September 2016 Surgeries

Options
13»

Comments

  • Irony
    Irony Member Posts: 46
    edited September 2016

    Reflect, I'm sorry your nodes are positive. What is your next step?

    I need to call my breast surgeon. My surgery on Monday was late afternoon and I have just been in and out of it for the past couple of days.

    From what my husband remembers the BS was not concerned at all and said this sometimes happens with prior breast surgery. She said she looked at the rest of my nodes and they didn't look swollen but to my husband's knowledge, she didn't test any.

    I need to call and get the full story because it doesn't make any sense to me.

    I don't want to walk around with positive nodes.

  • reflect
    reflect Member Posts: 576
    edited September 2016

    Hi Irony,

    Sorry you've been out of it. Hope you hear back from your surgeon today. I am sure that if nodes were taken, they will be biopsied. I got results 8 days post surgery, but mine was "complex" (multifocal, multicentric, 4 diff areas, oy) so you may have results sooner. Hang in there.

  • Bagsharon
    Bagsharon Member Posts: 200
    edited September 2016

    I woke up like this. Gotta admit, it hit me kind of hard. I loved my silver hair.

    image

  • Irony
    Irony Member Posts: 46
    edited September 2016

    NEW Question: Like most people, I think I have a high pain tolerance. I was told to stay ahead of the pain. I take a percocet every six hours, with keflex. Three hours after the percocet I take a valium, so that I stagger the pain meds so basically I am taking something every three hours. I have been sore, but ok. My surgery was on Monday.

    I will run out of percocet on Sunday. It works cway better than the valium. I called my BS. She said it is up to the plastic surgeon to give me more. The nurse at the plastic surgeon said she will contact the doctor to see if she will give me more.

    At this point, I really need the percocet. I am not a drug seeker. I don't even take advil, but I can't function in this pain.

    How long before you were cut off of meds. My surgery was five days ago.

    Thsnks

  • meg2016
    meg2016 Member Posts: 287
    edited September 2016

    I think I had enough meds to last a week, but I was on oxycodone. I did a similar thing with staggering but with Tylenol between. I started to notice that I needed the stronger meds less often and then just at night. I am a little over a week after surgery and no longer need anything other than the tylenol. I didn't really try to stay ahead of the pain after about the first 48 hours at home, though. I didn't love the way I felt on the pain meds, though, and the constipation they caused so I started trying to take them only when I had to. I'm hoping your dr. gets you some relief!

  • reflect
    reflect Member Posts: 576
    edited September 2016

    Hi Irony,

    I am a week and a day post op and have a really sore and swollen axilla. I saw the doc today and got another rx for oxycodone (15 pills). I take it with ibuprofen or aleve to give it a boost. My doc had no problem. I am also in a pain study, lol, those needle pricks are eeeeeasy. But I compare it to gallbladder attack and active labor (both "10"). Some docs are seriously worried about "drug seeking behavior". I think you just have to be straight with them and hope for the best.

    Is valium a pain med? I thought it was more for anxiety. It might not be so helpful for pain?

    Hope you feel better soon.

  • Irony
    Irony Member Posts: 46
    edited September 2016

    They gave me a new prescription for another week of percocet. I didn't know I could substitute advil or tylenol for the percocet.I would totally do that. I'm not sure why they gave me valium. They just said to stagger every three hours until my follow up in a week. Literally, all I do is sleep.

    I would love to stop the valium.

  • CourtneyS
    CourtneyS Member Posts: 4
    edited September 2016

    Hi guys,

    Age 33, dx with DCIS a few weeks ago and lumpectomy is scheduled for Wednesday. Not looking for anything specific from you other than following along with some people who know what it is like since most people don't :) Nervous about surgery only because then it is real and I don't want to be in pain

  • HouseDivided
    HouseDivided Member Posts: 21
    edited September 2016

    Hi Reflect - I live in the Phoenix area. I originally contacted Cancer Centers of America (they came highly recommended from a friend in Chicago) and they reviewed my reports and recommended that once I had the diagnosis to come to them for a second opinion and treatment. But they checked my insurance and it would cover me if I went to one of their out of state facilities but not the facility in my home state. That made so sense to me but they said they would fly me to Chicago and do treatment there if I had a cancer dx. Part of me feels like there model is excellent and I wish I could go there but I really don't want to do this away from home. But part of me feels like it is a well-oiled profit making center.

    We have an MD Anderson clinic here but my insurance didn't cover them either.

