April/May 2012 Chemo hang out

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  • lsharvey822
    lsharvey822 Member Posts: 257
    edited July 2012

    Good luck girl!

  • Stacie
    Stacie Member Posts: 607
    edited July 2012

    Cool  Hello everyone.  Hope you all have a good day.  My prayers are with all in the BGC today.  I am working pretty hard so not keeping up with everything. 

    When you are PFC please PM me your date in case I miss something in the thread. 

  • nofear2012
    nofear2012 Member Posts: 160
    edited July 2012

    Ok I am soooooo stinking bored. I am not working - took disability, but I have nothing to do during the day. What do u all do if u are not working?

  • IndigoMont11
    IndigoMont11 Member Posts: 1,095
    edited July 2012

    PositivityRocks - Yay for last A/C!!  Warrior Activated - love that!!

    Nofear - what do you like to do? I work but I can only imagine how bored I'd be without the internet.

  • dancetrancer
    dancetrancer Member Posts: 4,039
    edited July 2012

    nofear - I obviously spend a ridiculous amount of time on line.  LOL

    Otherwise, I have rented movies, read books, etc. when feeling really sick.  I did get really bored for a while there when I was super sick and couldn't do much.    When I'm feeling better, I do light exercise (yoga, walking), etc. and love to cook.  Of course there are always projects to work on around the house, but I put those off as long as possible.  LOL 

  • sandik
    sandik Member Posts: 482
    edited July 2012

    Im way behind here. Way behind at work too. Don't know what I've been doing! haha

    As far as my MO, she's a little too meek for me. But, I like her. I think she's confident, but doesn't come across that way. My surgeon and radiologist ooze confidence. But, aren't cocky. I like that in a dr. But, I see her before every treatment. She said she wanted to watch me with the new node development back before I started treatment. She did give me a choice in treatments. She said I could have done my TAC every 3 weeks, 4x or the ACx2 DD then Taxol x12 weekly. She said the second treatment would take longer, but it's the old proven most effective. So, that's what I went with.  She always tells me how good Im doing. Which should be a good thing, but I can't help but wonder why I am having it so easy? Is it not working on me like it should? I know I shouldn't think that way. But I do. 

    Chapter 4, Will be keeping you in my prayers.

    Allie, I am doing rads as well. I will throw anything I can at it I can.  

    Rose, hope the foot heals quick!

    Positivity, be careful this week. That last AC kicks your butt! Rest as much as you can.  

  • Fierro6
    Fierro6 Member Posts: 224
    edited July 2012

    Tomorrow is A/C three of four.  I saw MO and got blood work done today.  My blood results were better than last time and she said I'm doing great.  Since the headaches are not as bad and I can successfully control them with meds, she's not going to cut my steroids further.  I was relieved with that, since I was worried I'd get sick without them.

    As far as sleep, she sort of said I should be happy with six hours.  I know that a lot of people only get six always, but I want my eight!  LOL  She's very happy with my lack of a lot of common SEs (mouth sores, nail issues, nausea, etc) and said that I'm doing great, and Taxol will be easier (We've all heard this, right?  I'm SO hoping it's true for me.)  I only lost 2 lbs this time, so no lectures.   

    My BFF flew in from TX to surprise me, and will go to BGC with me tomorrow.  Tonight, DH and I decided we were going out for dinner (we VERY seldom eat out, and NEVER on weeknights) so I could pig out and eat red meat, etc before not having an appetite for 4-5 days.  We went to Texas Roadhouse and it was fabulous.  Mmmm, steak.

    OK, enough of the check in.  I guess I'll be happy that MO is happy with how things are going, and I'll count my blessings that I've been so blessed in the SE department.  After tomorrow, only one A/C left.  I can do this!  I AM doing this!

  • lsharvey822
    lsharvey822 Member Posts: 257
    edited July 2012

    Almost there Fierro!!  I just told my gf I'm eating like a pig in prep for chemo this week!! haha!  I hope it's a super easy round for you and so glad your onc says all looks well!

  • dancetrancer
    dancetrancer Member Posts: 4,039
    edited July 2012

    Yes, you ARE doing this Rachel!  Wahoo! 

  • Melrosemelrose
    Melrosemelrose Member Posts: 3,018
    edited July 2012

    Fierro6 - Yah Baby.... You got it right!!!! YOU ARE DOING THIS!!!!!!  Happy that your gal pal came in from Texas to see you!!!  Even more glad to hear that your onco says you are doing well.  Wishing you an easy time in the chair tomorrow-- getting your chemo and hanging with one of your friends at the same time..... what a great combo!!!

  • lisa2012
    lisa2012 Member Posts: 652
    edited July 2012

    Rose, heal up and enjoy your puppy!

