March 2012 chemo

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  • tc9876
    tc9876 Member Posts: 136
    edited March 2012
    Amy:  I had my heart checked because of the Herceptin drug which has heart damage as a side effect.  I don't think that it is a standard procedure.
  • brax
    brax Member Posts: 98
    edited March 2012

    Wondering if headaches are a side effect.  Terrible, terrible headache and some strain around jaw.  Not a normal occurence for me.   I'm 3 days out from first TCH treatment and this headache is something else.  Wondering if anyone else has gotten them? 

    And TC9876:   I also had heartburn.  For me days 2 and 3 after treatment.  So far, none today:)

  • Sissydi
    Sissydi Member Posts: 516
    edited March 2012

    Brax......yes! Headache after 1st treatment....for 5days straight! Tightness in jaw, for sure. My onc says it could possibly be from dehydration (are you drinking? I wasn't), or just a plain old side effect.



  • Sissydi
    Sissydi Member Posts: 516
    edited March 2012

    Also ladies, I told my onc nurse about my struggles with nausea, and she said get Canada Dry Ginger ale, and warm some up like a tea......it will really help. Also, the heartburn, I know what your saying! I chewed a few Pepcid tablets, and it helped.

  • GeorgiaMom
    GeorgiaMom Member Posts: 66
    edited March 2012

    So happy to find this group.  I just decided today that I will do chemo.  My oncatype DX came in at 20.  I was so hoping to avoid chemo but know that I have to fight it with everything I have and not look back, so here I am.  I was hoping to start on Friday, March 9 but have to see if I can get a port placed by then. I I want to start and finish as soon as possible. I believe that I will be getting TC X4.  Feeling very nervous but also relieved that I have made the decision and am ready to proceed. 

  • journey4life
    journey4life Member Posts: 517
    edited March 2012

    Sissydi - even though I don't have a start date, would you add me to the list? A/C x 4  T x 4  Thanks.

  • Sissydi
    Sissydi Member Posts: 516
    edited March 2012

    Hey girls, if I screw up on the list, let me know, as I have chemo brain, lol!

  • kokonut
    kokonut Member Posts: 9
    edited March 2012

    galena_79 - No, they haven't found a primary tumor.  I'm wondering if my MRI will find one Wednesday.  Mammo, CT Scan and PET Scan showed nothing in my breast.    I went to dr for swollen lymph nodes under my arm and had a sinus infection. They were thought to be swollen from that.  They just sent them to be checked because they took them out and it's standard procedure not expecting it to be anything else. 

    PET Scan showed all three levels of breast lymph nodes and also nodes in my neck and chest.

    I got my port this morning. All went well.  I'm sore now, but it's not as bad as the incision from the biopsy.  Chemo starts Thursday, still don't know what yet.  Will update as soon as I do. 

  • zillamom2
    zillamom2 Member Posts: 28
    edited March 2012

    Hi. I am new here. I just found out today i will be getting taxotere/ cytoxan x 4 on 3/15. I had idc stage 1 in march 2001. I was 28 yrs old and had AC x 4, lumpecomy, rads. On 2/6/12 i found out i have idc again on same side. Ucla tumor board reviewed my case and inconclusive as to whether it is local recurrence or new primary. If they were to stage it - onc said stage 1 again but if recurrence they dont normally restage. It has been 11 yrs since 1st cancer and i am 39 now. On 2/23 I had a bmx with immediate diep reconstruction. Up until i had the oncotype the onc didnt think i would need chemo based on path but onco score came in at 27. So joining your group if that is ok and glad there is a board to offer support. Even though i did chemo before it is still hard and ithas been a long time. 1 st time my son was 15 months old - now i have a 12 yr old and a 8 yr old who i had post treatment. : )

  • Alicea
    Alicea Member Posts: 36
    edited March 2012

    Hi Marchers,

    I am now able to fuzz my way through the haze I have been in for the past few days. Day 4 was a wash for me, I could not even keep my eyes open to eat, it wasn't tired but a feeling of complete helplessness. I am feeling much better today and was able to work from home for 5hrs. Still feeling a bit dizzy and light headed, a stray headache hear and there. The taste bud is completely shot. Everything taste of metal or salt. But all in all I was expecting much worst, so still happy with day 6. Has anyone else been passing gas, I spent all of last night in a fetal position just passing gas.



    Welcome to all the newcomers !!!! Margaret hopefully your have minimal SEs after your treatment.



    Wishing all minimal SEs and lots go HUGS!!!!!

