lumpectomy vs mastectomy - why did you choose your route?
Hi all,
i was wondering if anyone could elaborate on this question. i have multifocal, grade 3 DCIS, and am contemplating another lumpectomy vs a mastectomy. my surgeon is confident she can clear the margins with another lumpectomy, and recommends radiation afterward. BUT anecdotally, so many women I’ve talked to, even with a Grade 1 single foci lesion, opted for mastectomy. I don’t want to undertreat OR overtreat but I am struggling to figure out why women would make this choice and what am I missing? I'm at a very cutting edge cancer hospital if that matters. I'd love any perspective on this. Many thanks in advance.
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Hi Ealga,
While you wait for the ever-helpful advice from the other members here, you may be interested in checking out the main Breastcancer.org site's page on Mastectomy vs. Lumpectomy.
We hope this helps!
--The Mods
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Hi Ealga,
I choose lumpectomy because my BS was also very confident he could achieve clean margins. Based on the original stereotactic biopsy we were going after a fairly small area of grade 1 DCIS. However after the surgery during which he did 2 excisions, I now have grade 3 DCIS and I have positive margins. We were unable to get the clean margins we thought we were going to (can't take more tissue). I have come to understand that the imaging prior to surgery really does not tell the whole tale. After surgery we did more imaging to see if any microcalcs remained since I had positive margins. There were none. After a long conversation with my BS I decided to do radiation instead of going back for a mastectomy since there was no real evidence of remaining cancer (i.e microcalcs) and my BS & RO thoght radiation should clean it up. Hind sight being 20/20 though....for me anyways....we removed so much tissue (one piece was 9.2cmX7.6cmX1cm, the other piece was 1/2 that size) now that the swelling is down I wish I had had a mastectomy and reconstruction. As my BS puts it, I have a shark bitten appearance. Also, since I had positive margins I will be doing 5 years of tamoxifen. Initially I was not going down that route, but with the positive margins it is the only thing that really makes sense.
Just my tale....hope it helps.
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Hi Ealga: These are the reasons I chose BMX (1) my mass was misshapen so it was going to leave me needing reconstruction anyway if I had done lumpectomy (2) Doctor told me it would be hard to get clean margins the first time-I wanted one surgery, not several, even if it was a bigger surgery (3) I did not want radiation (4) though it was initially thought I only had DCIS, an MRI revealed an area suspicious for being invasive-at that point I felt my breasts had to go. I did not want ticking time bombs in me, (5) I knew of a couple of women who had had local recurrences after having lumpectomy and (6) I chose BMX instead of just SMX because I wanted to end up looking better, not worse, after having to go through the crappy experience of having BC. I have not regretted my decision at all. I think I may be different from a lot of women in that I was not "attached" to my breasts. I have really thought about this. I am very grateful I was able to breastfeed my children but other than that, for me, losing my breasts is not like losing an arm or a leg. Had I kept my breasts I would have been reminded more often that I had breast cancer because I would be looking at them worrying that something else unwanted had grown in there and might still be in there. I honestly feel I am less worried because most of my breast tissue is gone my chance of local recurrence is way less. Sure there is no guarantee some loose BC cells didn't float away to cause more problems, but my faith keeps me from stressing about that possibility. And because I had BMX, which thankfully I have not had any complications with, I am not dealing with the aftermath of radiation and any possible problems that could bring, nor am I taking any hormone pills because for me personally, the risk outweighed the benefit (4%) So while a BMX is a "bigger surgery" I am done other than needing to finish my reconstruction, which I also have had no complications with. I know I am really one of the lucky ones who have had no complications. By the way my final pathology report did find another tiny, tiny area of invasive growing at the other end of the DCIS (1 mm) so if I had had a lumpectomy that might have been missed so I am truly grateful I had a BMX. That's just my experience - I know this is a very personal and hard decision. I actually found that when I had made my decision then I was ready to roll and it was way better than being in the "waiting" and "undecided" phase.
