March 2015 Surgery Sisters

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  • Valentine99
    Valentine99 Member Posts: 75
    edited February 2015

    Hello ladies. I am meeting with my surgeon on the 5th and will hopefully have surgery in mid March. I will be having BMX. I have multi-focal tumors on the left side and one lymph node involved, and there as a spot that showed up in the MRI on the right side but they couldn't find it to biopsy. But since it showed itself I don't want to risk it and am going for both. I have so many things running through my mind about surgery and afterward it's starting to be a problem. I can't help wondering how surgery/recovery will be, trying to get someone to be with me the first week I am home while my husband works, and worrying about the cancer coming back. I did find a great a great board on here with suggestions of things to take to the hospital, things to do to prepare for afterward and things to have to make after surgery easier.

    I hope everyone's surgery and recovery are easy, and we can get on with our lives!

  • DiveCat
    DiveCat Member Posts: 968
    edited February 2015

    deb1267, I have added you to the list!

    March 4th will be here quickly, I can relate to that wish to be on the other side of surgery though mine was purely prophylactic. I hope your pathology comes back with no more surprises.

    Valentine99, I have added you too, date pending. With my PBMX, I did need a little help first few days with some things as I could not lift/open/reach much due to restrictions and weakness, but was able to do more than I thought I would be able to, and felt better than I imagined I would too, and was quite mobile overall. After a few days I did not really need any help during day. I had no nodes removed though and I understand that can add more to recovery and of course everyone is different!


  • ladyduffer
    ladyduffer Member Posts: 40
    edited February 2015

    Good luck to you Deb!  I hope and pray everything works out better than you think it is going to.  Hang in there and keep us posted.

    Jacquie

  • hummingbirdlover
    hummingbirdlover Member Posts: 421
    edited February 2015

    Our support group is growing!!  Welcome everyone!  As Divecat mentioned earlier, and I agree - I truly did not think the BMX was horrible.  It took time to recover (I took 5 weeks off of work) but I could do more than I thought I was going to be able to do, even right after surgery.  I slept in our recliner for at least a week, maybe 10 days.  It felt good to be propped up.  Everything was pretty much numb after surgery (which was kind of nice) and honestly, I still have a lot of numb spots across my chest.  I'm hoping that numbness will help ease some of the pain from my TE surgery.  The underarm area where the SNB was done was sore (it's still tender) and the drains were a drag but it was totally do-able.  My siter, who is a nurse, stayed with me for a week and helped me keep track of taking meds and helped me strip the drains, that was super helpful.  I laughed at first when she drew up a med chart, but you forget when you took your pain meds last and you're kind of in a blur anyway, it's nice to have someone help you remember to take your meds - you want to stay on top of those.  The waiting is absolutely the worst part.  You wait for surgery, wait for test results, it all just stinks!  I promise, you'll feel so much better when there is a clear treatment plan. 

  • angmom41
    angmom41 Member Posts: 27
    edited February 2015

    The waiting is really hard. My very supportive husband is drafting a schedule for family to come visit and help after surgery (I have 3 kids, youngest is 3) which is very comforting, but I just don't know what I will need and when. That makes me the most anxious, I'm not used to having others help me. I'm used to hearing mom, mom, mom all day.

    Two more weeks until the surgery and starting to feel more prepared for it, but not for the emotional aspect of it. Just starting to think about that now....how will I feel afterwards trying to snuggle my youngest and seeing the worry in my kids faces? Ugh I need to be strong, and I will be....it's just the unknown that is terrifying. How is everyone else feeling?


  • Coblndie
    Coblndie Member Posts: 36
    edited February 2015

    I'm set for direct to implant double mastectomy March 4th

  • DiveCat
    DiveCat Member Posts: 968
    edited February 2015

    You have been added Coblndie. That is the surgery I had in April 2014; us direct to implant women are still in the minority around here compared to those doing TEs, but we are growing. Feel free to ask if you have any questions about experiences specific to direct to implant reconstruction.

