Chemo May 2011

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  • ---
    --- Member Posts: 197
    edited June 2011

    Goodmorning Everyone,

    Jut checking in to say hi to all.  This is my chemo-off week.  Generally, i am doing well.  Scalp is itchy every now and then, but nothing terrible.

    I hope everyone is doing well and hanging in there.

    Laureen

  • Patriotic
    Patriotic Member Posts: 281
    edited June 2011

    Candice, I am sorry you're having a bad day. The hair issue stinks. I am off to find some cute scarfs today. We finally have some sun this week. Hope you're feeling better soon.



    The Look Good Feel Better is really good. Got some really nice make-up and tips, especially for the eyebrows (when they are no longer there). Also, they gave a great demo for scarfs and turbans, etc.



  • ksmatthews
    ksmatthews Member Posts: 812
    edited June 2011

    38years old- dont be depressed it is just hair it will grow back.  I lost mine 14 days after my first chemo.  God knows we wont feel well enough to deal with hair issues is why we lose it.  This time nxt year it will be back!  Stay strong and positive!!!  ((hugs))

  • neecee
    neecee Member Posts: 663
    edited June 2011

    Back from treatment!  Everything went fine.  Slight headache, but nothing unbearable.

  • ksmatthews
    ksmatthews Member Posts: 812
    edited June 2011

    great to here Necee, I hit the chair nxt week.  I have 2 more to go.  I actually started chemo in March.  You can do it!

  • neecee
    neecee Member Posts: 663
    edited June 2011

    ksmatthews - this is number two for me, and so far it hasn't been as bad as I had thought it would be.  I am working full time (retail) and only missed 5 hours last treatment.  Two of those were for a doc appt, the other three because I wasn't feeling well.  I think I'm doing pretty well, considering.

  • rondajean
    rondajean Member Posts: 74
    edited June 2011

    patriotic, you can do it too!!

  • bak94
    bak94 Member Posts: 1,846
    edited June 2011

    neecee, your picture is so cute!

    Laureen-doing great here, but my next chemo was moved up a day again, so I go in on wednesday. I had the choice, one day early or 3 days late. I would rather get it done sooner than later and I don't want any extra days for the cancer to grow!

     CT scan on wednesday also to see if chemo is working.....I asked my doc when he would have the results, he said to head up to his office after the scan and he would get the results asap. He did that with the pet scan and bone scan. Got the results of the pet scan the day I had it and the bone scan the very next day. All the scan techs know to get my scans read quickly by the doctors and results to my doc asap as he is not patient waiting for scans, got to love him for that! Just hope they aren't missing anything when they read them so quickly!

  • neecee
    neecee Member Posts: 663
    edited June 2011

    bkj66 - thanks!  Good luck with everything Wednesday.

  • 40-years-old-now
    40-years-old-now Member Posts: 309
    edited June 2011

    The feel good look good thing went well tonight.  I had to leave a bit early but there were only 2 people there. I had to go and have a MRI , because my leg is not working. I cant seem to get it to move.

    It seems to be one thing after another.

    Candice 

  • Cyborg
    Cyborg Member Posts: 848
    edited June 2011

    Good luck to all the hurls going to chemo this week! I am pounding the water. Tomorrow is Neulesta shot I am ready with Claritin. I feel good now, but know I am going to crash. BKJ66: I will thinkof you on Wednesday.

    Dang it, Candice. I hope your leg stops giving u grief.

  • blondelawyer
    blondelawyer Member Posts: 327
    edited June 2011

    Had my first AC treatment today.  I also had an echo and physical therapy.  I got the neulesta shot and also a lupron shot.  I'm tired--it was a long day--but otherwise okay. I'll be taking steroids and anti-nausea pills for a few days to keep the symptoms at bay--hopefully.  

    My biopsy site from last week is leaking like crazy--and therefore driving me crazy.  But it is a minor thing compared to everything else.

     I am pampering myself this week and have a professional organizer coming by to help me set up my office and then a cleaner on Wednesday.  I have decide to use my energy for things that I enjoy and outsource other things! 

  • 40-years-old-now
    40-years-old-now Member Posts: 309
    edited June 2011

    blondlawyer,

    I think that is a great idea. Enjoy as much as you can!!