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I chose lumpectomy, for several reasons.
Keeping my breast was important to me (for sensation, more than appearance).
I had a very small area of cancer and mastectomy seemed overkill. My surgeon offered it as an afterthought, but didn't particularly recommend it. Had the area of cancer turned out to be larger than expected, mastectomy could always be done at a later point, but once chosen there is no going back. By the way, it is possible to have reconstruction after a lumpectomy if the cosmetic outcome isn't good. I think it's important to realize that, because it seems not everyone is aware.
I think that many people who choose mastectomy in similar situations do it because they are afraid of doing radiation, but I had no particular risk factors for complications from radiation and in fact tolerated it very well. Now if I'd had some other risk factors, that might have made my decision harder. I'm also taking Tamoxifen, which my MO says will benefit me most in terms of preventing a new primary (as opposed to recurrence of the original cancer, which he feels has been dealt with effectively already), and having 2 breasts does increase the total area at risk of getting more BC but even a double mastectomy doesn't remove the possibility entirely.
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thank you, i will!
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I didn't have a choice - I had so much DCIS in a small breast that the only way to remove it all was with a MX. But given a choice, I would gladly have gone with a lumpectomy + rads. Like Annette, I had no risk factors that would have made rads more difficult or risky for me and I simply was more concerned about the side effects from the MX than from the rads. Since I didn't have a choice, I had a single MX.
Sometime ago I created a list of considerations for those making the lumpectomy vs mastectomy vs. bilateral mastectomy decision. I've reposted this many times now, and I've added input from many other women. Going through this list might help you come to terms with how you will deal with either of these options and what the best decision is for you:
- Do you want to avoid radiation? If your DCIS isn't near the chest wall, then it may be possible to avoid radiation if you have a mastectomy. This is a big selling point for many women who choose to have mastectomies. However you should be aware that there is no guarantee that radiation may not be necessary even if you have a mastectomy, if some DCIS is found near the chest wall. Radiation might also be recommended if it turns out that you have a large area of invasive cancer in addition to the DCIS and/or if it turns out that you are node positive (which is only possible if you have invasive cancer).
- Do you want to avoid Tamoxifen? For those who are ER positive who have DCIS, this may be possible if you have a mastectomy and particularly if you have a bilateral mastectomy. Tamoxifen provides 3 benefits: 1) It reduces the risk of local recurrence; 2) it reduces the risk of the development of a new breast cancer in either breast; and 3) it reduces the risk of a distant recurrence. For most women, a mastectomy will reduce the first risk to a low enough level that the benefit from Tamox will be minimal. For most women, a bilateral mastectomy will reduce the second risk to a low enough level that the benefit from Tamox will be minimal. The third benefit, protection against a distant recurrence (i.e. mets), isn't a factor for women who have DCIS, since by definition DCIS cannot move beyond the breast. However for those who have invasive cancer, this is a crucial benefit and is not affected at all by the type of surgery. So if you have an invasive tumor that is ER+, usually Tamoxifen (or an AI) will be recommended whether you have a lumpectomy, mastectomy or a BMX. However if you have DCIS (and therefore face virtually no risk of mets) or a very small non-aggressive invasive tumor (and therefore face only a very small risk of mets), it may be possible to pass on Tamox with little change in your long-term prognosis.
- Do you want to avoid having node removal? For those with any amount of invasive cancer, an SNB is necessary. But because DCIS cannot travel to the nodes, an SNB is not required for those who have DCIS. For DCIS women who have a lumpectomy, if some invasive cancer should be found in the lumpectomy pathology (as happens in about 20% of cases), an SNB can be scheduled later as a separate surgery. However, an SNB is difficult to do after the breast is removed, so for women who have DCIS who are having a MX, usually an SNB will be done during the MX surgery just in case some invasive cancer is found. Therefore the requirement to do an SNB with a MX is a significant difference vs. lumpectomy for those with pure DCIS. Any node removal presents the risk of lymphedema; after an SNB, the risk is estimated to be in the range of 5% to 10%. Once nodes are removed, lymphedema can develop at any time (even years later) and once it develops, it remains for life (although it often can be managed). (Note that sentinel node mapping is a new procedure, developed by Pink Lotus, that may allow DCIS women having a MX to avoid an unnecessary SNB, but this method is new and not yet widely used.)
