Fill Out Your Profile to share more about you. Learn more...
Take Our Poll: What’s most important to you for your overall health?
Share your story: Your reflections about Mother's Day

Stage II w/Lymph Node Involvement

Options
1…7172747677

Comments

  • roareus
    roareus Member Posts: 68
    edited December 2019
    Options

    can i ask... if your mammo and ultrasound were negative, what made them do a MRI?

  • peregrinelady
    peregrinelady Member Posts: 416
    edited December 2019
    Options
    Actually, I was misdiagnosed for 20 months after the negative mammogram and ultrasound. That is why I think you are lucky they are suggesting further testing to be on the safe side. I am in a small town and my pcp did not suggest further testing which is supposed to happen after both are negative with a palpable lump. I had the MRI after diagnosis to check the other breast.
  • roareus
    roareus Member Posts: 68
    edited December 2019
    Options

    Got it. While I am grateful they are being conservative even with a normal clinical exam, I am also terrified...

  • peregrinelady
    peregrinelady Member Posts: 416
    edited December 2019
    Options
    Try to keep yourself busy and let us know how it goes. If the MRI comes back clear, you will have peace of mind.
  • HoneyBeaw
    HoneyBeaw Member Posts: 150
    edited December 2019
    Options

    Same here did not show up on mama and had a hard time finding on ultrashould . Mine was right under my nipple right in the middle. I sill swear if it had not been for my nipple being inverted and and me being hell bent something was wrong I would have went another 2 yrs with that damm thing. I had clear mama 2 mts before finding it myself

  • roareus
    roareus Member Posts: 68
    edited December 2019
    Options

    I got my MRI results and it was fine. Thank you everyone for your support. Will go back in 2-3 months for a follow up to make sure it does not happen again. Greatest Christmas gift I could have asked for. Hope everyone has a happy holiday.

  • llilly
    llilly Member Posts: 3
    edited January 2020
    Options

    Anyone had their Oncologist suddenly state they no longer need to be seen and can be transitioned back to regular doctors. I am 8 years out from surgery and on Year 8 out of 10 for taking Arimidex. It was my understanding that I would be followed until completing Hormone Therapy (long term surveillance of bone and cardiac issues) and would still want my tumor markers reviewed after completing Hormone Therapy for comparison, especially since I had one positive lymph node. At this point, I need to be working on my Survivorship Plan. Thank you.

  • nancy2581
    nancy2581 Member Posts: 407
    edited January 2020
    Options

    Hi llily though I am not 8 years out only 5 1/2 I am wondering if you were transitioned back because they (according to my oncologist) are recommending 7 years of hormone therapy now instead of 10. Not sure just a thought.

    Nancy

  • Pittiemama
    Pittiemama Member Posts: 1
    edited January 2020
    Options

    Hi All! I love reading this thread, but I am curious what the ratio of pre-menopausal vs post-menopausal is? I've been diagnosed as IIb with 2 involved nodes and at 43 years old I am only pre-menopausal. Everyone I've talked with so far all seem to lean on a more aggressive treatment because of my age and want me to do 4 rounds of chemo. Have any of you had success at a younger age without chemo? My RO is already planning 30 rounds of rads with hormone blockers as well. Thanks in advance!

  • pebblesv
    pebblesv Member Posts: 486
    edited January 2020
    Options

    HI Pittiemama - I have a very similar case to yours, and hopefully its encouraging to hear that my first mammogram post-treatment in October came back completely clear and cancer free! In fact, they just said, "Everything looks good, see you next year." and the visits with my oncologist have gone from every month to every 3 months to 4 months and now 6 months.

    I was also diagnosed at 43, ER/PR+ and HER2-, 2 involved nodes, also (and still) pre-menopausal. I did the surgery (lumpectomy, not masectomy), radiation and am currently on tamoxifen (hormone therapy) treatment. I DID NOT DO CHEMO. The saving grace was the Oncotype DX test which I highly recommend you insist on getting (seems you would qualify for it) where results came back to say that the risk of recurrence for me was the same whether I did just tamoxifen or chemo too, and at that point, my oncologist who had been assuming chemo would be part of my treatment prior to the Oncotype results, said - and I quote - that he would "no longer recommend chemo due to the EXTRA TOXICITY IT WOULD INTRODUCE for no benefit".

