Mother terrified of Adriamyacin
Comments
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I know nothing about 'cold caps' or icing fingers/hands or toes/feet. I did neither, nor ever thought about doing.
I've had problem with being cold all my life as my usual temperature has been below 'normal' for as long as I can remember. One SE I had during Chemo (more so on Taxol than on A/C) was very low temperature - dropped below 94 during one Taxol infusion while cover in warmed blankets and in a glassed in cubicle with the room heater turned to max. Had I been 'icing/cooling' any extremities (head, hand, feet) this could have been possibly catastrophic. Obviously that was me and not what everyone experiences but there is nothing that is absolute. We are each unique.
There are many who have done Adriamycin with no nasty/long term SEs. There is no way to know what any of us will experience because somebody says 'you will'. We can each only speak for ourselves.
4 DD A/C neoadjuvant (Adriacmycin/Cytoxan before surgery every 2 weeks) was 'easy' - did not slow me down at all. 12 weekly Taxol adjuvant (Taxol every week post surgery) was nasty - completely/utterly EXHAUSTED the entire time. Of course there were some other SEs but it's all in the past and I'm still here as active as ever.
BTW - I was 63 when DXd - now 70, living and loving life everyday.
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Older physicians are (with some exceptions like my PCP) more confident with the technologies they’d been using for a long time and are often resistant to innovation (even long after that innovation has become standard-of-care). I read an article not long ago by a bc survivor with a tiny tumor who back in 1998 insisted on a lumpectomy with sentinel node biopsy, followed by radiation, rather than modified radical mastectomy (with full axillary node removal and dissection). Her surgeon told her she was playing Russian roulette and refused to treat her unless she acquiesced to his preferred protocol. She was then operated on by Dr. Susan Love—lumpectomy, SNB and radiation. She’s still alive—that’s how her reminiscence got published—and recurrence-free.
There are two scales of Oncotype DX, both (as BarredOwl says) 0-100; but the scores for DCIS (to determine whether lumpectomy alone without radiation is a safe choice) usually run much higher—the same numerical score considered high-risk in IDC (and which usually determines the need for chemo) may be a much lower risk for DCIS (which is not treated with chemo; and would indicate whether radiation could be safely skipped).
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Gina, between the poor communication on AI/tamoxifen, and now their refusal on cold capping or at least icing fingers/toes (if your mom wants to try them), are you really sure you want to use these folks for your mom? I get that it is very inconvenient to start at a new place, but really, neither cold capping or icing fingers/toes are new things. And both can make immeasurable differences for the patients who are willing to deal with the expense and inconvenience. While keeping your hair is not assured with cold capping, the proven systems (Penguin for one) work at least somewhat for most, and the icing of fingers/toes can not only save your nails, but prevent neuropathy (post treatment numbness and/or pain) which can be life-long after effects of treatment. Keeping ice in the mouth can prevent sores. They need to get with the times.
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Hi everybody,
I wanted to give an update. Mom starts her chemo on Wednesday. We went to a different cancer treatment clinic and they are wonderful and had no problem with her using the cold caps. So fingers crossed that that works.
Mom decided to go against using the Adriamyacin and she is doing 12 weeks of Taxol. Her new oncologist, even though he recommended AC, he respected her decision and ordered the Taxol for her. She is also going to be doing the AIs instead of Tamoxifen after treatment is finished, so thank you so much to everyone who told me about those. Oh, and I may have mentioned this earlier, her first six month mammogram came back clean as a whistle. No sign of recurrence so far.
She's scared though and she told me that she's positive the cancer will come back in a year. I think mostly it's gearing up on the anniversary of my dad's death - one year on 4/27 and a lot of that has been weighing on us both. I broke out in severe hives all across my chest and shoulders, FUN. So anyway, enough of that. Sorry!
I will be back with more updates over the next several weeks. Thank you all again!
xoAbby
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Gracie,
Icing of fingers and toes??? Is that for neuropathy? I have never heard that before!
And nope! We left that place and went somewhere else and they are fantastic!
