Man Of Metal

WARNING! – This blog contains a request for your money, again

I am not sure why anybody would call an event the ‘Ironman’. I think, ‘Man of Steel’ would be more appropriate because the event is ridiculous and frankly, it sounds impossible to somebody who always found a way out of PE. Hang on, I am being sexist and I am a female; ‘Human of Steel’ would be better. Everybody is equal. Regardless of the political correctness issue, I should try and get to my point…

Neil has decided that he is going to run the Ironman Wales in September 2013 to raise money for Myeloma UK. He is clearly crazy. The Ironman is 2.4 mile swim, followed by a 112 mile bike ride and then, because you might as well commit yourself, a full marathon. Back when I was a morbidly obese healthy person I could swim 1750 metres, fall off a bike when I attempted to turn a corner and run 10 paces for the bus. So…

It is 10 months away, and so my plea for cash is coming early (and anticipate that I will request again) but he needs to raise £2000 to be able to participate. They really do make you jump some hurdles…. As I am sure you will appreciate that there is a considerable amount of training and commitment involved, and I imagine blisters. You don’t have to experience it though,because he will, but you can donate if you are that way inclined. I am not talking megabucks here, every little helps, it really does. I know I keep hitting you up for cash, but Myeloma UK help fund new treatments for Myeloma. I have Myeloma and I want there to be a cure. I am not ashamed of asking people to help in anyway they can. To date, I have donated a measly £55 to Myeloma UK. I intend to donate so much more if My Myeloma allows it.

Neil’s JustGiving page explains why he is doing it, but in case you still need to be persuading, I will tell you why he is doing it. Neil’s father-in-law, who just happens to be my dear friend Rachael’s dad, also has Myeloma. He was diagnosed seven years ago and he has had two relapses. Huw, the man in question, has handled his illness with strength and courage, and his family have been both an inspirational and a support to me since I was diagnosed in August. Rachael, for example, just today, braved driving down Holloway Road to see me. That really is something else. To find out more about my views on the family, please revisit the blog post below:

https://ejbones.wordpress.com/2012/10/07/aspiration/

It’s late now, so I will leave you with the link to Neil’s page.

http://www.justgiving.com/Neil-Whitney/?utm_source=Sharethis

Many thanks for your time and the warmest of regards,

EJB x
Lazy Arse

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