    I personally felt like a cloud had lifted when I learned I did not need chemo. To be honest, I was already leaning towards not doing chemo, but I knew if I didn't have the data and tests to back up my decision, it would be very, very hard to hold my ground amongst family and friends and doctors who would be pushing me to do chemo. Yes, they say that because you are "younger" (the only place early 40's is young LOL), that we can better tolerate chemo and go for a more aggressive treatment. But I saw it the opposite way - that because I am younger, I am less willing to introduce debilitating side effects, many of which can be permanent (like a permanent neuropathy, or hair loss as has happened for some on taxol) into my life when I have such a full life ahead. Now, plenty of people do chemo and get through it just fine and make a full recovery. That said, I saw too many cases close to me where people did chemo and it came back anyways, or did chemo and suffered some very permanent side effects as a result, and in almost all cases, for someone pre-menopausal, chemo would push them towards menopause. Whereas on tamoxifen, for better or worse, I still get that time of month very regularly every month - and my oncologist actually thinks I'm tolerating tamoxifen so well BECAUSE I'm pre-menopausal, and far from menopause, so he says I'm not confusing any menopause symptoms with tamoxifen. Not getting hot flashes, not getting joint pain, had a little nausea when I started but it passed in a week and now I've adjusted to it. Did gain weight and much harder to lose weight but I'm trying to break through that now.

    Anyways, I have no regrets on the path I chose because I've been able to get through all the treatment (including a fairly aggressive radiation treatment!) with minimal to no side effects, feel like I didn't lose any part or sense of myself along the way, and came out of it a year and a half later completely in the clear and feeling healthier than I did when I was first diagnosed! I'm a big believer that you have to do your research, be informed, trust your gut and choose the path that you feel is best for you and move forward with confidence. Everyone has a different risk/benefit scenario in terms of what risk they are willing to tolerate for what benefit, you just have to know what you're stepping into, what risk you are willing to take for what benefit, and go with it. For me, I said yes to some things and no to others. I was not OK with the risk of a full axillary node dissection with my surgeon told me had a 40% chance of lymphedema (a permanent condition) but was OK with an aggressive radiation treatment that still carried a 15% risk of lymphedema. Such were the chances I was willing to take, and I felt I could control how I reacted to radiation better too as my nodes are still there (yes they still treated all the nodes with radiation since I had 2 positive nodes). I was fine with tamoxifen and researched a lot how to manage and avoid side effects and am still taking it, and lucked out with an Oncotype score that validated my not needing chemo, but I was already leaning towards saying no to chemo, lots of stories behind that I can share another time or over messaging. There is another on this thread who had a high Oncotype score, still said no to chemo, and is thriving and healthy 6 or 7 years later.

    Anyways, since we have really similar cases, I'm happy to share more insight - feel free to reach out to me over message. Best of luck with your journey, please keep us posted, and know that this is a very beatable and survivable thing. And its fully possible to get through this while maintaining your sense of self, not suffering, and minimizing side effects. I did it! I know others who have too!

  • jrnj
    jrnj Member Posts: 407
    edited January 2020
    Options

    Pittiemama, Your Dx does not appear correct. LCIS and DCIS do not spread to nodes. Did you have lumpectomy? Mx? Were they not able to find the primary invasive cancer? Maybe that's why they want to be aggressive? What is your Onctotype Score? I am 54, but my Dx is similar to yours and I am a "young" 54, totally pre-menopausal with very active hormones. With Drs. these days they really rely on Oncotype Score with Estrogen positive Dx. With a 15, I was in the low risk/gray area. I went for three opinions, 1. I don't know, 2. No chemo 3. Yes chemo, but since you are "low risk" CMF (from Sloan). It is not that common and most of the people on it were recommended by Sloan or a hospital in CA. Dr. said it is about 2% less effective than AC, but has lower risks of permanent side effects especially neuropathy and hair loss heart problems. I am on it now. They said my hair would "thin", but after 3 treatments I've lost about 60%. I feel pretty crappy the first week, but pretty good the second week. But not worst case scenario, to my surprise no nausea, but some chemobrain, fatique, slight headaches, slight digestive issues. Although it is better than TC and AC, it is still chemo and I am not working. And it is 8 rounds every other week, so takes longer. Just wanted to let you know there was another option. Also depending on if you have ILC or IDC, two of my Drs. recommended skipping Tamoxifen and going to AIs, which are supposed to be more effective, especially for ILC. Sloan recommended Lupron for ovarian suppression, but I am going to get my ovaries removed. I've had two periods already on chemo, nothing can stop them.

