Abraxane

Kandy
Kandy Member Posts: 1,461

Anyone else out there doing this chemo. I'm starting it on Tuesday. Let's join together and form a group. Wishing everyone the best.

Comments

  • Christina313
    Christina313 Member Posts: 27
    edited January 2017

    my mom just finished this chemo. She did really really well on it. We won't know until next week until we get the scan. Her breast tumor is gone completely and her liver one they couldn't feel it. It was 6 cm. She didn't feel sick at all. Just kept her awake at night sometimes.

    In addition to this she drinks beet juice. One glass a day. I also make her carrot juice and I buy those dried golden berries from Costco. My father's co-workers wife had breast cancer over 10 years ago. They told her to get her affairs in order. They said she had three weeks to live. She said " we will see about that''. She changed her diet to include very juice among other things. She had daily chemo. Now she is Cancer free. She isn't on any medication whatsoever. So there always hope for each and everyone here.


    All the best to you

    Christina


  • Kandy
    Kandy Member Posts: 1,461
    edited January 2017

    Thank you Christina, I was thinking I must be the only one taking this. I hope your moms scans are good. Wishing you and her the bes

  • Sherriw
    Sherriw Member Posts: 47
    edited January 2017

    I'm on a clinical trial, abraxane or abraxane + trial drug. The abraxane is three weeks on one week off. I ride the line for white counts most cycles and am battling the neurapathy. Good news is that scans show mets are stable to better. Tomorrow is day 8 of cycle 7.

  • Kandy
    Kandy Member Posts: 1,461
    edited January 2017

    What is the trial drug? Have you had any side effects
  • Zillsnot4me
    Zillsnot4me Member Posts: 2,687
    edited January 2017
  • Kandy
    Kandy Member Posts: 1,461
    edited January 2017

    So I got my first treatment today. It went well. They said I was going to do 2 weeks on, then a week off. The PA said not everyone loses their hair, that it will definitely thin but some people don't lose it completely. She said we would know in 3-4 weeks. Wishing everyone the best.

  • Southernsurvivor
    Southernsurvivor Member Posts: 632
    edited January 2017
    Hi Kandy,

    I was on Abraxane for a few months in 2014 and did lose most all of my hair within a month. My hair is naturally thin so ended up shaving what was left. I wish you the best of luck on Abraxane and pray it kicks your cancer to the curb!
  • Nan812
    Nan812 Member Posts: 289
    edited January 2017

    Hi Kandy, they told me that too...about it thinning and not everyone looses it....well it was a beautiful day and i went out shopping with DD to a lovely outdoor mall. I bought a new scarf that day just in case cuz I was a first timer...went to the ladies room...ran my fingers thru my hair...here comes the walking dead!!... it came out in handfuls!...It wouldn't stop (and I had just shampooed that morning) I was filling up the trash!!...my eyes were filling with tears... I couldn't get the scarf on without pulling loose more hair...a angel walked up and said..."let me help you" she tied it on, it looked great..then when I told my daughter about what happened we laughed our heads off on what a site I must have been...we still laugh about it...I wish you much better luck than me :)

  • Kandy
    Kandy Member Posts: 1,461
    edited January 2017

    Awww, how traumatic. I'm sure I will lose mine too, which I hate the thought. I've done that one other time and I really didn't like it at all. I find it humiliating and I feel I lose my feminine side. I know it's crazy to worry about the way you look when you are fighting for your life. But it's a big deal for me. I really don't have good luck so even if they said only 2 % lose their hair, trust me I would be in the 2%. I wish you the best.

  • Nan812
    Nan812 Member Posts: 289
    edited January 2017

    Kandy, yes at first it was a shock but it really was kinda funny when I told the story... I kept thinking bout the poor cleaning lady, she must have thought someone changed their identity in there...and the ladies walking past must have thought I was contagious...and when I got home and shaved the rest, I thought yup kinda funny :) I have to admit that I'm typically very vain and I know just what you mean about liking how you look and feeling better. I couldn't wear a wig, my head was to tender and I missed my eyelashes the most. Something told me that this was just part of it and if I was gonna pull off this new look I better act like it doesn't bother me. I know, it's a goofy way to think and I'm so sorry if any thing I've said bothered you. I sincerely hope you don't loose a strand and that you breeze right thru this. You've been in my prayers all day.

