For those starting TAC in March/April 2006....

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  • MarciaA
    MarciaA Member Posts: 178
    edited April 2006
    Julie and Shineonme, welcome to the TAC thread. It is comforting having a thread with women on the same protocol. It is very hard and the effects seem to be hard on most all of us. For diarrhea I take liquid immodium. It seems to help calm my stomach too. For constipation I take colace every day and senokot-s when I need more help. I got a sample of aciphex to take daily for the burping and esophagitis and it has made a world of difference for my. I am day 15 from my second tac and I am experiencing some pain in my back and in the bones under my ears (mastoids) Occasionally I experience pains in the breast where my surgery was. I also have a dull headache today. But then I have read where Chemo is cummulative and that some days you actually feel worse than the day before. Julie I hope your temp goes down. I was told to call if my temp went over 100.5. I had fever with my first treatment but not with this second one. And shineonme, I use OTC eye drops and it helps the eyes. Also saline nasal spray for that burning sensation in my nose.
    I will keep you all in my prayers. I light a candle each night I am able for all of us that have cancer, in hopes that we will be given the faith and strength we need to get through this.
    Take care and everyone try to have a restful and enjoyable weekend!
    MarciaA.
  • peejay
    peejay Member Posts: 131
    edited April 2006
    Today was my bad stomach day. Couldn't keep anything in all day, jsut went right thru me. I took Immodium and called the doctor, to make sure that I would be ok getting my port done Monday. He said it would be no problem. Now I just have to get that over with, lucky it's at 6am, so hopefully I can come home and sleep it off.

    Yeah the diarrhea is a killer. Don't even want to drink for fear of "that" pain. And it makes me depressed and feel like a failure. At least I should be ok by next weekend for Easter. Is it Easter already??!

    This board has been a lifesaver for me, and probably my onc too, he's not getting 40 million calls in the middle of the night. Glad to have you all with me, and be with all of you.

    Paula
  • notready
    notready Member Posts: 5
    edited April 2006
    Hi Sherri,
    I am scheduled for my 6th TAC on 4/21, then on to radiation. Did you have radiation? How long did it take for you to get your energy back? When did your hair start growing back. Are you taking Arimidex or anything like that? It must feel so good to have all of this behind you now. I can't wait.
    Thanks,
    Sue
  • MollyK
    MollyK Member Posts: 70
    edited April 2006

    I start TAC this Friday the 14th. 6 rounds every three weeks. Can I join you discussion group? Good to talk with people on the same plan.

  • jpsgirl96
    jpsgirl96 Member Posts: 240
    edited April 2006

    Welcome, Molly. I'm having TAC#2 on Thursday; this is a good thread and seems to cover a good range of the TAC experience. I'm at the lucky end of the scale so far; one totally 'on the couch' day, no nausea (I should say, thanks to good drugs), flew and went back to work on day 6/7. Expecting some cumulative effects, especially fatigue, but had an easy first one. Hoping the same for you. Leigh

  • MarciaA
    MarciaA Member Posts: 178
    edited April 2006
    Anybody else on TAC feeling tired as the day goes along? I am finding I tire so easliy. I am due for my third TAC this week, I hope I can bounce back. It took me two days longer to pep up last time. I read somewhere that it is safe to take Ritalin to help combat chemo fatigue! That would be a rough way to lose the chemo weight! Anybody else feeling tired?
    MarciaA.
  • jpsgirl96
    jpsgirl96 Member Posts: 240
    edited April 2006

    Hi Marcia, Not every day, but maybe 1/3 of the days I definitely hit a fatigue wall, from maybe 3:00 on, and then the energy just doesn's seem to come back. I'm only on #1, and it's the one side effect I expect to persist and get worse. My onc said TAC had three things for sure: hair loss, low wbc (thus Neulasta) and FATIGUE...everything else happens to some, some of the time. Her experience. Leigh

  • peejay
    peejay Member Posts: 131
    edited April 2006
    Marcia, I found that this time I'm having trouble getting energy back also. I'm not sure if it's becuase I had the flu the week before chemo, or the chemo, or both! And now I go for surgery tomorrow for. my port, and I'm terrified. After all the cutting open for the biopsy and then the SNB and clearer margins.. and I'm scared of a little port. Like literally shaking. Blah. I think the worst is the thought of recovering from the surgery AGAIN!!!

