March 2017 Surgery

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  • Sitti
    Sitti Member Posts: 230
    edited April 2017

    Raven, hope your drains have slowed down and "Elphaba" comes out today!

  • raven4mi
    raven4mi Member Posts: 562
    edited April 2017

    2FUN, sorry that the word is now definitely more surgery. Keeping you in my thoughts on that. Good on you for 10K steps! I can't do any kind of exercise with Elphaba still in me and it's making me nuts.

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

    Hi everyone:

    Hope everyones weekend was relaxing.

    2Fun: I am so sorry you need more surgery. That sucks. On the other hand, I am impressed and inspired by your 10,000 steps already. Holy macaroli! What a fighter.

    sjl: Thank God your surgery is over and that part of treatment is done. It is mind relieving, I agree. I used to live on the west coast myself eons ago and took ferries everyday, so I know what its like to wait for a ferry. What an ordeal to have to go that route after surgery though. It can be tiring.

    Scottie: so sorry about your burning pain too. Has it subsided? I find if I am too active (and I don't mean to be) I get burning pain by the end of the day. If I am not too active, I am mostly pain free except for the odd twinge. It frustrates me because I want to get on with it. I am not a patient patient. LOL. I hope your pain is resolved Scottie.

    Raven: I too hope you get your drains out. Fingers and toes crossed.

    And to everyone else.. hugs to you all.

    I am getting weird aches and pains now. Twinges of pain in my fat grafting side. Weird.

    wallan


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

    Sitti, I was at my son's robotics competition, and it was a 10 minute walk to the stadium from the hotel. I did that 4 times, and then 2 bouts of laps around the stadium. Each about 15 min. I'm 3 weeks post MX as of today, so that is usually when I am able to do more. Normally I walk 60-90 minutes daily. And I'm still overweight by a ton. Ok, obese. I go back on femara today, so say a prayer my joints tolerate it, and it doesn't make me gain weight. I was just at the store and stocked up on veggies, so I am trying to get a good start to the week. DH has a bad week coming up with work. I hope he is still employed at the end of it.hugs to all, sorry to be a debbie downer!

  • raven4mi
    raven4mi Member Posts: 562
    edited April 2017

    My goodness, 2FUN, that's a lot of walking just 3 weeks post-op. The robotics thing sounds awesome, though. I wish my two boys would get into that; I think they'd really enjoy it. Sorry to hear about your DH's works woes - just what you need! Don't worry about being a downer, girl. We're here for ya!

    wallan, I had pretty extensive FG back in October and I had pain from that for a looong time afterward, but mostly from the donor site. Is your pain where they put the FG?

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

    Hi Raven:

    My pain is from the donor site too a bit if I sit for too long. My thighs hurt which is the donor site.

    As for the pain on my chest where FG is, I get weird twinges of pain every now and then that are intense for about a half second or so and then go. Mostly, its pain free. This just started in the last few days. Weird.

    I hope you get your drains out Raven.


    2Fun: I am inspired by your walking so much as routine. This is amazing. Sorry about your hubby's job stress. That is stressful to deal with for sure. Hugs to you. (PS I agree with Raven, you are not a debbie downer. This site is wonderful for being able to vent and get what really bothers us off our chest. Its healthy and necessary I think)

    wallan

  • raven4mi
    raven4mi Member Posts: 562
    edited April 2017

    F/up with PS again this morning: Elphaba, the bitch, is still with me. Next appointment is in another week, although the PS said that if the drainage slows down by Thursday to go in and have the drain removed then, but I just know I'm not that damn lucky.

    I did get another 100 CC fill today, though, and he did explain that the reason he's going so slow is not to put any undue pressure on the incision while it's still healing. He said once he's 100% confident the incision is healed he'll start filling me faster. So right now I'm at 300 cc on my way to 750.

  • KimE
    KimE Member Posts: 53
    edited April 2017

    I just heard back from my surgeon, my lymph nodes were clear but my lumpectomy margins were close so they have to go back in and remove more tissue. Just as I was feeling like I could go back to work! But, on the bright side, I probably won't need chemo!!!

  • Tappermom383
    Tappermom383 Member Posts: 643
    edited April 2017
    Good news on the nodes, Kim. Sorry about the margins. It's this constant unknown that's so exhausting, right? No chemo but will you have radiation? I'm still waiting for my pathology report but the surgeon already told me I'll have radiation (what's confusing about that is I've read radiation is not usually prescribed for women 70 or older - what? We don't have years of living left to do?). Best of luck on your second surgery
  • Yvonne_M
    Yvonne_M Member Posts: 72
    edited April 2017

    2Fun, so it's called a dog ear? Huh, good to know. You said you were back on Femara, any tips for me? I've been on it a week or so. I take joint pills, so hoping that helps. Did your joint pain happen right away or was it after you had been on it awhile?

    Raven, so sorry your Elphaba is still in your life. Prayers that it slows down on the draining!