  • marguin
    marguin Member Posts: 10
    edited January 2020
    Options

    Hi, does anyone have info on how/why a BC surgeon decides how many lymph nodes to remove during a mastectomy?

  • peregrinelady
    peregrinelady Member Posts: 416
    edited January 2020
    Options
    With me, they injected a dye that goes to the sentinel node (where the cancer usually spreads first). My first node was clear, but the surgeon took the 2nd node as well, and it had micromets. Has anyone mentioned the sentinel node biopsy to you? Some surgeons take more, but I am not sure what they base that on.
  • vidal1993
    vidal1993 Member Posts: 60
    edited March 2020
    Options

    Hello Everyone:

    My wife is now 44. She will have axillary node dissection next Thursday March 19.

    Anyone wanna share their experiences? We are concerned of course about lymphedemia. How was it post-surgery? For how long?

    My wife had her lumpectomy last September, and 2/2 nodes were positive. She has just finished chemotherapy on the FEC-D regimen.

    The pathology reports from her surgery last September indicated macrometastasis, and extranodal extension of about 2.5 mm.

    After this she will have radiation, and then hormone therapy.

    Looking forward to the replies. Thanks in advance.


  • pebblesv
    pebblesv Member Posts: 486
    edited March 2020
    Options

    Vidal1993 - I’m only just seeing this now (haven’t checked in lately), I guess your wife had the axillary node dissection today? I hope she is well.

    A bit late to share my perspective and experience but I also had 2 positive nodes and declined the axillary node dissection due to the high risk of lymphedema. Radiologist later told me they could treat my nodes with radiation which carries far less risk of lymphedema (15% for radiation vs 40% for axillary node dissection according to my surgeon). Happy to report that I had a completely clear and cancer free mammogram recently! It’s almost 2 years post diagnosis for me.

  • jrnj
    jrnj Member Posts: 407
    edited March 2020
    Options

    vidal1993, I suffered a lot of anxiety over this issue. I thought my Dr. would take more nodes due to 2 positive and she didn't. And when I showed her the NCCN guidelines that recommend node disection for mastectomy, she got mad and refused to do it. Drs. are split on this issue. So after time, it didn't make sense for me to seek out another Dr. to do another surgery, if I was going to get radiation. But lots of women are fine with the dissection, so hopefully your wife will be too and will have peace of mind they are out. I'm still having anxiety that radiation won't get it all and node invasion won't show up on any scans under 5 mm, and they tell me I won't get any more scans with mastectomy anyway.

  • sivatej
    sivatej Member Posts: 4
    edited April 2020
    Options

    Hi everyone , it's so nice to see you all doing great!

    My mom was diagnosed in November of 2018 and the imaging showed N2 nodal involvement , Level 1 and Level 2(er- pr- Her2+)

    She first had 4 rounds of AC, then surgery (which showed T2N1, 3/12 nodes) then she had 4 rounds of Taxol+Herceptin then continuing herceptin for an year finishing this February(2020) and she is doing great as of now.

    My question being , is it usual for people to have surgery (or atleast , is it not very unusual ?) after 4 rounds of AC ? I see that mostly either people have surgery before or after 8 rounds of AC+TH. Also , now which is the staging that I have to look at for her diagnosis, the one before or at the time of surgery?

  • vidal1993
    vidal1993 Member Posts: 60
    edited March 2020
    Options

    hi jrnj and peebles. Thanks for your replies. As it turns out, my wife’s surgery was postponed due to the Coronavirus crisis. I understand she is at the top of the list, but it is causing us tremendous anxiety. The pathology reports after her lumpectomy showed extensive lymphovascular invasion.

    She is starting tamoxifen now, any comments about that?

  • mariadelpilar
    mariadelpilar Member Posts: 37
    edited May 2020
    Options

    hi ladies,

    My oncologist is adamant about not drinking alcohol. I just finished radiation after surgery and chemo and will start ET. I enjoy drinking a couple of glasses of wine every night as I sit on our deck and visit with my husband. I am scared to death of a recurrence because of the alcohol. Where are you all on this subject? Also when the research says that every drink increases your recurrence rate by 7 to 10%, what does that mean ? 7% of what number?

    Thank you all for being so supportive

  • GoKale4320
    GoKale4320 Member Posts: 580
    edited May 2020
    Options

    I pretty much gave up alcohol. I didn’t drink a lot before- one craft beer a week, so now I will have a sip or two once in a great while. I am doing several things to try to prevent a recurrence such as plant-based diet, time-restricted eating, better sleep, dial-down stress, more exercise and little to no alcohol.

