March 2017 Surgery

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  • StillBlessed72
    StillBlessed72 Member Posts: 12
    edited June 2017

    hello. I am new here. I wish I joined presurgery but there was so much to process decide and organize. In any event, I had a bilateral mastectomy with diep flap reconstruction on 3/14/17. I returned to work 9 weeks later and over the past 5 weeks I have become increasingly fatigued. I finished PT last week and have no energy to do anything. Anyone else going through this?

    Also, I am scheduled for Stage 2 reconstruction on 8/9. Anyone else scheduled for Stage 2?

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

    Hi stillblessed

    Fatigue may be tied to the type of surgery you had. Have you checked the thread in the reconstruction forum for DIEP? Those ladies know a lot.

  • Tappermom383
    Tappermom383 Member Posts: 643
    edited June 2017

    Hello, ladies. I haven't checked in here in a while - been focusing on my radiation thread. How is everyone doing? The numbness in my tricep has subsided but not gone away completely. I've had 24 of my 33 radiation treatments. I'm getting red now and have an itchy rash. My two incisions are red and sore. But it's the fatigue that has really gotten to me. I'm hoping it will vanish when I finish my treatments.

    I see my surgeon on July 13 for another follow-up. I have no idea if he'll continue to see me or if I'll only see my RO and MO in the future. I had an appointment with the MO in mid-July but got a message from his office that he didn't want to wait that long to see me. What???? I see him on Tuesday and I'll find out then what the hurry was (I tried to find out on the phone but had no success).

    My surgery seems so far in the past now. Hope you're all doing well. The camaraderie that has developed among us on the forum is wonderful.

    MJ

  • EastcoastTS
    EastcoastTS Member Posts: 864
    edited June 2017

    Nice to see some activity, March 2017ers!

    I'm doing well. Exchange surgery coming up in Sept. TEs are a joy! Actually, they aren't that bad. Once I got over BMX healing and fills, they calmed down. Went back to work in May -- and though I often feel there are two groups now and it somewhat affects my view of life: Cancer and non -- work is going well enough, too. I just may not care as much about it. Idk. ;)

    Hugs to all of you!!!! I hope everyone is doing well.

  • Rrobin0200
    Rrobin0200 Member Posts: 433
    edited August 2017

    I had my BMX on 3/31. Surgery was 9 hours, which included reconstruction (direct implants) I didn't qualify for DIEP flap surgery (too thin) but will be having stage 2 surgery in the fall which consists of fat grafting. Any insight to this fat grafting? They will take a little fat from stomach, thighs and butt areas.

  • StillBlessed72
    StillBlessed72 Member Posts: 12
    edited June 2017

    Thanks Molly50. I will check it out.



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

    Hi ladies, nice to see you all. I am doing really well. Life with implants is much better than TE's. Tappermom, did your RO give you something for the itching?

  • Tappermom383
    Tappermom383 Member Posts: 643
    edited June 2017

    I see we're both awake in the middle of the night, Molly!

    No, because it started itching over the weekend. I have some hydrocortisone ointment and put that on. It helped.

    I only have two stickers now but one is really bothering me. I'll ask the tech today to take it off.

    MJ


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

    Nice to here from the March 2017 ladies again. I'm still working on my recovery from the March revision for CC. I have been slowly able to lift some light weights again, but my LE kicked back in from the March surgery and then again somewhat when I got my 3D tats two weeks ago. I've mostly been posting on the exchange board. It's a process for us all and these boards are such great support.

    Scottie

  • Dafne
    Dafne Member Posts: 104
    edited June 2017

    Ladies, nice seeing you moving on with treatments and everything. I m on a much needed short vacation, but things dont always move along with our plans. My right expander is leaking the last couple of days. It has lost all the last fill so far, which was the first over-expansion fill (100ccs overfilling). Dont know why or how this happened and i just hate the idea of another surgery to replace it, especially in the middle of this very hot summer. I just hope my ps can find some other way....

  • EastcoastTS
    EastcoastTS Member Posts: 864
    edited June 2017

    Oh, Dafne! I'm so sorry. Hope your PS can find another way, too.


  • raven4mi
    raven4mi Member Posts: 562
    edited June 2017

    Dafne, are you close to being completely filled? If so, my PS said that if I were to "spring a leak" they would just fill more often and refill until exchange time.

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

    Dafne. Hope your PS comes up with a solution. Can I ask a dumb question? Why do they overfill and not just put in a bigger expander?

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

    (((Dafne))) I hope your PS comes up with a solution. Tappermom, my RO prescribed something for itchy rash. It really worked. How's the redness?

  • Tappermom383
    Tappermom383 Member Posts: 643
    edited June 2017

    I'm slightly red but not too bad. I put hydrocortisone ointment on last night and it helped. Starting to get itchy again so guess it's time for more. I see the RO on Thursday so if it's not better, I'll get something from her.

    Thanks for the support.

