Lumpectomy Lounge....let's talk!

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  • MLP3
    MLP3 Member Posts: 534
    edited February 2016

    moondust- I like Swanson organic, non gmo and Aloha Chocolate pea protein. I also like Vega a lot too! All of these are low in sugars, whey and dairy free and great with address banana;)

  • Grammy4
    Grammy4 Member Posts: 56
    edited February 2016

    MLP3- I too had fluid build up in breast and underarm. The breast fluid was reabsorbed however, the underarm became inflamed and infected. I ran a fever, went to ER and was hospitalized three days. I did have cording... It was vertical. It went away with exercise and some PT massage. Please have yourself checked out.

    I really didn't know how bad it was. The underarm fluid burst while in the hospital and then I had to have wound care daily at home for two weeks. Not fun...

    I learned the hard way. If you have a concern... Call your doctor...


  • PontiacPeggy
    PontiacPeggy Member Posts: 6,778
    edited February 2016

    ORKnitter, we're all entitled to pity parties. Totally understandable. Good for you for going back to school!

    HUGS!

  • HappyHammer
    HappyHammer Member Posts: 1,247
    edited February 2016

    MLP- these comments from others are of concern....please get things checked out!

  • Melclarity
    Melclarity Member Posts: 388
    edited February 2016

    OhGosh I am so far behind I have no hope...I just wanted to say I'm different to anyone I've heard about HAIR GROWTH, I'm 8 weeks PFC and my hair is growing in even, it just looks like I currently have a crew cut. I have no patches at all, I was very fair before Chemo, so not dark haired or thick. I havent even worried about any of it, Im focusing on everything else.

    Life is good, am working, feel so incredibly normal, my birthday is in a few days and YAY I did it, I will make 48yo. I have to have scans and u/s in 3 months, but looks like Im facing mastectomy :( but means most likely I'll never have to worry about any of this again. What a long hard road, but Im going to keep moving and leave this behind me. I wont be getting it done if I agree until early 2017, so for now live live live....and Wine?? a few glasses here and there is me, a social drinker nothing much. I sure as hell am not going to stop living and deprive myself. I eat a healthy diet and am exercising.

    Stay positive ladies, one foot in front of the other and do what is right for you, and enjoy your life. BC doesnt define us, its been a part of our journey...good things come from bad. I feel lucky and blessed for so many things..

  • ChiSandy
    ChiSandy Member Posts: 12,133
    edited February 2016

    Interesting evening at tonight's Super Bowl party at our neighborhood restaurant/wine bar. Stayed pretty much on the straight & narrow carbwise--though I did try a few potato & tortilla chips and the amazing pickle-brined fried chicken (haven't had fried chicken since I visited KC in 2012). There was cava and a great Russian River Valley red blend from the winery whose winemaker we met last week. (As to how much, I take the Fifth--at least I didn't “drink the fifth"). No wine-bottle giveaways this time, but we hit the jackpot--we each won $50 on our squares and Bob won $25 in the final “Sack sack" pull (everyone signs a dollar bill, puts it in the paper bag, and each time a QB gets sacked there's a drawing and the winner gets the contents...but has to put back his own dollar for the next pull).

    But the most interesting was my conversation with the hostess (the sister of the co-owner). She's a 6-yr. survivor of ER+ IDC (5mm, grade 1) whose treatment was just like mine except she had standard-dose whole-breast rads for the full 33 tx. She's been my mentor and guru through all of this, ever since that first “focal asymmetry" mammo report that shook my world. We were comparing LE Medic-Alert bracelets, and I was surprised to find out she too had LE--breast more than arm--because she's petite and slender. She said hers actually went away (if there's such a thing as lifelong remission of LE, that's heartening). But the big revelation is that she, too, has never been to a support group, for precisely the same reasons as I gave. I told her I'm going Wed. night, because perhaps even those who may not need support might have a duty to give it. She's thinking of going with me.

