onco appt ....recc chemo

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  • Alicethecat
    Alicethecat Member Posts: 535
    edited November 2013


    Hello Paulette


    In case this helps, I'm 22 months ahead of you with a Stage 2 Grade 3 tumour and went through chemo - as well as radiation and Herceptin.


    Like you, I was lucky not to have any spread to the lymph nodes - and I didn't have it in the blood either.


    My docs tell me I'm cancer-free after my treatment and hopefully you will be too!


    Good luck!


    Alice

  • Paulette23
    Paulette23 Member Posts: 499
    edited November 2013


    praying for the best! I saw two doctors they both recommended the same treatment, considering my medical history which is complex.cytoxin/taxotere followed by tamoxifin. including nulasta and antibiotics. ....sounds like a sick cocktail....yeehaaa...all Ill want for Christmas is a head of hair! guess ill be sporting a glitter filled baldie look!! gotta laugh somehow!!!!

  • Melrosemelrose
    Melrosemelrose Member Posts: 3,018
    edited November 2013

    Paulette- Wishing you the best with your treatment plan.  I know the mere thought of having chemo has probably overwhelmed you but keep taking deep calming breaths in.  You will get through your time in chemoland.  I had 6 rounds of Cytoxan/Taxotere with a Neulasta shot chaser ( those Neulasta shots started with my 3rd round of chemo because I developed a high spikey fever/chills after the 2nd round).  I've been on Tamoxifen for 14 months ( I started taking Tamoxifen a month after I finished chemo).  I did what I could do to help myself while in chemoland... kept a daily log of my food intake, my drugs and symptoms, ate well, slept and rested as best I could... iced my fingernails and toe nails, went for walks, etc.  These are things that are in one's control.  Yes, my hair fell out and I never buzzed or shaved my head.  I did cut off my hair into a short pixie.  I had decided that I wanted to see if my hair would really totally fall out from the chemo.  Believe it or not, I was left with a very very thin veil of hair on my head.  I finished chemo in August 2012 and my hair, eyebrows and eyelashes all returned.  If you have any questions, please feel free to private message me.  When you start your chemo, please come to the Cytoxan/Taxotere ladies February/March 2013 thread http://community.breastcancer.org/forum/69/topic/800978?page=47#idx_1388... ( that thread is always open to anyone and has continued past that start date with new people all of the time!).  You may also want to join a chemo discussion thread that begins the  same month as you are start your chemo.  Good luck..... hugs!!!

  • KBeee
    KBeee Member Posts: 5,109
    edited November 2013


    Paulette, The Feb/March 2013 TC thread is not only for people in those months, but is for people in the midst of TC anytime, and is very active. If you read through some of it, it'll give you a good idea of what to expect. I am on TC now, and have completed 3 rounds so far. It is not a walk in the park, but it is doable. In some of the most recent posts, a few of us described our common side effects for someone else about to start. We're all here to guide each other through...good days and bad.

  • Paulette23
    Paulette23 Member Posts: 499
    edited November 2013


    I'm loosing it.......

  • Paulette23
    Paulette23 Member Posts: 499
    edited November 2013


    I am soooooooo alone.....I don't think I can overcome this....after 40 years......I'm tired....

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