December 2014 Surgery Sisters

Options
11214161718

Comments

  • Scottiemom11
    Scottiemom11 Member Posts: 1,298
    edited January 2015

    Quiggy, hugs to you. I wish I had an answer for the pain. That sounds like something you should call your BS about.

    Pink & Knm: I still can't side sleep and I'm 5 weeks post BMx. I want to badly because of neck and back problems from sleeping propped up. I'm also still having some pain but had to get off pain meds because whole digestive track is wonky. I'm returning to work on Monday and hoping for enough energy to get through most of the day. I can work shorter hours for a bit but really have to get back in the swing.

    So ready to start feeling more normal again. I guess I just have to accept that normal will be different from now on.

    Scottie

  • Chloesmom
    Chloesmom Member Posts: 1,053
    edited January 2015

    Saw BS 2 1/2 weeks ago to get drains out and he said he didn't think I'd need chemo as low grade tumor etc. Saw onco yesterday and she wants to see what oncotype number is. Now will be in limbo for next 2 weeks. Didn't realize PRneg increases the chance oncotype number high enough to warrant chemo :(. They are only sending for test now 4 weeks post op! Was making plans to return to work and now might be on hold. The 2 weeks wait isn't as the 3 between diagnosis and BMX but I'm still losing sleep. Just had to rant. The good news is I went for a massage today. A the massage therapist said my incisions look wonderful. He did an amazing job!

  • hopefulmomof3
    hopefulmomof3 Member Posts: 24
    edited January 2015

    Knmtwins-Thanks for the info and suggestions. I will look for the Jan chemo group. Most of worries do come from being "functional" & productive for my kids (8 year old twins and 11 year old boy). My husband has been doing a great job picking up the slack around the house. But he has returned to work and now sees how challenging it is to work full time and then come home to handle the kids and all the other housework,  etc. 

    I see that he is overwhelmed. And now with me starting chemo next week,  I know he is worried but isn't saying anything about it.  Like you said,  I think we do have all those images in our heads of what chemo will be like (Thanks Hollywood). I'm sure it may not be a walk in the park but your words reassure me-Thanks! Have a GreaT weekend!

  • knmtwins
    knmtwins Member Posts: 598
    edited January 2015

    Hopefull - my b/g twins will be 11 on the 24th and I have a 7.5 year old son - so yea - I get it. Most moms can function to the level necessary to keep their children healthy. My husband's hours are all over the place, so many days other people would drive to and pick up my kids from school. Worst comes to worst, there will be some days you don't check their homework and they might have to make a sandwich for dinner and they will have to buy lunch Might be time to teach the 11 year old to make microwave dinners. It will work out. Your kitchen floor will be dirty, the laundry won't be put away, there will be toothpaste on the sink and the underside of the toilet seat won't get cleaned and let's not even start on the dust. Just keep an eye on the dog's water dish, as they all forget that.

    As to husband's not talking... yea... good luck with that... Concentrate on YOU getting better!!!!!

  • SweetHope
    SweetHope Member Posts: 439
    edited January 2015

    Hopefulmomof3, my DDIL sent me this link. I'm sure DH and your dear kids are doing a great job helping, but who couldn't use this?

    Cleaningforareason.org

    "Fighting cancer is difficult enough, but living with it is even tougher and that's where Cleaning For A Reason steps in. As a nonprofit serving the entire United States and Canada, we partner with maid services to offer professional house cleanings to help women undergoing treatment for cancer, any type of cancer. To date, we have provided more than 17,000 cleanings for women with cancer with a value of more than $4.5 million in donated cleanings, and partnered with over 1,100 maid services."

  • Scottiemom11
    Scottiemom11 Member Posts: 1,298
    edited January 2015

    Sweethope,

    Thanks for posting this link. What a great resource. I am blessed to have some help with the basic house cleaning and had great friends who helped with meals while I was recovering from surgery. I have two special needs kids, and TG that my 12 year old waited until twof week after surgery to get ill (croup & asthma). At least I was able to go to doctors with him. DH bless him, for all his help, can't remember the meds and doses.

    I hope to pay forward some of the help and blessings we've had for the past two months. As for the housework and homeowrk, it's going to suffer for a while while I get back to work.

    Scottie

  • pamfightson
    pamfightson Member Posts: 9
    edited January 2015

    Just posting for the first time. I had my left side mx and full axillary dissection on 12/2/14. I only had one drain that I got pulled on 12/8. I was allowed to drive at 3 weeks and am allowed to wear a bra with a fiberfill poof.