    And Mel, Happy Birthday in advance!

  • PontiacPeggy
    PontiacPeggy Member Posts: 6,778
    edited February 2016

    MelClarity, you sound so much better than last week! You seem to have hit your groove. I'm so glad. LIVE!

    ChiSandy, I went to one support group meeting. It was terrible. One gal dominated the discussions. Didn't matter what anyone said, hers was bigger, worse, more life-threatening than anyone else's and she was totally obnoxious. The moderator was a wimp and didn't do a thing to shut her up. My little BC with a lx and rads was so minor in comparison I felt out of place. I've found the support here that I need from Day 1. No one ever made me feel out of place or weird because I had so little treatment. I'll stay here and share the little I know and enjoy the great friends I've made here.

    I've not changed my diet since dx. I am not a vegan (though my niece is) and I'm still drinking a glass of wine with dinner most nights. This works for me. Sandy, I'm glad you were able to enjoy some chicken and good wines last night!

    HUGS!!!

  • Jclc83
    Jclc83 Member Posts: 246
    edited February 2016

    I went to one meeting of a breast cancer support group. The conversation was more about one person's family than anything else. I didn't feel fulfilled when I left,so I never went back. I don't get support at home, very little at work. On most days I find some support here. Honestly, some days I feel invisible.

  • PontiacPeggy
    PontiacPeggy Member Posts: 6,778
    edited February 2016

    Jan, you are NOT invisible here! My DH wasn't able to give me much support (he was too ill). I am retired so that didn't figure into things. But here, I've made good friends, met some of them in real life, and been so glad to have found this group.

    HUGS!

  • bluedog
    bluedog Member Posts: 212
    edited February 2016

    Peachy, thanks!! 🐾


    Jan, I see you.

    Brithael, how are you doing? Have you started this round of chemo yet? It stinks that it takes such a toll on you.

  • MLP3
    MLP3 Member Posts: 534
    edited February 2016

    Thanks girls!

    No swelling just the cord and a spot that's very tender. Although, I iced it all last night during that BORING Super Bowl after massaging it on the 2.5 hr drive home from NH and it feels a little better. I think the hiking did it. I got the name of a great lymphedema pt this am and have a call into my bs nurse. I did a lot of stretching too.

    Mel- you did your best to keep your girls! The mx sounds like it's non-negotiable. You have the greatest attitude about it and I have a very good feeling that you'll put all of this behind you and live a very long and fulfilling life. We need to know your exact bday so we can send cakes and flowers via emojis!!;)

    RE: support groups... Nice moderators... Not! Remember when I told all of you ladies about someone in town making light of my situation? One-upping my lx and SNB to her double PROFALACTIC mx. And how lucky I am to only have what I had. Cancer is cancer. How and what we choose is our decisions. How can you tell a woman with dcis not to be scared because another woman's dx is more involved.?? It starts with that phone call "the biopsy was positive". Before they tell any of us anything else... We all got the same call and we all felt the same fear. Some of us cried, some of us curled up in a ball and me... I just pulled out of the parking lot after a great day of skiing, got the call, cried and then went and got lunch!! I should be a support group moderator... I wouldn't tolerate that bullying😉

    We are just starting a blizzard here, second big storm since Friday and people are complaining. It's still winter....❄️

  • Molly50
    Molly50 Member Posts: 3,773
    edited February 2016

    Jan, you are an important part of this group and definitely not invisible. I wish you got support at home and work like I do. Unfortunately my DS has such huge needs my own needs get put aside. It's okay because I don't think about my own problems as much. Mel, so glad you are doing better!! I have no desire to do in person support. When DS was little some ladies tried to get me to join their support meetings. I had already found plenty of support through email groups and had no desire meeting in real life.

  • MLP3
    MLP3 Member Posts: 534
    edited February 2016

    Mel- can you kindly refresh my memory? Why do you need the bmx after chemo and rads?

