Good news Katie, I felt less weird too but slept all the way home and during the infusion 😂.
GorgyS, you sound like you’re doing great on the AC. My Oncologist told me the opposite…… as in the side effects get easier, so far for me, this is true.
Coastiejas, that AC is not fun! From the bad taste, nausea (24/7), cravings, peeling hands and feet, no energy and all round yukniss!
For me the Paclitaxel has been very kind and I’m having double dose fortnightly infusions (5 hours). I almost feel normal!
Let us know how you go and try not to worry.
I’m off for my second infusion tomorrow and I’m not worried one bit, I’m actually looking forward to having a good sleep with the antihistamines they give me 😂.