It has been several years since my dad died from Corticobasal Degeneration, a largely unknown, incurable, degenerative neurological condition. 

It was hard to find hope. We knew where the path ahead would lead.

But I am running for hope. I am choosing to hope that in the future, through research, trials, donations and awareness, that a cure will be found. Step by step we will get there and in the here and now, the PSP Association are on hand to support - to support individuals living with PSP and CBD,  their families, and to fund research into a cure. 

I have never ran a half marathon before. My toddler, who never knew my dad, has been my training companion on runs with the buggy around my local town in Scotland. It has taken a lot to reach this stage. On the harder days, I think of dad, who inspires me to keep putting one foot in front of the other, particularly when the going gets tough - and not just when training. He is my inspiration. 

 Together, step by step, we will get there. Because when you choose hope, anything is possible. 

Thank you taking the time to read my story. Please share my story if you can.

If you would like to make a donation, the link is below. 

Many thanks

Fiona

PSPA is the only UK charity dedicated to improving the lives of people living with Progressive Supranuclear Palsy (PSP) and Corticobasal Degeneration (CBD). We provide information and support for people affected by PSP & CBD whilst funding research into the causes, treatment, and eventually a cure. Together we can stop PSP & CBD in their tracks.