- Does the length of the surgery and the length of the recovery period matter to you? For most women, a lumpectomy is a relatively easy surgery and recovery. After a lumpectomy, radiation usually is given for 6 weeks. A mastectomy is a longer, more complex surgery and the recovery period is longer. How do you feel about going through a longer surgery and a longer, more restricted recovery period?
- If you have a lumpectomy, how will you deal with the side effects from Rads? For most patients the side effects of rads are not as difficult as they expected, but most women do experience some side effects. You should be prepared for some temporary discomfort, fatigue and skin irritation, particularly towards the end of your rads cycle. Most side effects go away a few weeks after treatment ends but if you have other health problems, particularly heart or lung problems, you may be at risk for more serious side effects. This can be an important consideration and should be discussed with your doctor.
- If you have a mastectomy, do you plan to have reconstruction? If so, be aware that reconstruction, even "immediate" reconstruction, is usually a long process - many months - and most often requires more than one surgery. Some women have little discomfort during the reconstruction process but other women find the process to be very difficult - there is no way to know until you are going through it. Are you prepared for this?
- If you have a MX or BMX, how will you deal with possible complications with reconstruction? Some lucky women breeze through reconstruction but unfortunately, many have complications. These may be short-term and/or fixable or they may be long-term and difficult to fix. Common problems include ripples and indentations and unevenness. You may have lingering side effects (muscle pain, spasms, itching, etc.) on one side or both. If you don't end up with symmetry (symmetry is not a sure thing by any means, even if you have a bilateral mastectomy with reconstruction done on both sides at the same time), will you regret the decision to remove your breasts or your healthy breast? Are you prepared for the possibility of revision surgery?
- If you have MX or BMX, how you do feel about your body image and how will this be affected by a mastectomy? A reconstructed breast is not the same as a real breast. Some women love their reconstructed breasts while some women hate them. Most probably fall in-between. Reconstructed breasts usually looks fine in clothing but may not appear natural when naked. They may not feel natural or move naturally, particularly if you have implant reconstruction. If you do choose to have a mastectomy, one option that will help you get a more natural appearance is a nipple sparing mastectomy (NSM). Not all breast surgeons are trained to do NSMs so your surgeon might not present this option to you. Ask your surgeon about it if you are interested and if he/she doesn't do nipple sparing mastectomies, it may be worth the effort to find a surgeon who does do NSMs in order to see if this option is available for you (your DCIS can't be right up near the nipple).
- If you have a MX or BMX, how do you feel about losing the natural feeling in your breast(s) and nipple(s)? Are your nipples important to you sexually? A mastectomy will change your body for the rest of your life and you have to be prepared for that. Keep in mind as well that even if you have a nipple sparing mastectomy, except in rare cases (and except with a new untested reconstruction procedure) the most feeling that can be retained in your nipples is about 20% - the nerves that affect 80% of nipple sensation are by necessity cut during the surgery and cannot be reconnected. Any breast/nipple feeling you regain will be surface feeling only (or phantom sensations, which are actually quite common and feel very real); there will be no feeling inside your breast, instead your breast will feel numb. For some, loss of breast/nipple sensation is a small price to pay; for others, it has a huge impact on their lives.
