November 2017 Surgery Group

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  • Hariry
    Hariry Member Posts: 138
    edited December 2017

    I feel your pain RoamingStar, it's definitely tough. When I got my reports (of IDC 1.7cm) I asked the BS if it would be better to start chemo first but she said we'll remove it then chemo. She even did IORT for me, which was not supported by evidence. Then the detail of triple neg revealed itself after surgery. The onc did query why was it done such a way. Seems that triple neg would respond better to chemo and a lot others are doing neoadjuvant chemo.

    Life, unfortunately, is lived one way. No u turn. Stay positive darling. There are many recurrent cases who responded ultimately and got healed. You are in my prayer.

  • Roxy13
    Roxy13 Member Posts: 148
    edited December 2017

    Don’t say this, @roaming star. If the chemo made the tumour in the breast shrink substantially, I don’t see how it could have spread to more nodes. The cancer cells must have been floating around outside the breas for a while. I’ve been doing some reading and asked the oncologist when trying to decide whether to do adjuvant chemo and my understanding if that there is always a possibility cancer cells escaped even when nodes are clear.

    Lots of hugs and please feel free to vent here.

    And happy new year, ladies!

    XO

    R

  • DownNotOut
    DownNotOut Member Posts: 99
    edited January 2018

    RoamingStar I'm sending hugs and hope to you this new year. Hang in there and you will get support here as you struggle with your diagnosis and so many unknowns and scary things. I heard a great sermon yesterday and it was about how we all need HOPE and where hope comes from.I'm glad you have family & friends to love you through this and you have us, too.

  • swg
    swg Member Posts: 461
    edited January 2018

    Hey everybody..I hope you all had a great holiday season!

    I've been doing great. Had my first (and probably only) fill of my TE the other day. I'm amazed at how good my fake boob looks now. I'm excited to get the implant exchange..my PS says it should be in a couple of months.

    Been feeling really great. I was so fatigued and low energy before my surgery--I feel like once they got the dang cancer out I was back to normal. Been eating well..I make sure I get 5-6 fruits vegetables a day ( I make a lot of smoothies and cook my own food), and walking a lot. I think that's helped my recovery.

    I'm also taking vitamin D supplements (1 per day), 2 tbsp flaxseeds a day, and eating lots of broccoli sprouts as I read they are anti-carcinogenic.

    Pretty much back to work--still modeling and acting.

    I'm probably gonna volunteer for Unite for Her--they-'re a great organization that gives breast cancer patients and survivors funds to do acupuncture, yoga, reiki, and other alternative therapies, as well as help fund counseling and fitness memberships. I also get a free membership to a CSA that starting in Feb., I can pick up a box of produce from, once a week for 6 weeks.

    When I went to the Unite for Her wellness day, they gave us a box of produce as well as "The Cancer Fighting Kitchen", which is a great cookbook I've been using.

    You really can eat healthily and still enjoy your food.

    I took in a roommate because I needed the financial help, and that's going well. I'm influencing my roommate to eat healthy, and it's nice to have someone to cook for regularly.

    Sorry it took me so long to post back--just was very busy with the holidays!

  • Roxy13
    Roxy13 Member Posts: 148
    edited January 2018

    Hello, @swg! Glad to hear you are doing well!

    And thank you for sharing your health tips. I was doing so well before and after the surgery (juicing, green smoothies, whole grains for breakfast, no alcohol etc. etc.) Things slipped around the holidays, however, and now I think I’m addicted to sugar. Your post motivated me to get my act together. That and the fact that my jeans got tight (and they are stretchy!!!)

    I will try that cookbook as well. I’ve been reading a lot about nutrition, foods to eat and what to avoid. As expected, there is a lot of contradictory information out there (yes turmeric? no turmeric?, this mushroom or that mushroom - you get the idea), so I thought it’s best to use common sense. A good cookbook, however, gives you some structure. So thanks for sharing!

    I’ve been doing ok too. I decided to do a bit of chemo, starting next Friday. I’m not convinced that it’s all that beneficial in my case, but it improves the odds somewhat, so I took it. Hormonal therapy will start a little later.

    Also - I met with a physiotherapist. She told me that I didn’t need to come anymore (I only went once, as my mobility is back to normal (I attribute this to the daily yoga and pilates classes I’ve been doing, and strongly recommend exercising). She gave me some exercises to help prevent lymphedema. Supposedly they activate other lymph nodes and redirect the flow of traffic to spare the affected side. I’m not sure that I buy too much into this. I’ll ask my MO.

    Hope everybody is doing well!

    Stay warm! (If applicable :)

    Hugs

    R



  • Hariry
    Hariry Member Posts: 138
    edited January 2018

    Hi everyone,

    Hope you ladies are doing just fine. Roxy13, mind if I ask what do you mean by "bit of chemo"😂 full/part of standard regime?

  • Roxy13
    Roxy13 Member Posts: 148
    edited January 2018

    Hi, @hariry. I’m doing 4 rounds of TC (taxotere and cytoxan). I think this is standard for TC. I keep saying “a bit” so I don’t get so scared, but I didn’t ask to shorten the cycle :)

    Hope all is well with you!

  • Hariry
    Hariry Member Posts: 138
    edited January 2018

    All the best to you too,Roxy

    Am now lying on the bed in daycare waiting for my blood count- #2 AC today!