  • DiveCat
    DiveCat Member Posts: 968
    edited February 2015

    angmom,

    Yes, I have no doubt you are strong, but do not be too strong to accept help, you know? As I said earlier, I really was a lot more "able" than I thought I would be, but, it WAS still nice to have someone around to put something together for me to eat, or to go for walks with me, or to run out and pick up stuff I could not, or to make me tea (I could not lift the kettle at first!):) I don't have kids, but I imagine that help will be even more necessary when it comes to them. Not because you might not be able to do it, but because it might be a better choice...so you can rest and recover....to have someone else do it.

    As for myself, I am not really thinking about my surgery much at all yet, which I now note is about 2 1/2 weeks away. I don't expect to be nervous about the surgery, I am more anxious about the planning around the surgery with work, "time off" from the rest of stuff I have going on, and getting certain things done before I go into surgery as I won't be able to do them for a bit after, etc.

  • JustAJennifer
    JustAJennifer Member Posts: 85
    edited February 2015

    Hi all,

    I've mainly been participating in the February boards, my surgery was 2/6. I want to share some advice with you as you prepare...

    - little ones: I have a 10 and 7 year old and I had help from family and friends getting their lunches prepped, brought to the bus stop, help with homework, and driving them to activities for 2 straight weeks. Toward the end, I was managing ok by myself. But if you have the opportunity, let someone help with this.

    - meals: a neighbor set up a page for me on meal train.com for people to sign up to bring a meal 4x per week for 4 weeks. Many people will ask you how they can help. Let someone do this for you. Meals provided means fewer dishes, few grocery store runs, less expense during your time of healing.

    - candy: bring it for your nurses and medical staff while you are at the hospital and offer it to everyone. It makes you a person instead of a patient and brings a smile to the faces of those caring for us.

    Be brave, fellow warriors!


  • angmom41
    angmom41 Member Posts: 27
    edited February 2015

    Divecat, thanks. I think seeing a schedule of the time I might need help kinda freaked me out. I am back to feeling lucky that so many family and friends can help me and want to be there for me. The stress of not knowing how long I will need help is also less. Bottom line is it doesn't matter, it will work out! I am not working right now, but can imagine that is a huge stress trying to get time off and getting things done before your surgery. How much recovery time are you anticipating for the implants?

    Jennifer, thank you! Definitely going to bring some candy with me to the hospital. We always have an extra supply of candy.

    Twelve more days.

  • windingshores
    windingshores Member Posts: 704
    edited February 2015

    I see the surgeon today and oncologist next Wed. I assume I will have surgery in March, in 2-3 weeks, and hope so. Three biopsies showed invasive ductal carcinoma, approx. 1cm, grade 3, estrogen and progesterone positive and HER2 positive. Radiologist said lymph nodes looked okay on ultrasound. I hope testing shows they are.

    I know I want a mastectomy. My breasts are dense (even though I am 63) and I have the high grade and HER2+. I don't care about cosmetics, just want to be here as long as possible for my two daughters who have some special needs. A double mastectomy would be my preference but it may be too long and too much stress for my body; if so my insurance will cover this later. I expect the surgeon to want to do a lumpectomy and am ready to try to advocate for myself. We'll see.

    Thanks for the info on MRI on the apparently healthy breast.

    I am somewhat fragile and have a lot of sensitivities and reactions to meds (and foods) and require very low doses. I have neurological and spinal issues (my head cannot be bent back, the center base of my skull cannot be pressed), and a diagosis of lupus (reacted to surgical lights in the past).

    Has anyone with similar issues worked successfully with an anesthesiologist to minimize anesthesia reactions, or even the amount of general?

  • ladyduffer
    ladyduffer Member Posts: 40
    edited February 2015

    Good luck to everyone with all appointments, scheduling surgeries, and trying to stay calm throughout it all.  There is certainly a lot of good advice on here.  I really like Jennifer's suggestions about the candy and the meal train.

    I think I've made a final decision to go with BMX, finally got appointment set up with plastic surgeon on the 3rd, and a surgery plan appointment on the 10th with breast surgeon.  I hope I have my surgery before the end of March, I don't think my nerves can take too much more waiting, thinking about it, talking about it, and researching it.

    May God be with us all!

