Sunday, 12 May 2013

Day Seven - Not quite going to plan

I do apologise, as I said I'd try to keep this blog going on a daily basis and have so far failed miserably. In my defense though, since my infusion on Monday, it's been a shit week. I was hoping that this final bout of chemo would go like the first one, ie: first and second sessions quite easy, soaking in nicely with no major side effects, and the final session being the worse, with all the sickness and fatigue in the last 20 days. That's not what's happening. From the outset the fatigue is there already. My energy levels are really low. The feeling of sickness is quite pronounced. I'm off instant coffee again, food is a struggle and the urge to retch at the slightest thing out of the ordinary is ever present.
That all came to a head on Saturday when I spent most of the day in bed, hardly ate anything and just generally felt rough. Joh called the Christie hotline and asked if there was anything we could do to alleviate the sickness, and they recommended changing the anti-sickness tablets I was taking. So off Joh went to the doctors on saturday afternoon to pick up my new medication.
Now that seems to have done the trick for now. I've felt well enough today to eat 3 meals and a little bit of snacking in between, and even managed a half serving of pasta carbonara at the italian in romiley this evening.
It must seem odd to a waiter when this 6 foot 1 inch bloke orders a half portion of food off the menu.

My weight seems to be holding steady around the 208lb mark at the moment. My fitness has taken a real tumble though in the last week. Today was the first time I've been out for a walk all week. Time to do something about that I think. The sooner I start trying to get fit again, the easier it will be in the long run.

So, there you have it. Progress so far. I'm not promising any more daily updates, but I will update when I feel the need to let you know how it's going.

Take care xx

1 comment:

  1. You don't know me, but I know Jo, just want to say I'm thinking of u all and hope the remainder of your treatment is easier Sharon D x