Hi Jo,
So glad that Rob is nearly there. when I was close I got really excited for a while but then the final rounds were just so exhausting that all i did was collapse in a heap after the 5FU jetpack came off each fortnight. My onc had warned me that the final stretch would be tough. He was right but we made it!Just a quiet warning for these last few weeks.
Rob is lucky to have you go to the long treatment with him. I used to do the first couple of hours on my own but my parents always came up for the last coupole of hours and chatted while we watched the stuff drip through! They then took me to lunch before I was too sick to eat anything!
One of the hardest things I found was the sense of being disconnected when I finished treatment. You may have noticed this sentiment being expressed before. You seem much more astute to feelings than my family was so I am sure that you will be aware that "back to normal" doesn't exist. I am now up to 12 month CT scans but annual colonoscopies and 6 month checkups. I am still scared S******s every time.Bloods due in MArch.
Can you, Rob and your lovely boys manage to get away for a holiday when Rob is more settled? I promised myself somewhere that I could "swim with the pretty fishies" as I was really dirty about not being able to swim all summer 2007/8 due to the picc line. We went to Hamilton Island and it was perfect.
For now, you stay in bed, drink plenty of green tea and take copious amounts of vitamin C.
HAng in there, S
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