 100,000 people, and often misdiagnosed as Parkinsons Disease or Stroke. Pete was lucky in a sense, that his Neurologist suspected this at an early appointment. More information can be found here.

Pete expressed a strong wish to help and support other PSP/CBD sufferers in any way he possibly could. For this reason, as a family we have decided not to host a formal funeral. Instead, Pete is to be cremated, followed by private celebrations of his life, at a later date.

We are asking of people who remember Pete fondly, to kindly show your respects by sending a donation to the PSP Association - the only UK Registered Charity providing research and support into these rare conditions. We will be fundraising for PSPA on a regular basis going forward, and would love to have your support.

Please share far and wide - awareness is desperately needed into these conditions.

Kind regards

Pete, Pat and Family

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Donation summary

Total
£3,349.88
+ £721.75 Gift Aid
Online
£3,349.88
Offline
£0.00

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