Last chemo in a few days but afraid to ask onco what comes next
Very emotional and excited at the same time at the prospect of DD #8 in a few days. Radiation consul near home is tomorrow( Hospital is 110 miles away. I asked onco twice she told me only last week i find my own RO)
My questions are, 1. How early can I be freed from my Damed port?
2. Any scans to be done before Rads start?
6 month ckup w BS scheduled late August.
Any reply is appreciated.
Mimi
Comments
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Reb - every doc is different. You haven't posted your diagnosis & treatment, so we have no idea what chemo you have been doing? And have you already had surgery?
My MO ordered a bunch of scans at the end of chemo, and again after surgery. I wanted to keep my power port so I didn't have to deal with book work or contrast in my veins.
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It must be my chemo brain or my subconciousness keeps my info private.
IDC both stage 3A and 1A
Grade 2 w some 3 mixed in
Very High ER PR + HER2 -
BMX done
4DD AC
4DD T
Thank you.
P.S. rad consul in 2 hrs can't wait
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I would have wanted scans along the way. I would have insisted if my MO didn't order them. Usually had CT with & without contrast before each new step. There was an MRI thrown in twice. Good luck.
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Mimi.
You had mentioned having palpitations during AC, I would appreciate if you could tell me when they started and how long it lasted. Message if you prefer. Thanks
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tesse,
I had palpitations right after AC #2 which SE came a lot faster and stronger. My heartbeat went to 110 from the usual mid 70. Ativan and sleep lowered it after few hrs.
Mimi
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Hi there, thought I would chime in.
I had 2 MRIs of my breasts before my BMX/immediate recon--which happened about a year after chemo ended. Haven't had any further scans since then, but my PS wants me to get an MRI in the next few months to make sure there isn't any breast tissue left--and if there is, so we know where it is and can follow it.
My MO doesn't think scans are necessary (PET, CT etc.) she believes that is overtreatment, and can more than likely offer up a false positive than report something. She says that I'll have other signs and symptoms that will indicate a problem, and she knows I'll run to her asap if that happens.
My MO follows up with CBC blood work every single time, so I have to get labs done before I see her for my regular checkups. She looks for elevations in particular areas, and probably lower than normal status in others (in my pathology).
She also now gives me Prolia 2x a year--I have mild osteopenia, perhaps from the Aromasin I take (or it could be because I'm post-meno--chemo put me in menopause 5 years ago--and I'm 58 y.o.). The Prolia also can protect my bones from any potential metastases, which I like. I've have no side effects from it at all so far.
I would ask your MO if you'll be rx'd Tamoxifen or some kind of aromatase inhibitor.
Also ask about regular checkups--3 months the first year for me, then 4, now I'm up to 5, but I'm considered "high risk" so I'm followed more closely. And if there are lifestyle changes (diet, exercise, etc.) that you can do. My MO wasn't very well-versed in any of that, actually I've found more helpful and credible information on this site than from any doc.
I had my port taken out as soon as I was done with chemo. Didn't want the reminder pulling me back into the past when I wanted to move forward. My surgeon took it out in his office. I kept it and made recycled art with it.
Good luck and congrats on getting through!
Claire in AZ
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I'd love to see that recycled art!
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Mimi,
Thanks, so your heart was racing, did you feel it pounding too? And only the one dose?
Theresa
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Tesse,
One dose of Ativan did slow palpitatiom. I have been on low dose Ativan since DX. Ativan is good for sleep, anxiety and mild nausea. Nausea help was huge because I only took about 3 compazines for the entire 4DD AC.
Mimi
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Pingpong, I'll try to take a photo and post it somewhere on bc.org. I used it in a shadowbox artpiece. I'm a former river guide, and dx/tx/recovery felt rather like running a river, complete with rapids, so I used my port as my boat, and placed myself on the port as I traveled "downstream" in my shadowbox collage. It was a symbolic piece of art, designed to help me make sense of the whole life-changing journey
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Mimi - thanks
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Claireinaz - that's really beautiful! And a great way to look at it....especially for someone like me who's just pushed off from the shore. Thank you for sharing.
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Rebamacfan - yay for you! Made it thru chemo! My MO ok'ed for me to have my port removed when I had my LX and SNB. Typically she said she has you keep it in a year, but mine never worked well so she said ok. So wonderful being deported!!!! Every dr is so different. I had chemo before surgery. I had ultrasound midway thru chemo and again before surgery. No scans etc. I will see BSO every 3 months now for 2 years. Getting ready to start rads in July.
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ML1209,
My initials are ML. My last chemo is tomorrow and I cannot think of anything else right now. I know I have to exercise today but heat outside and my nerve gave me excuse stay inside. I walked 13000 steps and had a teeny heat exhaustion issue at a church w no AC yeasterday.
Yes deportation is coming for me along w more scans and rads. Tentative start date is July 26th.
Mimi
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