- If you have a MX or BMX, how will you deal emotionally with the loss of your breast(s)? Some women are glad that their breast(s) is gone because it was the source of the cancer, but others become angry that cancer forced them to lose their breast(s). How do you think you will feel? Don't just consider how you feel now, as you are facing the breast cancer diagnosis, but try to think about how you will feel in a year and in a few years, once this diagnosis, and the fear, is well behind you. Keep in mind as well that most women are pleased with their decision to have a mastectomy or bilateral when it's first done - they are relieved that the cancer is gone and the surgery is over and in most cases it wasn't nearly as bad as they feared. For women who are affected by the loss, the real impact usually doesn't hit until many months or even years later. That's why trying to think ahead to a time when this diagnosis is long behind you is important.
- If you have a MX or BMX, will removal of your breast(s) help you move on from having had cancer or will it hamper your ability to move on? Will you feel that the cancer is gone because your breast(s) is gone? Or will the loss of your breast(s) be a constant reminder that you had breast cancer?
- If you have a lumpectomy, how will you deal emotionally with your 6 month or annual mammos and/or MRIs? For the first year or two after diagnosis, most women get very stressed when they have to go for their screenings. The good news is that usually this fear fades over time. However some women choose to have a BMX in order to avoid the anxiety of these checks.
- Do you know what your doctors estimate your recurrence risk will be if you have a lumpectomy and radiation? Is this risk level one that you can live with or one that scares you? Will you live in constant fear or will you be satisfied that you've reduced your risk sufficiently and not worry about it except when you have your 6 month or annual screenings? If you will always worry, then having a mastectomy might be a better option for you; many women get peace of mind by having a mastectomy. Be aware however that while a mastectomy will likely significantly reduce your local (in the breast area) recurrence risk, a recurrence or the development of a new BC is still possible after a mastectomy. Lots to consider.
- Do you know your risk to get BC in your other (the non-cancer) breast? Is this a risk level that scares you? Or is this a risk level that you can live with? Keep in mind that DCIS cannot recur in the contralateral breast so your current diagnosis doesn't impact your other breast. However, anyone who's been diagnosed with BC one time is at higher risk to be diagnosed again and this may be compounded if you have other risk factors. Find out your risk level from your oncologist. When you talk to him or her, determine if BRCA genetic testing might be appropriate for you based on your family history of cancer and/or your age and/or your ethnicity (those of Ashkenazi Jewish descent are at higher risk). Those who are BRCA positive are very high risk to get BC and for many women, a positive BRCA test result is a compelling reason to have a bilateral mastectomy. On the other hand, for many women a negative BRCA test result helps with the decision to have a lumpectomy or single mastectomy rather than a bilateral. Talk to your oncologist. Don't assume that you know what your risk is; you may be surprised to find that it's much higher than you think, or much lower than you think (my risk was much less than I would ever have thought).
- How will you feel if you have a lumpectomy or single MX and at some point in the future (maybe in 2 years or maybe in 30 years) you get BC again, either a recurrence in the same breast or a new BC in either breast? Will you regret your decision and wish that you'd had a bilateral mastectomy? Or will you be grateful for the extra time that you had with your breasts, knowing that you made the best decision at the time with the information that you had?
- How will you feel if you have a bilateral mastectomy and no cancer or high risk conditions are found in the other breast? Will you question (either immediately or years in the future) why you made the decision to have the bilateral? Or will you be satisfied that you made the best decision with the information you had?
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I hope that this list is helpful. The thing to remember is that everyone's experience with surgery is different, everyone's pro vs. con list is different and everyone's emotions are different. Additionally, there is so much in this situation that you can't control..... how you feel about your breasts after reconstruction..... whether you have pain from your mastectomy or reconstruction or not... whether the fears you have now, just after you've been diagnosed, will still be as strong in 6 months or 2 years..., etc.. So don't make your decision based on what someone else did or the experience that someone else had or how someone else felt. Make the decision based on knowing yourself. Do what's best for you. Good luck with the decision!