    I do have a large hematoma above and below my incision that is hard and very slowly going away. It extends into what used to be my armpit and is really uncomfortable. It's making wearing a bra/poof really suck so I'm back to either going without anything at home or lightly wrapping myself in the ace bandage. It's times like this I wish I had bilateral. While I'm glad that the cancer is gone, I'm missing being even on both sides more than I admit. I think both sides gone would be easier to practically deal with. Plus I'm having phantom boob feelings so it's sometimes a surprise to look down and not see anything.

    I'm doing the exercises given and am getting my range of motion back. My elbow won't go back super far but I can reach over my head to my right ear. I still get flat out exhausted and I have to watch that my blood sugars don't tank.

    No reconstruction as I also have type 2 diabetes and aplastic anemia.

    Hope everyone is doing well!


  • Luckygirl27
    Luckygirl27 Member Posts: 16
    edited January 2015

    Hi everyone,

    These boards have been so incredibly helpful. I had bmx with diep reconstruction on December 17. I had IDC IN both breasts and BS also found dcis during surgery. Snb showed no cancer in lymph nodes.

    I am healing really well except for a lot of soreness in my arms. Not sure what to do. Does anyone else have arm and shoulder pain?

    Today I have my first oncology appointment to meet the doctor. Originally, my treatment plan did not include chemo or radiation. Now that one of the tumors is larger than biopsy showed my BS said chemo may be needed. I am very worried. Oncoscore results have still not been received. Insurance must approve test first. I want to return to work but worry about chemo brain.


  • Chloesmom
    Chloesmom Member Posts: 1,053
    edited January 2015

    lucky girl had the same thing happen Thurs. Was looking to go back to work and now waiting 2 weeks for oncotype! Feel like life is in limbo. This too shall pass. Spending a fee days visiting a cousin who had chemo last year. They look wonderful Very reassuring that it if it has to happen it will be another speed bump but then we will be on our way again.

    Hard thing for me is being self employed. No income ouch. But if I don't live I won't have any income for my family in the futureeither

  • waitingtoexhale15
    waitingtoexhale15 Member Posts: 12
    edited January 2015

    Funclassygal - I was not able to get my planned reconstruction on DEC 10 since I acquired an infection. I was planning on getting permanent implants without having to do Tissue expanders but now will need to re-arrange in 6 months Sadly, I will now need tissue expanders since the rest of my skin is shrinking and will need to be stretched with expanders and filled with saline. I am so fearful of another infection!

    Good luck with your reconstruction I wish you the best.

    Anyone have swollen side boobs? I have side boobs now since the skin was trying to be saved. I am getting used to the extra bumps under my arm but today I feel like both sides are big. Both sides have flabby bumps but today I feel very swollen and my left arm is swollen. I did a lot yesterday. Do you think this is from coming over working it. Went food shopping and although I thought I did not lift anything heavy, I think I overdid.

  • Scottiemom11
    Scottiemom11 Member Posts: 1,298
    edited January 2015

    Luckygirl,

    I'm almost 6 weeks post BMx. Still have some shoulderrands and arm pain although some is probably do to TE fills which I stopped last week. I also have an old shoulderror injury that sugery may have aggravated. It's frustrating. I did go back to work today and made it fr om about 9 - 4. Sore and resting now that I'm home.

    Scottie

  • Luckygirl27
    Luckygirl27 Member Posts: 16
    edited January 2015

    hi scottie,

    I spoke with my BS today and she said the arm/shoulder pain that I am experiencing is called cording. There is some info on this site. She said I will need some physical Therapy but can't start until at least 6 weeks post surgery. Also, said the pt would need to specialize in breast cancer.

    Stay well.

  • hopefulmomof3
    hopefulmomof3 Member Posts: 24
    edited January 2015

    Knmtwins-you really do get me. :-). Going to have to start getting my 11 year more involved. Thanks for hearing me out. 

    Sweethope-Thanks for the link! That sounds awesome. 

    I had my port put in this morning. Doing ok besides feeling loopy/sleepy. I'm going to make it a Netflix night. Have a good evening ladies! ♥

  • Chloesmom
    Chloesmom Member Posts: 1,053
    edited January 2015

    My BS gave me an Rx to see PT at 4 weeks as I was having some lymphedema and cording I found mine by going to the APTA website. The link find a PT and then the link for cancer specialist. Awesome PT at Hopkins Greenspring Station in Lutherville MD. Had me do very gentle treatment. Feels muchbetter.