    Candice

  • Cyborg
    Cyborg Member Posts: 848
    edited June 2011

    Blondelawyer- good to hear that!!!!!!

  • Oma11
    Oma11 Member Posts: 1
    edited June 2011

    Here goes, with my first post - so glad I found this site. Hoping to stay positive throughout this journey - can't help but think of my mother and her dx in the late 1950's - chemo was unheard of at that time (far as I know) and she received her dx when she came out of radical-mastectomy surgery. No wonder she didn't want to talk to us when we came to visit that night - she was an R.N. and knew what her future held, (not much hope back then). Am waiting for my BRCA results any day. Have TCH every 3 weeks and just Herceptin the 2 weeks in between - Wednesday will only be my 2nd 'big' chemo dose. So grateful for my wonderful oncologist - love her! - and the outrageously thoughtful nurses at the infusion center.  Hair almost gone - keep scrubbing it in the shower then slathering with conditioner to get it over with - cut it short on week 2 in anticipation, then the 'wig place' buzzed it 5 days ago. Relieved the scalp pain stopped. Hate that scratchy wig so made several scarves/hats to wear most of the time and/or around my grandchildren,(2 of them freaked out when they just saw the first haircut). Main worry was/is the nausea, but oncologist said she would prescribe meds to resolve that - so far it's tolerable. Thank you all for your posts - have spent a few hours reading lots of them. Best wishes for us all!

  • Beaglesgirl
    Beaglesgirl Member Posts: 287
    edited June 2011

    Heading for the chair this morning. I had a fill yesterday so I was uncomfortable last night added stress to a sleepless night. This is my 3rd A/C after today I just have one more.... I feel like I'm going to be dragging myself over that finish line. Then onwards to taxol



    Hugs to all

  • MamaV
    MamaV Member Posts: 907
    edited June 2011

    Beaglesgirl - you can do it!  I crawled over the A/C finish line and physically the Taxol has been so much easier (the weekly dose is much milder - I hope that's your plan).  I will warn you though that Taxol depression is tough (at least for me, and I've heard from others too).  Hang in there!  Be strong!

    Oma11 - welcome; sorry you have to join us!  You will find great support and information here!

  • neecee
    neecee Member Posts: 663
    edited June 2011

    Oma11 - welcome!

  • Beaglesgirl
    Beaglesgirl Member Posts: 287
    edited June 2011

    Thanks for the reply MamaV! I can't believe that I feel this horrible a few hours after treatment. I am so glad for those that don't get this ill you are truly blessed! I am a little worried about the taxol depression... What have you done to battle it or wish you had done? I seem to hit 9 out of a possible 10 SE so I want to look ahead.



    I wish I didn't have to back for the nuelasta shot tomorrow... 5 days of in bed with pain meds, writhing in pain



    BUT..only one more AC left AND my counts continue to be good.... I happily do this for more years with my family...I got home and I could taste the chemicals in my mouth, I can smell them on my skin, I can choose to believe that it's the sweet taste of future. So although my complaint list is long it's really only because it helps me to talk about it and I hope it helps someone reading it too.



    Love to all!

  • Cyborg
    Cyborg Member Posts: 848
    edited June 2011

    Oma11- they make soft caps to wear seam side out under the wig to create a very soft barrier between scalp and scratchy underside of wig.

  • bak94
    bak94 Member Posts: 1,846
    edited June 2011

    Cyborg, with that cap does it feel like your wig is going to pop off? I tried it and thought my wig would slide off, maybe I'm paranoid. I always feel like I am hiding something when I am wearing my wig, yeah, my bald head! I pretty much only wear my wig to work, can't go to a hair salon without hair! Everyone is really nice about it,  they say it looks real, but I feel kinda wiggy and I think it makes me move cautiously-kinda stiff. Not looking forward to ct scan and chemo today, but hoping numbers are good enough for chemo, so I guess I do want chemo today!:) Mixed emotions......

  • MamaV
    MamaV Member Posts: 907
    edited June 2011

    Beaglesgirl - Sorry to hear the Neulasta causes you so much pain.  That worries me for you about Taxol b/c that can do the same thing.  I didn't have any pain with Neulasta and very mild pain with Taxol.  The depression and anxiety have been tough for me - I am on antidepressants and anti-axiety meds.  Sometimes they help, sometimes they don't.  Today I am struggling again!

