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Taxotere, Carboplatin and Herceptin

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Comments

  • dragonfly1
    dragonfly1 Member Posts: 516
    edited May 2011

    Sharonann How are you feeling at this point? I hope the side effects are beginning to ease...

    Marylou Welcome to our group. I hope your first chemo went well today. Are you receiving TCH including Herceptin i.e. are you HER2+?

  • lilylady
    lilylady Member Posts: 478
    edited May 2011

    sewingnut-I have chemo envy-I go for #4 tomorrow. So happy for you!! Doing that happy dance thing!!!  Lots of TCH girls have finished up here in  the last 3 weeks. Hope this last one treats you well.

  • pasmithx2
    pasmithx2 Member Posts: 224
    edited May 2011

    Another TCH down. The end seems so much closer now that #4 is over and done with.



    We have a chemo bell that people ring after their last infusion. I find that signal that someone is finished makes me emotional. I had my sis-in-law welling up along with me. I guess I just wish it was me ringing the bell.



    I got my Carbo which was a relief. I was worried that I could be delayed or they would want to catch up the Carbo at the end. The shortage is still a problem but they're using what they have for those of us already on it and new people might get an alternative for the time being.

  • AmyIsStrong
    AmyIsStrong Member Posts: 426
    edited May 2011

    Sewingnut - CONGRATULATIONS. What a wonderful day. You made it!!!

    Pasmithx2 - congrats on #4 being behind you. Only 2 to go.  My chemo room did not have a bell, but my rads office did.  I also found it very emotional when I heard it ring.  When it was my turn, I broke down and sobbed with relief, even though rads were not difficult at all for me. I think there was just so much pressure built up inside of me through the whole ordeal.  In NO TIME at all it will be you ringing that bell. BE SURE to have someone there to take pictures. Or better yet, photos AND a video!

    Amy

  • libraylil
    libraylil Member Posts: 325
    edited May 2011

    And happy dance for b9 lymphy. Libraylil

  • pasmithx2
    pasmithx2 Member Posts: 224
    edited May 2011

    amylsStrong--I'm not sure I want pics, let alone video, of me melting into a puddle at the chemo bell. I imagine the DH will have the ever-present Blackberry and will make sure there's a pic or two.

  • specialk
    specialk Member Posts: 9,262
    edited May 2011

    I am glad someone else's husband has an ever-present Crackberry and mine is not the only one!

  • pasmithx2
    pasmithx2 Member Posts: 224
    edited May 2011

    SpecialK--Mine is a Crackberry pusher. He brings them home for us to play with too.

  • gasurvivor2011
    gasurvivor2011 Member Posts: 150
    edited May 2011

    My office doesn't have a bell- but I can understand the emotion. It's all tough- that chemo room and chair and experience is gut wrenching emotionally for me each visit. Sometimes I can block that out more than others...

    Definitely happy dance for those finished! So ready for TCH 6 to be done. Feel so much weaker overall. I went to the MO this week- and they said "you are still working? most people on this do not especially this far along." 

    Not up to par in anything in my opinion. I feel like a 90 year old and a 2 year old- 90 in my speed and 2 year old in that I have to have my rest/sleep/naps when I can to stay going...

    Hanging in and hanging on by a thread.

    Lisa

  • specialk
    specialk Member Posts: 9,262
    edited May 2011

    pasmithx2 - DH just got a new one - I called and left him a crucial voicemail yesterday while I was out.  He called me back from home (the message was to meet me downtown!) and tells me he has not yet figured out how to retrieve the voicemail!  I wanted to kill him!  Today he called me to ask if I left him a voicemail - he knows when he gets one, just can't listen to it!  Arrggg!

  • pasmithx2
    pasmithx2 Member Posts: 224
    edited May 2011

    SpecialK--Do you have your own bberry? We use BlackberryMessenger all the time. I hardly ever call the DH or my kids. You can even see that, yes, they did read your message.

  • karebear76
    karebear76 Member Posts: 150
    edited May 2011

    Hi ladies.

