2 more days to the end of my radiotherapy. So far it didn't give me much trouble, only darkened skin colour at the treatment / surgery area and slight hardened muscles there as well. It kinda encourages me to keep up with my physio exercises daily — Allow me to find some positiveness in every thing I do :)
I saw the radio-oncologist as well today as part of the weekly check-up. I was happy to hear everything seems fine. I need to see him in mid May. The 3 musketeers (in my own interpretation: my surgeon, oncologist and radio-oncologist) will be seeing me alternately in the coming months and years.
About 9 months of ups and downs, treatments and tests, surgery and therapies so far, I think it's time to move on, like REALLY move on!
The current goal is to prep myself to go back working, to prep the kids that mummy can't be spending so much time at home playing or studying with them while recuperating, so they'd better well discipline themselves!
....
End-note:
Started Tamoxifen for about a week now. Two changes I noticed are:
– slower bowel movement, a little constipation it seems.
– disturbed sleep at night (waking up to either really slight noise, or that urge to the toilet). This is quite noticeable cos I have been sleeping well and through the nights after I complete my weekly chemotherapy
