February 2014 Starting Chemo Club

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  • tangandchris
    tangandchris Member Posts: 1,855
    edited March 2014

    Hi ya'll....princessrn, I am using Clearning for a Reason too, they actually came yesterday. It's so nice :)

    I'm kind of annoyed, I called MO this morning and left a message. Didn't get a call back till late this afternoon and was told to come in tomorrow for blood work if I wanted to. I haven't been dizzy since, but I'm havig bad stomach cramps today. Also, when the nurse called me back it went to vm, so I didn't actually get to talk to her. Not sure what that means...if I want to come in for blood work. I mean do I need to or not??

    anyway, purple...I took advantage of my feeling good last round too. I really am hoping that starts soon for me. I'll be 7 days out tomorrow....soooo soon right? :)

  • purpletron
    purpletron Member Posts: 9
    edited March 2014

    And now it's suddenly busy around here! Ha ha, hi everyone.

    lago, I sure hope I'm like you and find it easier as I go!

    tangandchris, I HATE it when they leave things like that up to us. I'm very happy when they present evidence and arguments for and against and include me in the decision-making process, but things like this... ugh. Either way, I hope you'll be feeling better in no time!

  • princessrn
    princessrn Member Posts: 370
    edited March 2014

    tangandchris...  I'm on different regimen but I had severe abdominal cramps for days. I asked for Bentyl. You could ask your MO and see if this might help you too.  

  • Sicilian
    Sicilian Member Posts: 49
    edited March 2014

    I am officially 3/4 of the way there! Had my treatment today. Had a new nurse. He was good, but he kept asking ME questions about the treatment!

    I was hoping to be able to skip my Neulasta shot, but my white count went from 13 to 7 in the last two weeks. While the 7 was perfectly fine to go ahead with chemo, my doc considered it a downward trend that made it too potentially dangerous to skip the shot. So disappointed.

  • KAT4856
    KAT4856 Member Posts: 67
    edited March 2014

    Hi Macintx,

    Just checking in with you. How did your second treatment go? Hope everything is well

  • tangandchris
    tangandchris Member Posts: 1,855
    edited March 2014


    Morning ya'll!

    I just started having some eye twitching over the last couple of days. I think I'm blaming everything on chemo, but is this a chemo thing? Has anyone had this? It's not terrible, but annoying you know?

  • lago
    lago Member Posts: 17,186
    edited March 2014

    I had that with Taxotere (known as Taxotears). It's really annoying when your eyes are out of sync. I also had watery eyes at the end too. Made it really tough to read a book or look at my cell phone.

  • dancetrancer
    dancetrancer Member Posts: 4,039
    edited March 2014

    Yep, you can blame that one on chemo, too.  I had it as well.  So very annoying! Along with the dry eyes (systane eye GEL helped me a lot with the dry eyes).  Just gotta wait the twitching out. 

  • Macintx
    Macintx Member Posts: 118
    edited March 2014

    My second AC went well.  Day 3 was the only day I felt strange last time, and it was this time too, so far that is.  Don't want to jinx it!  But, I didn't feel quite as tired or weird this time.  I just kind of had a lull in appetite yesterday and took a long nap.  By the end of the day, I felt like I needed to burp all the time but couldn't.  That feeling is still lingering today, but it isn't really stopping me from eating.  I've never had indigestion before, so I don't know what it feels like, so maybe this is a little indigestion?  Not sure if a prilosec would help or not.   Overall, though, I will take these minor SEs over anything else.  I'm venturing out with my new buzz cut and baseball cap today.  I thought about just rubbing my head with a towel til it all came out, but I kind of want to keep a little hair on my head while I can.

  • KAT4856
    KAT4856 Member Posts: 67
    edited March 2014

    Macintx,

    Glad to hear it went well again. I know what you mean about keeping some hair. I never did buzz mine. I was left with just a little on top that made me feel a little better. Just could not bring myself to buzz it.

  • KAT4856
    KAT4856 Member Posts: 67
    edited March 2014

    Macintx,

    I had the burping with the Taxol chemo and found that Gas X helped.

  • Njmom3
    Njmom3 Member Posts: 143
    edited March 2014

    Had my second round of iron yesterday. I hope it works!  I'm still feeling tired.  I have a runny nose and when I cough or breathe in my chest hurts, so I don't know if I have cold or something else going on. I'm petrified to get sick!  I have some antibiotics left from my surgery and tempted to take them, but then again I don't know if I should.  I also have a headache, but that is a se from the iron infusion.  I'm tired if feeling like a hypochondriac!

