Chemo May 2011

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  • Patriotic
    Patriotic Member Posts: 281
    edited September 2011

    Hi everyone! I am so happy for those of you that are closer to the end of this nightmare journey.



    I have been taking a bit of a break from the boards. I finished chemo on Sept 6th. I feel so good. I had almost forgotten what feeling great felt like. Now, I am preparing for surgery followed by rads. Yuck. I just resumed Herceptin today and have that to look forward to every 3 weeks until May.



    So glad you are all doing great. Hang on there. Congrats to those who have finished chemo and/or rads!!

  • Cyborg
    Cyborg Member Posts: 848
    edited September 2011

    Just wanted to post that I am now done with chemo and rads. I have a weird kind if amnesia when it cones to remembering the chemo. I am back at work and trying not to get twisted up in stress. Working is moving me forward, I guess. Love and hugs to all the wonderful peeps on the boards.

  • MargieC
    MargieC Member Posts: 394
    edited September 2011

    Patriotic --  I am right there with you.  I haven't been on the board lately.  I finished TCH on Aug 30 and now just have herceptin every 3 weeks till May 2012.  I have surgery (BMX with recon) Oct 4.  Hopefully I will not need rads we will know for sure after surgery/sentinel node biopsy.

    Congrats to all the ladies that have completed chemo and rads.  It is hard to believe that 4 months have pasted.  I hope everyone's hair is coming back (mine hasn't started yet but I am hopeful).

    Margie

  • ---
    --- Member Posts: 197
    edited September 2011

    Cyborg,

    Congrats on finishing rads!  It seems like that went fast for you!  I'm still doing chemo, 2 more sessions! 

    Laureen

  • MamaV
    MamaV Member Posts: 907
    edited September 2011

    Laureen - 2 more!  You are almost there!  Keep up the fight girlfriend!

  • justme1
    justme1 Member Posts: 223
    edited September 2011

    I got my report back from the mamagram ultra sound and MRI. The mamgram didnt even see anything. The ultra sound and MRI 2.6cm x 2.1 down to 1.0 cm x 0.4cm my onc. said it was a 75 % shrinkage . He was happy with it. I was so sick at the time i didnt really respond i was hoping for a 0 left i guess but i was sick.I got some fluids /steroids/nausea meds and was better after the 2 hours of letting that get in my body.I am better today my feet still hurt but i guess theres nothing we could do bout that . I go see the surgen monday to schedule the surgery .I am excited and nervous i dread it but look forward to it. OH meee

  • bak94
    bak94 Member Posts: 1,846
    edited September 2011

    Justme-that sounds like great news, it shrank down to teeny weeny! My breast and chest, oh they did liver mri also came back good. I met with the surgeon today and my surgery is scheduled for Nov. 30. I still have 5 abraxane to go, well 4 after the one I am receiving right now. Were you sick from the chemo or flu? I have had a terrible cold and am going on antibiotics for a second time, as I am coughing up green gross stuff. Are you done with chemo? I know that even though my mri and ct is clear that cancer could still be lurking somewhere and I guess the path report after surgery will tell me, but he is not removing the im nodes, but will do a snb. I agree with the excited nervous part! I think I am ready to get this stuff out and gone! Then hopefully radiation and my body can take care of any stragglers!

  • justme1
    justme1 Member Posts: 223
    edited September 2011

    I had a upper respiratory infection but  i think the chemo i had last week just wouldnt let me goooooooooo.I was weak /neaseated just sick .I couldnt get out of bed much at all .I do feel better today.Thank GOD! I dont know till i have surgery if i am done .My oncology doc said he would have to see if i get clean margins and no lymphnode envolvement .So i might have to do 6 more taxols lest i get a break . I do pray its over i cant stand the thought of going back to the chair but i willl i dont want to.

    So happy for u urs came back good too !! Guess we are bout the same place right now. I dont know until monday when i get to get surgery but i think it will be soon like oct. if i get mine before u get yours i will tell u everything bout it if u want me too.

  • bak94
    bak94 Member Posts: 1,846
    edited September 2011

    Justme-Sounds good, I would like to hear of your experience. I hope you get clean margins and no  more chemo. Will you do tamoxifen or ai's since you are er pr pos? Since I am er pr neg and do not have any options other than chemo, I am almost thinking if they find any trace of cancer in me at surgery that I will probably have more chemo. If they don't find cancer, I am not sure, I kinda wonder about doing a mild chemo (if there is such thing) as an extra caution. There is talk of putting me on tamoxifen as I am weakly positive, 3%. Chemo feels like my safety net and I worry about what will happen when I am off of it :(. Just have to hope for the best and be as healthy and stress free as possible!