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Bessie, thank you so much for all the information. I was diagnosed in April 2013 with dcis right breast and surgeon, and oncologist both recommended lumpectomy after stereotactic needle biop. I had the lump. last Friday and today was told margins were positive and another lump. is suggested. Ugh. I had been leaning toward a masc. (not sure what all the abbrev. mean) but docs talked me out of it. Now, I almost wish I had. Wondering if I should go to another surgeon; did this one miss something. But looking at this blog I see many women have had 2 lump. before a mast. Oh, the indecision. I'm 67 and relatively healthy and active. This has been a real surprise.
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ealga, I'm in the same boat.
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Beesie, that was a great list of considerations. I've said it before but will say it again - you are a Godsend on these boards. Thank you.
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I chose lumpectomy+ radiation + Tamoxifen. So far no regrets, but at the time I remember feeling overwhelmed and unable to process statistics on risk. What-if's, what-if's, what-if's. For me, the kicker was that my long term survival rate was the same either way, and mastectomy just seemed so severe in light of that. I felt like mastectomy would remain as a choice if I wanted or needed it down the road, but I couldn't "undo" one once done.
I am just a month or so out from the end of radiation, I'm feeling more like my old self again, and most importantly, I don't feel defined by DCIS. The experience will always be a part of me - always - don't get me wrong. But it isn't always THERE (I'll also add there was a time I didn't think that was possible.)
If you are seriously thinking mastectomy, ask your surgeon if you can have a consult with a plastic surgeon to discuss the process, phases, timeline, recoveries for mastecomy, as well as look at photos of women who have been through it. See if there are patients at your facility who will talk to you about their experiences.Also, you'll see from my signature that I had a re-excision. It was more draining emotionally than physically. I was warned ahead of time that re-excisions are not uncommon with DCIS, though I don't have a good sense of how common or uncommon. I knew it was a possibility, but it was disappointing nonetheless.
Good luck with your decision.
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I had a single, very small bit of high grade DCIS, and I chose lumpectomy+partial breast rads. I carefully considered all of my options. At one point in my decision process my emotions took over and I thought the best thing to do (as a mother of a young child) was to make sure I am there for my child in the long term and 'cut them both off'. i also saw a mastectomy as less obtrusive than taking tamoxofin, which has a huge list of known side effects...and maybe other unknown ones. (I hate taking any sort of medicine/drug.) After research, i realized that having a mastectomy was not as simple as having a boob job...there were a lot of potential long term discomforts. I also looked at my relatively low recurrance rate and decided the best thing for me was a lumpectomy (without Tamox). If i have a recurrance, i have no doubt that I will have a mastectomy.
Good luck whatever you decide. Both of the BS that I talked to were OK with either mast. or lump. What is right for me (or anyone else on this board) might not be right for you.
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I had a large area of high grade DCIS removed via lumpectomy on June 5th and expect to start radiation in about 3 weeks. I had very large breasts so the option for a lumpectomy for an area 13cm was still a viable option for me. I had a reduction on the other side so they would match. Many people simply panic and just want the cancer out of their body and choose mastectomy, single or double, some, don't want to or don't have close access to a hospital that does the radiation, while others cannot fathom chemotherapy. Everyone is different. The important thing to remember is that you have to live with your decision. And you should be comfortable and at peace with your decision. I opted for a lumpectomy. I am waiting for the pathology results. If this doesn't work, I will have new options to consider. The same person with the same family history and diagnosis might have chosen a different treatment option, but for me, this was worth a try and even if it doesn't work out like I am hoping it will, I still am comfortable and at peace with my decision. Good luck with your decision(s).
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A warm hello to all of you. I am sitting here all teared up, not only at your thoughtful and incredibly insightful replies, but also that you've all been through this emotional wringer. I am going to re-read all of your posts now (lately it takes me so much longer to process things - is this normal?!?)
I have a meeting with my surgeon this afternoon. My leaning at the moment is to try for another lumpectomy and see where we're at, and I know that's what my surgeon wants to attempt as well. I may regret this decision, or I may not, who knows?
