January 2013 surgery

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  • BrandieMcAdams
    BrandieMcAdams Member Posts: 44
    edited January 2013

    Good luck Hope and Jenni! Praying for you all.

    Abitmuch: Reading about seeing your sweet one move reminded me of seeing my darling Anna at 12 weeks. We had thought we had lost her, so when I saw her (husband was deployed) all I could think was she's really there, alive and MOVING! It's amazing how much they look like babies at 12/13 weeks! I'm praying for your node surgery. I don't know which date would be better, so I'm just praying that whatever is suppose to happen (tomorrow or Valentines) happens!

    Hope everyones recovery continues to improve!

  • Lmimp64
    Lmimp64 Member Posts: 219
    edited January 2013

    Best for everyone having surgery today and tomorrow.



    FYI - I went to oncologist today and oncotype was not back. More waiting. My case is going to tumor board for the second time next Wednesday. They are also running receptors on the other 3 tumors - only two were biopsied and only one was oncotyped. The concern is 5 tumors even though they appear not aggressive. Hmmm. Officially stage 2a.

  • Mirmirpanda
    Mirmirpanda Member Posts: 89
    edited January 2013

    Good luck today Hopex3 and jenimomof3!!!



    Hoping everyone out there is having a wonderful day :)



  • MameMe
    MameMe Member Posts: 425
    edited January 2013

    Peeking in on this topic, as I am at home recovering from a second round of cancer tx. What I have noticed is in some ways I know what to expect, which helps me have a sense of control, but that knowledge also has set off some ptsd (read MAJOR anxiety at every single contact with treatment providers) which has been a huge drag. I am 61, and its been a good ten years since the first dx and tx. From my reading I feel quite strongly that I have had cancers that are unlikely to grow quickly or metastasize, and tend to feel like most of the tx recommendations are overkill for my situation. However, facing this fairly low grade situation a second time is stressful, nonetheless. My heart goes out to all of you who are feeling sore or scared or preoccupied or overwhelmed. The bus drops me off at those neighborhoods, just when I think I am over myself and able to focus on the rest of my life again. As I recall, it will get better as the days progress past the last formal treatment day.

    Hugs all around, Mame

  • peanutsgal
    peanutsgal Member Posts: 161
    edited January 2013

    Hi, everyone! So glad to see everyone is progressing so well. Have not had phone, TV, or Internet for the last 3 1/2 days!!!!!!!! GRRRRRRR. Do you have any idea how boring it is to not be able to do anything and to not have those necessities? You can only read books and watch so many movies! Thank goodness my son and lovely DIL made me an entertainment basket for after surgery! Anyway, I survived and came back to see several new January sisters on here. Hello and welcome to all of you. For those of you who have had surgeries during my hiatus, you were in my thoughts and prayers. Sympathies to those who are still dealing with drains and happy dances for those of you who were able to shed that burden!



    Saw PS on Tuesday and he did my first fill. I was terrified of how I would feel that night and the next day since I had read that the more athletic and fit you were, the more you would hurt. I had a really hard time right after surgery with just the initial fill of 50cc's, so I almost fell out when he said he was going to do 100cc's on each side! Apparently my TEs were wrinkled and he didn't like that. Fast forward to later that evening...my back and shoulders were really pulling, but nothing that some muscle relaxers and the heating pad for my back couldn't handle. Today is much better and even though I'm only 150cc's I feel almost like my old self. (My TEs are only 350cc's)



    Will have you in my prayers tonight and tomorrow, BrandieMcAdams!

  • robinlee76
    robinlee76 Member Posts: 27
    edited January 2013

    I was going to ask is anyone was having the tight chest/soreness but from reading above I am not the only one.  I told my husband the pain last night was worse than it had been at the beginning.  I am trying not to take pain meds because I want to DRIVE!  I have become addicted to HGTV.  I could move to Canada now and find half the houses that have been renovated and sold.

    This is why I like this blog.  It reminds you that you are not alone.