  • Kandy
    Kandy Member Posts: 1,461
    edited January 2017

    Nan, thank you for the prayers, I really need everyone I can get. You certainly didn't upset me in any way. I find it most beneficial to hear others experiences since this is is always new to us as it changes. My hair is like a security blanket to me, I feel confident with it, only if it is long so I can hide under it, lol. When it's not there, I feel very exposed and vulnerable. I know it's silly and you would think after losing it before I would be okay with it. But actually it bothers me more. And the fact that even if someday I come off of chemo, it will take forever to get it long again. The realization that I may never live long enough to have hair again, bothers me a lot. Probably more than the first time around. But it is, what it is, and I'm not ready to die yet, so I guess the hair will more than likely go. Thanks for responding, caring, and sharing your experiences. Wishing you only the best

  • Sherriw
    Sherriw Member Posts: 47
    edited January 2017

    the trial drug is atezolizumab. Technically I could also be getting a placebo but we have lots of evidence that I'm not.

    My hair is long gone. I can say it doesn't bother me too much, but the eyebrows and eyelashes do. I spend more time trying to paint on some eyebrows now that I ever did doing my hair.

    Good luck with the abraxane

  • Christina313
    Christina313 Member Posts: 27
    edited January 2017

    My mom finished this chemo. I believe it's the red one right? Well she's Ned. She's also triple negative. She did loose her her hair within about two weeks. They were absolutely shocked with her scan. Her liver tumor was 7cm, the breast tumor was 11cm. She had had it in several nodes. So I think you will have some luck with this one. :) It's powerful and potant.

  • Kandy
    Kandy Member Posts: 1,461
    edited January 2017

    You might be referring to Adriamycin , but I'm happy your mom got great results.

  • hansaim
    hansaim Member Posts: 278
    edited January 2017

    I had 6 cycles of Abraxane last year. Xeloda failed and lung mets appeared last spring and my MO suggested Abraxane. Fatigue and hair loss were the worst for me. The infusion time was only 30 min and no pre-meds, so quick in and out for treatments. Hair started coming out after the 2nd cycle so I shaved it all off. It did wonders for the lung mets; some shrunk and some disappeared. I wish you the best outcome.

  • lulubee
    lulubee Member Posts: 1,493
    edited February 2017

    Kandy, I have just started Taxol - three weeks on, one week off. Had my second infusion today. I was slated to start Abraxane but then wound up in a clinical trial for Taxol so we changed horses at the last minute. Since the two drugs are essentially the same except for a solvent in Taxol that is not in Abraxane, I think I will tag along with you here if that's okay.

    I'm watching my hair like a hawk. It's my one major vanity. I'll be honest, I have really good, thick hair with lots of body, and it is kind of my trademark, you know? I bought a wig last weekend and a couple of cute caps, and I have a lifelong collection of beautiful scarves, so at least I feel prepared now. That does help. Maybe go wig shopping with a friend, if you can? Get your onc to write a script for it. I took my young, stylish adult daughters and let them pick out the right wig for me-- they know what looks good on me. We can't change what is going to happen anyway, and probably soon. But you might be surprised how much better you feel about things with a pretty long wig on standby.

  • Kandy
    Kandy Member Posts: 1,461
    edited February 2017

    Hi Lulubee, please tag along with me. It's great to have company. I'm also watching my hair like a hawk too. I have thick long hair that I call my security blanket. Take it away and I'm vulnerable. I had chemo in 09 and lost it then. I hated that year. I wish I could be like others and not let it get to me but it does. I feel ugly and very old without it. I was so hoping I could hold onto it but I'm thinking probably not. I started thinning a couple days ago and everyday gets a little worse. My MO said that I would know after the second cycle. I just finished the first cycle. And being it's already started coming out, I'm thinking I don't stand a chance. I have the wig I wore in 09. It actually looks pretty good but they are so uncomfortable and I guess I'm fond of my own hair. But it is what it is. So far MO thinks I'm doing rather well. I have waves of nausea and am exhausted but overall pretty good. If I have to lose my hair this had better do some good, lol. Are you having any side effects? I wish you the

  • lulubee
    lulubee Member Posts: 1,493
    edited February 2017

    Kandy, thanks, I think I will hang here with you. Some of us Taxol metsters are trying to rustle up some new activity on the "Weekly Taxol for Stage IV" thread. You should add it to your favorites, too. Can't hurt to have more camaraderie, right?

