March 2017 Surgery

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  • Tappermom383
    Tappermom383 Member Posts: 643
    edited April 2017

    Woo-hoo! My anesthesiologist was a rockstar - Zofran did the trick. Woke up in recovery with a completely calm stomach. The injections of nuclear isotopes for the SNB hurt like a mother! The radiologist was pretty cool - "I'm going to hurt you," he said. And he did. But that didn't last long. I have no idea what went on in the operating room but I'll find out in two weeks when I return to the surgeon. Anxious to hear the pathology results. Just some discomfort now so it's not bad at all. I had read about a breast cancer navigator on this site but didn't know what that meant. Well, I met my navigator, Michelle, at registration yesterday morning. What a doll! She'll call me on Monday to check on me. I was pretty wiped out (lack of sleep and food!) when I got home. Rested, relaxed, thought I'd sleep well but no such luck! I had a terrible time falling asleep and then worke up two hours later. Still awake! Guess I'll be resting a lot come sunrise.Thanks again, everyone, for your support.

    MJ

  • Sitti
    Sitti Member Posts: 230
    edited April 2017

    Tappermom383 glad everything went well and you woke up with a calm stomach. Nurse navigators are wonderful, I love mine. Hope you are able to get some needed rest now.

  • 2FUN
    2FUN Member Posts: 956
    edited April 2017

    tapper. Glad you are home resting. I didn't have a navigator, so that sounds really helpful. Get lots of rest, and keep chugging water to get all that surgery stuff out of your system.

  • TenMarie
    TenMarie Member Posts: 3
    edited April 2017

    This is my 1st time posting. I had BMX with TE placement 3/3. 2 weeks later had incision revisions bilaterally due to necrosis. PS says due to compromised blood supply from the surgery. For the past week it seemed that the new incisions were doing great (except for the bottom corner of the TE making its way through the bottom, PS says skin is extremely thin ) but as of this morning the left one is leaking again. The fluid is enough to soak through the abdominal pad. I'm so upset and frustrated at why I am not healing! I have been on high protein diet the past 4 wks, which hasn't seemed to make a difference. PS says just have to be patient and allow to heal. I see him tomorrow so I'll find out about the leaking again. The only thing he has me do is wash with soap and water and dry dressing under ace wrap. All I can do is cry.

    Last week he said it will be a while until I am fully healed that we can even think about starting to expand. He placed them with 150cc. He also mentioned that the skin is so thin it will only stretch so much. The skin will dictate how much I can expand. Feeling like I should have not tried reconstruction at all!

    Sorry for venting!

  • Molly50
    Molly50 Member Posts: 3,773
    edited April 2017

    Welcome TenMarie. I am very sorry for the necrosis. You must be very frustrated. I will be praying for you. Tapper, woo hoo for a good anesthesiologist!

  • 2FUN
    2FUN Member Posts: 956
    edited April 2017

    tenmarie, sorry to hear of your difficulties. Don't second guess yourself. You are making a lot of decisions. ..all you can do is make the best decisions you can, given the information you have at the time. Hugs! This is a good place to vent, that's what we are here for.

  • Xtina78
    Xtina78 Member Posts: 6
    edited April 2017

    Y'all. My reconstructed breasts HURT. They appear to be healing well, and they look good...but they are KILLING ME. My PS said I really wouldn't experience much pain in my breasts because they'd be numb following surgery, but that I would have a lot of abdominal pain because he sewed my muscles together for the tummy tuck, and because there would be far less nerve damage in my abdominal area. It's been exactly the opposite. My belly is completely numb, and what little muscle pain there was is pretty much gone now. But my new breasts have plenty feeling, and I suppose the nerves are regenerating because they feel like...a weird combination of electricity and mild ant bites...only way I can think to describe it. Anyone else experiencing this?

  • Scottiemom11
    Scottiemom11 Member Posts: 1,298
    edited April 2017

    tenmarie. . .hang in there. It sounds like you have a good PS. Recovering from BMx with TEs definitely takes awhile. Hugs and sorry that you've had complications. We are here for you,even if you just need to vent.

    Xtina. . .the pain you are having definitely sounds like regenerating nerve or nerves that were cut and can't find thier pathways. Mine has been burning pain is the best way to describe it. Hang in there.

    Tapper. . .yeah for the good anesthesiologist. My second two were great and I learned from the first one to insist on what works for me.

    Today I was finally allowed to get up and walk about. Just one store without even carrying my purse did me in. Uggh I hate laying around. Oh we'll babysteps.

    Scottie

  • Yvonne_M
    Yvonne_M Member Posts: 72
    edited April 2017

    Tapper, that's great on your anesth! Never heard of a nurse navigator. Sweet you have one.

    Welcome Ten!

    Scottie, great on finally being able to move around a bit. Felt good, right? Now get back in bed. :)

    I took my first real walk today. Put in my knitted knocker and walked with my head held high. I'm at 3.5 weeks and I think I had a bit of a fear to go out and do it, like everyone would know. So it was good physically, mentally and spiritually. Such a gorgeous day too.