  • smethot
    smethot Member Posts: 161
    edited January 2013

    Ladies!  Just met with the surgeon...the news is good!  I am staged as a IIa...woo hoo! with 2/25 nodes and clear margins.  MY warrior princess nodes did the job.  Superheros extraordinaire!  I love my now-defunct nodes...a formal thank you for doing your job beautifully...my eternal gratitude.  No receptor info back yet but my cat scan today came back with an all-clear so i am feeling cautiously optimistic (insert Snoopy's happy-dance here).  Only iffy note was the "possibility of a BRCA associated cancer" due to the high grade (3) and "medullary-like features and a very high mitotic count"...so i'm gonna get tested to rule it out.  That said, keep your fingies crossed- NO breast or ovarian cancer in my family so i'm hoping for a GIANT RESOUNDING NO on the BRCA.

    So overall...a damned good night...just what i was hoping for..yeah!  And if there are any cellualr insurgents out there...watch out...I'm coming for your asses...chemo starts mid-Feb.  Nowhere to run...nowhere to hide...just annihiliation.  Die cancerous bastards, die!  (I feel like G.I. Freaking Joe!!!  I am Canadian...this is so out of character...)

  • kkuziel
    kkuziel Member Posts: 191
    edited January 2013

    Best of luck to those having surgery today. Went to my surgeon today, but test results are not in yet. I do know that the three lymph nodes all came back negative which is good. Don't know about the margins, but surgeon felt confident they would be good. Tumor size is small (not confirmed yet by path report, but has been measured by several mammograms and an MRI as being under a cm)



    So I was feeling pretty good that chemo would not be necessary. But the more I read and hear the more concerned that it might be part of my treatment, even for a small tumor with negative nodes. How often does a node negative tumor need chemo. I know there isn't a one answer fits all, but I'm curious as to how they determine this. Seeing an oncologist next week who I'm sure will have those answers, but I like having some input before I face that question. Guess I'm still trying to have some sense of control in a situation that seems to be completely out of my control.



    Wordgirl118 thanks for the words of encouragement. I do feel like I'm supposed to "get better" at all of this, but you're right this is my reality, and if I'm scared I guess I'm scared. Hopefully once all the answers are in place I will feel better, at least I hope so.

  • Lmimp64
    Lmimp64 Member Posts: 219
    edited January 2013

    Kkuziel - request an oncotype dx test to see if you need chemo. You have to be invasive, er+, her - and no lymph nodes to get it. I'm waiting for mine - It tests invasiveness, receptor status, proliferation rate to determine effectiveness of chemo. Here is a link with other good links at the end.



    https://humana-portal.dnadirect.com/pdf/patient-education/humana/oncotypedx.pdf

  • Lbwagner69
    Lbwagner69 Member Posts: 45
    edited January 2013

    Praying for all of you in surgery over the past few days and today...and upcoming. I went to my last personal training session and I am going to my last day of work tomorrow.  I am starting to have a little anxiety over my approaching surgery on Tuesday.  I have been strong...smiling...business as usual, however, I find myself with a wave of emotions over little things people are doing for me.  I know this is normal.  I'm hoping I can hold it together tomorrow at work.  I teach at a middle school and I think they're planning  something...wearing pink and giving the kids pink ribbons.  Of course, when I found this out...I lost it.  I'm sure I'll have more to post in the upcoming weeks...or at least I come out of the "fog" of the surgery.  Wishing everyone well!

    Laurie

  • Amy4978
    Amy4978 Member Posts: 473
    edited January 2013

    Prayers and positive vibes to all of you! Wishing you with surgery today and tomorrow minimal fears and a speedy recovery....hugs!

  • kkuziel
    kkuziel Member Posts: 191
    edited January 2013

    Lbwagner69: I too teach in a Middle School, and while we all know that 7th and 8th graders can be extremely difficult, I was amazed at how kind my students have been. My co-workers have been incredibly supportive and have gone out of their way to help. Overwhelming to be sure. I'll be returning to work on Monday after taking this week off. This week I've gotten flowers from each class, many cards, several emails and a couple of the students have talked to me about having a fund raiser. I don't want to discourage them, but I'd prefer if they want to do a fund raiser to do it for someone who needs the financial support for treatment. I've got a couple of girls discussing how to make that happen. It's gratifying to see them think of others. Hopefully your surgery will go well and you'll soon be back in front of your students.

