Tag Archives: Myeloma UK

The last post…?

Last Saturday was a huge day in my life history calendar. Six years ago I was diagnosed with multiple Myeloma. Each year that passes makes that day, 4 Feb 2011, more and more significant and makes me more aware how lucky … Continue reading

Posted in * Myeloma | Tagged , , , , , , , , , , , , , | 33 Comments

The sadness of so many losses

I began writing this a couple of months ago but didn’t finish the draft I’d started. Today though I’ve been reminded again of the sadness of loss; it comes and goes with a regular dull rhythm. On this Spring Equinox, … Continue reading

Posted in * Myeloma, Death & dying, Graft versus Host Disease | Tagged , , , , , , , , , , , , , , , , , | 21 Comments

Myeloma UK Clinical Trials

From time to time, I receive email updates from Myeloma UK, covering a variety of topics. To be honest, usually I take a brief glance and delete them without further ado. I tend to leave the medical stuff to the … Continue reading

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Kelsey and the Yellow Kite

I remember when I was first diagnosed, one thing I felt grateful for was not having young children… to worry about, to have to arrange care for while I was incapable of even caring for myself, to be upset about … Continue reading

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Flying high

So there we are, Colin & Deborah, Lorna & Mike and I sitting in the garden on Sunday afternoon after the party, talking about the party, the great music, the friendly people, the fabulous weather and the amazing raffle prizes, … Continue reading

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A pity party? No, a damn good myeloma party!

A pity party is one “in which you spend your time feeling sorry for yourself and whining endlessly about how crappy your life is.” (as defined by Urban Dictionary). It would be very easy and understandable for any of us … Continue reading

Posted in * Myeloma, Emotional health, Fun, play & adventure | Tagged , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , | 8 Comments

Stem cell transplant

I won’t be ready for a stem cell transplant for some months yet. I think they wait until the drugs I’m currently taking have made sufficient impact on the myeloma cells. I am also not emotionally ready to really face … Continue reading

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