    Jacquie

  • nlosgatos
    nlosgatos Member Posts: 14
    edited February 2015


    I'm on the 10th for BMX.  Glad to get it going but yeah, nervous, too.  My process started on Jan 3 with the bad mammo.  Yes, the waiting is the worst part.  Almost the same diagnosis as you.  Let's get this going!  Onward to healing and great health! :) 

  • nlosgatos
    nlosgatos Member Posts: 14
    edited February 2015

    I want to add:  I am one of those get er done independent single gal types.  I went thru the gen anesth biopsy recovery by myself.  Thought I could just get in bed and sleep it off.  Baaaad idea.  Nausea, wrong food, pain, etc.  I'm finding the pre surgery lists and what to expect threads are incredibly helpful.  Also, sharing my diagnosis and surgery date with friends and family has been so emotionally helpful.  All the outpouring of care and offers of help is really helping with my fear and anxiety. This website has been so awesome, too.  Very supportive in my decision to do the BMX.  Very sincerely wishing my March surgery sisters peace and health.  We can do this!  xoxo

  • ladyduffer
    ladyduffer Member Posts: 40
    edited February 2015

    That's right nslosgatos, to onward healing and greath health!  Good luck to you!

    Jacquie

  • nlosgatos
    nlosgatos Member Posts: 14
    edited February 2015


    Thanks Jacquie-  We may be missing the links (and tennis courts) for awhile, dang it!  Most of my relatives are in PA south of Erie. Beautiful state.   

  • bbbbun
    bbbbun Member Posts: 59
    edited February 2015

    Hi Ladies~ I would like to join your group! My exchange surgery WAS scheduled for 3/3 but my precious grandchildren came for my Valentine's Birthday and snuggles with my 3yo grandson resulted in bronchitis for me...wouldn't trade those snuggles tho :D So now exchange has been moved to June 2nd :( I am on cancellation list to be called....so I am praying!!!! In the meantime the info and support on this site is important to me with HOPES for a moved up March date!!!!!!!

  • bbbbun
    bbbbun Member Posts: 59
    edited February 2015

    Hi Ladies~ I would like to join your group! My exchange surgery WAS scheduled for 3/3 but my precious grandchildren came for my Valentine's Birthday and snuggles with my 3yo grandson resulted in bronchitis for me...wouldn't trade those snuggles tho :D So now exchange has been moved to June 2nd :( I am on cancellation list to be called....so I am praying!!!! In the meantime the info and support on this site is important to me with HOPES for a moved up March date!!!!!!!

  • hummingbirdlover
    hummingbirdlover Member Posts: 421
    edited February 2015

    Windingshores, I did have one issue that I knew about before surgery and I told everyone, and I mean EVERYONE who would listen to me about it.  I have always had a horrible reaction to pain meds.  They make me sick as a dog and I was so worried about waking up from surgery nauseous and puking and even MORE worried about taking the pain meds and being sick, once I went home.  The anesthesiologist came and talked to me before surgery and I told him all about it.  He assured me that he would pump me full of anti-nauesea meds for surgery and also wrote me a prescription for an anti-nausea med to take at home, called Zofran.  The Zofran was part of my medicine routine at home and I took it 1/2 hour before I took the Norco.  It all worked like a champ and I was never nauseous, not even once.  It was so awesome!  I would just say you are your own best advocate and be vocal.  Make sure all of your concerns are noted and known.


     

  • DiveCat
    DiveCat Member Posts: 968
    edited February 2015

    angmom:

    I am only planning to take about a week off from work for this revision. I don't need a lot, if any, pocket work so it won't be anything like the first surgery. I will probably be doing work from home though after 3-4 days, or get a ride to and from work as the main thing will be driving at that pint. I can make sure I don't have any thing really scheduled in that time so I can mostly just be at my desk. Recovery though for other things should be similar to before with weight restrictions for a few weeks, and so on. I had a great recovery last time and was up and walking several miles a day within 3-4 days, so hoping for similar fortune this time around.


  • DiveCat
    DiveCat Member Posts: 968
    edited February 2015

    hummingbird,

    I am one of those who gets horribly nauseated at many things, and I had 3 different anti-nauseatic drugs during surgery....woke up very nauseated and I guess I am one of those "lucky" ones who gets bad PONV (Post-Operative Nausea and Vomiting). Had several Zofran IVs while in hospital before it got under control! I am hoping this time around they can try something else during surgery so I don't wake up feeling like that again!