Beesie - your information is invaluable, thank you. I had no idea how unclear the path can be for DCIS. My first impression was that they cut it out and you're done! How wrong i was. Sending you all my gratitude, and healthy peaceful vibes.
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I honestly think Beesie's guideposts & focusing on what is best for you will lead you to the best result.
Everyone comes with a different set of factors informing their decision that are very personal & multi- faceted.
I had BMX. Is it a decision that was right for me? My gut says yes. Is it right for everyone? Of course not.
My decision was based on my doctors' advice (including a second opinion) about a huge amount of ER negative, premenopausal, aggressive grade DCIS in a relatively small breast.
I'd also had previous biopsies & calcifications in the other breast & an overall family history of very aggressive cancer, not just breast cancer. I have at least one family member who went the lumpectomy route with DCIS & recurred within a year with invasive breast cancer.
There are so many factors that went into my decision. My best advice is to take a deep breath & make the most informed, thoughtful decision you can. Every woman who comes on these boards has a tough decision to make. I did not take my choice lightly & I honestly do not regret the choice. Do I regret the circumstances of that choice? Perhaps, but I am still grateful that (unlike others who are diagnosed at a metastatic stage of cancer) that I had more options available.
Best of luck in both your decision & treatment!
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I had 3 lumpies till the docs gave the all clear. I asked before the last one if I should do a mastectomy, my surgeon who has an excellent reputation said no, I can get it all! She seems to have been right as it is now almost 5 years, yes I did rads and have been doing aromasin but no regrets. I do have a lot of boobie to start with~~
I think Bessie gives great advise but go with your gut. Best of luck
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Beesie, Thank you for your post. I hope I can find it the next time the subject comes up again. It really does hit on many/most of the questions we all need to ask ourselves when deciding which way we need to go.
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To Ealga, I've been wondering how you are doing? Did you need a second lumpectomy or get clear margins. As I posted earlier, I had to have a second and we got clear margins so I'm about to start radiation. I'm ready to get on with it and I'm feeling very positive.
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Hi bjham! Congratulations on your margins - that is great news - what a relief. I go in tomorrow morning for my re-excision. My surgeon is pretty confident (but not totally) that she can get what she needs, so i'm very hopeful. I feel good about both my hospital and surgeon. She is an ace.
She said something interesting to me when we were going back and forth about mast. vs. lump/radiation - I was leaning toward mastectomy simply because i was terrified. But she said that the lump-rads route is often considered as equally/even more agressively treating the cancer than mastectomy, because the radiation will hopefully kill whatever tiny cells are left, whereas with a mx there is still breast tissue left behind, and radiation is not optimal. Either way, the survival rate is the same. I hope she can clear them. Good luck with your radiation - i'd love to stay in touch with you as we go down this road together :-)
question for you: how was your recovery from re-excision? quicker than orig. surgery or the same? It took me awhile to feel back to normal after the first lump. and i hope it doesn't take that long this time. And, are you planning on tamox?
all the best to you.
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Best of luck, ealga, on your lumpectomy re-excision. I did it in three lumpies, but the first was done by another surgeon who didn't mark the margins, so the second surgery was done by visual guide and there was still a close margin. By #3 I had wide margins. So, it's even possible to do three and then rads. Some even do four, but it helps to have a large breast for that (I don't have that).
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thank you ballet12! i hope she is successful.
I'll repeat my questions for you: how was your recovery from re-excision? quicker than orig. surgery or the same? It took me awhile to feel back to normal after the first lump. and i hope it doesn't take that long this time. And, did you do tamox?
thanks so much.
