Friday, March 19, 2010

last week

So I have made it through chemo, and have just one more week of radiation left to go.
My Liver function tests are still improving, although I still have NO idea why they went abnormal. I would have put money on it being the chemo at the beginning, but it is so unlikely because they kept getting better while we continued the chemo. So they will probably remain as one of my bodies little mysteries.
I must say that it feels good to have finished chemo. I really didn't like it at all. (Not sure if any one does). The only good thing about chemo was the other patients. I was always with a good group of people and we usually spent a good part of the day laughing through it. What I really hated: the dexamethasone. Its a steroid drug (not like the body builders use) thats main job is to combat the nausea. And it was pretty good at it. But it also made me constantly awake, fairly grumpy, extremely achy on the days I wasn't taking it (they give it to you 4/7 days) and it has turned me into a chipmunk.
I can cope with most of the side effects of most things, but the fact that every time I look into a mirror I see a puffy, chipmunk "dex face" it really reminds me that I have cancer, and that I am a patient. I know it will go away, and in some ways should be grateful that I have put on all the weight that I lost (and maybe a bit more - also from the dex), but I really don't like it, and it is such a small thing.
Next week I have 4 more zaps of radiation and then I am done for a bit. There are a few more bits and bobs to do in a couple of weeks, then follow scans in a couple of months. It takes a few months to work out if the radiation has done its job so thats why we wait for the follow up scan.
In the mean time I have to work out what to do with myself. I get very tired doing even small things at the the moment and the fatigue will take some weeks to months to resolve.
So once more I guess it's a case of take it day by day and see where we end up.


  1. Hi Cath
    This is Chris and Garth here. Kate put us onto your blog site.
    We think of your journey every day . You are such a bright and beautiful girl and we are privileged to know you and Rob AND your fantastic family.
    Our love and prayers are with you
    Keep strong!

  2. Hi Chris!
    It was my last day of treatment today and when I got home a lovely bunch of flowers arrived. They are beautiful. Thank you so much.

  3. Hello,
    I have a question about your blog. Please email me!