Starting Chemo May 2008

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  • Roxi65229
    Roxi65229 Member Posts: 462
    edited May 2008

    Ladies,

    Good luck to all with your treatments tomorrow, this is my off week and I feel GREAT!!!! I over did it today and worked 6 hours so I'll be hitting the sheets after American Idol. Go David...Cook that is. Has anyone's side effects escalated after round 1? A couple of people have told me that the SE's get progressively worse.



    Thinking of you all.



    Roxi

  • familyroks
    familyroks Member Posts: 575
    edited May 2008

    Roxi - awesome!  Glad to see that you are feeling so well.  I too would love to know how the SE's are as we progress further into treatment.  Like you I felt fabulous my off week and my se's were pretty much non-existant, except for exhaustion on day 3 & 4.

    I know everyone is different but as I mentally prepare for treatment 2 I'm starting to worry that last week was just a lucky thing.  Keeping my fingers crossed for all of us.

    And I'm with you!  We're rooting for David Cook also!

    Enjoy your off week.

  • drcrisc
    drcrisc Member Posts: 836
    edited May 2008

    Hi all,

    I'm still a Grrrr monster - the only thing I heard today was that the pathologist at Stanford called the pathologist at the hospital.  WTH?!?  If I don't have a report by noon tomorrow, I'm calling the pathologist at Stanford myself.  Grrrr......Yell  Thanks, Rock, for the empathic grrrrr.

    flyrzfan - know how you feel.  At this point, I may be with you in June!

    Otter - hope you found something that was easy and tasted good. 

    Glad others are having minimal se's and good luck to Rock and Adrienne tomorrow. 

    Someone may have to come bail me out of jail as I may threaten the pathologist though (but it will only be a threat, Rock!)...

  • Leeayn
    Leeayn Member Posts: 40
    edited May 2008

    KristyAnn - I'm not super close, but I do live in the Dallas area and would love to chat. 

    I had my first does of Chemo on May 1, so this is pretty new to me, too.  I've done a lot of research and reading blogs like this help me, too. 

    I'm on:

    My Chemo drugs:

    Adriamycin

    Cytoxan

    5FU

    Anti-nausea drugs in my IV:

    Alozi

    Dexamethesone (steriod)

    I have had my 1st round, 5 more to go.  They are not fun, but I have to look at the big picture - the end result!  I want this beast gone for good!

    Feel free to contact me off-line - Leeayn_B@hotmail.com

    Fighting Cancer with Dignity and Grace

    <><  Keeping the Faith  <><

    www.caringbridge.org/visit/leeaynbyrd

  • gogators
    gogators Member Posts: 39
    edited May 2008

    Well, I started the dexomethasone pills this morning for my first treatment tomorrow.  I am hoping that the treatment will still be a go, the onc wants to look at my lump. incision before they decide if the treatment will go as scheduled.  I have already drank almost a liter of water this morning.

    One question, the Emend that they gave me says to take one hour before chemo.  Should I take it with me, since I have to have lab work and see the doc first or should I take it before I leave the house.  I called the onc office this morning, but I had to leave a message and "worry wart" me is paranoid that I won't get the call at work as I am in and out of my office so much during the day and out in the boonies, so cell service doesn't work out here.

    I'm rambling, I think it might be those pills I took.  Boy, do I feel like I'm typing at light speed.

    Tina

  • familyroks
    familyroks Member Posts: 575
    edited May 2008

    Tina - my nurses told me that as long as I have taken the Emend 30 minutes prior to treatment its all good.  Perhaps you can question them as soon as you arrive.  That way I imagine you'll have it in your system at least 30 minutes before they start treatment.  Good job on the water!  I go in for treatment 2 this morning.  I've started on my water and hope to get 42 ounces in before treatment and another 32 during treatment.  Good luck this morning!  Let us know how it goes.

    ~Adrienne

  • beachmom13
    beachmom13 Member Posts: 313
    edited May 2008

    gogators - my nurse said to wait and take the emend when I sat in the chair because if my bloodwork was low, they wouldn't do the chemo and I would have lost 1 pill.  I haven't had any problems with it so far.