  • CyndiNic
    CyndiNic Member Posts: 59
    edited February 2016

    Been following everyone but haven't been posting much - just exhausted all the time. Got approval to pretty much work the next few weeks with minimal physical sales calls.....hoping to not have to go on STD......I am so close to finishing chemo with #10 Taxol on Wednesday.

    I have never fully healed from my re-excision. Have dealt with a seroma ever since that has now been drained 3 times. After the last draining I developed cording down my abdomen and under my breast. Last night I started to feel tenderness on my left side on my side/back. BF gave me a great massage this morning but I'm thinking I'm going to need more than his touch to resolve this and I want answers before I start radiation. MO was not concerned with the cording down my abdomen when I showed him last week.

    MLP - can you send me the name of the lymphedema PT you found?

    Cyndi

  • Melclarity
    Melclarity Member Posts: 388
    edited February 2016

    MLP - At this stage could just be my left side and its purely because I had an aggressive recurrence in 4yrs, so precautionary. My thing is though, nobody will ever know if it will or wont come back...I dont want to do chemo again, so only way to avoid in the event it came back is be ahead of it and get rid of it. Super hard, Ive always loved my girls, my man was wonderful on Saturday, I got upset about it, but he's like I trust my BS implicitly, be guided by his opinion. It will erradicate worry of it coming back. My mum had a mx at 40 and regretted it,so Im struggling absolutely with it all and she's not here to talk to. So one step at a time will wait for 3 months and his opinion. My birthday is thursday so 2 days, its tuesday here.

  • LovesToFly
    LovesToFly Member Posts: 1,133
    edited February 2016

    Jan we see you!



  • Molly50
    Molly50 Member Posts: 3,773
    edited February 2016

    Melclarity, as kbeee would tell you mx doesn't 100% end the risk of recurrence. It should make it easier to find though. It is a tough choice. I keep going back and forth between wanting to keep my right breast and cutting my risks by having a prophylactic mx on that side and not wanting to lose my remaining breast.

  • Moondust
    Moondust Member Posts: 510
    edited February 2016

    Sandy, congrats on winning some $ on your squares. I won a big fat zip on two squares I bought.

    MLP, thanks for the pea protein recommendations, and good luck getting rid of that cord!

    Cyndi, I have not heard about cords down the abdomen. Great to hear you are almost through with chemo!

    My DH is loving and always helps if I'm physically unable to do something, but he's not supportive in an emotional sense. He has always been the emotionally needy one in our marriage. That used to bother me, but not any more. I learned to be pragmatic, strong, and do what I have to do. But it's nice to have all you ladies to talk to :)

    I might have a seroma and want to resolve it before radiation (or be reassured that it won't be permanent). I'm waiting for a call back from BS office.

    I made some progress organizing things at home, and that always feels good. But it never seems to make a dent in what I need to still do.

  • Sloan15
    Sloan15 Member Posts: 896
    edited February 2016

    CyndiNic -Out here in CA the term STD means something totally different! Haha, so yeah, you don't want any of that either way! I hope you can finish your last chemos without any problems.

  • MLP3
    MLP3 Member Posts: 534
    edited February 2016

    Cyndi- Lynne Sanford 781-581-0484 in Lynn, MA and Amanda King 617-461-7516. Not sure where Amanda is but I got her number from a friend of mine that's a masseuse and reiki master. It can go down your stomach...??!!

    We have a blizzard brewing here so I have to wait until tomorrow am for a call back from the nurse. I'm heading into Boston Wed anyhow for my wig fitting, so I'm hoping I can kill two birds in town with cording and wig... Who da thunk?

    Mel- thanks for the clarification. Sounds like the right thing to do at this point👍🏻

  • MLP3
    MLP3 Member Posts: 534
    edited February 2016

    Too funny Sloan!!!

  • HappyHammer
    HappyHammer Member Posts: 1,247
    edited February 2016

    Sloan- that was funny!