  • DebR53
    DebR53 Member Posts: 6
    edited January 2013

    I had a lumpectomy and SNB on January 18, 2013. I will not meet back with my surgeon until early Feb. He called to say lymph nodes are clear--I hope that means "for sure".  I have been experiencing weird sensations and numbness. Glad I found this website, so I learned the sensations are common.

  • CookieMonster
    CookieMonster Member Posts: 1,035
    edited January 2013

    kkuziel - as I understand it, before the Oncotype results are known, if you're ER-, PR- & her2- (aka triple negative) they generally want to give chemo. Also if you are her2+ same thing. Then with oncotype, it tells you how much chemo is likely to help your particular situation.

  • DebR53
    DebR53 Member Posts: 6
    edited January 2013

    hi kkuziel!

    I just found this forum and spotted you on the list of recent surgeries similar to mine. Like you, I had a lumpectomy and SNB on January 18, 2013. I was only diagnosed 4 weeks prior to that! So this is all happening so fast and my emotions are up and down, buried, then surfacing. I also was lucky--under 1 cm, margins cleared. But I couldn't get my follow-up appointment until Feb 4th. Glad my Dr. called me to tell me the nodes were clear. Hope that wasn't a pre-mature statement. Like you, I'm nervous. I actually found this forum, because I was getting creepy, tingly, and numb sensations. So I'm hearing this is common. My underarm feels quite strange. Are you having any of this?

  • shadytrake
    shadytrake Member Posts: 142
    edited January 2013

    Hi Robinlee,



    I agree. I am so glad I found this site too because I don't do in person support groups very well. They remind me of my mom who passed in 1997 of BC.



    Ironically I got a card inviting me to her old support group and the lady who leads it is the same from when my mom was there. Just can't go. Too many emotions there. Miss my mom so much right now. She was 49 and I am 42 now. I know mine is early but I am still scared.



    This group makes me feel like I'm not alone.

    -Melissa

  • wirdgirl118
    wirdgirl118 Member Posts: 231
    edited January 2013

    This forum IS wonderful! When I'm not up to talking or listening, I can read the posts and absorb the info and support at my own pace. I don't know if I will or should join a support group. You make a good point in your post ... I read what you said to mean that a particular support group, even a breast cancer support group, may not have a positive effect.

  • Amy4978
    Amy4978 Member Posts: 473
    edited January 2013

    Kkuziel... If your students.do end up doing a fund raiser for you or anyone I have a great idea for you! A good friends of mine did it for me and raised almost 3,000 in a month. We went to seven different chain restaurants and asked them to donate a gift card for 50.00 for a cancer fundraiser most of them did. If not we just purchased the gift cards from the proceeds. Anyway after we got the giftcards we did a raffle and called it the 777..... Seven days of eating out, at seven locations, valued at 350.00 . We made up raffle tickets and sold them for 20.00 each but you could do 10.00 or 15.00. We sold tickets for 4 weeks and picked a winner. This turned out to be a fantastic way to raise money cause if you do chain resturants you can sell tickets to people near and far. Anyway it was very sweet of the students to wanna help. Its got to feel awesome to have them supporting you!



    Hope everyone is feeling as good as we can be and you enjoy your day! We are suppose to get 4 inches of snow here in MI today! I cant wait.for spring.....

  • kkuziel
    kkuziel Member Posts: 191
    edited January 2013

    DebR53, our situations do sound similar. Especially the up and down of emotions. Went to my surgeon yesterday, but the reports weren't in so you not meeting until February will probably work okay. I knew after my surgery that my lymph nodes came back clean, but I thought that might change as they do more testing. He assured me that that will not change. Felt somewhat better about that. He did of course say chemo was not off the table (worst case scenario) so I've been in a panic about that. Just thought with negative nodes I had dodged that bullet.



    Haven't had any of the symptoms you described. My recover has been thankfully uneventful and painless. This forum is a great place to speak out about your fears. Everyone hear has been so wonderful that I'm sure you'll get a sense of support our your journey.



    Amy4978: thanks for the great fund raising idea. We don't have many chain restaurants in our entire county. It there are many local places that would eager to participate. I'll be back on Monday and shoot this idea past my students.



