How sick after first chemo treatment....?

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OxfordLady1
OxfordLady1 Member Posts: 18

I've just been diagnosed and might (after results from Oncotype DX) have to have chemo but I have a two week vacation planned mid-August - so my question is if I have the first treatment a week before I go away - and then have the two weeks away - will that work? Will I get really sick from first round? Of course I have fingers crossed that my number comes back low! Then this hopefully won't be an issue...thanks for whatever you can tell me - I'm 68 - very healthy otherwise - in good nick from swimming etc.

Comments

  • Spookiesmom
    Spookiesmom Member Posts: 9,568
    edited June 2015

    Hard to say, everybody reacts differently to chemo. I never had vomiting, but had the big D. Some work full time, some just can't. Keep your docs phone # handy, hope for the best.

  • Moderators
    Moderators Member Posts: 25,912
    edited June 2015

    Hi OxfordLady,

    We're sure some others will be by shortly to share their chemo experiences so you know how to prepare, but we wanted to stop by and say hi and welcome to our incredible Community!

    Please let us know how your Oncotype results come back and if you'll be having chemo or not!

    We're thinking of you,

    --The Mods

  • tamkay123
    tamkay123 Member Posts: 56
    edited June 2015

    I would agree that each person is so different. I've had one treatment of A/C. I didn't have a single side effect except my sleep was a bit interrupted but I know that's not the case for everyone.

  • shorfi
    shorfi Member Posts: 791
    edited June 2015


    I sent you a PM.

  • AmyQ
    AmyQ Member Posts: 2,182
    edited June 2015

    Side effects worsened for me after three rounds. The first two were fairly easy, only fatigue and diarrhea. Never had nausea with any of my chemo. Again, we all handle it differently. I think vacation is the perfect way to recover from your first treatment. Much luck to you.

    Amy

  • SelenaWolf
    SelenaWolf Member Posts: 1,724
    edited June 2015

    I took the antinauseants prescribed prior to chemo religiously and did not suffer any nausea or vomiting. However, I did have issues with gastric reflux which was relieved by otc Gavescon.

  • Kicks
    Kicks Member Posts: 4,131
    edited June 2015

    There is no way anyone can tell you how you will react to chemo. Not all react the same to the different chemos. For me, my neoadjuvant A/C did not slow me down at all, adjuvant Taxol had me completely and utterly exhausted. For some, it's the other way around - A/C nasty and Taxol nice. (I was 63 when went through TX - turned 69 today and still NED for IBC.)

    The time frame between infusions depends on depends on the chemo used. Some are every 2 weeks, some every 3 weeks and some weekly. Your Dr is the one who can answer your questions.

    "Getting sick" means different thing to different of us. Are you talking about your immune system being compromised? Nausea? Fatigue? etc.? Again there is no way of knowing beforehand. There is no "One Size Fits All".


  • OxfordLady1
    OxfordLady1 Member Posts: 18
    edited June 2015

    Thank you for your responses....Obviously need to talk to my surgeon about all of this...don't even know what kind of chemo I would have if I need it! Just feeling so anxious about getting away for this much looked forward to and anticipated holiday.

  • Kicks
    Kicks Member Posts: 4,131
    edited June 2015

    Your surgeon is not the one who makes decisions on what chemo may or may not be needed. The Medical Oncologist (aka MO or Chemo Dr) is the one who does chemo. It has been SOP to do neoadjuvant (pre-surgery) chemo for IBC for quite a few years but neoadjuvant chemo is becoming more usual for other types/stages more recently to get 'better' surgical results. Radiation - again not the surgeon's decision but the Radiology Oncologist (aka RO or Rads Dr) to make radiation decisions. It always surprises me how many jump into surgery without seeing a Chemo Dr and Rads Dr to get a complete overview of the complete TX plan first.

    Your ER/PR and HER2 status play into overall TX plan. Family HX? There are MANY 'things' that play into the best TX plan which include Surgeon (the one who 'cuts'), Chemo Dr (the one who does chemo) and Rads Dr (the one who does radiation) as they are each specialists in what they do and all needs to be coordinated.