    MJ

  • lrwells50
    lrwells50 Member Posts: 254
    edited June 2017

    My BMX was 3/9, and I went back to work about 3 weeks later, 20-30 hours a week. I'm still a combination of numb and can feel light pain on the sentinel node biopsy scar when I bathe. The other side is still slightly numb, but no pain. My TEs have been fine. They filled me with 120 ccs each time, and I had no pain at all. After my last chemo 7/21, I'm to call my PS and set up an appointment to see if I need any more fills, and to set up my exchange surgery. it's daughter #1s turn to come cook and clean for a week, so I'll have to coordinate the surgery with her schedule

  • raven4mi
    raven4mi Member Posts: 562
    edited June 2017

    2FUN, I can't speak for Dafne, but in my case I have the largest expanders available (650 ccs) so the only option for "evening out" is to overfill, which my PS did on the left by 100 ccs and it looks good.

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

    oh, that makes.sense raven. That wasn't a.thing for me, thus.the stupid.question !

  • Dafne
    Dafne Member Posts: 104
    edited June 2017

    Guys, i called my ps he said "oh, ok this can happen" and we ll discuss it when i see him next Thuesday. He asked me when was the day of my bmx, so i guesss he ll want to push the exchange surgery. I would prefer he ll keep filling it lets say every week instead of two to three weeks, till September as was the plan but we ll see. I know he overfills cause he always uses implants that are smaller than the expanders and in my case in 600ccs you could barely see some "breasts" forming due to my broad shoulders and rib cage. Volume of my te is 500ccs and he overfilled them to 600. I guess the right one did not like the overfill lol. At least it seems it lost only the extra 100, but kept the rest so i still have some foob showing under clothes.

  • Rubystar
    Rubystar Member Posts: 2
    edited June 2017

    As a trained psychologist (retired) and a pain patient for other reasons, itsn't it time for objective studies of pain level response to the nuclear injections? What is the variable that makes this a difficult for some and not for others? Why don't we start using the standard pain standard (1-10) in discussing our experiences? Why have do we not ask for studies to determine what is a determine factors?

    I had a Level 10 response. Others seem to be at level 1 or 2. It's time to shead some light on this issue since some patients have other considtions such as heart conditions that would be set of by high level pain. It seems irresponsible to not have scientific pain studies. Anyone agree?

  • Rubystar
    Rubystar Member Posts: 2
    edited June 2017

    As a trained psychologist (retired) and a pain patient for other reasons, itsn't it time for objective studies of pain level response to the nuclear injections? What is the variable that makes this a difficult for some and not for others? Why don't we start using the standard pain standard (1-10) in discussing our experiences? Why have do we not ask for studies to determine what is a determine factors?

    I had a Level 10 response. Others seem to be at level 1 or 2. It's time to shead some light on this issue since some patients have other considtions such as heart conditions that would be set of by high level pain. It seems irresponsible to not have scientific pain studies. Anyone agree?

  • Tappermom383
    Tappermom383 Member Posts: 643
    edited June 2017

    I'm with you on the Level 10 pain, Ruby. The radiologist looked me in the eye and said, "I'm going to hurt you. I could give you a shot of lidocaine but I think it's better to just get the injection over with." Not knowing any better, I agreed. Believe me, should I ever have to do something like that again, I'll be numb (and preferably unconscious!!!).

    MJ

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

    Dafne. . .hoping that you can keep your EX set for Sept as planned. Sorry you having to go through this but sending gentle hugs.

    Scottie

  • Dafne
    Dafne Member Posts: 104
    edited June 2017

    Scottie, i keep my fingers crossed. Rubystar, although I was lucky enough to avoid the shots, I fully agree with you, but I m not so sure they (medical community) will listen to us on this. Docs tend to underestimate mastectomyaand node removal pain, would they even care for the pain caused by an injection? In my opinion they just dont care.





  • lrwells50
    lrwells50 Member Posts: 254
    edited July 2017

    I can't remember how many injections I received before my sentinel node biopsy, but only one hurt, and it was very brief, but maybe a 7 on a scale of 10. He did give me some lidocaine first

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

    The nuclear radiologist who did my nuclear dye injection on the morning of my BMX was actually very apologetic. He used some numbing cream and told me he was sorry that it might feel like a bee string. I laughed and told him that it was hardly the worst thing I was undergoing that day.

    Scottie

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

    I can't remember when I last posted, but I had to share that I just got a good report from my last surgeries and I think I can say I am cancer free!!!!!

  • Tappermom383
    Tappermom383 Member Posts: 643
    edited July 2017

    Congratulations, 2Fun - that's great news!

    MJ

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

    2Fun!!! Wonderful news.

  • raven4mi
    raven4mi Member Posts: 562
    edited July 2017

    Haven't posted in a while but, Dafne - what did your PS ever do about your leaking TE? I'm curious to know because now I'm in the same boat.

    I went in for my LAST fill yesterday and the intern punctured the TE, so now it's quickly leaking out all the saline. I soaked through a feminine napkin last night and estimate at this rate that I'll be completely flat by tomorrow. My PS is in surgery on Tuesdays and Wednesdays but I have a very strongly worded e-mail out to his office that he better damn well call me today to let me know what we can do. Since my implants are over the muscle I'm frankly just hoping that he schedules the exchange ASAP. This whole thing has been freaking ridiculous and I can't wait for it to be over. Guh!

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