  • Sissydi
    Sissydi Member Posts: 516
    edited March 2012

    Was Margaret the only one that started today? Hope your doing okay sweetie!

  • Sissydi
    Sissydi Member Posts: 516
    edited March 2012

    Yes Alicea, gas was and still 7 days out, a big issue. Been taking a lot of Pepcid. I don't even remember day 4. Good for you, you were able to feel productive with 5 hrs of work done! Hope everyone else are dealing with gentle S.E. 's!

  • Sissydi
    Sissydi Member Posts: 516
    edited March 2012

    Welcome Zillamom!

  • QuinnCat
    QuinnCat Member Posts: 3,456
    edited March 2012

    So if chemo began on Thursday, is that Day1? If so, Day 5 didn't work out so well. :)



    Zillamom- i'm sorry you have to go thru this again. Welcome.

  • Kadia
    Kadia Member Posts: 314
    edited March 2012

    Welcome new Marchers!



    Brax, I still have an on and off headache 7 days in. Argh!



    Went back to work for the first time since the infusion today. Lasted 4 hours, then had to come home and vegetate. Am definitely feeling some fuzziness when I try to concentrate.

  • Masserz
    Masserz Member Posts: 92
    edited March 2012

    Hi ladies- for those asking the day of treatment is considered Day 1. It's good to know so you can communicate timing with your medical team because that's how they will think of it.



    For anyone worried about the TEs and implant, the TEs feel nothing like implants. I had implants prior to my BMX and so had space in my muscles for the TEs and even mine are super firm and uncomfortable. You can probably also feel where the different materials are or maybe even folds. Your implants will be soft and comfortable and because you have TEs they will feel more natural right out of surgery. I can't wait to get mine switched out. I'm going with silicone as I had saline before and know they won't look natural without any breast tissue over them.

  • Masserz
    Masserz Member Posts: 92
    edited March 2012

    Oops...I also meant to welcome our new friends. You've found a good place for support here!



    Oh and I finally got my chemo scheduled for this Thursday. I've been going through the older posts picking out all of the advice for what to bring or have on hand. Thanks again for your kind advice and willingness to share! My MIL made me the most beautiful tote bag to use for my chemo kit. I wish it were for a more fun purpose...

  • Msbelle
    Msbelle Member Posts: 235
    edited March 2012

    Alicea: you described me exactly. It's gets better. I felt like myself on day 8.

    Masserz: went to therapy for the first time today because of these TE. Very intense stretching by therapist of my entire chest. I hope I can move tomorrow. She said I am extremely tight. I can't wait to get these things out and get the implant. Thanks for the light at the end of the tunnel :) praying for you Thursday

  • Hannahsnana
    Hannahsnana Member Posts: 9
    edited March 2012

    Golly Gee Wiz..........can't leave you girls alone for a minute!  Worked my 8 today though not happy about it.  So much to catch up on!

    And unfortunately I see we are still growing!  Welcome to the new ones.

    Masserz, Margaret, Kokonut, Georgia mom wishing the best to all of you this week.

    Kam170 if chemo day was Wednesday, day 4 did not work out so well here.

    Sissydi, Alicea, I think gas was my worst problem of all since Thursday after chemo on Wed.  I knew I was not constipated at that point, but did end up that way and only today feeling a little better after a little action.  Took another laxative tonight, gonna knock it out one way or the other. My stomach flat out hurt bad yesterday!  Almost feel like wanting a different sort of action now!  Just teasing, not yet!

    Yes taste buds gone south, bannana pudding was the only thing good. My husband made it for me yesterday and I had more tonight for dinner.

    Msbelle, I am holding you to day 8 - 2 to go and not a day later. 

  • Masserz
    Masserz Member Posts: 92
    edited March 2012

    Thanks msbelle! Let us know how the PT goes. I may ask my PS about it too. I'm so tight I feel like it's hard to sit up straight. I just got the drain removed from my ALND so I'm only now able to do much stretching again. I have cording again already on that side now. So bummed!



    Lisajcj, how's your cording issue going?

  • galena_79
    galena_79 Member Posts: 107
    edited March 2012

    End of Day 9, and I'm feeling really sorry for myself. I'd had a good day, felt pretty normal. Then, at about 8.30pm, I started to feel nauseous and took 2x Domperidone pills. First ones for a couple days.

    Within half an hour, I threw up. :( I spent 2-1/2 hours sitting quietly, sipping on water, but then threw up again half an hour ago. :(

    I'm fed up with this. Really thought I was past the worst of the wacky gastric SEs, but apparently not. Perhaps I have to keep taking my anti-nausea / anti-constipation drugs every day until chemo is over.