    Paula
  • jpsgirl96
    jpsgirl96 Member Posts: 240
    edited April 2006

    Paula, Just a quick word of encouragement re: port placement. I had mine a couple of days before axillary node surgery. The radiologist was great, showed me the port, explained the procedure, answered my questions. The procedure itself was very manageable, only pain was the %#$&# local anesthetic but I was expecting that and it was brief. The pain in my neck was annoying but aided by pain meds, and disappeared in less than 24 hours. I'll be thinking good thoughts for you tomorrow. Leigh

  • svans
    svans Member Posts: 32
    edited April 2006
    Hey ladies, I had a pretty good weekend, felt really good considering where I was on Monday!!! I really would not wish any of this on my worst enemy!!!

    Hope everyone had a decent weekend and I will be thinking of all of you as a new week starts. Take care

    Sylvie
  • JulieMcKeehan
    JulieMcKeehan Member Posts: 11
    edited April 2006
    Hey Everyone:

    Did I just have a strange few days! I went in last Friday for my 1 week bloodwork. I'd come down with a fever the night before (101.9), and called the call center and they told me to get a culture as well with my blood work. The culture was to see if my port had gotten infected. After telling them about my 30 hour diarreha run, and horrifying stomach cramps, they started scrowling at me in a worried way and running more tests. In another hour I got admitted to the hospital where I've been till a few hours ago.

    I so didn't see that coming!!!

    So here is what happened to me, and what I learned from asking a lot of questions of the hospital staff about what things matter in terms of sides effects.

    I had a fever for more than a few hours. This really is what put me in the hospital. Here is what they said. Once they looked at my white count (.6) they couldn't let me go anywhere. If I got a bug I'd go down bad.

    The diarrhea along with the temperature probably meant an intestenial infection and that had them worried as well. So they spent three days pumping me full of three different antibiotics and daily shots of neutripina. My WC went up fast even after the first dose (2.6) and then to normal the next day. By today I felt wonderful, my stomach cramping was down to a minimum and the headache and other stuff was far more managable.

    The most important things to watch for:

    #1- Fever really, really matters. By 24 hours they need to take some action even if you have no obvious signs of an infection. (I didn't- no coughing, no sore throat, no anything but the diarrhea and stomach cramps.)

    This is the place were serious problems happen for people on chemo, so don't ignore it. From now on, I'm going to take my temperature every cycle on days 2-10.

    #2-Uncontrolled diarrhea after 1 1/2 days needs attention.

    #3-Look for mouth sores even if you don't feel things in your mouth. These are signs of serious infection and they need attention. They don't always hurt. (I didn't have any of these, but they searched my mouth twice a day).

    Everthing else is important but not as serious as this stuff , so this is what I am watching during those critical post infusion days.

    I hope this info helps. It is wonderful to be home

    Regards,
    Julie
  • MarciaA
    MarciaA Member Posts: 178
    edited April 2006
    Julie, so sorry to hear what you have been through. It is a reminder to all of us of how serious being on chemo really is. Thank you for sharing such good information. We will all be so glad when we finish our chemo.

    Paula, I hope your port placement went well. Just take it easy for a couple of weeks and let your body try to heal itself. I look forward to getting this chemo behind me and then to the day when I can get my port taken out. (I have herceptin to follow so I am a cyborg chick for at least another year).

    Leigh, My most annoying side effect now besides fatigue is tingling and numbness in my toes and tongue. It persists about 10 to 12 days post chemo now. I don't read where TAC ladies complain of that much but then I guess that is what makes us all have different experiences.

    Take care all and let's get another week behind us!
    MarciaA.
  • kburns
    kburns Member Posts: 37
    edited April 2006
    Julie--thanks for the info and so sorry you had to go through that.