    I had an eye twitch the day after my second chemo and I wondered if it had anything to do with it, now I know!  

    Hope everyone has a great weekend!

  • h0pe
    h0pe Member Posts: 125
    edited March 2014

    Hi All,

    Just had my #3 dd AC today. Feeling pretty fatigued, even with the steroids. Labs today were a little low, but high enough to still do chemo. My hemoglobin was low too; MO said it will probably only get lower since SE's are cumulative. That explains all this fatigue. I asked about changing my diet to help the counts, but he said counts probably won't go up until i'm done with chemo. They say your counts do improve on Taxol.

    Hope everyone has an uneventful, normal as can be weekend!

  • lago
    lago Member Posts: 17,186
    edited March 2014

    Njmom3 if you don't do a full course of antibiotics when you need them you  could make the situation worse. Call your onc. Let him/her know about  your chest/breathing issue too. You know when your body isn't right. This is NOT the time to think your a hypochondriac. This is a time when better safe then sorry is best.

    h0pe you're getting closer to that finish line!

  • tangandchris
    tangandchris Member Posts: 1,855
    edited March 2014


    I'm going to try the eye drops, I have noticed my eyes are extremely dry. I'm glad there is a reason for the twitch :)

  • KAT4856
    KAT4856 Member Posts: 67
    edited March 2014

    Hi Hope,

    I just finished my 3rd Taxol and it is true your WBC will go up on Taxol. Mine went up so high I did not need the neulasta for my 2nd Taxol

  • KAT4856
    KAT4856 Member Posts: 67
    edited March 2014

    I've been consistently drinking (8) 8 oz glasses of water through my chemo. I have completed seven treatments one to go. I find that the water helps fatigue, dry eye, constipation etc.

  • h0pe
    h0pe Member Posts: 125
    edited March 2014

    KAT4856 - congrats! you're really getting close to the end of all this and beginning of a new start! How'd you think the Taxol Se's are compared to AC? 

    Day 2 - actually better than day 1 of chemo. I lowered my decadron to 4 mg with ok from MO. That stuff got me too wired. Taste is going. i have dry mouth, but I knew that was coming. Feel kind of like I have a head flu. Neulasta shot tonight. Will update you all if there are any unusual SE's! 

  • KAT4856
    KAT4856 Member Posts: 67
    edited March 2014

    Thanks HOPE only one more treatment to go which will be in eleven days. I definitely found the Taxol SE's better. I was very lucky even with the AC treatments I only experienced fatigue, loss of appetite and no taste buds. With Taxol my appetite is back and my taste buds, a little fatigue around days 3-5 and some achy feelings from the Neulasta that Advil helps. But I can honestly say I feel much better on the Taxol than I did on the AC. I don't know if some of that is because I am closer to the end than the beginning but I'll take it either way.  Hope all goes well with your treatments

  • h0pe
    h0pe Member Posts: 125
    edited March 2014

    Kat - did you do dd Taxol? I'm doing 12 weekly taxols. will be done in June-Julyish. 

  • Sicilian
    Sicilian Member Posts: 49
    edited March 2014

    Feeling a bit blue today. Hate the weekend after a treatment. Between the queasiness, the exhaustion, the bone pain, the thrush, I just want to bury my head until Tuesday, when I finally begin to feel a bit better.

    Saw my surgeon for a checkup. She's amazing. She wants me to join her support group, but I've never been much of a joiner. It might be a good idea, though.

    In the meantime, since I'm such a boat anchor this weekend, I made reservations for me and my husband for next weekend at one of the nicest local restaurants. It's restaurant week, so you get a 3 course meal for $30, and the menu looks delicious. It will be nice to just get out and do something normal.

  • lago
    lago Member Posts: 17,186
    edited March 2014

    Sicilian After a while I too got that "I don't want to play anymore" feeling and at times blue but I made it through. You will too. I would be excited for restaurant week. Also you can always go to the support group and if you don't like it don't go back. You never know till you try. I've heard mixed reviews about support groups. I think it really depends on who is in the group.

  • Sicilian
    Sicilian Member Posts: 49
    edited March 2014

    Thanks, lago. It's just hard to keep chugging along sometimes, but it's not as if we have a choice, so chug, chug, chug (but not the fun kind lol).

    I AM excited about restaurant week. This restaurant is fantastic and extremely expensive, so this way we'll get a nice treat that we can afford (I don't need to tell everyone about the damn medical bills, even with pretty darned good insurance).

    I hope everyone has had a decent weekend. At least this was my last Neulasta shot! And only one more chemo treatment to go. My doctor assures me that radiation is a walk in the park after this!