    I've never worn a wig before so I'm really dreading it. I have a large head (I can never, ever wear women's hats) so I had to insist on trying only the wigs that came in large. I could seriously tell a difference when the gal plopped an average size wig on my head-- yowzer, so uncomfortable. So maybe you could try a large wig and see if that's better for you.

    Hard to tell whether I'm having side effects from Taxol because I have a lot of other challenges going on right now while I'm getting started on it. I was just released from a weeklong stay in the hospital because I developed a malignant pericardial effusion that dang near took me down. Had a catheter surgically inserted, drained off a big jug of junk, and now I'm trying to regain my ability to breathe on my own-- the pressure from the effusion caused some lung collapse and also caused some pleural effusion from the inflammation. I've been on oxygen for over two weeks now. So if I have side effects from Taxol, who could tell? LOL

    Right now tonight I'm navigating the lovely steroid crash from Thursday's infusion. Ay ay ay ay ay. I really hate steroids. Do you get them with Abraxane?

  • Kandy
    Kandy Member Posts: 1,461
    edited February 2017

    They do give me steroids although I don't think most people would get the on Abraxane. I was very allergic to Taxol and Taxotere when I had chemo in 09. I went into anaphylactic shock with both. Not a bit of fun. So I have a whole list of premeds they give me before chemo. My MO thought that hopefully he could get me to tolerate this, so far he has been right. I had a lot of anxiety starting it cause of my past experiences but I am tolerating this much better. I probably lost about half of my hair this week, so sad. But my hair is really thick, so now I have probably what most people normally have, lol. I'm not counting on keeping too much after seeing how much came out this week. My MO said we would know after round 2. I'm sure hoping this does some good, I would hate to think I lost my hair for nothing. I'm exhausted today but I guess overall this isn't so bad. Wishing you the best

  • illimae
    illimae Member Posts: 5,710
    edited February 2017

    Kandy-I too had terrible allergic reactions to taxotere and taxol. I started Abraxane weekly on Monday 1/30 and was so relieved to have no reaction other than some mild joint pains and an increased heart rate (still within normal range) for a few days. I am also having a Pergita/Herceptin combo every 3 weeks.

  • Kandy
    Kandy Member Posts: 1,461
    edited February 2017

    IIIimae, so glad you are doing okay with it too. I'm starting my second round on Tuesday. I wish you the bes

  • Sue2009
    Sue2009 Member Posts: 228
    edited February 2017

    hi Kandy & other BC sisters, I am starting Halaven tomorrow, but will ask my dr about abraxane. Halaven sounds similar to abraxane. Nan your hair loss experience would have made me cry too, & later I usually laugh at myself for getting so upset over things I have no control over. Kandy, like you, in 09 I went bald overnight. When I came out of my bedroom for breakfast and the shocked look on my 5 sons' faces were priceless, I had to laugh, which seemed to make them feel better. There is something about a bald head to make your dx real. I too hate wigs & am way more anxious this time thinking about it. I wore a pink, Uni of Florida ball cap mostly, I don't remember who gave it to me, but it turned out to be my favorite. I elected to wear it over a wig to my 20 yr HS reunion.

    My poor oncologist is probably going to drop me as a patient as I question her every move.


  • Wiegp22
    Wiegp22 Member Posts: 268
    edited February 2017

    where do you get the beet juice

  • illimae
    illimae Member Posts: 5,710
    edited March 2017

    I lost so much hair after my 4th Abraxane infusion that I just had my husband buzz off the rest. I'm finding that people are so nice and apologize for anything when your bald, it's very odd. I am currently having issues with food tasting bad but it's manageable. Everyone else doing ok?

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