Good morning It has been a quiet but lovely Christmas here, I was at the end of cycle two so felt more or less normal, which was great for me and the kids. (I am a single parent). I had my 3rd EC on Wednesday. I had a similar experience re: cold capping. I tried it for the 1st and 2nd and found ai had so much hair loss and bald patches so decided not to do it again. I bumped into a lady who I had met on my 1st session (her 2nd), she was going in for her 4th session and had what looked to be a full head of hair, she said it had thinned a lot but it looked normal to me. It reinforces that the cold cap had not worked for me and made me feel confident in my decision not to have it again. I must say that the treatment without the added pressure of the cold cap was so much better. Day 2 was a right off, I didn’t sleep at all the night after the treatment and just felt so hungover. Today is hopefully a better day. I have a scan booked for the 12th to see if it’s all working, the lump is definitely smaller to palpate go fingers crossed. sorry to hear about the heart fibrillations, and the struggle to be heard, hopefully the meds with work well for you. Is this a side effect of the FEC? I find I am wishing time away, halfway through the chemo treatment plan, I feel I can be mostly positive but wonder if that’s mostly trying to keep normality for everybody else. It’s all pretty rubbish really though isn’t it. But we push through! Xx
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