    Feel like I'm going to cry. I just want to feel comfortable and get some sleep!

  • tc9876
    tc9876 Member Posts: 136
    edited March 2012

    Hello Ladies, It's sad but I feel a strange sense of comfort knowing that I am not the only one suffering.  Today is Day 6 and I still feel like I am still in a fog but less so.  Day 2 of work and I truly do not want to be here.  No nausea or anything though...just general malaise.  I have been sleeping like a rock.  Heartburn went away, taste buds are subpar.  I've been eating a bit of junk to see what will stimulate the taste buds.  Nothing thrills them. 

    I keep reminding myself that this too shall pass.  We will make it through!

  • journey4life
    journey4life Member Posts: 517
    edited March 2012

    Galena - have you called your onc to see if he/she can prescribe something for your nausea? Maybe you don't have the "right" stuff that will work for you. 

    Masserz and Msbelle - I asked my PS about PT and he doesn't want me to do it right now. He told me to continue with my ROM stretches, especially on the right (ALND). I have to confess I'm not doing them as often as I should so I still have discomfort.

    I thrilled to know the implants will be nothing like the TEs! I envisioned a lifetime of repositioning myself in bed to find a comfortable position to sleep! As the TEs expand, do the folds go away?

    Prayers and hugs to those starting tx this week. WE CAN DO THIS!

  • Sissydi
    Sissydi Member Posts: 516
    edited March 2012

    (((((galena)))))))).



    (((((tc9876))))))). Hugs to you both. All this bragging about eating, and last night I had an episode like galena. And TC, my chemo brain is bad too. I had to take 2 Benadryl to knock myself out to get some sleep.



    Remember we are in this together. Your not alone. Hang tough girls.....it will all be over in a few months time. Remind me of that after my tx #2.

  • QuinnCat
    QuinnCat Member Posts: 3,456
    edited March 2012

    Galena - I'm sorry to hear you are having such problems with nausea. My heart goes out to you. Maybe just getting back on top of your meds and like you say, taking your anti- meds every day will get you back on track. Sending you positive thoughts {{{{hug}}}}}

  • kltb04
    kltb04 Member Posts: 1,051
    edited March 2012

    Hi all. I am new here and have only posted once. I am supposed to start chemo on march 12th to the best of my knowledge. I have a PET scan tomorrow, a MUGA and CT AND port insertion Friday and then onto the oncologist Monday for "education" and to get started. All the drug names went in one ear and out the other at my first meeting with the onco so I will post more when I know more. Oh and I am having neoadjuvant chemo bc that us the way my surgeon/onco proceed these days do the only surgery I have had so far is my sentinel node biopsy. Best to all.

  • KCB
    KCB Member Posts: 365
    edited March 2012

    Hi Everyone! I'm new here, first time joining any sort of online discussion board... but it is time. Starting chemo one week from today, and getting nervous. So good to know I'm in good company here, and there's a place to come to air out questions, issues, thoughts, triumphs, whatever...I'm in Canada, and will be doing FEC-D, 6 cycles. Anybody else?

    Also, anyone with young kids here?

  • brax
    brax Member Posts: 98
    edited March 2012

    Hi everyone.  I agree with TC.  I am also at ease that we all have this place where we can lean on each other and share our highs and lows!  I am right behind your TC, today is my day 5.  Still have the headache and the jaw pain comes and goes.  Another problem I have is I must have been in the bathroom 5 times last night.  I kept waking with stomach pain.  All together I must have went a dozen times yesterday.  What is up with that?  No more senekot for me. 

     I have been lucky in that I have not really had much nausea.  I made a scrambled egg this morning and I could taste the butter I melted in the pan.  It was "gross".

    Galena, my heart goes out to you.  Lisajcj is right maybe there is something more they can prescribe.  I am new and don't know all that you are taking, I had the tiniest bit of nausea upon waking.  I was very lucky.  I took emend, zofran, and compazine.  My nurse told me to interchange the zofran and compazine whether I needed it or not for at least three days.  Hope you have a better day today.

  • brax
    brax Member Posts: 98
    edited March 2012

    Welcome Katy!  I am on day 5 of my first treatment.  I am getting 6 rounds of TCH.

  • kltb04
    kltb04 Member Posts: 1,051
    edited March 2012

    I have an 8 and 11 year old Katy. Thank goodness they are old enough to understand somewhat and be a little more independent but worrying about them is the worst part of all this for me. How old are yours?

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