Ps I had a carbo reaction 2 weeks ago, the dr. said no more for me. I asked the nurses about that and they said the only way the dr. would do it would be at the hospital on a 24 hr. . drip, in a setting where a nurse would be monitering me the whole time. (?). I have heard of just doing slower drips but that seemed extreme. She is probably going to add something else, will know tomorrow.
I am on chemo 3 1/2 tomorrow for recurrence. I have not had a Ct this time since surgery in Oct, where I had pain from intestinal blockage. I have actually requested a head to ab ct for tomorrow, and they are going to do one. I just want peace of mind how things are.Last yr, I had a ct several times during treatment, I guess since my cancer was not visible this time is why they haven.t done one. Maybe I worry too much now about aches and headaches. donna
After my first-line carbo/taxotere treatment, I had a PET/CT and a contrast CT of abdomen, pelivis, chest and head. I'm sure it depends on the stage, the location of the cancer--we're all unique and hard to compare to each other. What worried me is my onc wanted me to do monthly follow-ups--both appointments and CA125 tests--when I thought the normal was three months. However, at stage iv and as long as insurance will pay for it, I can "live" with that. Best wishes for your Mum's chemo and results.
Also, I believe infections can cause a rise in CA125 levels.
Paula