April/May 2012 Chemo hang out

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  • lsharvey822
    lsharvey822 Member Posts: 257
    edited June 2012

    Fierro - I was told DD A/C + Taxol is the step up treatment from T/C x 6 or A/C x 6.  They may have stepped you up because of your nodal involvement.

  • RoulaG
    RoulaG Member Posts: 239
    edited June 2012

    Kjiberty - Western Springs is a suburb, funny enough just west of Chicago. It is a very small suburb so I just tell people, we are between LaGrange and Hinsdale, just east of Ogden Ave and south 294 tollway. I always tell people if you are on Ogden and blink you may miss us :-)

  • silkuk52
    silkuk52 Member Posts: 13
    edited June 2012

    Hi :) new to this forum as of now. Had Port put in yesterday. Did you have general anesthesia or "twighlight" sleep? VERY SORE today-know what you mean about your arm! Had to practically beg for something stronger than Tylenol!



  • RoulaG
    RoulaG Member Posts: 239
    edited June 2012

    I was completely under when they did my port, but I was also having a re-excision done for clear margins.

  • rgina
    rgina Member Posts: 100
    edited June 2012

    Evening all,

    I'm still here and trying to catch up again.  Had a busy weekend, Monday commute to the office and last 2 days have been work crazy.  I've felt good, tastebuds came back last weekend and have eaten everything in sight.  Even worked in the yard/barn 4 hours on Sunday. This Friday will be labs for me and 2nd Herceptin only.  Hair is still coming out very lightly and I'm 2 weeks today post 1st TCH, imagine that will speed up soon - but I'm ready with misc. pre-tied scarves, caps, hats, (no wig).  My skin which is dry anyway is like the Sahara Desert but found Mary Kay Extra Emollient Night Cream has really helped.  Also, went shopping on Saturday at Kohl's and picked up some Earth Therapeutics aloe moisture socks which I am sleeping in and aloe moisture gloves that I wear for awhile in the evening - those are helping too (just an FYI).

    Dancetrancer - that baby oil on a q-tip - tip last week for the inside of the nose - worked wonders.

    Hope everyone is having a good week or at the very least as good as can be expected with minimal SE's.

  • Melrosemelrose
    Melrosemelrose Member Posts: 3,018
    edited June 2012
    Isharvey822- What's up with that BP of yours?
  • Marcia1111
    Marcia1111 Member Posts: 368
    edited June 2012

    I had versed (I think that's the correct spelling) for my port placement.  From what  I understand, you are awake the whole time but don't remember anything.

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

    Hi Fierro - actually, I'm on A/C but on a regular (every three weeks), not dose dense, regiment. I have a friend on the March board who is also stage IIb like you but HER2 positive, and is getting the same tx as me (same regiment) on a neoadjuvant basis, to shrink her tumor before surgery. I don't know how/why they prescribe dose dense vs regular. I thought at first it had something to do with how aggressive the cancer might be but as you and I were both grade 2, that can't entirely be it either.

    I wonder if it's anything to do with the fact tha Jaxson delayed starting your tx. But I will see if I can look into it further; now I'm curious.

  • Fierro6
    Fierro6 Member Posts: 224
    edited June 2012

    They did my port placement at the same time as my mastectomy, and never told me I had a choice about where it went.  It's in my chest, and other than being weird (it's a party trick..."wanna feel my port?") it's never bothered me.  That could be because I was distracted by the MX trauma.  Who knows?

  • rgina
    rgina Member Posts: 100
    edited June 2012

    Marcia - I don't think I was awake during port placement - if I was, for sure I don't remember anything.  Actually, I do remember someone waking me up and me telling them I was having a wonderful dream, now that you mention it.  I checked into the hospital at 7:30 and was home eating a grilled cheese sandwich by noon.  Of all the poking/prodding/needles/biopsy/and the radioactive dye for the SNB before the lumpectomy (the worst) - the port was an easy procedure.

  • Melrosemelrose
    Melrosemelrose Member Posts: 3,018
    edited June 2012
    IndigoMont11-  I didn't realize you were having chemo every 3 weeks like me.  Three weeks is the recovery time for both our chemo regimens according to this website-- chemocare.  I like having the third week when I feel good before the next round!!!  Hope you are doing well this evening.  Glad we are kicking around in our big girl boots!!!!
  • vballmom
    vballmom Member Posts: 426
    edited June 2012

    Fierro, I'm on the same regimen, except I will follow up with Herceptin after Taxol. 

    My nausea is back. Bummer.

     

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

    Hi silkuk! I had IV sedation for my port but it was pretty mild. I wouldn't call it twilight sleep - I remember the whole thing.

  • kjiberty
    kjiberty Member Posts: 1,385
    edited June 2012

    Is anyone's blood pressure A LOT lower after the nuelasta shot?  Mine is about 93/63.  You would think I was in terrific physical shape and 21 years old!  (PS--normal for me is about 115-120/80

  • lsharvey822
    lsharvey822 Member Posts: 257
    edited June 2012

    @Melrose - good question! haha!!  I'm starting HCTZ 25 mg now.  Just what I need..more meds!  I feel like I went from 43 to the 73 in 3 months!  uggghh! 

    I have a red spot on the palm of my hand?  Kinda looks like the beginning of a blister but I can't think of anything that would have done that (plus it's off in a weird spot for a blister) and it has stayed like that for the last day or two.  It's a little tender but doesn't really hurt.  Don't know if it's something to do with the chemo or totally unrelated?