  • Lula73
    Lula73 Member Posts: 1,824
    edited January 2018

    Hariry- I’m sorry it took so long to get back to you in the choice to have oophorectomy. There is a family history of ovarian cancer in my dad’s side, prostate cancer on my mom’s side. (The scary part about ovarian cancer is that there’s no screening protocol and by the time they diagnose it it’s already stage 4 with few to no options on treatment.) I tested positive for a gene mutation that increases risk for ovarian cancer called BRIP1 and recommendation was remove them by age 50 (I turned 44 in 2017). I had pretty much made the decision to move forward with removing them at that point. Then the tamoxifen caused blood clots in my calf and both lungs so I had to discontinue it. Since I’m 100% ER & PR+ not taking an anti-hormonal wasn’t an option. I could’ve taken a Lupron or zoladex to shut the ovaries down so i could take an AI but by the time 5 years passed I’d be at that age 50 mark. So the tamoxifen debacle sealed the deal and I had the ovaries (plus all the other baby making parts) removed during my stage 2 DIEP recon surgery. I hope this helps

  • MBPooch
    MBPooch Member Posts: 229
    edited January 2018

    Hey All -

    Just wanted to check in, haven't been on for awhile and glad to hear that everyone seems to be doing well. @roaming star, I agree with Roxy and DownNotOut, I know the initial news had to be shocking and scary but there are so many advancements now and there are tons of success stories! @swg - love the health tips. I've been dabbling with a Paleo diet and am surprised by how easy and nonrestrictive it feels. Definitely over did it over the Holidays with sugar, carbs and alcohol.

    Overall I am feeling great, I think having the direct to implant really aided in my recovery. They look and feel surprisingly good. Still a little sore around the alloderm area but I don't feel the need to take anything over the counter. The 4-5 week mark was a huge turning point for me. Almost full range of motion just a little tight in the armpit area. We went up to Northern Wisconsin for New Years and surprisingly my PS gave me the green light to go snowmobiling. After hearing the trails were a little bumpy I declined but really am surprised by how good I feel.

    Happy New Year!

  • swg
    swg Member Posts: 461
    edited January 2018

    Hey Roxy13--glad you're doing well, too..I admit, I still like sugar. I put it in my coffee. One tip I got from the Unite for Her wellness seminar was--use cinnamon, instead of sugar, in your coffee.

    I haven't quite gotten there, yet.

    They made the point that yes, sugar feeds cancer cells...but it also feeds healthy cells, too. We need it, just..not too much of it.

    As for lymphedema, I had a friend who was a massage therapist who highly recommended lymphatic massage. I think there may be some science behind that.

    I might do Reiki, as it's one of the things my Unite for Her passport offers. I'll let you all know how it goes.

  • swg
    swg Member Posts: 461
    edited January 2018

    MBPooch

    That's so great that you're so mobile! I feel the same. Right after surgery, I remember really overdoing it and dealing with a lot of pain, but I'm back to normal now.

    Funny how surgery seems like a distant memory.

  • Hariry
    Hariry Member Posts: 138
    edited January 2018

    Thanks Lula, for sharing your experience. Hugs to all

  • swg
    swg Member Posts: 461
    edited January 2018

    Hey..where is everybody?

    I guess many of us have gone back to just living our lives, huh? Busy with work and family life and stuff..

    I am doing well..hope you all are too :)

    I haven't had my outpatient implant exchange yet..I need to schedule my pre-op appointment. For some reason, my PS wanted to wait a month or so. Is that common?

  • Ghionik
    Ghionik Member Posts: 101
    edited January 2018

    Swg, I got a call on Friday last week from my PS office to get me scheduled for my exchange surgery! Mine is March 12th. My pre-op is Feb 27. You were only a week ahead of me, so I’m sure you’ll be getting a call soon.

  • swg
    swg Member Posts: 461
    edited February 2018

    Cool! How is everything looking? My fake boob nipple is still inverted. I'm now used to it being numb. Took a while to get used to that.

    But people can't even tell it's fake! I took a topless pic and put little stickers on the nipple part, and asked my friends to tell me which one was the fake one, and they couldn't tell.

    I really lucked out with my plastic surgeon.

    I can't wait to just get the implant in, and be done!

  • swg
    swg Member Posts: 461
    edited March 2018

    Hey--just posting because my implant exchange surgery is finally set for March 21st.

    Has anyone from Nov. done theirs yet?

  • Ghionik
    Ghionik Member Posts: 101
    edited March 2018

    SWG, my exchange surgery is this coming Monday! Wish me luck.

  • Ceci-246
    Ceci-246 Member Posts: 50
    edited March 2018

    Hi swg - I had my BMX Nov 21 and the exchange to implants on Feb 14 - with fat grafting because my implants are above the muscle. The exchange surgery was only 2 hours — BMX was 5 - and I was home that afternoon. I was a bit bruised on my chest above my boobs, and a lot on my butt from the fat grafting, but that all resolved in a matter of days. I was surprised at how much better the implants feel. They are so soft! I was back to work at the office looking normal in a little over a week. Just need to wear compression garments (snug spanx) for 6 weeks. Sometimes my chest under the implants feels tender, but much better than the hard tissue expanders. My PS recommended that I wear band above my boobs to help the implants “drop and fluff” but my left one doesn’t need it. I can tell the right one will need more fat grafting in a few months - ‘she’ didn’t keep as much of the fat as the left one. But in clothes, I think I look pretty good.

    I hope all goes well for your exchange.

    Ceci

  • Ghionik
    Ghionik Member Posts: 101
    edited March 2018

    Ceci, did you have to have drains when you had the exchange surgery?

  • Ceci-246
    Ceci-246 Member Posts: 50
    edited March 2018

    Hi Ghionik - no, all I had was 2 strips of surgical tape on the 2 scars under my breasts. I was sent home with a front zip, not very tight bra. And the only med was Tylenol w/codeine. No antibiotics!

    I will caution against judging how you look right after surgery - I was quite swollen and was not happy. Even though I read here many times to withhold judgement, I did it anyway and cried. So, that wasn’t fun, but like most everyone else, I began to look better fairly quickly

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