    So I went to a local cancer clinic, Ironwood Cancer Clinic on the recommendation of a friend whose relative went there. The BS reviewed everything and said her first recommendation was to do the lumpectomy (which really I believe is more of an excisional biopsy), just taking the whole lump,which is small (1 cm). She did get back to me with the answer on seeing the RO and said that she wanted me to see him just in case we need to do radiation after surgery.

    While I am slightly worried about not following the standard protocol, I just want this spot out since it is small and only one spot and I had such a disaster with the biopsy. I really don't think I would need chemo prior. This may be stupid on my part but it's been six weeks already to get to this point.

    I'm not 100 percent sure that this is the right thing to do, but I am going to do the surgery Thursday and hope for the best. I really appreciate your help and advice and if anyone knows anything about Ironwood or other options for me in the Phoenix area, I would love that info, thanks.

  • HouseDivided
    HouseDivided Member Posts: 21
    edited September 2016

    Thanks Irony for the input. Very helpful. I had an incompetent radiologist do the biopsy. Even she wasn't sure that she got the right spot. It was really concerning. She said they'd bring me back again for free but I could never go back there.

  • reflect
    reflect Member Posts: 576
    edited September 2016

    HouseDivided, I'm glad you've decided on your plan. Once you get the pathology and know what you dealing with, what the plan is (radiation or not), you will feel more settled! Good luck & let us know how it goes.

  • bosterh315
    bosterh315 Member Posts: 8
    edited September 2016

    Have had a few surgeries now. Had rare ovarian cancer 10 years ago. They weren't sure how I got it but did a complete hysterectomy and have been cancer free ever since. Had genetic testing in 2014 and found out in February of this year I am BRCA1+2 positive. Had bilateral, nipple sparing mastectomy with immediate reconstruction in May. My right drain and implant became infected so had surgery to clean everything out and remove the implant. Did my 3 months of healing and just had surgery two weeks ago to put in the tissue expander. My thoughts and prayers are with all of you and I wish you all the best of luck. I stay positive because I know I'm fortunate. I understand that a lot of you beautiful women have been through a lot worse than I could even try to imagine. I do have a question. Anyone with experience in drain complications.. I saw my surgeon on Monday. Output was under 30cc for 2 days then a little spike to 50cc's (I did a lot that day) then back down to under 30cc's the following 2 days to my appointment. She decided to keep it in for another solid 48 hours of under 30cc's. That night I must have not given the tubing enough slack when I taped it down and bled from the drain site. I would say at least 2 tbsp on the dressing. I have not had anything come from the site up to this point. The site is irritated and have had less fluid from it today but it's still there. Now my output is gone up to 50-60cc's! No change in fluid. Same color, thickness, no odor. In fact, what started coming from the site is exactly the same as what I get in the drain. Kept an eye on any temp or swelling and that is all fine. I have been and still am taking two different antibiotics. Does anyone have any ideas as to what might be going on? I really want my drain out but I don't want to cause myself complications either. Just not sure what my surgeon will want to do and if I should wait until Monday to notify her. Any help is appreciated. God bless all of you and I wish you all continuing strength and stamina. Stay positive

  • Irony
    Irony Member Posts: 46
    edited September 2016

    Okay. So nothing ever happens to me in a normal way. I had my bilateral mastectomy on September 19th for cancer in my left breast/prophylactic on the right.

    During the surgery, they could not find a sentinel node at all on the left side. They said they looked at my other lymph nodes and they looked fine so they didn't take any nodes at all. The pathology came back on my actual cancer. And that too was gone. So the cancer was taken out during the ultrasound guided biopsy. With no residual cancer left in. No cancer in the other breast either. That is great news.


    My problem is that even though they didn't take any nodes from under my left arm I'm having swelling in my left arm from my elbow up until about my shoulder. It is painful it is a little red and kind of warm to the touch. Nobody seems concerned about this at all. They say it cannot be lymph edema because it is too soon. They say it may just be post surgical swelling. But my breast surgeon never saw it. It's been over a week and it isn't getting any better.

    When I called my breast surgeon today. The nurse told me to call the plastic surgeon. I told her the swelling happened prior to seeing the plastic surgeon and that I had been dealing with the breast surgeon. She told me to call the plastic surgeon anyway. I called the plastic surgeon and the nurse at the plastic surgeon's office called said that I should call the breast surgeon.

    I had my surgery out of state, so I'm wondering if I should go around them both. I'm so dissatisfied by the lack of care.