    I think the 7-10% reduction in risk is really something like: if your risk of recurrence is 15% for example, 10% of that would be 1.5%

    I suggest doing some reading and decide for yourself what your plan will be. There is tons of information out there. It could motivate you to make changes (versus just doing what you’re told).



  • bravepoint
    bravepoint Member Posts: 232
    edited May 2020
    Options

    Mariadelpiler - My oncologist told me that 2 glasses of wine a week was OK. I used to enjoy a glass every night with my husband but have cut back to just weekends.

  • smiling_brenda
    smiling_brenda Member Posts: 24
    edited May 2020
    Options

    My MO (@ Stanford) said the limit is 3 drinks per week, but up to 7 (1 a day) is "probably ok".

    I generally have 5 drinks a week but it is always organic wines (less sulfites, pesticides, alcohol) etc. I get it from dryfarmwines.com


  • mariadelpilar
    mariadelpilar Member Posts: 37
    edited May 2020
    Options

    thank you, smiling Brenda! Looks like I’ll have to cut back!!!!

  • mariadelpilar
    mariadelpilar Member Posts: 37
    edited May 2020
    Options

    I thought that was the math, but wasn’t sure. thank you

  • Onlyme64
    Onlyme64 Member Posts: 12
    edited May 2020
    Options

    How big of a risk on recurrence if one drinks. With the covid-19, I been drinking about 3 drinks a day over the past 2 weeks. I have been out of treatment one year, my following up appointments have been rescheduled due to the virus. I don't want to over drink and go back my old habits. but don't want to freak out just because I had 2 bad weeks of drinking. Because from what I read my drinking, being overweight, and bad eating habits could have given me my bc, Again, don't want to over think or freaking out just because I had bad weeks.

  • GoKale4320
    GoKale4320 Member Posts: 580
    edited May 2020
    Options

    Justme1964- don’t beat yourself up over a couple of bad weeks. Instead, think about all of the good changes you’ve made and try to build on that. If you still need to make some improvements , there is a lot of good information out there. Tons of stuff online to read until the library opens again. I took small steps to a better lifestyle over many months.



  • mariadelpilar
    mariadelpilar Member Posts: 37
    edited May 2020
    Options

    dear just me, I agree. Don’t overthink it....I am also trying to cut back to one drink a night, but it is hard! We are very social and wine has always been part of our lives. I do read a lot and get conflicting answers on drinking and breast cancer recurrence. Is anyone has a cause and effect type of research data on drinking and breast cancer recurrence, please share it. All the research seems to be observational.

  • santabarbarian
    santabarbarian Member Posts: 2,310
    edited May 2020
    Options

    I too have been a lot of carbs eating lately-- since sheltering at home-- though this has not been my habit for a long time. I agree, do not beat yourself up. I am considering it reaching for a simple dopamine comfort in a time of emotional trauma. I think like you I am already feeling the need to go back to more veggies though because of how I feel on more veggies. Simple carbs produce a general/subtle inflammation in my body, that I feel. Healthy eating plus supplements is so much better in terms of how I feel.

    An apple or some nuts to snack on is my normal. Not bread & butter! I need to get back to a whole foods vegan basis. I have luckily stayed with intermittent fasting which to me makes a huge difference no matter what I am eating.

  • claireinaz
    claireinaz Member Posts: 680
    edited May 2020
    Options

    Here's are two link to b.c. recurrence and alcohol consumption. It looks like (according to the study) some research reports no increase in recurrence, and others do.

    I share concerns. I like wine. I do believe that regular exercise, meditation, eating habits, weight, environment, etc. all counter drinking alcohol (that is my story and I'm sticking to it).

    https://www.fredhutch.org/en/news/center-news/2016/06/new-study-on-alcohol-use-after-breast-cancer.html

    https://ww5.komen.org/BreastCancer/Tables/Alcohol-and-Breast-Cancer-Survival.html

  • mariadelpilar
    mariadelpilar Member Posts: 37
    edited May 2020
    Options

    I agree. Vegetables, exercise and a healthy weight should counteract the effects of wine. I have specifically looked for research on alcohol and recurrence, but I have found a lot of conflicting information. I will google next the recurrence rate of women in countries that consume a lot of wine like Italy, Spain, and France!😜

Categories

Join Us on Zoom: Upcoming virtual meetups. Read more...
Give your account some personality! Add a profile photo.