That’s all folks

cheers

This is going to be my last blog post about my 2013 London Marathon adventure. It’s been emotional!

I started this blog because I wanted to capture the experience of running a marathon and fundraising for charity. I happen to have Ulcerative Colitis and Dilated Cardiomyopathy which (until now) I’d never really told anyone. I hoped that I’d raise awareness of the diseases that effect me and my family and in turn possibly help others suffering. I didn’t expect to have quite so many things to write about and would never have imagined the blog to be as popular as it has been. I have always hated the way that I write and have very little confidence in it but I would recommend blog writing to everyone, just jump in and do it!

I want to say one final massive Thank You!!!┬áThank you if you’ve sent me a nice message, sponsored me, asked me about the diseases, donated to the auction, cheered me along the marathon, cuddled me at the end of the marathon, hugged me when I’ve been upset or if you’re one of the thousands of people who’ve read my blog. I’ve never felt so supported in my whole life and I can’t believe the power of a blog!

The PR is still coming in and we’re hopefully going to be in some women’s magazines in the near future, so look out for us! I’m going to have a little break from silly exercise challenges and fundraising for a bit and work out how best to focus on the things I’m most passionate about when it comes to hearts: organ donation (opt out campaigning), heart screening of young people and research into turning heart disease around. I’ve enjoyed the blog so much that I’ll start a new blog soon, probably called ‘Lucy Lives Life’ – watch out for it on my social media.

Please don’t forget that when this blog’s long gone, there’ll still be young people dying of heart problems every week and there’ll be people dying while waiting for organs that are out there, just not on the donor list. Please continue to spread the word and use my family’s story as an example of how tragedy can be turned around simply by filling in an online form and telling your guardians. Today is Jack’s 3rd anniversary of his heart transplant and just writing that has made me burst into tears quite hysterically. You’ll never know how meaningful that silly organ card is until it happens to you, so please keep talking about it.

Thank you and bye for now xxx

Advertisements