#crowdeyslegacy
Paul Crowdey is raising money for Motor Neurone Disease Association
Participants: Fighting the fight and raising awareness and funds for the rest of my life.
Story
I// 'This will be my Legacy' //
In memory of Paul Stephen Crowdey Paul passed away on 22nd September 2016 after a short but heroic battle with motor neurone disease. He was only 37 years old. I have picked up the baton and in his name will continue to raise awareness and money for mnda. We miss him more than words can ever say.
My name is Paul Stephen Crowdey and I'm 37. On Wednesday 28th January 2015 I was diagnosed with Motor Neurone Disease.
I promise you this, I will fight and be here for as long as I can. With the support of my beautiful wife George, my girls Annie (17) and Emily (7) and my entire family, we'll enjoy whatever time I have left (hopefully many years).
I don't want pity, I just want you to help me make sure as many people know about this wicked disease.
Unfortunately MND is severely underfunded in the UK and this has to change. It's clear that it doesn't just affect old people as most people think, it can affect anybody at anytime. It also doesn't just affect the person living with it, It affects all those around us that we care for most.
Please visit my blog https://paulcrowdey.wordpress.com and follow our social media accounts. With your help we can make a difference.
Thank you,
Paul.
Instagram
#crowdeyslegacy
@__p.c__mnd__
Twitter
@paul_george_mnd #crowdeyslegacy
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