On Saturday 21 September, Duncan Neil and I will be running 20km (including the climb and descent of Mount Errigal), cycling 41km and kayaking 2km... all across the wild, hilly terrain of Donegal! This type of event is completely new to both of us and beyond anything we've ever done before. 

Why, I hear you ask...?

Almost 2 years ago my father in law was diagnosed with Progressive Supranuclear Palsy (PSP). This is a rare disease for which there is currently no cure. I know there are many horrible diseases out there, but watching this illness take hold, knowing things can only get worse, has been heartbreaking for all the family. It is slowly taking away his movement, his communication, and his independence. 

Watching this has cemented the immense appreciation I have for what my body is capable of. 7 months ago I gave birth to Ronan... I was so lucky to recover quickly from the pregnancy and birth, and I made a pact to myself that I would make the most of my physical ability, almost as a gratitude practice, and be thankful for every training session I was able to complete - even the really hard ones! 

At the point where I was starting to think I'd bitten off more than I could chew, less than 4 months ago, Duncan Neil accepted the challenge to complete Gaelforce too.  At that point he had done no cardio or strength work for many years...but his dogged determination has seen him complete a forest 10k, a half marathon and an open water swim. He now cross trains 3 times a week, runs at least twice a week and cycles in between. 

At the time when I have become only too aware of how quickly the body can deteriorate, Duncan has been an amazing, inspirational reminder of what our bodies can also be capable of if our minds send the right messages.

I don't know how long the event will take us (estimates may be around 6 hours) but we are both totally determined to finish (or else be carried off the mountain!!) as we are both quite stubborn 🤣🤣 

We would love it if you were able to sponsor us, however small the amount, with all monies going to the PSPA to help other families coping with the impact of this horrible illness. 

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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. We aim to improve the lives of everyone affected by PSP and CBD. We rely entirely on voluntary donations, and that's why we need your support.