    CookieMonster: that is the one thing that no one has right now - the hormone status. It was never faxed to my first surgeon and my second surgeon got the copy sent to the first. He said they redo all of that so it will come in with all the others surgical results. That's all going to the MO who I have an appointment with this Thursday, so I guess then finally all the pieces should fall into place. My surgeon again reminded me that this test and wait, test and wait is the toughest. Once I have everything in place i'll feel better. I sure hope so I'm driving myself and my poor husband insane.

  • wirdgirl118
    wirdgirl118 Member Posts: 231
    edited January 2013

    I'm also getting tingly, creepy and numb sensations, my left arm and underarm feel weird like i got novocaine, and so when my bs said I could start massaging the upper arm on the left, given those sensations I've been having, I thought massaging would hurt, but it actually feels good. Last night I got a brief sharp zap where my left breast used to be, and I was like, oh no, here we go, but that was it. Nothing acts like I think it should! It is confusing it's like I traded my old body for a different model!

  • dnadebbs
    dnadebbs Member Posts: 82
    edited January 2013

    those tingly and numb feelings are normal and will most likely last for a long time.   i had my surgery last year in march and i still had them at times but they do minimize.   at first i couldn't even wear a necklace because it was soooo irritating just touching my skin right there.......but it only took a few months and i was good to go.   what's funny is that you will have an itch on one spot of your chest and have to search around to find where that particular nerve really is to actually relieve it.  like it i would feel a sharp sensation where my nipple used to be and have to massage under my arm to relieve it!  lol!   it was hilarious to me.   crazy stuff.   

  • Tamiami
    Tamiami Member Posts: 396
    edited January 2013

    Good morning ladies~

    Today is the day I see my PS and hopefully get these drains out!  It's been 3 weeks with them in, and even though they are still draining at 35-40cc's I'm really hoping she will take them out anyway!  I honestly feel like they are bringing me down.  The more I sit in this house (stuck here), the worse I feel.  It is completely against my nature to feel like this...I WANT to feel good!  When they come out, I plan to take the longest shower ever, and start back to the gym...I can't wait to have something to do every day again. 

    Does anyone know if PS will start fills with drains in, or will fill the day the drains come out?

    Those of you that mentioned the tight feeling...I am feeling that too.  It is getting worse everyday.  I think it might be that the swelling is pretty much gone now except for the "side boobs" I'm rockin.  LOL!  So with less swell (less cushion?) I can really feel the TE's.  I can see and feel where they are stiched in now and it kind of pulls there when I stretch or move.  Is anyone else experiencing this?

    Hoping everyone is healing well, and that the upcoming surgeries go smoothly.  Thanks for being there for me!  Smile

    Tami

  • Morningsun1
    Morningsun1 Member Posts: 649
    edited January 2013

    @ dnadebbs - I will have to remember that one for my post-op, when nipple area hurts, massage under arm to relieve it Wink

  • AuntieEm
    AuntieEm Member Posts: 30
    edited January 2013

    Good morning ladies!



    Well got my port placed yesterday. Feeling groggy but better than I thought. Chemo starts next Friday. 8 sessions (4 Adriamycin Cytoxan then 4 Taxol) every other week. I hope it goes quickly. Ready to get this over with.



    Tami- congrats on the drains! Enjoy that shower! I hope you do better than I did with the TE fill. It was very uncomfortable for me. But keep in mind we are all different. You might not look at it as such a big deal. Best wishes!





    As always warm wishes and prayers to all you strong ladies!

  • dnadebbs
    dnadebbs Member Posts: 82
    edited January 2013

    tammyT.....definitely......it will crack you up just trying to find "the" spot!  lol!