  • jbokland
    jbokland Member Posts: 890
    edited March 2014

    Now that I finished the 4 rounds of AC, I am cautiously looking forward to Taxol for the next 12 Fridays.  I met a chemo nurse from another state, (Michigan) and she said that her patients keep their finger tips in ice during treatment to minimize any neuropathy in fingertips...anyone here of this?

    I am getting married the end of June (3 weeks after last Taxol tx).....I wonder if I will have any hair then or if I shall continue to bedazzle my head.

    BTW...I enjoy the bedazzling.  I wore some on my head yesterday and stopped at the grocery and by the hospital to visit someone in the ER....it opened up lots of conversation with strangers and supportive comments.   Embrace the bald!

  • Atiteca
    Atiteca Member Posts: 7
    edited March 2014

    Sicilian, thanks for your chug, chug, chug comment, it made me laugh and is so on point.  I'm having such a hard time and it makes me feel like I'm somehow wimpy because I'm getting all of these SEs.  My onc made it seem like I would have no problem working, but I've been so sick and missing so much time even on my non-chemo "off" weeks.  I've had fever again all weekend and am on my 3rd antibiotic for this mystery fever that they assume is viral but they want to keep me on the antibiotic to be cautious, but they really don't know.  It's been on and off (mostly on) since the 28th of Feb. and it's really wearing on me.  And now I can't eat,  everything that goes down just gives me stomach pains, even water.  I was able to just get down a few saltines, so that's a small victory.  I promise ladies I'm normally a very positive person, but this is a comfortable space for me to vent so thanks for listening.  I have my 3rd AC this Thursday. I can't wait until I get to Taxol as well. I'm really hoping it's a big improvement over the AC. I'm not sure if adding Carboplatin in will increase my side effects though?  My Onc is recommending since I'm triple negative.  Any insight on Carboplatin ladies? 

    h0pe and Kat, I'm also curious about DD taxol vs. the 12 week regimen.  I'm scheduled for DD, but if the 12 weeks is easier I think I may want to go that route at this point.  Not sure how the carboplatin will fit in with that though...

  • KAT4856
    KAT4856 Member Posts: 67
    edited March 2014

    Hope,

    Yes I did the dd Taxol they never mentioned to me about weekly Taxol. Maybe because the drive to Boston takes 1 1/2 to 2 hours each way so that would be hard to do every week. I would expect the SE's to be even better with weekly Taxol.  June sounds like a long way off but you will be surprised how quickly it goes by.

  • KAT4856
    KAT4856 Member Posts: 67
    edited March 2014

    Atiteca,

     The only SE I have had with the dd Taxol is aches in my bones and joints when I have the Neulasta shot the day after  the Taxol. The 2nd Taxol treatment I did not have the Neulasta shot and I did not get the aches.  I had the discomfort Saturday and Sunday (3rd & 4th day after treatment) had to take 3 Advil last night but it really is not bad. Other than the aches I've had a good appetite and good taste buds, no naseau, some fatigue.

  • Macintx
    Macintx Member Posts: 118
    edited March 2014

    Kat4856, glad to hear about your minimal side effects with the DD Taxol.  Since the Nuelasta doesn't seem to give me the aches and pains that a lot of people experience, I hope I do as well as you on it!

    jbokland, I asked my MO about icing and he didn't seem to think it would make much difference.  I know a lot of people do ice, but I do know of people that were told that they should only ice if they start seeing changes to their nails or if the neuropathy is bad.  So, I guess, different docs make different suggestions.

  • h0pe
    h0pe Member Posts: 125
    edited March 2014

    JBok- I've heard of many people icing with taxol; however, my MO didn't suggest it. The only thing he suggested for me to ice is my mouth with sore gums.

    Kat- Thanks for the encouragement! Plan is to do 12 weekly taxol. MO says it's supposed to be a lot more tolerable. Can't wait to be done with all this. So tired of no energy and no taste! one more dd AC to go next week. 

    Hope everyone is doing well/better. 

  • lago
    lago Member Posts: 17,186
    edited March 2014

    Atiteca I did Carboplatin with Taxotere. I think the Taxotere was causing most of my issues.You have to stop beating up on yourself. Adriamycin is really tough stuff. Most of my friends that were on it got wiped out from it too. I don't think I could have done Taxol. I had some neuropathy on Taxotere (Not bad but I still have some in my left heel) and all my nails were ruined on it. Taxol has a higher risk of neuropathy so be one the watch for that. If it's bad they will reduce your dose.

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