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Gina, icing fingernails and toenails is to protect them from what can be negative effects of chemo, including lifting and even nail loss. Like hair, nails are fast growing cells and prone to chemo damage. Something as simple as a bag or two of frozen peas works great, and doesn't melt the way ice does. Just hold them on nails to cut down on chemo circulating where it isn't needed anyway.
And so happy to hear your positive news about a more accommodating onc! Hope all goes smoothly! If you haven't yet, you or your Mom may want to join the BCO thread for those starting chemo this month. It's helpful to compare notes on SEs, etc, and feel supported by others dealing with the same initial fears and concerns.
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Gina, congrats on the new place. As dlb mentioned, icing can help protect the nails and also can help prevent or lessen neuropathy, which is numbness, pain and or tingling in the hands and feet caused by some chemos. The icing slows down the blood flow so less of the chemo gets into those areas. Hands and feet are not normal sites for cancer to travel to, so most docs don't have an issue with patients icing if they care to, and since neuropathy can really be a long term problem for some, many patients are willing to deal with the discomfort of icing.
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Abby,
Congratulations to you and your mom for following your inner wisdom. Like you, I went with my 2nd opinion. Even though I experience SEs from the AC+T, I have no regrets.
With lots of support, I got through it. Now I am working through my survivorship care plan. Things are tough, but I feel like I am on the other side. It's been 8 months since I completed treatment. It's so good to hear that you are by your mother's side through this very intense journey.
Best wishes.
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I did not 'ice' my nails! I used OPI Nail Envy on my nails with them being fine thoroughout 4 DD A/C and 12 weekly Taxol.
For me - 'icing' would have been impossible (IF I had wanted to do it) My temperature was dangerously low throughout chemo. I had to have one of the gllassed in cubicles with it's individual thermostat cranked up as high as it would go with piles of warmed blankets to stay at least 94F.
Did/Do not have any neuropathy issues either.
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For several year of reading these threads, icing the nails does help to keep the nails in place. It does not really help with neuropathy. I iced every time. I did not loose my nails. I did get permanent neuropathy in my feet & intermittent in my fingers.
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hi Gina, I was also stage 1 with negative nodes but had a night oncoscore but I did taxotere/ cytoxan Tc x6. And most woman stage 1 Posotive did the TC regiment. Ask the MO
Hugs
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Speaking of neuropathy, if your Mom starts to experience any tingling in hands or feet, B6 can often help. I did that when I had the start of it in my feet -- used just 50 mg., as I recall --- and I was fortunate that it nipped it quickly. Here's a helpful article on it, but, of course, always ask your (or your Mom's in this case) onc for guidance.
https://cancer.uvahealth.com/images-and-docs/neuro...
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I didn't read all the comments here so this might be a repeat, just wanted to weigh in that for me, the Adriamiacin was easier than the Taxotere. I know this isn't the case for everyone. I had an allergic reaction to the Taxotere and in general found myself having fevers, etc after almost every cycle. The side effects on Adriamiacin were more predictable, easier to manage with prescriptions and I did it dose-dense, so it was over faster. The neulasta shots I got every cycle, I think this helped a lot. I was also fearful going in, but I would just advise to not fear the side effects unless she has them.
I did cold caps, kept my hair through treatment (both types of chemo) but lost 80% after my final Adriamiacin and ended up cutting it short. But I was never bald and never needed wigs. But the cold caps are a commitment.
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Gina, I don't know if there's anything new in this article, but I thought of your Mom when I saw it, so thought I'd share it here. http://www.news-medical.net/news/20170419/Scalp-co...(hair-loss)-approved-by-the-FDA.aspx
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Hey ladies!
First chemo treatment of Taxol was yesterday and it went really well. No allergic reactions or any side effects so far except for fatigue. The hard part. was getting used to the cold caps. It is definitely a two person job working with those things so hopefully they work the right way. The treatment itself took about an hour and a half including the pre drugs. We both didn't get to bed until five am this morning after being so wired from the day. She gets her first labs done after treatment next week so fingers crossed everything is going to be looking fine.
dib823, B6 for neuropathy? I have never heard of that. She's had light neuropathy for a long time due to injuries to her left hand from a broken glass and then a screwed up surgery on her foot. I wonder if that will help her now. Thank you for the tip!
Gina
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