    Sounds like a couple of october surgeries for the May Chemo gals! Margie

    Margie-Good luck with surgery! Do you mind me asking what type of reconstruction? I can't have immediate reconstruction, but am hoping for diep at some point!

    Any more October Novemember surgies? Mine bmx is scheduled for Nov. 30.

  • justme1
    justme1 Member Posts: 223
    edited September 2011

    My feet are really bad can hardley walk on them and my  fingers tingle i am thinking neuropathy  .I keep telling the doc but he really dont give me any advice on what to do . Does anyone have any ideas as to what will help? Should i try to walk more or less? They hurt some this morning but by the afternoon they are really sore . I hope and pray this goes away.

  • Beaglesgirl
    Beaglesgirl Member Posts: 287
    edited September 2011

    Justme1,

    that sounds like neuropathy. I am so sorry your doctor is not helping with suggestions- mine really didn't give any either but he was really took action asap when it happened-- They actually reduced my dosage by 20% a couple of weeks ago. Ask your onc if you can take acetyl l carnitine as a supplement.  It has worked for many women on the boards. 

    sending you healing thoughts and prayers 

  • bak94
    bak94 Member Posts: 1,846
    edited October 2011

    Did you say your onc won't agree to l carnitine? I swear it has helped me. I still have problems, but not near as bad when I started carnitine. I also take glutamine. My doc told me to take bothe!

  • justme1
    justme1 Member Posts: 223
    edited October 2011

    he pretty much says it will get better.I am a week and ahalf out from last chemo (last chemo for now) and i thought i would feel good by now .But my feet hurt and i have no energy .I go to my surgen monday and I willl ask him about it.

  • justme1
    justme1 Member Posts: 223
    edited October 2011

    glutamine i have took that from the start

  • bak94
    bak94 Member Posts: 1,846
    edited October 2011

    I'm pooped. I only worked a few hours today and feel like I cannot stand to work anymore! i posted why on the triple neg thread, but having personal issues. 4 more abraxane, 4 more, can I make it? I am so emotional today. Oh, I just realized it is my decadron crash day! That make me feel a bit better.

  • justme1
    justme1 Member Posts: 223
    edited October 2011

    I am almost 2 weeks from last chemo and have no enegry go from bed to chair .Thats about all the energy i have right now.Is this normal ? I had hopes of having a couple of good weeks before my surgery .Guess i was wrong I am just as tired  maybe even worse than when i was on weekly taxol the steroids give me a couple good days now i am just wiped out. : (

  • bak94
    bak94 Member Posts: 1,846
    edited October 2011

    Justme-I wonder if the doc would give a low dose steroid for energy after the treatments? It does seem like if you were doing weekly taxol that after the first week off you would feel better, but maybe not. Just the accumalation of all the chemo for 12 treatments can probably take awhile to recover from. I am worried about going into surgery weak also. I will have 4 and a half weeks between my last chemo and surgery, is that about the same amount of time as you? I had a 4 week break in between ac and abraxane, and I really didn't feel much better until after the 2nd week, 3rd and 4th week I was starting to feel a bit better with a little more energy, but not back to normal by any means.

  • justme1
    justme1 Member Posts: 223
    edited October 2011

     i had a 3 week between a/c and that taxol .I had 6 taxol .Today i see my surgen and i think he will give me a date today as to when my surgery will be. I feel like i might freak out once i get a date ,OH the mind games my mind plays. I feel a lil better this morning not alot but some.

  • bak94
    bak94 Member Posts: 1,846
    edited October 2011

    For some reason I felt a little better knowing the date, but maybe because mine is further off than yours! I am sure I will start to freak out as I get closer. I think I am starting to have somewhat of an acceptance now, kinda like lets just get this over with! I know I will be emotional before and after, that is just the way I am wired!

  • justme1
    justme1 Member Posts: 223
    edited October 2011

    I met with my surgen and he wants me to meet with a plastic surgen and talk about reconstruction.I dont want it but he wants me to at lest talk to one. I think that app is friday.He said i will have to feel better before he does surgery anyway so i have a few weeks to get to feeling better.

  • bak94
    bak94 Member Posts: 1,846
    edited October 2011

    Justme, I was the opposite of you! I wanted immediate reconstruction but both my bs and mo said I need to wait. I have to have rads and already had rads on the otherside plus the fact that I have locally advanced bc they want me to wait:( I am not a good candidate fot te's and implants so I have to do diep and not for about a year.