    I am day 13 from TAC #1 and feeling pretty good. Still having some heartburn, but Pepcid complete helps. MY WBC on Friday was 17000 (is it hundred, thousand??) and the onc said it looks like the Neulasta is really working. Which is probably why I feel pretty good! I actually worked in the garden some yesterday (with gloves on)...not sure if I should be doing so, but just had to pull out a few weeds and plan some herbs!

    I really want to get into some kind of exercise routine...espeically during week 3, but it is hard. Even though I feel so much better, I am still fatigued and just a little bit seems to take a lot out of me.

    How's everyone else doing? I know we had lots of TAC # 1 last week.

    Take care and talk later....Karen
  • kburns
    kburns Member Posts: 37
    edited April 2006
    Ooooh...forgot to mention...I am supposed to go to wig lady tomorrow for the buzz cut! Not really seeing any hair coming out yet (and some strange part of me thinks maybe it won't), but I guess I am going.

    DH came home Friday with a total BUZZ! He wanted to be supportive and actually it made me a little less fearful to see him bald first! What I really noticed was how WHITE his head is!

    NOT looking forward to tomorrow.....
    Karen
  • MarciaA
    MarciaA Member Posts: 178
    edited April 2006
    Karen, I think we all secretly hoped we wouldn't lose our hair. I was anxious about losing my hair but didn't realize it until it was buzzed and gone. After that It was a relief because it was one less thing to worry about. You are lucky to have such a supportive husband.
    Have an enjoyable week and good luck with the hair cut and wig!
    MarciaA.
  • MarciaA
    MarciaA Member Posts: 178
    edited April 2006
    Dear TAC Ladies....I have been reading the March chemo thread and feel so envious that some are almost finished with their A/C treatments. And here I am not quite half way through my 6 TACs. I am somewhat comforted there are others like me on the same schedule. Thank you for listening and understanding.
    MarciaA.
  • peejay
    peejay Member Posts: 131
    edited April 2006
    Port placement went well. The surgeon said it went right in, and is all fine. Well aside from the fact that it feels like someone is poking a stick thru my arm there! I'm very relieved, but the tension is going to take a few days to leave my body, it's jsut how I am. At least next chemo I won't be there an extra 30 minutes, nor will I have to worry about being stuck a million times.

    My chest hurts right now, but I took my pain meds like I good little girl, so I'm off for some sleep.

    Paula
  • jpsgirl96
    jpsgirl96 Member Posts: 240
    edited April 2006

    Paula - Thanks for the update - glad to hear it went well. Don't freak if you bruise - I did (big and ugly) but no totally healed. Sweet dreams! Leigh

  • jpsgirl96
    jpsgirl96 Member Posts: 240
    edited April 2006

    Hi Marcia, I have a sort of numbness JUST inside my lips; was worse at the beginning but I still feel the 'weirdness'...my husband jokes that I have no circulation in my extremities anyway so wouldn't KNNOW if they were numb LOL. Starting to prep mentally for #2; hair is shedding like mad (I had it cut really short a month ago but now need to shave or my keyboard is going to clog) Leigh

  • JulieMcKeehan
    JulieMcKeehan Member Posts: 11
    edited April 2006
    Paula, Glad the port is in and mostly okay. I remember that stick feeling!!! It does go away. Mostly now I don't notice (that's 1.5 weeks after). It is actually the stich above where they threaded the tube that really bugs me. The surgeon pulled the skin too tight and its a bump that won't go away. So I fiddle with it.
    Marcia, I wonder about the numbness. Do you have to be super careful when you cut with knives??

    Ohh and the hair thing!! You know, I would say I've accepted the diagnosis with very little denial and went quite practically into the business of what it meant. But this hair thing is the absolute opposite for me.

    I steadfastly refuse to believe that it will fall out. (--Yes I know somewhere in my left brain that it will) The 12 year old girl who also lives up in my mind who has always wanted to be Rapunzel is running around screaming "Touch my hair and you will all die, die, die!!!"