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

    @Melrose - yep, I think I just started maybe four or five days before you did, but otherwise we're on the same schedule, if not the same cocktail.

  • kjiberty
    kjiberty Member Posts: 1,385
    edited June 2012

    Vballmom:  I hope the nausea is very short-lived.

    Roula:  I live in a very small down outside of Peoria--Dunlap.  There's about 500 people here (was 250 and we had a lot of growth due to our wonderful school district--growth in property taxes too!).  

    Silkuk52:  Welcome to this board with some great, smart and beautiful ladies! 

  • lsharvey822
    lsharvey822 Member Posts: 257
    edited June 2012

    @Vball - hope it's short lived!  Go away nausea!

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

    Isharvey-I'm on the same bp med with the diurectic in it and havne't had any problems with it.  It has really helped my bp stay down.  Hope you are getting the Hand-Foot Syndrome which is a side effect of chemo.  Look at the main BCO section under chemo side effects.  It is no fun for sure!!!!

     IndigoMont11- There are so many gals on this thread now, it is hard to keep up when everyone is having her chemo but i won't forget when yours is anymore, girlfriend!!!!!

    Vballmom- OH NO!!!! Hard to believe that the nausea is back..... call you onco to see if he/she can give you different meds before it gets worse.  Gentle hugs.....

  • Fierro6
    Fierro6 Member Posts: 224
    edited June 2012

    vballmom - I was to start a few weeks ago.  We would have been nearly identical in treatment for a while!  (stupid JP drain, literally "hanging around" for too long.)  I was offered the Herceptin as a clinical trial (because 2+ is negative?) and the Herceptin would have been paid for by the trial, but my insurance would have had to pay for the infusion of the drug, and it won't.  Ass hats.  

    Ohh, somebody is getting moody.  Time to get offline?  Or time to get a beer before my liver has a more important job to do?  Maybe both. 

  • Melrosemelrose
    Melrosemelrose Member Posts: 3,018
    edited June 2012
    Fierro6- You are too funny....  lol.  I never asked my insurance if they would pay for the Herceptin clinical trial infusion.  The infusion center just submitted the bill with the Herceptin infusion charge and the insurance paid whatever it billed, no questions asked.  Go figure.
  • Marcia1111
    Marcia1111 Member Posts: 368
    edited June 2012

    HELP!  My MO said that my meds would be very clear about what to do tomorrow for my first day and the instructions are as clear as mud!

  • FightingLikeAGirl
    FightingLikeAGirl Member Posts: 69
    edited June 2012
    Silk...welcome! I have my port in my arm. I had a local and I was totally awake listening to music and chatting with the surgeon and nurses...I felt nothing just a little pressure when they were pushing it in. However it was really annoying for the first couple of weeks...now I hardly notice it.

    VBall...so sorry you've been having such a tough time with the nausea. Do any of the anti-nausea meds help?

    Indigo...so glad your husband is doing okay. You really do have a lot on your plate.

    Lisa...So sorry you're feeling crummy...hope it's short lived. Just this morning I was thinking about a trip I took right before I had my mammogram that found this cancer. It was such a great trip with my boyfriend and 2 other couples. We went wine tasting up North to the Santa Ynez Valley. I was so unaware of what was happening in my own body...just having fun and not worrying about anything...its just so amazing how life can change in a snap. Funny that you were telling your story about being in Santa Barbara...do you live in CA?

    Cindy
  • Melrosemelrose
    Melrosemelrose Member Posts: 3,018
    edited June 2012
    Marcia1111- What meds were you prescribed by your MO?  I'm sure one of us can help you decipher what you are supposed to take and when!!!
  • Fierro6
    Fierro6 Member Posts: 224
    edited June 2012

    Marcia, ask away.  I was put off for a bit and had confused some things and forgotten some others, so I finally freaked out and called the MO's office.  A VERY understanding nurse answered every question and calmed me right back down.  I wonder if any of my answers apply?  Ask!!!

  • kjiberty
    kjiberty Member Posts: 1,385
    edited June 2012

    Marcia1111:  I don't know how far you live from your treatment center (I live 5 minutes away), but I take an atavan (lorazapam .5 mg) 1/2 hour before I go.  I am given an oral steriod to take 2x/day the day before (today), the day of, and the day after.  Saturdays are when my crashes start.  I also take B6, L-Lysine (for prevention of mouth sores) and am given compazine to take in case it's need for nausea.  I have to take a multi-vitamin and calcium supplement as well.   

  • Marcia1111
    Marcia1111 Member Posts: 368
    edited June 2012

    I just called my husband who was with me at the education session.  He says she said to bring everything with me, but I think I will call the MO and get someone on call.  I'll let you know the results.

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

    Vballmom - hoping the nausea doesn't escalatecand goes away soon!

  • Marcia1111
    Marcia1111 Member Posts: 368
    edited June 2012

    Okay, I called the MO and am waiting for a return call.  I have Emend, Dexamethasone, Prochlorperazine, and Lidocaine.

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

    Good idea to call the onco because one usually takes anti-nausea meds the day before the actual infusion.  Let us know what you find out .  If not, call the pharmasist to ask him to explain when you are to take the drugs.  I got confused on my Decadron, steroid drug as to how long to take it..... I took it for 3 days instead of just 3 doses. When my onco found out, she said it was fine since I didn't have any nausea and it is how she used to prescribe the drug--- twice  a day for 3 days (old way) versus twice a day for a day and 1/2. 

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