    Kim, sounds like good news right?

    Tapper, oh you live in Lake Arrowhead? How nice! We used to live on the other side of Wrightwood, but loved driving up to your neck of the woods (literally). :)

    Prayers and love to all!

  • Dafne
    Dafne Member Posts: 104
    edited April 2017

    Just to say hi to all the ladies here. Seven days post op today, three drains out of four gone, one more left. Still sore and in pain at times mostly under my arms. Hope I ll be home soon

  • Superbody
    Superbody Member Posts: 17
    edited April 2017

    Hello all,

    If you're interested in scar therapy treatment, please read my post! It's been a while since I posted to the community; I guess that's a good thing which means I'm healing (physically and emotionally). I wanted to share with you BC warriors who are dealing with surgery, and scars, that there is a very good silicone device product to help with post-surgical scar healing. I had a double mastectomy, was scared of nasty scars, and through much research found, through medical peer-reviewed journal articles, the product "Embrace" which reduces tension-load on the skin to reduce scar formation (haven't found other products that can do that; see product and before/after pics here: https://www.embracescartherapy.com/shop-now/breast-reconstruction-scars/). My PS highly recommended it and being overly zealous I bought twice the recommended amount (4 months supply instead of 2 months supply). Well, I ended up having a radiation side effect 3 months post-surgery on my right breast which led me to have hyperbaric oxygen treatment. I was so bummed because I had to stop using Embrace (I was already on the second 2-month supply) and the scars were healing very well, especially the non-radiated breast. After hyperbaric treatment (5 weeks), I was happy enough that I did not resume wearing the remaining 2 months supply, so I'm wanting to get rid of the extras for a small price. The two month supply comes with 12 silicone devices (6.3 inches each silicone strip) and is recommended to start wearing 2-4 weeks post-surgery. I ended up using 2 (one for each breast) before my radiation skin breakout, so I have 10 devices left, which you can stretch to last 2 months by changing them out 12 days instead of the 10 days they recommend (I left them on sometimes more than 10 days to get more wear for my money). I'm happy to privately share pics of my scars. These devices can be used for tummy scars, too. Send me a private message if you're interested. Good luck with surgeries, ladies, and know there is life with new breasts!image



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

    Raven: Sorry to hear your drain is still there. Dammit! Hopefully its out before next visit.

    Kim: Great news on the nodes... sorry you need more surgery though. No chemo would be awesome.. that is for sure.

    Dafne: Great news on your drains disappearing one by one. One week is quick for the drains to come out. Are you still in the hospital?


    wallan


  • raven4mi
    raven4mi Member Posts: 562
    edited April 2017

    kimelliott65, sorry you have to go back in for clear margins. That happened to me when I was first diagnosed several years ago but they got good margins the second time. Yay for no chemo. Will you have to have radiation?

    Dafne, have you been in the hospital for the entire seven days post op??? Sorry about the pain but it will get better each day.

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

    2FUN sending positive thoughts and hugs. If you have more surgery ask about radiation again. I would have had radiation if lumpectomies, but avoided it with BMx. Probably depends on the margins but it's possible. Way to go on the steps. I'm not very mobile yet. Yeah on the robotics competition (my ds is a total geek and would love to do that). Prayers for your dh. Vent away when needed.

    Tappermom. . .have you considered a second opinion on rads? Lake Arrowhead is beautiful.

    Raven, fingers crossed the Elphaba dries up. Raven it sounds like you're doing okay with the fills. Better slow and go than too fast.

    Sjl. . .wow on riding the ferry after surgery. 45 minute drive home was alot for me. Take it easy.

    Kimelliott sorry about the need for more surgery but yeah on the nodes and hopefully no chemo.

    Wallen, I think you're right that I may have to give it more time. Sounds like we both need to keep taking it easy for a bit.

    Welcome Dafne. . .sounds like you're doing well. Keep us posted. Are you still in hospital.

    Hope I didn't miss anyone. . .


    My udpate: Yesterday was better and woke up just very sore this morning. Burning pain back this afternoon, but no swelling, redness or fever. If it continues for a couple more days will call PS, although my surgeon is currently out of town. I've had nerve pain issues with each surgery so it may just be me. Bad storm's here today so mostly just hanging in bed with arms propped up. Pain is manageable just frustrating at 2 weeks post op.

    Scottie

  • raven4mi
    raven4mi Member Posts: 562
    edited April 2017

    Scottie, sorry you're having so much trouble with pain. A quick call into the PS may alleviate some of the worry. I just noticed that you're near Atlanta. Are you impacted at all by the bridge collapse? What a nightmare that must be.

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

    HI Scottie:

    Take it easy. It is frustrating to have these setbacks and have to sit with our arms propped up.

    Heres hoping your pain is subsiding.. and you can get at it once again.