    Hope you are all doing well today, amidst the crap going on in our bodies.

  • TenMarie
    TenMarie Member Posts: 3
    edited April 2017

    Thank you!! Just feel like DH and family don't understand and they must be so sick of listening. Lol.

    Scottie and Yvonne so glad you are up and about!! Keep up the good work.

  • raven4mi
    raven4mi Member Posts: 562
    edited April 2017

    Tappermom383, sounds like you're coming through this really well. I've never had a nurse navigator but it would have been really helpful. I seem to get a lot of "the right hand doesn't know what the left hand is doing" at my facility. There's a competing system here that advertises nurse navigators all the time; I'm kind of jealous.

    TenMarie, so sorry you're having such a difficult time with the healing process. I would encourage you to up your Vitamin C as well. If you have access to high-dose IV vitamin C that would be even better. And feel free to cry and vent away here – it's a safe, supportive place.

    Xtina78, sorry you're experiencing so much discomfort. I'm sorry I don't have any advice for you but hopefully others here will be able to chime in.

    My drain drama continues………Elphaba put out 45 yesterday and 35 today – so it went UP instead of down! Arghh!!!! I'm currently trying to dehydrate myself with alcohol. LOL!

  • wallan
    wallan Member Posts: 1,275
    edited April 2017

    Hey everyone;

    Sorry to hear about the difficulties.

    Xtina: So sorry to hear of your pain. I think doctors don't realize how much it hurts. Hugs and vent all you want.

    Tappermom: I am jealous of your nurse navigator. LOL. I would use her all you can. Its good to hear you are doing well.

    Tenmarie: Hugs to you. So sorry about your complications. Hang in there.

    Scottie: Its great to be out and about! Take it easy though. I feel "fatigue" if I am too active and walking around a store will do me in. But its so worth it. LOL

    raven: Sorry to hear about your drains. What a pain. Hopefully they are removed soon.

    YOu know, I lurk on this particular surgery forum alot and I can't keep up with everyones "handle".. alot of us had surgery in March. Holy macaroli!

    You are all in my thoughts and prayers though.

    wallan



  • EastcoastTS
    EastcoastTS Member Posts: 864
    edited April 2017

    Xtina: I think it's normal. I'm almost 5 weeks out and still have lots of what I'd call "burning". The sharp, somewhat painful "zings" are getting better as is (I think) the bullsh*t/ TE pain between my breasts and/or over ribs. I don't know how to explain it. But the burning remains. My PS said this is nerve regeneration. My nipples (spared) also burn and I don't even know if that is real or just my mind. LOL I think surgeons and doctors in general discount pain to a large extent. Idk why.

    It does get better though.

    Hugs to all!!!

  • EastcoastTS
    EastcoastTS Member Posts: 864
    edited April 2017

    Also should add that a bunch of my burning is kinda above my breast fold incisions. I think I've read that Alloderm can cause burning. In any case, no one seems alarmed when I tell them this is happening.

  • Sitti
    Sitti Member Posts: 230
    edited April 2017

    TenMarie, Xtina78 - So sorry to hear about the difficulties you are having.

    Raven, sorry to hear about the drain. Hoping Monday is the day it comes out.

    Yvonne, glad you got a good MO that you like. Hopefully he'll more than make up for the BS.

    Does any one feel like theirTEs are almost in/under their armpit? I can't tell if it's swelling or TEs or both. 10 days out from BMX, I too have burning, like a sunburn, even my shoulder blades feel like they are sunburned!? 😕

    I've been keeping up with reading but haven't been responding too much. Even though I've never met any of you, I do carry you in my thoughts.

    Hope everybody is able to have a restful weekend.

  • 2FUN
    2FUN Member Posts: 956
    edited April 2017

    my TE feels like it's under my clavicle, and more to the side, but not under my armpit.HTH

  • Sitti
    Sitti Member Posts: 230
    edited April 2017

    2FUN Now that i think about it I guess I would say to the side, not under the pit. Guess that's the nature of TEs.

  • 2FUN
    2FUN Member Posts: 956
    edited April 2017

    anatomically speaking, I would think there would be less room for an expander closer to the center of your body . That is said with knowledge of the structure of the chest, and NO KNOWLEDGE of expanders!

  • Bluebirdgirl
    Bluebirdgirl Member Posts: 115
    edited April 2017

    Sitti, my right TE always seemed to be close to my armpit, and I had a dog ear (think that's what they call it.). Since exchange, that has gone away and breasts are a natural shape instead of the "football" shape of TEs. Hope that makes sense. So it does get better!

    To everyone with the little stinging/burning sensations, I had that really bad the first few days after surgery and doctor said yes, it's your nerve endings going haywire. It has eased up quite a bit, surgery was 3/21, and now just getting the occasional zap that makes me go "OW" out loud and my family looks at me like I'm nuts lol.

    Tenmarie, sure hope you get better soon!