  • reflect
    reflect Member Posts: 576
    edited September 2016

    Irony, that's not cool that your docs are not answering your questions. I would push hard on your BS and contact a lymphedema PT for an eval. I've had swelling and pain (I had 17 nodes removed so no surprise) and my BS said ice and elevate. It is finally beginning to resolve (sx 9/14).

    Congratulations on your truly wonderful results.

  • Irony
    Irony Member Posts: 46
    edited September 2016

    Thanks reflect. I'm still on keflex, so they said to finish that. I meet with both surgeons on Tues. If it is still swollen on Sat, I'm gonna,head to work and ultrasound it myself to make sure there is no clot.

  • Miskatonic
    Miskatonic Member Posts: 9
    edited September 2016

    I am having bilateral masectomy tomorrow. I still feel not back to myself from the chemo. I am worried how I will tolerate it, my only previous surgery was emergency Csection.

  • Numbalina
    Numbalina Member Posts: 17
    edited October 2016

    The anxiety post surgery was a real shock for me. I was just throttled with all-consuming anxiety stress for a solid week after the surgery. Not sure if it was a combination of the anesthesia and the unknown pathology results. Anyone else get post surgical anxiety? It has happened to me previously post-surgery, when there was no report to be stressed about.

  • Numbalina
    Numbalina Member Posts: 17
    edited October 2016

    Reading Irony's posts about trying to manage the pain brought back the hell I lived through a few weeks ago. I have a lot of sympathy pain for anyone who goes through breast surgery. I wish there were more options for pain management since it clearly plays an important role in the recovery process.

    I learned that I cannot take pain medications (any of the opiods) from previous surgeries (cold sweats, shakes, nauseousness, turning greenish-gray, and the pain doesn't decrease!) and so this time around I tried to cope with ice, and staggered doses of Advil and Tylenol. Needless to say it was a pretty horrible and sleepless few days. I tried the non-opiod, Tramadol, that I was prescribed for post Neulasta bone pain, but it did nothing. Usually that drug would at least make me sleep, durn it! I ended up taking a muscle relaxer on day 4 since I was getting unbelievable back spasms, and I finally slept for a solid 8 hours. Not sure if it was from pure exhaustion or the drug.

    Anyone else have problems with taking pain meds? How did you deal? Reconstruction surgery is not something I want to think about, since coping with the pain is beyond what I am willing to go through.

  • KentRunner
    KentRunner Member Posts: 25
    edited October 2016

    So glad to find this group! For as much as you hear how often people are diagnosed with breast cancer, I sure did feel alone with mine. My surgery was September 7, and I am happy to say my healing has gone very well, and my pain was well managed. I'm even very pleased with my reconstruction process. It sure makes a difference having a medical team you trust...and good insurance! My thoughts and prayers are with all of you as we figure this whole thing out!

  • Irony
    Irony Member Posts: 46
    edited October 2016

    Hey How is everyone? Reflect, I went for follow up and my arm swelling is lymphedema. I have to see a specislist for therapeutic massage and PT. This process is so frustruating. My arm is now swollen from my shoulder to my hand. My BS says she thinks it is reversible but she also said it wasn't lymphedema.

    I'm so pleased with my diagnosis that I know I have no right to complain about my arm.

    Numbalina, I am currently only taking advil. I cannot function on those pain meds at all. BTW, I fell flat on my face while I was taking valium and percocet. I broke my nose and have to get it reset.

    I am truly a disaster. Lol

    I hope all my fellow September fighters are doing well.

  • berrylvr
    berrylvr Member Posts: 5
    edited October 2016

    Hello Sisters!

    I had a bi-lateral mastectomy w/ TE placement on September 15-- almost 3 weeks ago! I'm feeling much better as each day goes by, but am slightly troubled by my elevated heart rate and BP. I normally have a resting heart rate of around 70-- but it has been between 90-110 at my follow-up appointments. My BP is also a little 'off'-- it's normally on the low side, but now is w/i the higher range of normal.

    Has anyone else noticed post-surgery heart rate and BP changes-- could it be due to the anesthesia still working it's way out of my system? I haven't started exercising in earnest yet, but when I go for a walk I can feel chest tightness if I take a deep breath and I seem to get winded fairly easily...

    Wishing the best to you all.