    I have been to Boston and to my Onc and we have decided that I will do herceptin, radiation and then do navelbine (mellow chemo) with the herceptin!! So so glad that it won't be tch!!! 

  • lago
    lago Member Posts: 11,653
    edited May 2011
    Great news karebear. Glad they won't be abusing your body too much and you'll get Herceptin. How long on chemo-lite?
  • karebear76
    karebear76 Member Posts: 150
    edited May 2011

    Not exactly sure. Poss 12-16wks. It is given 1x week.

  • lago
    lago Member Posts: 11,653
    edited May 2011

    Do you get to keep your hair?

  • lilylady
    lilylady Member Posts: 478
    edited May 2011

    Just got home from #4 and I am really bummed out. I went from my feet not touching the ground because of great scan reports to total depression from the onc visit. He was extremely pleased with the scan results but then told me he was going straight to the phone to call my 3---three???-surgeons to schedule appointments. Breast, liver and lung. WTF??? My tumors shrank so dramatically I guess I just assumed we would melt them to death. Kind of always knew i would have the breast tumor out but didn't think I would need the other ones. he said I get 1 month to recover from chemo #6 and then he wants the surgeries done back to back. Breast first, then liver then the lung. He said they will go in the order of which are the easiest to tolerate. That would be Aug 8. He wants all surgical consults done in the next 2 weeks. I am not even going to listen to the answering machine toight. Bummer. Guess that fall beach vaction isn't going to happen.

    Next great news-I have to go back for bloodwork next week. Dangerously close to transfusion level. Each tx my counts have come back up to almost pre-chemo level. This time they have dropped like a rock. I have never had to have a Neulasta or Neupagen =probably also wasn't pre-approved thru insurance togo get 1 tomorrow. They want me on house arrest til I go back. I feel fine so  I will probably ignore that. I am notlanning on a rock concert or anything other than friends and family.

    OK enough of that-anyone want cheese with my whine? Have a happy 3 day weekend.

  • lago
    lago Member Posts: 11,653
    edited May 2011

    lilylady I know you don't thing it's good news but I think it's great that they are going to surgically removal all that cancer and so quickly. More cancer removed less likely cells will get lose and hang out somewhere else.

    BTW I felt great too but my immune system was weakened by chemo and that's why I got shingles. I would listen to your doctor and don't expose yourself to crap.

    Just found out about this stuff today (speaking of whine/wine)

    http://chocovine.com/images/chocovine-flat_r7_c3.jpg 

  • Ang7
    Ang7 Member Posts: 568
    edited May 2011
    We did not have a bell at my chemo place BUT I did do 2 cartwheels down the hall after my last Herceptin.  You cannot keep an old gymnast down...Wink
  • libraylil
    libraylil Member Posts: 325
    edited May 2011

    Lilylady. I know you are bummed. Whining is accepted here, you are entitled. I went into whine mode over my re excision in feb. It seems that your onco is slapping the krap out of your cancer and being very aggressive. Let this all sink.in. You were sort of blindsided with your diagnosis and have had a load to deal with recently.



    My levels always rebounded well until about 4. Ended up having neupogen 3 times. That was all I needed to kick it and they rebounded for the next chemo. I did not have any SE from the neupogen.

    Keep us posted on the surgery info. Try to relax and think they will be taking sout the cancer and that you are kicking butt. You can enjoy the beach a little later. We have good weather at the nc beaches on up until sept. Libraylil



    PS. I am going outlet,junk, thrift shopping today!

  • pasmithx2
    pasmithx2 Member Posts: 224
    edited May 2011

    Ang7--I will have to be satisfied with the chemo bell. I'd likely end up in traction if I attempted a cartwheel! But it sounds like it would be more fun.

  • pejkug3
    pejkug3 Member Posts: 277
    edited May 2011

    Lily - reschedule that fall vacation for spring.  I agree with the others, while surgery is never really a good thing, ridding your body of cancer IS.  And the sooner, the better!