  • rock
    rock Member Posts: 1,486
    edited May 2008

    Chemo #2 (A/C) went fabulously.  Unlike Chemo #1, though, this one featured a fire alarm gone haywire and -- on the 1 train home -- a mariachi band. (On the subway, I leaned over to my friend and said, "Are you seeing the mariachi band too?")  Adrienne, I hope yours went as well as mine did!

  • familyroks
    familyroks Member Posts: 575
    edited May 2008

    I'm back!  Gee rockthebald...a mariachi band just for you!  How cool is that.

    Treatment too also went very well for me...not quite the excitement that you had apparently.

    Bloodwork was also great.  WBC and Neutrophil are back in normal range...YAY!  Doc was suprised to see that I still have my hair.  I told him that I know that it is gone any day now.  He also said that, contrary to things that I've read on the Internet, following treatments are easier than the first (meaning side effects).  Yes, you'll still have the exhaustion but the other stuff gets better.  So I'm pumped about that because treatment 1 was good for me for the most part.  I'm hoping that holds true.

    Really glad to see #2 went well for you as well.  We're halfway through A/C!!  Woohoo!!

    ~Adrienne

  • rock
    rock Member Posts: 1,486
    edited May 2008

    All the details (with pictures) are posted at:

    www.boobity.blogspot.com

    (I'll probably delete this post later, but wanted to share the silliness.  Yes, silliness.)   I was going to point out who I am in the photo but um, I guess you can figure out as I am the one hooked to the machine.  Pitchy faints at the sight of needles, ergo the thing draped over my arm.  What a trouper!

  • craftygal
    craftygal Member Posts: 31
    edited May 2008

    Hi All,

    I was having a pretty good week and hardly any se's. Until the  fallout began Tues morning (Day#16/Tx#1). Its right on time but still the pits. Pillow has more each day and it comes out like little paintbrushes in fingers or comb. No real bald spots yet, but soon I guess. 

    I had wig styled yesterday and I liked it. It slides abit (on my hair underneath?) which "reminds" me that its there. Friend feels it won't slide once hair is gone. It seems to sit back further than I would like and shows alot of my already high forehead. Any tips to keep it in place? I've ordered a wig hugger. Will that do trick? If I can get it to sit still and in lower position, I'll like it and wear it more. If not, I'll be glad to get the hat/scarf I ordered from tlc this week.  

    I have a picnic in VT Saturday. If tlc arrives in time, I may wear hat instead of wig. Its a casual picnic, but my first public event. I also see what you all mean about the fallout being nerve wracking. I'm sure once hat arrives (if not sooner) I will cut fringes and be done with this mess.

      

    My 2nd swim in pool is 10am Tues. Glad to hear the s/e's may be less as txs continue. Hope that's true for all of us. Other than my cold (which I don't expect to repeat) I had very mild #1. 2nd (last?) fill is Thurs, but I already have ride there if I need one.

    Good luck to all and hope we can enjoy the holiday weekend.

    Janice   

  • collector
    collector Member Posts: 193
    edited May 2008

    Well, i'm on Day 3 of first T/C treatment and had my Neulasta shot yesterday.  I forgot that I was supposed to take Claritin last night and went out to buy some today.  Do you get the nondrowsy formula?  That's all I could find and it seems stupid to take that at night when sleeping is problematic as is.  I have a call in to the nurse but they aren't in a hurry to get back to me.  (the waiting game as usual)

  • robink
    robink Member Posts: 336
    edited May 2008

    Happy Wednesday to all!

    I have my ticket to...not Hawaii or Mexico but for four courses at the infusion bar, arrival 9 am Thursday. 

    Appetizer:  Benadryl 

    1st course: Taxotere 

    To Cleanse my palate:  Zofran 

    Grand Finale:  Cytoxin

    Since I'm taken this trip once before I'm not very apprehensive.  If I'm not too drowsy from the Benadryl my dh and I may go see a movie, otherwise renting "National Treasure" sounds like a plan.

    My best to all of you. See you on the other side!