    Anyway, she is definitely in charge of when we cut the hair, not the practical one as I keep trying to tell my sweet beloved family. Everyone from my mother who brings out a pair of scissors and a sweet smile and thousands of silly comments about how cool my head will feel with all that nasty hair gone," to my beloved husband who keeps telling me how very terribly sexy a bald head sounds, to my six year old who now greets me each morning with a kiss and the exclamation, 'Hey, how come you still have hair????" GRRRRRRR. Rapunzel wants these guys to all go away and leave her in her fairy tale.

    Hope you all have a lovely night. See you tomorrow,

    Regards,
    Rapunzel
  • peejay
    peejay Member Posts: 131
    edited April 2006
    Julie- thanks for making me laugh a little this morning. That little six year old must be a real riot!

    I won't get to see my actual port site until this afternoon when the gauze comes off. But I can see where it's gonna bruise like heck. Anyone else have a little numbness in the arm on the side they did it in? Like mostly in the thumb. Like it hurts up that shoulder and straight down the inside edge to the thumb once in a while. what a pain. literally! I'm still nursing a migraine from late last night too..

    Paula
  • MarciaA
    MarciaA Member Posts: 178
    edited April 2006
    Rapunzel, Miracles happen all the time, maybe keeping your hair will be one of them. I had a bump where my port was threaded also but 4 weeks after my port was put in it went away. It must have been those stitches that dissolve. Maybe yours will dissolve also.

    Leigh, Regarding the numbness. I saw my oncologist today. He told me to take 100mg of B6 daily. It helps the digestion and the tingling and numbness. I had my period last chemo and now I am having wicked hot flashes that wake me up. He told me to take 1000mg of vitamin E daily and that should help. I am er/pr- so tamoxifen wouldn't help. He said these vitamins were compatable with TAC. I will let you know if they work. I also got a prescription for acifex so I am hopeful TAC #3 tomorrow will not be too rough.
    Take care all and best wishes in our battle!
    MarciaA.
  • jpsgirl96
    jpsgirl96 Member Posts: 240
    edited April 2006

    Hello Marcia, Thanks for the tips. I got rescheduled to Friday b/c there won't be any doctors on site at the center tomorrow...sigh. Some brain-dead person in the center LEFT ME A CELL PHONE MESSAGE (that I got in DC today) to tell me my chemo had been moved to...TODAY! Oh well...got the onc nurse I had for #1 and she was great, so 8 on Friday. Lucky husband gets to be my chemo buddy this time. Thinking good thoughts for you tomorrow. Leigh

  • peejay
    peejay Member Posts: 131
    edited April 2006
    Marcia - I had my last period on my first chemo treatment.. and I haven't gotten it again. But I have hot flashes at night, its driving me nuts!! I'm going to have to ask what I can do about them.

    Port site looks good, and is healing well

    Paula
  • mindyk
    mindyk Member Posts: 87
    edited April 2006
    Has anyone broke out from either the chemo itself or from the decadron? I don't know if this is one of the side effects or if something is wrong?

    Hope all is getting along ok!

    Mindy
  • peejay
    peejay Member Posts: 131
    edited April 2006
    I had a huge honkin' white head on my face the first time through. I'm still not sure what caused it.

    Paula
  • kburns
    kburns Member Posts: 37
    edited April 2006

    My face is all broken out. Hope it is just from first chemo and not something to deal with throughout! Karen

  • svans
    svans Member Posts: 32
    edited April 2006
    I broke out too, my head and face broke out with red spots. No they are not pimples which is what I thought it was at first, they are just little red spots.
    Driving me nuts.

    Sylvie
  • mindyk
    mindyk Member Posts: 87
    edited April 2006
    Driving me nuts too. Have them on my face, back, neck and in my EARS!!! Called the onc to see exactly what it is from and what I can do fro it! Will post when I find out.

    Take Care,
    Mindy
  • svans
    svans Member Posts: 32
    edited April 2006
    I know, the ears are driving me more nuts than anything else. At least on my head I can wear a hat!! he he but my face and ears and driving me bonkers!! Yes please post and let me know if this is normal!!

    Sylvie

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