    Dancetrancer, I think the same will happen to me. Tomorrow it is 3 weeks and I envision my body starting to say, whoa, I get to keep recovering and getting back to health. I also had a small cup

    If coffe this morning- first in 3 months, tasted good !!

  • RoulaG
    RoulaG Member Posts: 239
    edited July 2012

    Hello ladies - I hope everyone has a great week. Good luck to all those in the BGC, I wish you minimal SEs. And for those finishing treatment, a big hooray!

  • hopeful123
    hopeful123 Member Posts: 191
    edited July 2012

    Hello everyone. Haven't posted in a while as i am on to weekly Taxol which has it's own issues. But have been trying to keep up with your posts. I do have a question for the Her2 positive folks here.

    I am a little confused. I am getting weekly Taxol but herceptin every three weeks. Some studies have suggested Herceptin every week for the 12 weeks of Taxol. For those Her2 positive here what are you getting, Herceptin ever three weeks or weekly. Any info or papers that you are aware of as to which is better. Also I am getting 6mgs/kg since I am on the three week schedule. Do you know your dosage. Thanks for your help.

  • RoulaG
    RoulaG Member Posts: 239
    edited July 2012

    Hopeful - I am getting TCH x6, every three weeks. During the 18 weeks of chemo I will be receiving herceptin weekly. After chemo is done I will then be switched to herceptin once every three weeks for the rest of the 52 weeks, for a full year of herceptin.



    Herceptin works better when given with chemo. I actually started herceptin (the loading dose), one week before I actually started chemo. I hope this post makes sense.

  • SadeSurvivor25
    SadeSurvivor25 Member Posts: 119
    edited July 2012

    Hi Hopeful, I'm Her2+ and I'm getting weekly Taxol/Herceptin for 12 weeks then Herceptin every 3 weeks for a year. My onc had originally chosen weekly Herceptin but he said there was no real evidence showing a difference in weekly Herceptin or Herceptin given every three weeks.

  • hopeful123
    hopeful123 Member Posts: 191
    edited July 2012

    Thanks Roula and Sade. That's very helpful. The steroids make me hyper and I tend to freak out about such issues on the day of Tx.

  • nofear2012
    nofear2012 Member Posts: 160
    edited July 2012

    Thx for all yur suggestions. Problem is I really do not have any hobbies or stuff I like to do to keep me preoccupied. So I guess this is a good time for me to start something.

  • SaturnRing
    SaturnRing Member Posts: 36
    edited July 2012

    Hello Ladies,

    It has been some time since I posted, so lots to catch up.

    Positivity - Congrats on the new baby

    Rose- Hope your foot feels better fast.

    Yay to all the ladies who are finishing up with the chemo.

    I am starting the weekly taxol tomorrow. Question to the ladies undergoing / undergone weekly taxol....

    From your posts

    - I have estimated a possible dull body ache on the 3rd day which lasts for a couple days

    What else can I expect with Taxol ?

    - Do you guys have absolutely no queasy stomach at all ?

    - How are your taste buds ? Mine is now 50% shot, I still have appetite, but my portions have largely reduced.

    - How r ur energy levels ?

    I am a little scared to start something new, but I hope it is easier than AC.

    Have a good week ladies.

  • hopeful123
    hopeful123 Member Posts: 191
    edited July 2012

    Saturn-Weekly Taxol SE's for me- sore mouth, slight D, fatigue (exaggerated by my low hemoglobin levels). No nauseau and no real full down days look AC. Pretty able to eat everything except spicy food ( due to my sore mouth). No bone pain or neuropathy yet or me and I am done with four weeks of this. hope this helps.

  • babysammy
    babysammy Member Posts: 74
    edited July 2012

    Apparently I had a reaction to the neulasta.  Bloated up like a pufferfish.  I figured it was the steroids, but my home RN and cancer centre RN says it was neulasta.  Now they want me to take benadryl, I feel like I am over it and dont really feel like adding more drugs into my system.  My mouth is quite sore too, see how the sulcrate works.  Went to the ER last night with fever.  I had just taken tylenol and ibuprofen 45 min before for aching, so was worried about it masking, but my neutrofils were good.  That was a relief.

    Hope everyone is having a good day.  Having a hard time resting today, this sucks.

  • IndigoMont11
    IndigoMont11 Member Posts: 1,095
    edited July 2012

    Babysammy, I'm sure sorry you've had such a rough time. Glad at least your neutrophils were okay. Sending you big hugs and purple energy to feel better soon!

  • lisa2012
    lisa2012 Member Posts: 652
    edited July 2012

    Ditto Babysammy- neulasta reaction AND ER visit, that's a lot. Hope you have un-puffed by now...

  • PositivityRocks
    PositivityRocks Member Posts: 35
    edited July 2012

    Day 1 post last AC and steriods sure are working. Can't get to sleep. And when I do doze off baby Ethan is up n ready for his bottle! DH is working with the bottle feeding also. But somehow I still wake up.