    Wallan

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

    2Fun, sorry about the margins but I am glad you have a super careful surgeon. HUGS

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

    Scottie, I am very sorry about the pain. I am doing really well. Just get a momentary shock each time I see my right frankenboob. That is the side with the mastopexy. Superbody, I need to check with my PS first but maybe...

  • raven4mi
    raven4mi Member Posts: 562
    edited April 2017

    Molly50, sorry, but I had to laugh at your "frankenboob" comment. I remember the first time I went into see PS after my mastectomy and I asked him when I would stop looking less like "Bride of Frankenstein" and more like "Bride of Dale" (my DH's name) and he totally cracked up. That reminded me of that moment.

  • Yvonne_M
    Yvonne_M Member Posts: 72
    edited April 2017

    Molly, that is so funny you said frankenboob. I was writing a friend this morning and I called it Frankenstein Boob, I like your version much better.

    I was reading some of you ladies signatures with all the stuff you have done (that sentence didn't sound right) ... wow. So many years dealing with this beotch. Here's to us all being warriors!!!

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

    Raven. . .we're not directly effected by the interstate collapse but it's messing up traffic all over and once I got back to work it will make the commute harder. Uggh

    Scottie

  • Sjsparks
    Sjsparks Member Posts: 20
    edited April 2017

    Hello Ladies,

    I am having a hard time focusing so I didn't go through and read all the post I missed, sorry. My surgery went great, I was in the hospital only 1 day. Coming home was rough, but now I have my pain under control. I am emptying my drains every 8 hours and I feel like I am not getting much. I have 4 tubes. Tubes 1 and 3 rarely have more than 5 cc per dump. Tubes 2 and 4 I can dump any amount from 7.5 cc to 14 cc this evening. Do I add the total cc dumped for the day, Is that how they gage the amount coming out? I think I worked up the surgery and recovery in my mind way more than I should have. Yes I am uncomfortable and yes I hurt but not what I was think it would be like. I go for my follow up on my reconstruction doctor on Thursday. She told me she was able to fill 300 cc in both TE. I look so awkward, I know the end result will be nice but for now it just looks so weird. She said she won't do another fill until about 4 weeks out from surgery. I've been able to shower every day since surgery which is nice. But my limitations are driving me crazy. I can't bend over, lean over, and I can't reach for things. Relying on ;someone 24-7 is tough.

    I am so glad this phase is over!!

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

    Sjs, it's a record of each drain individually. Each total for the day usually need to be under 30 ml to be removed. Glad you are doing well.

    It's funny but my incision on my two mastectomies didn't bother me but wow now I have my original scar and an upside down T. I'm sure in time it will be better. Calling it Franken boob at least lets me find the humor in all this.


  • DiV
    DiV Member Posts: 231
    edited April 2017

    Hi! For all who are having difficulties with their surgery know that you are in my prayers and thoughts every day. For all who have had their surgery I wish you a speedy recovery and take it easy on yourselves.

    As for my own up date 1 week after release from the hospital for arm amputation I'm learning to adapt to one arm. My pain is mostly in my scapula where the surgeon did most of the work to remove the tumor by cutting a window in my ribs #2-5. I also get shooting pains that runs length of amputated arm to fingertips like shock waves (phantom pain) hurts but I can deal with it. I will talk to Orthopedic surgeon on the 7th about pain management and finding the right drugs for me and my symptoms to manage the pain. I start a therapy group for amputees friday. The therapist mentioned a mirror program they do to tell the brain that the arm is no longer there, she said alit of people benefit from the mirror program. All in all doing pretty good considering.

    Raven I too can't wait to get my drain out. I had 4, 3 chest drains and I breast drain. Still have the breast drain. Hoping to get it out on the 7th.

    Hugs and prayers to all!

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

    DiV, so glad you checked in. I know it's got to be pretty rough, but you are tough! I have read a lot about the mirror therapy, and have friends that have used it with good result. Are you going to have a prosthesis at some point? I wish you speedy tissue healing, and quick emotional healing.

  • DiV
    DiV Member Posts: 231
    edited April 2017

    2Fun the only prosthesis I can have is for looks only cause I have no joint to attach a working prosthesis to. It doesn't bother me it's part of my battle scars. I really don't even think about not having my arm i just adapt and do the best I can. I think attitude has alot to do with recovery process.

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

    Hey sjs:

    Glad you are at home now and doing well. It sounds like your drains will be out sooner than later. Which is great.

    It is frustrating being incapacitated sort of. Time to rest up and pamper yourself.

    Hugs

    Wallan

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

    DiV, I agree, it's 99 % attitude, and you will master all the skills you need b/c you have the right sttitude. I have a friend who is a physiatrist at Cleveland clinic if you need a referral ( doctor who specializes in physical medicine and rehsb). I was in Cleveland last weekend, I didn't notice until today that you are located there!


    Hugs to all and keep beating cancer! We can!!!

  • DiV
    DiV Member Posts: 231
    edited April 2017

    2fun thanks for all the great advice. Where are you from?

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