I met with my oncologist today to review the results from my CT scan last week. Overall, the results were positive as there was no change since my scan in August which means STABLE!! This was the goal. My next scan is in 3 months and I’m told that no change on that scan would be good news too. I selfishly want to see shrinkage, but that might not be reality yet. Patience is hard. My oncologist is focused on my whole self and is pointing to the lack of oxygen usage as another sign that Enhertu is doing what we want.
My 3rd infusion was also today and that went smoothly. Side effects continue to be limited to GI unrest. Lovely, right? Hopefully I can address that by being more proactive with meds. I have a tendency to take something when it is too late.
The hip is recovering well, but I’m having pain in my knee, ankle and toes that is being attributed to arthritis. Sara thinks the new hip leg might be slightly longer so I’ll need to try an insert in my other leg too. I’m trying out a cream that just moved from prescription to over the counter for the arthritis. If that doesn’t work, I have a script for a non-steroid anti-inflammatory. It can also upset the stomach so I’m trying to avoid that. Overall, I don’t like taking anything. But, I have options which is good. Keep trying until you find what works…I guess I need to be ok with that for chemo too.
I got a strong dose of steroids today with chemo, but want to avoid them as much as possible hoping my moon face will go away. I’ve been off daily steroids for a week now. I can hide the cheeks if I take the pic from the right angle :) I’m getting used to the wig and feel less self conscious with it, but I’d love to find something short and funky. My eyebrows and eyelashes are back…and my mustache!! Ugh! I also have fuzz on my head, but it is nowhere near covered. And the areas that were radiated are seriously lacking. Maybe I’ll have enough to ditch the wig and hats in the spring?
No comments:
Post a Comment