  • Jule
    Jule Member Posts: 250
    edited May 2008

    Adrienne,

    Thanks for the update on what to do before chemo. What a great resource? Is anyone taking TAC?  Adriamycin, Cytoxan, and Taxotere. I just wanted to know if there was anything I should prepare for. Thanks

    Julie 

  • drcrisc
    drcrisc Member Posts: 836
    edited May 2008

    O.k., I finally got the 2nd opinion path results...and I did NOT have to harm anyone!  It was a good day for all.  The results basically confirm the first one, which is what I was looking for.  They disagreed about the grade of the cells (they said 3 instead of 2), but that's about it.  So I have my barstool ready for next Thursday at 9:30. 

    Whew...just made it to stay with you gals.  Moving to a new board would have been just as depressing as some of the other stuff that's happened!  I have come to think of this one as my "home board" and generally check here first. 

    Glad to hear that everyone's chemo was relatively uneventful (well, except for the fire alarm!) and Rock - love the blog and pics! 

    Robin - sending thoughts of uneventfulness your way for tomorrow!

  • gogators
    gogators Member Posts: 39
    edited May 2008

    Good middle of the night y'all.  It is 3:18am and I CAN'T SLEEP!  It's got to be the doggone steroids.  I took some Tylenol PM, worthless.  I have been contemplating getting on the board for the last couple of hours, thought that if I start reading and typing maybe I would get things off my mind and it would stop racing.

    Tommorrow is my first tx, so long as onc thinks my incision is healed enough.  It looks much better than it did when it busted open saturday night and the drainage is very minimal now.  My mind is not racing so much about the tx, but more about the disease and my lack of family and friend support (parents dead from cancer and friends have all moved away because of the job market.)  I miss my parents so much, I have been without my mom since 21 yo, I am 34 and lost dad in Aug 06 kinda quickly.  I really need them right now and that has really been bothering me tonight.  I don't think it helps that my onc was my fathers as well and it brings back the horrible memories.  I have been wondering all night, if I will "sit in his chair" tomorrow. 

    I don't know, I feel like I'm rambling, I don't mean to be a downer.  I have been so busy and tired from the 3 surgeries, but tonight the idleness has really gotten to me. 

    Big day ahead of me tomorrow.  First tx, then to the wig store and then wal-mart for last minute things I forgot about to make this weekend smoother.  If it weren't for the boys sleeping, I probably would have went now to get the stuff.  As for the wig shopping...the girl who does my hair (used to be my clubbing buddy back in the day, but she is now married and settled down) and I were supposed to go together.  BUT, and I swear Murphy and his law have a secret hiding place in my house, she was pregnant and went into labor 3 weeks early, yep you guessed it, labor pains Friday night, baby born Saturday a.k.a. wig shopping day!  So, now I will be going by myself, but called the store yesterday and set up with the Manager my own session with her.  Problem is, I have no idea what I want.  I thought I found on one the internet, emailed it to Carolyn - my hairdresser - she said "Oh, Tina, that looks soooo 80's."  So, I will need all the help I can get from the store manager. 

    Well, this has probably been long enough....sorry about that.  I hope everyone has a great day tomorrow, I feel a bit better already, I even yawned...yeehaw!

    Tina

  • gogators
    gogators Member Posts: 39
    edited May 2008

    Update:  I went on myspace and posted a blog to my far away friends that have moved from here, I feel better.  My alarm went off 30 minutes ago, so I must get up, shower (well, bathe, I still can't shower until they look at this port today), get my son up and to his bus (the school is two miles away, but I have to drive him 7 miles to catch the bus, weird huh?), eat something and off to tx I go! 

    I will check in later today.  Enjoy your day!

    Tina

  • familyroks
    familyroks Member Posts: 575
    edited May 2008

    (((Tina)))  Will be thinking of you today.  I'm so sorry you couldn't get a good nights sleep.  On top of steroids you have a million thoughts screaming through your head.  Check in and let us know how you are doing and if you found the "perfect" wig!

    Robin - good luck today!  It sounds like you are as ready as you can be.

    Cristine - finally!  Another hurdle passed.  I'm glad your wait is over and you can start planning ahead for your treatment.

    rockthebald - how are you doing today?