    Taxol #9 for me tomorrow.  Also, finally got insurance approval for the BRCA genetic testing - now just on more thing to be anxious about.  Great.

  • mccrimmon324
    mccrimmon324 Member Posts: 1,076
    edited June 2011

    bkj66 - Just had my first treatment last thursday, my hair is still here but everyday I worry more and more about how I'm going to handle it coming out then having to shave.  I have a wig for work also, I wanted to know if yours bothers your head, is it scratchy?  Does it move around alot?  Thankfully I have a desk job so I won't be moving around alot but I'm soooo paranoid it's going to slip.  Good luck on your chemo tomorrow, Are you almost done your A/C?

  • Cyborg
    Cyborg Member Posts: 848
    edited June 2011

    Bkj66- I wore the wig to short outings with a scarf in the car for back up. Wig stayed in place.

    MamaV- keep moving forward sweetheart. I had a crying drag due to steroids yesterday. Love on yourself. Let yourself be loved.

    Beaglesgirl- claritin helps, sweet sister for my bone ache due to Nuelesta.

    Mccrimmon- good to see you here, Girl.

  • Patriotic
    Patriotic Member Posts: 281
    edited June 2011

    Beaglesgirl, I just had Taxol #7. I am doing Taxol first. I have had very minor SE's. I am not diminishing SE's anyone else has experienced, by any means. I am just saying that you might be fine. Everyone has a different experience. I have another friend who did the regimen in this order and she also stated she had minor SE's with Taxol and things didn't really get difficult until AC. I hope this helps you with any anxiety about it. Congrats on only having one more AC. Yeah!



    Yesterday, my Onc mentioned having a 2-week break between DD Taxol and AC. I told her I preferred only 1week and wanted to start sooner, if possible. Does anyone have any opinion on this?

  • neecee
    neecee Member Posts: 663
    edited June 2011

    mccrimmon - I wear my wig at work, and I have a very active job (retail).  I have yet to have it slip on me.  Most wigs have adjustment straps inside to get it the right amount of snug so it doesn't move.  I tried the wig with a liner, but found that I prefer it without one.  That may just be me.

    I wasn't sure how I would handle the hair loss and shaving, and at the time the hair loss was so annoying that shaving was a relief.  It was also liberating and empowering to make the decision about when my hair would go.

  • DebRox
    DebRox Member Posts: 437
    edited June 2011

    MammaV and cyborg: hang in there! I have also been crying a lot due to the steroids. They make me feel so low, like giving up. I hate the feeling. I'm going for my first neulasta shot today as I was in the danger zone far too long after my first infusion. I'm so anxious and worried about having it.



    Well I guess I am just a basket case right now due to steroids. One more day on them, ugh!



    MammaV: try not to stress about genetic testing. I'm sure all will go well.



    Neecee: sounds like you're doing fine since your Monday treatment. Great for you managing SEs.



    Beagles girl: I'm sorry to hear about the pain you've suffered with neulasta. Have you tried the claritan and aleve to help. I'm trying that today for my first shot.





    Everyone: hope all is best as can be. I find this so much more emotionally draining than physically. I want to be me again, feel happy and alive. Right now I feel I'm stuck in a nightmare, just getting thru one day at a time. It doesn't help that I dream that I'm drowning, at least I do make it to the surface, so that means I'm fighting. Better stop here, I sound too depressing. Going for neulasta in 20 min.

  • mccrimmon324
    mccrimmon324 Member Posts: 1,076
    edited June 2011

    I know I've only had one treatment and one Neulasta shot but I did take a claritin and an aleve on the day of the shot, then an aleve every eight hours for 3 days total and a claritin on day 2 and 3.  I had absolutely no bone pain at all.  I kept waiting for it to happen and it never did.  I was tired and felt funny but no pain.  They say Aleve can lower your platlettes so now I'm back on Tylenol if I need to take something. 

  • Cyborg
    Cyborg Member Posts: 848
    edited June 2011

    Cellulitis returning... Ugh

  • Cyborg
    Cyborg Member Posts: 848
    edited June 2011

    I can't believe it. I actually threw up my anti nausea medication. Ugh.

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