  • reflect
    reflect Member Posts: 576
    edited October 2016

    Irony, I'm sorry you are dealing with lymphedema. But catching it early and seeing a PT is supposed to give good odds to reverse it. My swelling is definitely going down. Now my breast is worse than axilla, or maybe I'm just noticing it more as the arm & axilla resolve! I have a temporary sleeve and will order a custom sleeve & gauntlet soon. By far my biggest issue is my fatigue/depression. I am letting everything slide, getting up with best intentions but then retreating to Netflix, books or bed. Or BCO. lol.

    berrylvr, welcome to our thread! I have not had heart rate/BP symptoms, I would call your BS (or MO) and ask about it. Hope it's nothing and resolves soon!

  • meg2016
    meg2016 Member Posts: 287
    edited October 2016

    berrylvr My surgery was the day before yours- same surgery. I actually had the reverse, my BP was running a little low after surgery (they almost kept me longer at the hospital because of it.) It consistently got higher over the past weeks and at my follow-up last Friday was back to my normal (but I am on the low side normally.) I would check with them on it being elevated, hopefully its just anesthesia side effect. I will say I do feel like I have more shortness of breath. They told me that should improve after I exercise more, but also that sometimes after having a breathing-tube in surgery that can happen and because of the pressure of the tissue expanders the tendency is to shallow-breathe. So I try to focus on really taking deep breaths (which actually do hurt a little with my expanders if I am truly breathing as deeply as I can.)

  • 4girlsmom
    4girlsmom Member Posts: 27
    edited October 2016

    Berrylvr,

    I definitely noticed very low stamina and got extemely winded just after going to greet someone for one minute- I would then have to dive right baxj into bed. Only today- at 3 and a half weeks post surgery - did I feel normal- two doc appointments, up and out all day, and tonight I just like my self (albeit wirh one boob that feels like a balloon about to explode

  • berrylvr
    berrylvr Member Posts: 5
    edited December 2016

    Thanks for your responses everyone! A quick update-- in case anyone searches this thread with they same concern in the future. Shortly after my post my BP and heart rate they started to come down and eventually resumed normal levels-- which are typically on the low side.

    Best wishes to all on this journey!

  • Irony
    Irony Member Posts: 46
    edited December 2016

    Hello my fellow Sept surgery survivors! It has been a while. I just wanted to catch up and see how everyone was doing.

    When I last posted, I thought i had lymphedema. It turned out I had a deep vein thrombosis (dvt) that clotted from the jugular vein in my neck, down my left arm. I'm very lucky it did not travel to the lung. I am currently on bloodthinners for three months.

    The dvt really pushed back my recovery . I go to a lymphedema clinic for PT to get range if motion back. (I had to wait two months until the clot was stable. ) I'm feeling so much better now and range if motion is greatly improved. It also pushed back expander fills and subsequent reconstuction. Looking at implant exchange in March.

    I start back to work on Monday after a 12 week leave. I'm really nervous.

    How have you guys been?

  • reflect
    reflect Member Posts: 576
    edited December 2016

    Hi Irony! I've recently finished rads and am finally starting to feel better (normal? I don't know!). I started back at work PT at beginning of rads, stopped out towards the end, and this week I am almost back to FT, and it feels great. I had forgotten that I am a competent productive person! Hope your return goes well. I was very glad to ease back in. Good luck!

  • KentRunner
    KentRunner Member Posts: 25
    edited December 2016

    Hi Irony! I'm gearing up for my exchange on December 21. Things have been a bit quiet, and I could "almost" forget that I am a cancer patient. HA! I have my pre-op with my PS on the 13th and my 3-month follow-up with my BS on the 14th. I feel extremely fortunate to not need chemo or radiation at this time. I'm only on Tamoxifen, and so far I haven't experienced any side effects. Not sure if the medication needs time to build up in my system before side effects occur, but my oncologist said if I didn't have anything yet, I probably wouldn't get anything too severe. I know things can change in an instant, so I'm just enjoying my time right now surrounded by good news. Looking forward to getting the TE out and my implant in place. On to the next step!

  • Irony
    Irony Member Posts: 46
    edited December 2016

    Reflect, you have been through so much. I'm do glad you are done with radiation. This site has been so helpful to me but at times actually made me more anxious, so I haven't been on as often. I just didn't like not knowing how people I've connected with are doing. Congrats at getting back to work.

    Kentrunner, My case is similiar to yours in that I don't need further treatment. Tamoxifen is not an option for me due to the blood clot, so I'm just gonna roll the dice and hope for the best. I hope you implant exchange is uneventful and your recovery, quick.

    Thanks for writing back ladies!

Categories