Chemo still sucks on taxol
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@melclarity that is so tough!! I agree they don’t tell u what can happen. I have had lots of weird little things happen that I didn’t expect, and possibly even more continuing things could happen post chemo. The only reason I know it’s “normal” and I’m not alone is from this forum. One thing I found was that losing your hair hurts/is very uncomfortable which is something I never would of expected but is normal. I’m seeing my oncologist next week for my finished chemo chat so it will be interesting to see how interested she is in the list of symptoms and questions I have.0
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@Kiwi Angel Mine was not remotely interested. Which is not pleasant as a patient, but maybe as a doctor every patient is more or less the same and it's so it's just not pertinent, and almost certainly boring. Doesn't make us feel good though.0
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@kmakm I get sick of the fact some of them just treat us like we are on a production line. They get so jaded they forget we are all scared and confused and actually do have feeling.0
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@Kiwi Angel And then when you get one that isn't like that it's such a nice experience. I count myself lucky that my breast surgeon is so caring and personable.0
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@kmakm It is so lovely when U get someone that treats u like an individual and not a production line person - almost makes up for all the other a holes1
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Just saw my oncology and he said that how I'm geefeel is very normal but that I'm doing well. Extreme tiredness is due to suppression of bone marrow and if bloods show it's mecessarn down the track, I will have a transfusion. He also said that I can expect it to get worse as I go along. Really happy with the honesty even if it doesn't change the outcome.
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Good. I hate being 'handled'. I much prefer the straightforward telling it like it is approach.0
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I'm sure my phone does the opposite of autocorrect after I've hit post comment.0
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wow I wish I didn't read this post @Sister :-) I start my first T tomorrow, weekly for 12 weeks after seeing the onc today she warned me it will be different from the ac which I handled well, but what bugs me at the moment, I have to give blood on a weekly basis, I think i'm running out of the red stuff0
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@Matt just make sure you convey absolutely everything to your Team each week you go in, as they keep a record of everything. If you handled AC pretty well, you may just be ok with Taxol, you'll only know as you go along. Fingers crossed for you. M1
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@Matt Sorry to have alarmed you. You will get there - it's just a real drag. I actually feel better (mentally) for knowing what is going on with my body. The onc telling me that what I'm feeling is par for the course because I'm not having a chance to repair before the next dose and that the extreme fatigue is because I'm so low on red blood cells (and it will be treated if it gets too bad) makes me think that I can get through it. I'm still emotionally low, but this is halfway through so next treatment I'll be on the other side of the hump.2
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He @Sister,
I haven't read the full post but it sounds like you are having a really tough time. Keep your eye on that goal post. You're nearly there lovely. I kept a calendar in my car so as soon as I walked out I could put a big red cross through another week, It's hard to believe when you are going through all this, but time flies and before you know it you'll be a year down the track. xoxo
Wholly shit @melclarity that certainly a rough trot to say the least. So glad you are feeling good now. What a lot of hard work to you had get back there though. xoxox
@Matt It's just another one of those things nobody knows. You might get through without too much trouble.
It's so strange how differently everyone responds to different treatments. I had next to no problems with Paclitaxel, but am getting an absolute flogging on the HT. Fingers crossed for you.0