  • hummingbirdlover
    hummingbirdlover Member Posts: 421
    edited February 2015

    Divecat, that makes me wonder what they have me before and/or during surgery and whatever it was, I want it again because I agree, that vomiting thing is horrid. I'm a huge fan on zofran, I wonder if we can have it before surgery too?

  • windingshores
    windingshores Member Posts: 704
    edited February 2015

    Thanks for the response hummingbirdlover. I had a great appointment. I had an appointment at a different cancer center last week where I did not feel listened to. But yesterday the surgeon and oncologist were very understanding and made careful note of my sensitivities, my neck problem and were respectful of my choices. I wanted a double mastectomy but due to the fragility of my immune system decided on a single one first, and then can go back (the surgeon agreed to do the other one later if I like). Part of me wants to call back and say, if I am doing well in the surgery, maybe they could keep going! At any rate, after being belittled last week for wanting a mastectomy, yesterday's appointment was a breeze: in fact, due to the effects of radiation on a person with autoimmune problems, they were relieved that I wanted a mastectomy versus lumpectomy. For anesthesia, there are some alternative ways to go including the paravertebral block so I will talk to the anesthesiologist in a consult.

    So did anyone do a single then go back for a prophylactic mastectomy on the other breast? Do you think the stress of having them both done at once would be greater or less than doing a single, twice, for a person with some of my issues? Thanks!

  • Jenga60
    Jenga60 Member Posts: 24
    edited February 2015

    jenga60- scheduled for surgery March 23rd. Just need to decide whether it Lump + rad or Masectomy. Got core biopsy back yesterday to confirm cancer. 2cm but feel it's growing. I have very dense breast with a lot of unknown areas. They could be precancerous or just my milk drying up as I just finished breastfeeding a couple months ago. I'm 38 years old and had part of my cervix (precancerous cells only) removed 6 years ago as well and was able to have my beautiful daughter since then.

  • robinblessed54
    robinblessed54 Member Posts: 578
    edited February 2015

    jenga, I don't know what your diagnosis is(type of cancer) but I would go with a BMX because of size alone and you already experienced cancer elsewhere. You don't want to go through it twice down the road. Are you considering immediate reconstruction? Blessings, R

  • angmom41
    angmom41 Member Posts: 27
    edited February 2015

    jenga-you are definitely facing a hard decision...take your time and get at least a second opinion.

  • windingshores
    windingshores Member Posts: 704
    edited February 2015

    Scheduled for March 6th. Sooner than expected. Right now planning single mastectomy with agreement from surgeon I can come back for the other one. With my age and health status everyone feels one at a time is better, but I am still not sure!

  • DiveCat
    DiveCat Member Posts: 968
    edited February 2015

    robinblessed, just to clarify, pre-cancerous cells in the cervix is NOT cancer. I had pre-cancerous cells in my cervix as well in my late teen years, and after treatment have never had an issue since. They may or may not develop into cancer, if left untreated, but treatment is considered VERY successful...both preventative and curative.

  • AudreyB
    AudreyB Member Posts: 377
    edited February 2015


    Hello all!  I'm joining and also hopping over from the February 2015 Surgery page.

    My SNB is scheduled for next Tuesday, March 3.  Getting nervous.  My core needle biopsies came back benign, so when I had excisional biopsy on Feb 6, I had not yet been diagnosed, so nodes were not removed.  Now I have to go through another surgery :(

    I was originally told I would need a double mastectomy, but path came back hormone responsive, so now I am thinking about keeping the girls and doing radiation.  I am constantly second guessing myself if I am making the right decision.  At least the SNB is buying me some time to think.  It is horrible how you are poked, prodded, squeezed, operated on, given diagnosis and have to make major life changing decisions all in a few weeks time.

    Wishing you all a wonderful weekend, stay positive ladies, as hard as it is to do. 

     

  • kabana
    kabana Member Posts: 6
    edited February 2015

    Add me to this list as well, I am scheduled for a lumpectomy and sentinel node on 3/26. As of now it appears I won't need chemo, only radiation (thanks to the sharp eye of the radiologist who noticed the small asymmetry between my right and left breast) . My tumor is only 5mm.

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