  • Lmcqueen
    Lmcqueen Member Posts: 21
    edited January 2015

    Well 6 weeks post op with two drains still in and they admitted me to the hospital for infection/cellulitis. I am receding IV antibiotics. Wondering if I should make the PS pull these drains. They are doing cultures on the output. I have to believe that this infection came from the open wounds from these drains. So conflicted. Is it that bad to have the fluid manually drained? Thanks for any help you can provide.

  • Bippy625
    Bippy625 Member Posts: 890
    edited January 2015

    luckygirl, sorry you may need chemo, it sucks but it is doable. I am interested in diep vs. implants and TEs. If you are willing to share, I would love to hear.

    I am going to get some pt too, always great info on this site


  • Mecsmama
    Mecsmama Member Posts: 20
    edited January 2015

    Hello, all. Today I have my second post op with my surgical oncologist and an appt. with my medical oncologist. I am feeling pretty good physically. I feel like I might have turned a corner in the healing process the last few days. The TEs are still not terribly comfortable, but definitely livable. The swelling under my arms is starting to go down quite a bit. The right is definitely still more swollen, but that is where they took the nodes. I am hoping my MO gives me some answers today about whether I will need chemo or not, since the final pathology found a micro-met of .49mm. The onco-type was ordered so she may say we need to wait for those results. Just wanted to check in. I have been reading the thread everyday, but hadn't chimed in in a few days. 😀

  • knmtwins
    knmtwins Member Posts: 598
    edited January 2015

    Mecsmama - hoping all goes well today. I think you are amazing to be feeling pretty good today. 23 days after my surgery was the day I stopped the percocet, not because I didn't hurt, but because I was constipated. I (BMx w/ TEs 12/2) didn't start driving until last week and pulling the seatbelt down or turning the wheel full circle is still tough. You are going to rock this cancer thing. 'feeling pretty good physically' 3 weeks post surgery. You rock!

  • Straitlover
    Straitlover Member Posts: 124
    edited January 2015

    Lmcqueen, I also ended up in the hospital w/ cellulitis 2 weeks after my original surgery 7/30. They left the drain in because it was a way to keep a check on the fluid to see if there was still infection (purulent pus - yes gross!). I was in the hospital 6 days and then on home IV abx for a month (!!!), still w/ one drain. Hopefully the hospital stay will be enough for you, cause I ain't gonna line, home IV abx sucks! :)

    Hope you feel better soon!

  • farmerma
    farmerma Member Posts: 83
    edited January 2015

    Quiggy - I had my first lumpectomy surgery on 12/19, a second surgery on 12/31 because they didn't get clear margins. I just saw my surgical oncologist yesterday and asked about the numbness I still have under my arm (3 nodes removed according to the pathology report I finally got a copy of). I also have had pain in my elbow, although not always all the way down my arm. He explained that one of the nodes removed was next to one of the nerves and that I may or may not get feeling back there. I am starting to do some arm exercises now that he has okayed that. I see a little improvement, but would like to be able to feel things when I'm shaving my armpit! Hopefully given time yours will feel normal again. We just want to be back to normal NOW!

    I had a drain put in at the second surgery but removed after 5 days as the output was minimal. Of course, I've felt that full, tight feeling again and he confirmed that now I have hematomas on the right side. Not sure if the tube clotted and didn't let it all drain or what. He says they will liquify and either be reabsorbed or he will aspirate them. I asked him if anything would help (massage, heat, etc.), he said just time. Anybody else deal with hematoma? Anything help?

  • quiggy
    quiggy Member Posts: 315
    edited January 2015

    Hi farmerma;

    Sorry you had to do the second surgery, one is bad enough! I've heard that any node removal can cause long term issues. You're right we want to feel normal. I am did the seroma thing, that was no fun! Numb AND pain and sensitive skin; strange and hard to explain to people not going through this. I'm still having more pain then I think I should but then, I haven't experienced this before so ????

    Hope you get some relief soon and that we all find "normal" again!!

    So hard not to sink into depression.

  • sandra4611
    sandra4611 Member Posts: 2,913
    edited January 2015

    One of my armpits is numb but not the other 17 months after 1st surgery. Same number of nodes taken during BMX in Sentinel Node Biopsy - 4 on each side. Apparently more people have problems if they have an incision in their armpit for an ALND, Axillary Lymph Node Biopsy, which is often done with a lumpectomy or done in a separate operation before a mastectomy.


