Thursday 28 June 2012

Slightly disappointing visit to the clinic

I was hoping to have a good result from my latest chimerism test, namely that I would be 100% donor; but sadly, a small amount of my host T-cells remain. Due to a slight mess-up by the lab we did not have the graphs, only a textual description of the results. My doctor will reserve judgement until she has seen the graphs, but it is likely that I will need another treatment of donor lymphocytes (a DLI). Harry will not need to donate any more cells, as they took enough for four doses, and froze them. The precise timing of the DLI is not important, so it will probably be at the same time as my next clinic.

I continue to be in good health, and I have decided to stop recording my blood results as they are totally normal. I am still gaining weight; modesty forbids me to reveal it! However, I have reached a watershed, and the time to cut down has arrived :(

I am now waiting for my last scheduled intrathecal dose of methotrexate. I hope the doctor is as skillful as the last one ... or maybe even the same doctor!

Saturday 23 June 2012

One year old

It is one year since my transplant. June 23rd has become my second birthday!

It is hard to describe how I feel. On a simplistic level, glad to be alive and well. More philosophically, it has made me think about "luck". There is an expression "you make your own luck", which means that we can take choices and make decisions whereby good and bad luck just dictate the level of success we achieve. A very famous example of this kind of luck was when Gary Player played out of a bunker and into the hole, and someone watching said he was "lucky", to which Gary replied "the harder I practice, the luckier I get".

But getting leukaemia is a different kind of "luck". It was a random event, something that cannot be planned for, nor predicted. Similarly, my brother being a match for me as a donor is another kind of luck again. And us both being CMV negative.

Some things which were lucky I did have some control over. I was lucky not to get a bad infection after the transplant; but then I was very careful! I am lucky to have Rose to look after me :)

I know that my life expectancy is still not normal, but I do feel this is an important milestone. I will continue to blog after each of my clinic visits; at some point they will become quarterly rather than monthly.

Thank you all for your kind wishes and support over the worst times of my illness.