    Side effect: heavy eyes, insomnia, slight headache. No nausea so far and never had with previous treatments. Occasionally get a slight metallic taste in my mouth. Appetite is as normal, or sometimes even more than usual. I wonder if its the steriods. Extreme fatigue!



    Wishing every1 a very restful night.

  • lsharvey822
    lsharvey822 Member Posts: 257
    edited July 2012

    Big hugs Positivity!!  If I was closer I would totally help you with baby Ethan!!  my youngest is almost 12 so I haven't had good baby time in forever!! :)

  • LyndaMarie
    LyndaMarie Member Posts: 92
    edited July 2012

    I haven't posted during most of my treatment so far. I have just finished 12 weeks of weekly Taxol with Carboplatin every three weeks and ABT-888 [PARP inhibitor for clinical trial] orally twice a day. I start 8 weeks [4 treatmentsts] of DD bi-weekly AC tomorrow. The taxol phase went quite smoothly. I had gome fatigue, was emotional, minor neuopathy and metal mouth. It was all worse on carboplatin weeks. During that phase I also had thrush and a very mild case of shingles. They both cleared up quickly.

    Tomorrow, however, is the start of something new and the unknown is difficult. I managed a small vacation [3 days] after my last taxol infusion last Friday and just wanted to run away and skip the whole AC part. Obviously that is not an option so here I go... onto chemo phase 2...AC.

    I hope you all don't mind my jumping in here so out of the blue. I welcome a place to discuss all of this. I am very optimistic but, as I said, the unknown is scary. I hear that AC is harder than taxol and I do not like that idea. I will try to check in regularly and answer any taxol questions I can.

    My chemo is neoadjuvant so I have not had surgery yet. I have that coming up in September. Rads are also still up for discussion, possibly yes, possibly no... Many decisions still to be made.

     Hope you all have a fabulous evening!

    Lynda

  • lsharvey822
    lsharvey822 Member Posts: 257
    edited July 2012

    I have a completely different protocal Lynda but I can tell you you couldn't have landed at a better place then here.  We have some amazing ladies here that can help quide you.  and in the meantime I can tell you that one consistent is that the unknown scares us but often times more then it really should.  And we have a motto here - no sister left behind!  so we are here to carry each other thru no matter what!

  • Fierro6
    Fierro6 Member Posts: 224
    edited July 2012

    Lynda, welcome.  First: You have landed in the midst of some of the most knowledgable women I've ever come into contact with (seriously answers in layman's terms within an hour, instead of technical jargon that may be outdated online or waiting for a call back from a medical professional that's never had cancer.)

    Second:  They are also the most welcoming bunch of women!  I was nervous at first because so many of them seemed to have formed friendships already and I felt like I was crashing the party.  After my FIRST post, I felt loved, helped, and a part of the group.  You pop in and ask whatever questions you have.  SOMEONE will have experienced it, or done hours of research on it.

    I am on DD A/C, which will be followed by DD Taxol, so we're opposite.  I've been told that Taxol is easier, but you've described the side effects that I'm having on A/C.  Some fatigue, headaches, and emotional.  No metal taste or neuropathy for me yet. 

    Hang in there.  You just added a LOT of friends/help to your arsenal. 

  • IndigoMont11
    IndigoMont11 Member Posts: 1,095
    edited July 2012

    Lynda, I just finished A/C three weeks ago. I didn't have an overall awful time. I do have the bitter taste off and on, took all the meds to prevent nausea and avoided trouble every time but one. Worst for me has been fatigue and emotional ups and downs. I hope your SEs will be minimal, too, and that the neuropathy improves. Welcome aboard.

  • bcbarbie10
    bcbarbie10 Member Posts: 319
    edited July 2012

    Hello, ladies! I have just been lurking the past months but i started AC last April 26. Now im halfway done with my chemo!!!! I will be doing taxotere x4 every 3 weeks starting two weeks from now with weekly herceptin x12. I prefer to see the cup half full. Im halfway through!!!

    I cant help but feel apprehensive about my next step, though. I have heard that generally taxotere se's are gentler than AC, and im hoping this will be so for me.

    I have learned a lot from this thread, and i feel im not alone.

    God bless us all.

  • vballmom
    vballmom Member Posts: 426
    edited July 2012

    Lynda, I just finished A/C last week.  Someone used the word "manageable" to me and I think it's a good one.  One day at a time, one side effect at a time.   We will help you get through and since none of us sleep, one of us is usually covering here 24/7!

    bcbarbie, we are a no girl left behind group.  You are definitely not alone!  Halfway is a great milestone.  I'll be on Herceptin for a year, so we'll be in together for the long haul!

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