     

  • Gingercake
    Gingercake Member Posts: 31
    edited January 2015

    Hi all,

    I've posted this on another forum but I figured I'd ask here as well since so many have had chemo. One annoying SE I have is that my eyes run constantly. It started somewhere around my 3rd treatment and hasn't stopped. My tear ducts have narrowed and closed up from chemo. I've been to the eye dr and he wants to put stents in my tear ducts. Have any of you ever had this done? It seems like it's my only shot at getting this corrected but there are no guarantees.

    Any feedback/experiences/tips are appreciated. I really don't want to spend the rest of my life dabbing at my eyes and explaining to people that I'm not crying!

  • waitingtoexhale15
    waitingtoexhale15 Member Posts: 12
    edited January 2015

    Need some advice from my Dec surgery sisters - My nerve ending are starting to heal and both breasts are starting to ache a lot. My sagging tissue and side boobs are starting to hurt when I walk or pick up something from floor. Raw, nerve ending pain. PS says it is normal but I am swollen and it is very annoying.

    Anyone else have achy boobs? My underarms are still quite numb, although my side boobs ache and back and shoulders are throbbing. I was feeling great a few weeks ago despite the open wound in left breast. Now, I am in more pain and exhausted all the time.

    Anyone else having these issues after BMX?


  • knmtwins
    knmtwins Member Posts: 598
    edited January 2015

    Gingercake - the joys of runny eyes and nose. For most people it goes away when chemo is over. My eye doctor said I needed lubricating drops, that the eyes were dry from the chemo, hence over producing, he recomended Systane. I didn't ever get them, as it was the least of my symptom concerns, and I always would forget to purchase them. Personally, I'd wait for chemo to be over before having a stint put in, but as you can see, I didn't even get the drops, so obviously I wasn't going to do anything more. BTW - I stopped chemo, TCHP on October 29th. I'm not sure when my eyes and nose stopped running, but they don't anymore. Also, they both just seemed to be running 'water', the dried tissues were never 'crusty' like when you have a cold. My MO said for my eyes, any saline (not 'get the red out') eye drops would work and for my nose my MO said to buy Simply Saline MIST in the metal can, not the plastic squirt bottle. Doesn't have to be that brand, but get the mist not the spay, much nicer. It will run out of your nose, so have a tissue ready, but this helps moisturize higher up, so the nose doesn't do it. You will run less for a bit afterwards.



  • knmtwins
    knmtwins Member Posts: 598
    edited January 2015

    waitingtoex… - are you still on the muscle relaxers? Mine are every 8 hours and I'm only taking 1 or 2 a day, not the 3, and definitely notice it when I wake up, as I'm not taking the night pill, although even when on them there is a constant issue, but the Flexeril helps bunches. Not sure if you did recon. I have tissue expanders in. I had bunches of issues with bending down, felt like tearing, so I would hold my breasts, but if I held them, bent and reached, OUCH! Side boobs - hurt if I push my arms down to my sides, hence push them forward. Hopefully all this will get better soon.

  • goodprognosis
    goodprognosis Member Posts: 251
    edited January 2015

    Hi farmerma.  I too had a re-excision after my lumpectomy.  It's been 2 and a half years now and my breast is still a little sore if I lie on my tummy.  I also had a huge hematoma and a second one in the other breast (also lumpectomy where they found atypical cells ).  I felt it took a good year (sorry to have to say that as it seems a long time) for the hematoma to desolve (it's always made much worse because of a second surgery in the same place) and in that time it felt hard and swollen but dr said it would go away and it has - more or less.  So hang on in there.

  • goodprognosis
    goodprognosis Member Posts: 251
    edited January 2015

    Hi Sandra4611.  How is your husband?  Any diagnosis for his feeling so unwell before Christmas?

  • sandra4611
    sandra4611 Member Posts: 2,913
    edited January 2015

    Hi Good,

    The news on my husband is horrible. He has a type of blood cancer called high risk Myelodysplasia Syndrome and they gave him a little over a year to live. His one chance is a bone marrow transplant. We are looking for a donor.

  • SpecialK
    SpecialK Member Posts: 16,486
    edited January 2015

    Sandra - so sorry to hear about your husband.  Does he have any living siblings?

Categories