jet black living My life with Myeloma And learning that life isnt about waiting for the storm to pass, its about dancing in the rain.
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Friday, 24 June 2011. Just to let you know that I have now moved to word press. blogger was just very old fashioned! Give me some time though. need to do a few other bits first! Links to this post. Bone Marrow Biopsies, Peripheral Neuropathy and Wigs. 65279; On from there to the Bone Marrow Biopsy.
Wednesday, 7 March 2018. Thank you for the party, b. Ut I could never stay. Any things, on my mind. Ords, in the way. my head is above the water. I want to take the opportunity to acknowledge the group of people who are quietly, unobtrusively propping us up, right now. You know who you are.
Before she passed away we discussed her blog. So, here I am. Goodbye Helen, I love you.
I wish I had the words and muscle to help bear your load. You have borne your distresses with such amazing grace. Caring for the elderly becomes much like the labor over young children and you are pressed on all fronts with little margin to tend to your own needs. Ariel Levy, staff writer at.
Thu, 12 Apr 2012. Tue, 20 Mar 2012.
The infernal ramblings of a myeloma sufferer and his beloved.
June 29, 2014 in fun.
Make an Ok Cupid Profile- Part 1. Two days ago I walked down the high street of the rural town I live in, carrying a bouquet of roses for my girlfriend. This town is a community in transition. I lucked out in my first handful of intimate experiences w.
We still had a little time left. We cast our eyes around the library we were writing in, and Nicki found the perfect source for the next free-write. Perhaps because all that determination. Gets a girl nowhere in the end. Except up to her elbows in muck. Grit in the hoover, grit in the bath.
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The site had the following in the homepage, "My life with Myeloma And learning that life isnt about waiting for the storm to pass, its about dancing in the rain." I noticed that the web site stated " Mon, 5 Feb 2018." They also stated " This anniversary post is to recognise that Im still here, in remission, seven years on from the day 4 February 2011 when I was first diagnosed. So if anyone reading this has any thoughts of signing up to a stem cel register, she and I would both like to encourage you to go ahead. As a recipient, I can vo."ANALYZE MORE BUSINESSES
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