Separates

You know that feeling when you wake up knowing exactly what you are going to wear that day and said outfit is going to be the best outfit you have ever worn in your life and not only that, it will be the best outfit anybody else has ever seen? Well, that is exactly how I felt up opening my eyes this morning. I was going to wear a dress and I was going to look hot. H-O-T hot. I was very excited and pleased to be giving this gift to the world.

And then I remembered…

Today was a day I had to wear separates. The Medically Trained People made it so. Not only did I have to wear separates, but I also had to wear something with an elasticated waist. It was at that point I knew the day was going to be a let down.* I had not planned for this when my eyes were closed. I was going to have to look daggy. I was also going to have to have a bone marrow biopsy. My outfit upset me more.

I know it is a price one has to pay on Biopsy Day, at least on Velcade Days I do not have to lower my being to elasticated and ‘comfy’, I just begrudge it.

Nobody warns you when they tell you everything else about it, that myeloma dictates your dress, even, occasionally, forcing one to become sartorially challenged. At least once a fortnight, I dress for myeloma and not for me. Imagine that. It has been 17 months, and still, every time it happens, the few times it happens you understand, it smarts. It really smarts.

Oh, and I really cannot believe that it has been six months and four days since my transplant.

EJB x

* except for the fact that I was accompanied to my biopsy by two fine ladies and a foetus, and had a scone, I love scones.

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3 thoughts on “Separates

  1. Deborah says:

    Hi Emma
    That time seems to have gone quickly. My remission thanks to the PADIMAC trial only lasted 5 months so back in chemo now and the stem cell transplant to look forward to sometime 😦
    Deborah

  2. Terri J says:

    Tomorrow you can be HOT.

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