  • bak94
    bak94 Member Posts: 1,846
    edited October 2011

    This has turned into the bak and justme thread:)

    Blondelawyer, how are you? Did you skip town before starting rads or are you already doing rads? I know that going daily for rads and all the other appointments keeps one very busy!

  • blondelawyer
    blondelawyer Member Posts: 327
    edited October 2011

    Hi ladies.  I'm still here, just haven't been checking in.  I've been overwhelmed by everything.  I had my rads set up appointment today and will start next Tuesday.  I am now doing 35 instead of 33 treatments and will be doing Xeloda along with it. My onc also confirmed that I am going to have to do more chemo after rads--another 3 months.  I thought that I would be okay with all of this, but for some reason this radation thing just hit me today.  I think that it is because I had to cancel my thanksgiving plans.  I am SO tired of cancer ruling my life.  And it looks like it will be this way until at least the end of February and that doesn't even include reconstruction!

    The rib issue is still up in the air and that stresses me out because I'll be stage 4 if it is a tumor.  The plan is to zap it with radiation and then rescan when I'm done.  If it is gone, then they will call it a tumor.  I don't know if I can accept a stage 4 dx after all of this.  I may just completely lose it.

    In good news...my hair is growing back and it seems to be growing quickly.  There is a spot in the front/middle that isn't growing in as well, but the rest of it is.  I told my MO that I was going to be mad at him if I had a bald spot :) 

  • 40-years-old-now
    40-years-old-now Member Posts: 309
    edited October 2011

    So tired. Oh if any one is bed ridden dont always sit with your feet up. I did and now if I sit having my feet down for longer then 3 hours (or standing or walking) I feel I ran a marathon. I am so worn out.

    I am all done with chemo and rads. Atleast for now. I have a PET end of month to see where everything is at.

    My physical therapy is done too, now I just have to do the exercises at home myself. I cant wait to drive again. and then walk.

    Take care everyone.

    Candice

  • bak94
    bak94 Member Posts: 1,846
    edited October 2011

    Blondelawyer, will it be a different chemo than xeloda? Do you know which one? Glad you finally get to start rads! That is exciting about having hair again, the bald spot will go away, it seems like mine came in uneven the las last ime  i did this. I still only have some grey thin fuzz, it's kinda funny.

    Candice. sorry you are so tired. I too have been pretty tired and it is no fun. I started walking on the treadmill, but just trying to do it most days is difficult. I just tell myself to do 10 minutes, most of the time I do 15-35, but find myself doing the lesser amount most of the time. I have been thinking of you and glad you checked in. I hope your pet scan goes well.

    4 more abraxane for me. seems like it is dragging now. went pretty quickly in the beginning. SSDI had told me I would have an answer by oct 4 and I didn't so I called back. Now they said they have until the end of the month to give me an answer. Good news is I saw my primary physician for my now high blood pressure and fast heart rate and she said she would help me get ssdi, so if I get denied I am suppose to let her know and she will write something up! I thought that was so nice, as I think my mo thinks I can work, I think he forgets what I do for a living even though I tell him all the time how hard it is on me.

  • 40-years-old-now
    40-years-old-now Member Posts: 309
    edited October 2011

    According to SSD you can work up to $700/month and still receive benefits. I know it is not much but it is something. SSI is more strict. You also have asset limits with SSI

    I hope all goes well

    Candice

  • Beaglesgirl
    Beaglesgirl Member Posts: 287
    edited October 2011

    I rang the bell on Tuesday! I am thankful for all of you and pray for the May chemo ladies everyday. Of course I wrote about the experience on my blog but I will tell you for me it was bittersweet because what I wanted was absolution of the whole thing. But all you get is whatever hope and faith you brought with you to the fight. 

    I see my RO on 10/14.  

  • MamaV
    MamaV Member Posts: 907
    edited October 2011

    Congrats Beaglesgirl!  I have been waiting for you!

  • lifelover
    lifelover Member Posts: 553
    edited October 2011

    Hi May Ladies,

    I haven't posted in a long time mostly because I'm so tired of feeling unwell and having no hair.  I just wanted to avoid even thinking about cancer, no matter how positive and upbeat you Ladies have been on this thread.  But I'm happy to say I've finished chemo and I have some white fuzz on the top of my head here and there.  No rads for me as I had my lifetime limit 17 years ago.  I'm on tamoxifen now.

    Thinking of you all and wishing us quick healing and positive attitudes as we finish our treatments and become disease-free.

  • MamaV
    MamaV Member Posts: 907
    edited October 2011

    Congrats on being done lifelover!  You made it!  You crossed that bridge!  You will start feeling better soon! 

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