    MLP- hate that about the cord thing... but you are on it! Warrior on. Another blizzard...wow. Stay warm! Day 1 of reboot- so far, so good. I did not give up the 2 morning cups of black coffee. Figured it's my re-boot. :)

    Mel- you sound great!

    Cyndi- sorry you are possibly dealing with LE! SO glad that you are almost finished with chemo, though. The last ones xan really be hard because of the cumulative effect...no wonder you are exhausted! Your body has been through so much!

    Sandy- awesome win! Maybe we should have a Lump Lounge Lotto group and get you or your DH to pick our numbers!

    Pea protein????? Nah! I'll pass.

  • MLP3
    MLP3 Member Posts: 534
    edited February 2016

    HH- great on the reboot! I had coffee this am too;)

  • CyndiNic
    CyndiNic Member Posts: 59
    edited February 2016

    Sloan....LMAO!!!! I needed a laugh today!!

    MLP - from what I can tell and have been able to research what I have (the cording down my abdomen part of itanyways) is very uncommon. Thanks for the names - I am in West Peabody so at least the woman in Lynn should be convenient.

    Very grateful to hear a neighbors plow in my driveway right now......no way could I shovel this year!! The kindness of others has made such a difference in getting thru this nightmare!!

    Cyndi


  • ChiSandy
    ChiSandy Member Posts: 12,133
    edited February 2016

    HH posted:

    "Pea protein????? Nah! I'll pass.

    OMG--just did a classic Danny Thomas spit-take! That’ll teach me to go online while drinking coffee.

  • MLP3
    MLP3 Member Posts: 534
    edited February 2016

    Cyndi- I'm in Marblehead... We should meet up one day

  • blamoms
    blamoms Member Posts: 113
    edited February 2016

    it's been a busy week. Last Tuesday I met my oncologist. She is amazing very down to earth and went over my pathology report in great detail.we talked about my treatment plan. I am triple negative so I will be doing chemo every 2 weeks for 4 cycles with 2 kinds of drugs and then switching to another drug and going every week for 12 weeks. I get three weeks off and then do radiation for 3 weeks and 1 day and then 4 months off to recove.

    She said I couldn't work that the drugs they are using I will manage to take care of the house but that would be it. I am having a PICC line because the drugs will wreck my veins. Anyone on PICC line? How do you like it? I met the radiation Doctor last week, had a bone scan, mugs test.CT sthis coming Friday. Next week more appts PICC line class,PICC line inserted and chemo starts. Feb 19. I also get the immune booster shot in between. I think that's it

  • MLP3
    MLP3 Member Posts: 534
    edited February 2016

    blamoms- That's quite a plan! But, isn't it great to finally have one?

    I found a great website for comfortable and stylish head coverings. One I know well because it's a ski inspired company and we have many of their hats. They actually donate to many cancer centers in VT and NH. It's called Skida and I can attest to the comfort of their fleece lined hats. The other is buffusa.com They are cool cotton infinity tubes that can be worn several different ways. I actually found chemo patients posting YouTube videos on them.

  • bluedog
    bluedog Member Posts: 212
    edited February 2016
    I wore a buff all summer when I walked in the woods with my dog. I tied it in a kind of pirate do, with a knot in back. I'm here in the humid mid-Atlantic, and it was the coolest option around.
  • MabelJo
    MabelJo Member Posts: 25
    edited February 2016

    Back to work todat...my excision spot itched like crazy! And I was sore. I quit taking the tylenol 3 because it left me feeling so hungover.

    Ladies, I am biting my nails waiting. I think its giving me a stress headache. This surgery wasn't all that bad, tho I feel like I should still be recovering.

    How has everyone coped with explaining things to your friends and family. I have a wonderful support group of both, but for some reason they all expect me to be in the depths of despair (Anne of Green Gables has the best lines). I am not, and luckily, if I do have cancer, its most likely in early stages. Like someone said, sorta feel like a fraud.

    Love reading all your stories!

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