  • lilylady
    lilylady Member Posts: 478
    edited May 2011

    Dear girls, thanks for your encouraging words. am over it now. it was just such a total shock. All i have heard from the beginning is at stage IV you are not curable. The BS and the liver guy both called me at home last night after 7pm.Pretty awesome to do that on a Fri night before a holiday weekend. they both said my onc is so passionate about my case that they wanted to touch base with me and not leave me worrying over a long  weekend.

      The BS said i have fallen into a very small category for Stage IV people (less than 2 %) that are curable. She said the name but I was too out of it to ask her to spell it. I have tried numerous spellings but can't get anything to pop. I am going to ask a couple of the ladies that seem like cancer PHDs to see if they know it. it sounded like oglimentary or aulimentary or something like that. I had a real good talk with her. Will save that for later. I will want to hear how you guys did after your Mx. I have lurked on the April and May Sx threads-doesn't seem all that bad. (Easy to say if it isn't you with drains hanging out of you)

    Liver guy just talked briefly but also said my Onc was very excited and really wants to move forward so they will call me tues to set an appt. he said he has my records but I have to get him copies of the scans. he said judging by what he sees I would be in for a minimally invasive procedure. Maybe RFA where they stick a probe in and burn it or possibly laproscopic. All good to hear. he would be the second surgery.

    I did not hear from the lung doc but that is OK. That is the one  am worried about. My mom had some histoplasmosis in her lung and when they tried to remove it they ruptured her pulmonary artery and she ended up in a coma for a month. it was a hellish 1 1/2 yrs getting her back on her feet. They had to rip out the entire lung to save her life. I know the odds are small for that happening. that surgery won't probably happen til Oct anyway.

    I am curable-who the hell would have thought that and how could that not be the focus instead of worrying about throwing up from anesthesia. What a butthead.

    Well,its outside to cut the grass-and PRAISE GOD I am woman enough to do it.

  • dragonfly1
    dragonfly1 Member Posts: 516
    edited May 2011
    Lilylady Wow!!! Stage IV and curable-now that's some great news. I know you are facing a lot of surgery but being in that 2% will be so worth it:)
  • libraylil
    libraylil Member Posts: 325
    edited May 2011

    Lily that totally rules. The Docs are total babes to call you. My bs called to tell me the re excision margins were clear so I would not have to wait. At that point i felt like he was an really awesome human being as well as a dr. Cute little butt as an added bonus...in scrubs:) Sorry I am encouraging all of you to misbehave and check out the Docs rear view. Libraylil

  • dragonfly1
    dragonfly1 Member Posts: 516
    edited May 2011

    TCH #6 - I'm in the chair and finishing today-hooray! Even though I'm facing my usual 10 days of side effects, it's the last time!!! On to rads on June 20th and or course the Herceptin will continue. I'm celebrating by going skydiving on my Birthday on June 18th. I'll post a video to share the experience afterwards:) Congrats to others who are finishing soon as well. I know LisaGH and SpecialK are finishing in the next two days...

  • nmoss1000
    nmoss1000 Member Posts: 324
    edited May 2011

    Yay!!! Congratulations Dragonfly! I am thrilled for you !

  • omaz
    omaz Member Posts: 4,218
    edited May 2011

    Yay Dragonfly!!!!!!!!  Can't believe it!!!  I am in the chair too with herceptin number 14.  You'll be here before you know it!

  • AmyIsStrong
    AmyIsStrong Member Posts: 426
    edited May 2011

    Congratulations Dragonfly. And congratulations-to-come for Lisa and SpecialK.

    Can't wait to see the skydiving video. You really know how to mark an occasion!

  • pasmithx2
    pasmithx2 Member Posts: 224
    edited May 2011

    Congrats Dragonfly1!! May the last 10 days surprise you and be easy.

  • lilylady
    lilylady Member Posts: 478
    edited May 2011

    Congrats Dragonfly-.hope the SEs are kind

    Have you done the skydive thing before? Coolest (scariest) thing ever to celebrate with. Can't wait to see the video. Seems like it would be the ultimate cure for the Big C-standing in the door of a perfectly good airplane and jumping out.