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i just did a biopsy yesterday, because of my first bilateral mammo one year after finding the cancer in my right breast, there was found in my left breast a branching linear microcalcification. i had just stopped arimidex 2 weeks before, because of excruciating bone and joint pain. also had just seen an arthritis specialist there who has ordered a bone scan, to find out what maybe going on there, had baseline a year ago, only pre-arthritic changes in both ankles! in my life, i have really pushed my bod! Glad i did! will always have memories of extraordinary leaps and bounds, catching a train boxcar and jumping off when it got close to my work, impressed the hell out of my co-workers, when they saw me jump off a moving train! not scared to move and use my body. am scared about how could i possibly have something wrong with my other breast, already? i did take a three month break from herceptin, oncs advice, since LEF fell greater than 10 %. So am waiting for results, and havent started tamox yet. they havent even done the blood test to find out if i am a metabolizer of tamox, plus i have fibroids, plus, in a lymphedema book i have read, tamox makes le worse. i am just disgusted. i am slender, and have been really healthy all of my life barely caught a cold. blech.
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Hi ealga,
I had no issues with recovery from any of the lumpectomies, in terms of the early recovery period. The re-excisions were no different. I had the surgeries on a Friday and I was back in my ballet class on Wednesday and my other dance class on Thursday (and I'm 61-lol). I even had stitches still in me from the first surgery when I was exercising, although the last two surgeries had steri strips. I modified raising the arm and didn't do any weights for awhile. I did have issues after the third surgery, in that I have swelling in the breast (seroma and maybe even lymphedema), which became more prominent after radiation. So, I have very mild discomfort in the axillary area from that. You have to know that I have had a total of six surgeries on that breast over the years, so all of the scar tissue and tissue distortion is probably greater than most. Cosmetically, ironically, the swelling has improved things. I will say that I do not regret doing lumpectomy at all. I still have that breast.
About the hormonal therapy, my oncologist was offerring Aromasin. At this point, because we have somewhat of a choice with DCIS, I am holding off on taking an AI due to potential side effects. I could also take Tamoxifen. I feel great and want to continue feeling that way. If I did take Tamox I'd like to take that test to determine if I do metabolize it.
Best of luck to you. I hope you don't have problems and you get the "all-clear" to go on to radiation.
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Hi kathec,
I am praying that they don't find anything in your other breast. You have suffered enough.
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Hi Kathec.
I'm thinking of you and sending you all my best. I hope things improve for you soon.
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thanks Ballet12 - that's good to know that you recovered so nicely. i hope tomorrow goes well and i don't have the dizzy spells that i had after the first one. those lasted for more than 2 weeks. it was hard to walk around the city because i was afraid of falling and hitting my head. Anyway, so glad to hear you feel great! that is encouraging. all my best.
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Hi ealga, if you find you aren't in much pain, stay away from the opiate pain killers that they hand out like candy. They can make you feel dizzy. Stick with Tylenol if you can, as well as local icing of the breast (bags of frozen peas work amazingly well). Also, compression with a sports bra 24/7 for a long time (month?). I'm sure you know all of this stuff, but it's the meds that likely make people feel dizzy. I don't know if you took those the first time around, and if so, maybe they stayed in your system for a long time.
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thanks, yes, i only took the oxy for the first day and half of the second day, and couldn't take any more. I still felt seriously dizzy for so long afterward. I'm going to try to avoid those drugs this time around. thanks again!
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Thank you, ealga, and ballet 12. i am truly impressed, ballet12, that you returned to dance class so quickly, (and @ your age! Naughty girl!) Wow! i am 53 now and hope to do as well! dontcha love BCO? i Dooooo!
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Hi Kathec, just to let you know, that my dance instructor, for these classes, is 62 years old She is a 17 year survivor of IBC in one breast and triple negative in the other (brca 1 carrier). She has severe lymphedema in one arm, among many other long term side effects from all of the treatments (including a bone marrow transplant--done at that time). You wouldn't know it by watching her. Full of energy, never complains, amazing. A true inspiration to me.
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Thankful for this thread. My lumpectomy is July 18th, I've been wavering about my decision to have a lumpectomy. I've read many other threads and its seems there are a lot of women who opted for LX only later having a mastecomy. My lump is 1.6 cm and my cancer is grade 3 Triple Negative...hope I'm making the right decision.
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