    Hugs to allof you!!


  • 2FUN
    2FUN Member Posts: 956
    edited April 2017

    Glad to hear about the dog ear (if you have an upper or lower extremity amputation the stick out to either side, thus dog ears. With a MX you only have a dog ear). My PS did not answer my question directly when I asked if all of that tissue under my arm was going to be eliminated by the time the exchange surgery was complete.

  • Bluebirdgirl
    Bluebirdgirl Member Posts: 115
    edited April 2017

    Also, talking about nurse navigators, I receive a publication from Living Beyond Breasr Cancer, LBBC, and this month they have an article about nurse navigators. Hopefully this link works!

    http://www.lbbc.org/news-opinion/navigators-can-he...

  • Tappermom383
    Tappermom383 Member Posts: 643
    edited April 2017

    That's an interesting article, Bluebirdgirl. And a helpful site. I signed up for their email alerts.

    MJ

  • Scottiemom11
    Scottiemom11 Member Posts: 1,298
    edited April 2017

    My turn to vent. . .I was up yesterday and supervised moving ds' old bedroom furniture out and new in. I barely used my arms and did no lifting. Woke up at 2am with excruciating bilateral burning pain. What the #@)(/*$!) $@(/&;*&$#!!! Pain meds worked after an hour or so but I've been trying to stop them. This bites!

    Currently sitting on a bench just supervising Dh and ds planting lots of stuff.

    Hope everyone else is doing well.

    Scottie

  • lrwells50
    lrwells50 Member Posts: 254
    edited April 2017

    The funny thing for me, is that the burning pain is in my right thigh! Don't know if it was a little traumatized or what. Hasn't been unbearable so far, and only happens when I'm in bed.


  • TenMarie
    TenMarie Member Posts: 3
    edited April 2017

    Thanks all for the hugs and thoughts, will update tomorrow after PS appt.

    Bluebird-girl thanks for the link. I have also signed up for the email.

    Scottiemom sorry to hear about your pain, and I feel your frustration. Just when you think you are doing / feeling better something will flare up (or in my case leak out ) and you feel as though you just took 3 steps back. On the bright side at least you can sit outside, here we still have snow, ugh!

  • 2FUN
    2FUN Member Posts: 956
    edited April 2017

    finally spoke with BS on the phone. He is concerned about the small margins on my last path report. He's going to contact pathologist, and he is thinking of going in and taking more skin. I am figuring I won't worry until he gets more info. I see him in person on tuesday. Yay, more unplanned surgery. Not sure how that will work with TES. Wonder if I will get back to work B4 end of school year at the end of June. DS graduates HS in 8 weeks. Hmmmm, it will all be interesting.

    So sorry u r having pain scottie. What did dr say about it? Although u r only 2 weeks post. I really started feeling a bit better about 2.5 weeks after.

    Hang in there everyone. Just keep putting one foot in front of the other! We will get to where we need to go!

  • SJI
    SJI Member Posts: 69
    edited April 2017

    Had lumpectomy Thursday, March 31 at noon. Surgery took a bit over two hours. Was on the ferry headed home at 5:30 pm. (It's an hour from surgery center to ferry). Both my older daughter and my 6 year old grand daughter have been here from out of state helping me.. They leave tomorrow. I've felt more relaxed since having surgery - maybe just the thought that the cancer was removed but most likely due to having family around. Getting anxious about pathology results. Waiting seems to be the most stressful part of bc. At preop appointment surgeon said he was going to consider my cancer multi-focal. Said if the lumpectomy didn't get it all we may be looking at a mastectomy and either way I would need radiation.

    Post surgery I have found the sentinel biopsy area more painful than the lumpectomy area. But it hasn't really been that bad. I have been really tired and have slept a lot. Am ready to work tomorrow.

  • raven4mi
    raven4mi Member Posts: 562
    edited April 2017

    Scottie, sorry about the pain setback. It's so annoying, isn't it? Just when you think things are going along okay, then BAM! Something new to deal with.

    SJI, sounds like things are going OK for you post LX. Would you still need radiation if you went for the mastectomy?

  • 2FUN
    2FUN Member Posts: 956
    edited April 2017

    SJI, I can believe you rode a ferry home. Hope u r able to rest.

    I finally spoke to.BS about my narrow margin, and he wants to go back and take more tissue, mainly skin. He said he needs to get more info from the pathologist. Argh, like I need more surgery.

    DH also told me this weekend he thinks I'm going to have a hard time getting back to my previous job. I think he doesn't realize that any job in my field is physically difficult, but not impossible. The more surgery the longer before I return.

    I was able to get to my usual 10,000 step count over the weekend, so I hope I can keep making improvements.

  • Sitti
    Sitti Member Posts: 230
    edited April 2017

    2FUN, sorry to hear that it looks like you are looking at more surgery, that has to be disappointing when you're thinking that part of the surgery is done. On the other hand, 10,000 steps.....way to go! Most I've done so far is 1,685. :o/ How long did it take you to to there?

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