    Tami!   i'm soooo where you are right now.   my drains have been in for 3 weeks and i getting more and more depressed.  i feel like my a$$ has fused to my recliner becaused i was told to do little activity.   my drainage is a little more than yours but i developed an infection at 2 weeks and had to go back on antibiotics so not sure if that extended my time or not.   but gosh i'm praying you get to lose yours!  i too cant wait to take a REAL shower.....and then hit the hiking trail!  it calls to me every single day!   i have an appt next Tuesday so i donned my compression band this morning to hopefully help slow the drainage down before then.   i had the same question tho.....i was supposed to get a fill next tuesday but will they do it with the drains still in?   you'll be able to tell me that when you get back here!

    good luck hun!      Wink

  • DebR53
    DebR53 Member Posts: 6
    edited January 2013

    Jen, Hope you are doing well since your surgery a week ago. It's funny how passing time becomes your friend! (Normally I fight the "time goes by too fast" thing!) If you want to add me to the list: On Jan18, I had a lumpectomy and SNB. Deb

  • DebR53
    DebR53 Member Posts: 6
    edited January 2013

    Thanks for responding kkuziel!  Glad to hear you aren't having those numb and prickly sensations. I guess that's why they don't warn you about all the possible side affects--we are worrying too much already. Like you, I was hoping chemo was not a consideration for me. When I see my surgeon next week, hopefully I will have less anxiety. I'm surprised they set you up with the follow-up before the pathology report was ready. I have yet to see my reports. Others on this forum sound so much more informed than I. My doc just explains everything and writes it down as he talks/sketches, then gives me a copy of the notes. It's kind of cool--I was all ready to take notes the first time, and then he started writing everything down. Consequently, I'm not as informed on details and terms. Maybe I'll ask him for a copy of the report next week.

    So, I'm a teacher too! I also go back this Monday and as luck would have it, it's a professional day so it's a physically easy first day back. My student teacher will be starting--she's is happy to lift heavy stuff for me! (I teach art!). Since I teach elem., I got some adorable handmade cards from students, but was advised not to share the details of my absence with young students. I got a bunch of cards that had a white hand print that had a rabbit face drawn on and read "Some bunny loves you", hand-writtten on the front, with a note inside. I was getting all teary as I read each one, when I came across one that read, "some dummy love you." It really made me giggle! I

    t's so sweet that your kids want to do a fund-raiser--I love middle-schoolers--usually teach that age at summer camp. I agree with you that helping an individual struggling with costs would be such a blessing to that person. I was upset that my insurance did not cover the $85 cost of a pill that completely took away any nausea from general anesthesia. No vomiting for once! My health coverage is not as good as it used to be, but at least I have coverage!  Good luck to you going back to work. I think it will be a good distraction for us! deb

  • Tamiami
    Tamiami Member Posts: 396
    edited January 2013

    Well I'm home from the PS, and I still have drains. Frown  She filled the TE's and said that will either cause them to drain more and then taper off, or it will cause them the dramatically decrease.  Either way, I am supposed to go back on Tuesday and if they are under 30cc's (and she thinks they will be) then her PA will remove the drains.  I go back for another fill next Friday.  I was surprised at how much saline she put in...210cc's on each side! Most of the posts that I had read on here were between 50-100cc's per fill.  It didn't hurt at all, but it did feel really weird when she let the air out of the TE's before she started to fill!

    So yes dnadebbs, you can get filled with drains in.  I hope they pull yours on Tuesday AND fill you up!

    Emily~ I'm gald you are doing ok with the port, and have a plan as far as the chemo goes.  I will be thinking about you next Friday, and hope it will not be too bad.

  • Tamiami
    Tamiami Member Posts: 396
    edited January 2013

    DebR53~  It's a good idea to get a copy of your pathology report for your own records.  I have saved all of mine over the years and it's really helpful to be able to look back at them years later when you need to know something, and you don't remember the terminology.  Case in point...I had the pathology report from a tumor excision I had done in 1988.  I just remembered that it was a benign breast tumor, but the pathology report showed that it was ADH, which in 1988 was not recognized as a precancerous condition, but is now!  My BS was then able to get my insurance company to cover annual MRI's in addition to the annual mammogram and twice a year breast exams.  Without that MRI, I still wouldn't be diagnosed!  Make sure to get a copy!

    Tami 

  • jojo2373
    jojo2373 Member Posts: 662
    edited January 2013

    AuntieEm, already been through port placement and 4 AC 4 Taxol so feel free to ask any questions. Amy, Hopex, and myself are part of the Sept 2012 chemo thread. There is a world of experiences on this one and others for you!

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