Hello lovely friends!

 

Thank you so much for visiting our page - and for donating to PSPA.

 

We are honoured to work at an organisation that makes such a difference to so many people’s lives and every day we get to speak to many incredible individuals whose lives have been touched by this degenerative brain condition.

 

We are so inspired by their audacity in the face of this illness that we have decided to show them how much they motivate us, and we have all signed up for the Night Run on April 13th, Hooray!

 

However. We have swiftly realised our error, and having never run before, we are now starting to panic... This will not be a comfortable experience and we will be in pain. We will drag ourselves round the track, feet blistered, limping and out of breath in the hope that our struggle will inspire you to donate a little more to PSPA to fund the excellent work of the charity.

 

If you want to know more about PSP then please watch our video, as this really will give you an idea of what life is like for those affected by PSP. Once you’ve watched it, please dig deep and donate whatever you can to help us end the fight against PSP and find a cure for this disease, once and for all.