  • OxfordLady1
    OxfordLady1 Member Posts: 18
    edited June 2015

    Thank you Kicks....actually here in UK my doctor is an Oncologist/Surgeon - Breast Cancer specialist - they have different designations - She's the one who suggested Oncotype DX as I'm in a kind of "grey" zone based on pathology report.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited June 2015

    I recovered from the first tx pretty quickly. As I recall, I was sick (not throwing up kind, dopey from the benedryl given for allergic reactions, and hepped up from the small amount of steroid they give, also for allergic reactions) the first night. The second and third days I was simply mildly nauseated with no appetite and a little fatigued. It didn't stop me from walking the dog, going on errands, going to my bikram yoga class, etc.

    They did seem to be cumulative so the 3rd and 4th were a bit more hard to take. And yes, AC took me down and caused weight loss, hypersensitivity to food, food and other smells, even food commercials on TV made me ill! But I felt a lot better on Taxol.

    Good luck. I hope it works out in your favor. Let us know.

  • 208sandy
    208sandy Member Posts: 2,610
    edited June 2015

    I had no nausea but constipation was my constant companion (solved by warm prune juice) heartburn (solved by OTC Zantac 75 2 x day) and wasn't terribly interested in food but managed to walk the dog, exercise mildly, grocery shop, laundry, etc. was retired but would probably not have wanted to be working full time. Of course your vacation may be to somewhere that you might be in close contact with people and that's kind of a "no-no" . Definitely talk to your drs. Good Luck!

  • ruthbru
    ruthbru Member Posts: 57,235
    edited June 2015

    If you are planning a really active mountain climbing/camping etc. or heavy duty visiting tourist sites type of vacation, I would switch it to a relaxing, laze around vacation. No matter how little or big your SEs, most people are not going to be up for extra excitement. But even with SEs, a relaxing vacation would be good for the spirit. You generally get more worn out as you go along; that being said, I went to my niece's graduation out of state between rounds 3 and 4 of AC without any problems, other than feeling kind of creepy and 'off'. Best of luck!

  • waiting-to-exhale
    waiting-to-exhale Member Posts: 61
    edited July 2015

    I had very little sickness or tiredness with chemo, however AC devastated my white blood cell counts on my first round. I had to be hosptalized for an infection. i was in the hospital for 4 days. Be careful about travelling while you could be neutropenic. If you have a fever you need to get to a hospital fast. You will have no ability to fight off an infection without IV antibiotics.


  • OxfordLady1
    OxfordLady1 Member Posts: 18
    edited July 2015

    Thanks for your help....as it turns out I'm not having chemo as my Oncotype was 21 and there was no difference at all in terms of 5 year outcome if we added the chemo....so it's just going to be radiation and hormone therapy - neither of which I've actually started yet! Maybe my age had something to do with it as well - 68 this August.

  • msphil
    msphil Member Posts: 1,536
    edited July 2015

    hey sweetie everyone s different but i didnt get sick till my last treatment, believe it or not, the meds i was given before helped, good luck, that was 21 yrs ago, (Praise GOD)  hang in there. msphil(idc, stage2, 0/3 nodes, L mast, chemo and rads and 5 yrs on tamoxifen)

  • Hopeful82014
    Hopeful82014 Member Posts: 3,480
    edited July 2015

    OxfordLady, I'm glad you won't need chemo. If you have questions about radiation or wish for some camaraderie and support during the experience, please drop by the Summer 2015 Radiation thread (in the Radiation Forum). You'll find lots of useful information and support to help the time fly by.

  • OxfordLady1
    OxfordLady1 Member Posts: 18
    edited July 2015

    When did you start the radiation/hormone tablets....it's been almost six weeks since my surgery and so far I haven't had any other treatment - I'm getting worried that those little cells are multiplying while they faff around - I'm in the UK with NHS - not like being in the States in terms of being able to call the doctors directly....I heard nothing this week at all - a whole week with nothing happening....My care up til now has been fantastic but it seems like I'm falling through the cracks in the system at the moment! Thanks for your support and help!

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