In September 2011, almost 4 years ago, our darling Dad, Ian, was diagnosed with Motor Neurone Disease.

Since then, our lives have changed. Every day, Dad endures a multitude of difficulties and has been forced, by this horrific condition, to adapt the way he lives. Dad now has a stair lift, both manual and electric wheelchairs, ramps, a portable battery operated breathing machine, as well as other functional items; all of which make his life easier.

These have been provided by the Motor Neurone Disease Association.

Without these, Dad would not be able to enjoy some of the experiences that we have shared over the past 4 years, his quality of life would be greatly reduced.

He would not be able to whizz around the lounge, beeping his horn, chasing his giggling grandson Dara. He would not be able to travel. His beloved Ireland, Australia, America are just a few places that have remained accessible. He would not be able to work. He would not be able to continually support young people at a school in Medway for 3 days a week. In August, he would not be able to scoot my sister Alyce down the aisle on her wedding day.

Most of us take these experiences for granted, yet for my Dad, these are hurdles that he has to overcome. Thanks to the Motor Neurone Disease Association, we are still able to live well and enjoy these moments.

Motor Neurone Disease affects approximately 5'000 people in the UK. Sadly, my Dad is one of those people and we are one of those families that faces the heartache of this condition.

As a family, we can not put into words how inspired we are by Dad's spirit, strength and courage. For this reason, I will be running the London 10K on 12th July.

Please donate whatever you can. Every penny will be appreciated.

Thanks for taking the time to visit my JustGiving page.

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