    Happy se free day everyone (well as free as can be).  I'll be off for my Neulasta shot later this morning.

    ~Adrienne

  • Jule
    Jule Member Posts: 250
    edited May 2008

    Tina,

    Good luck today. I am rooting for both you and I that today is good with minimal complaints in the next couple of days.  I am hoping that it will be fine. Did they tell you that someone could come with you today? It has to be hard since both of your parents are gone, my thoughts and prayers are with you today.

    Julie 

  • familyroks
    familyroks Member Posts: 575
    edited May 2008

    Julie - Good luck to you today!!  You will do great.  Getting past the first treatment is a relief to some degree.  Please check in and let us know how you are doing. 

    ~Adrienne

  • familyroks
    familyroks Member Posts: 575
    edited May 2008

    rockthebald - I hope you don't mind...I cut and paste your Tips from page 4 over onto the June 2008 thread.  I think your lists will benefit so many.

    ~Adrienne

  • craftygal
    craftygal Member Posts: 31
    edited May 2008

    Tina,

    Sorry you couldn't sleep but here is a great place to come to. I did a 4am visit last week and it really helped. Our minds should have on/off switch installed during this process?? Guess not. 

    Good luck to you and everyone else for a smooth tx and less s/e's.

    Enjoy the weekend!

    Janice 

  • angelsaboveus
    angelsaboveus Member Posts: 298
    edited May 2008

    Hi everyone,

    Just a quick question,....I woke up this morning and my hair physically hurt, at the roots on the top of my head, is this my warning sign of great things to come? (or to leave...I guess would be a better way to put it !)  I am 14 days out today from first tx.

    Hope everyone has a great day! Innocent

  • beachmom13
    beachmom13 Member Posts: 313
    edited May 2008

    angelsaboveus - my head felt like I had my hair in a very tight pony tail the day it began to come out.  My guess is to start saying your goodbyes.

  • otter
    otter Member Posts: 6,099
    edited May 2008

    Yup, angelsaboveus, that would be it.  Mine didn't "hurt"--it itched a lot. Most women say their scalp hurts, with a tight pony-tail feeling like beachmom/Lee described. Day 14 seems to be D-day (B-day?  H-day?) for most chemo regimens where we lose our hair. (Tight hugs to you--this can be awful, or funny, depending on how you handle it)...

    Note added in Edit:  rockthebald, I spent all afternoon yesterday goofing off on-line and it was entirely your fault!  I followed the link to your blog and read the whole thing.  You are hilarious.  I wish I could write like you do--so witty and irreverent (that's a compliment).  Thank you so much for showing up on this ridiculous journey.

    Oh, and I wanted to tell a quick story about your blog post concerning "Saint Agatha," the patron saint of breast cancer patients--also described here:

    http://www.catholicspirit.com/stories/2006/feb/0206breastCancer.html

    http://saints.sqpn.com/sainta04.htm

    I am not Catholic.  I am not even religious (and don't want to go any farther than that).  But, I found this terribly ironic.  Her feast day is February 5th, right?  That's the day I had my mastectomy.

    otter

  • rock
    rock Member Posts: 1,486
    edited May 2008

    Post the Tips for Chemo anywhere you please!  The only ones I update, however, are listed on the "Tips for Getting through Chemotherapy" thread.  And if you run across any stupid or WRONG tips, please let me know. For instance, someone recommended Vitamin C supplements to me but my docs say absolutely no Vit C supplements ever, not during chemo, not afterwards, never.  So I took that one of my list and gave away my never-opened box of Vit C tablets!

    Muchos besos to everyone. (Or rather, hearty hugs. My nurse told me hugging my friends is probably better than shaking hands anyway.  That made me happy!)

  • EyesOTex
    EyesOTex Member Posts: 194
    edited May 2008

    I hope everyone is feelin OK post-treatment.  I go tomorrow for my last chemo of round 1; 3 more rounds to go....assuming today's blood work is ok, anyway.

    Muchos besos, indeed, since they are virtual!

  • otter
    otter Member Posts: 6,099
    edited May 2008

    rockthebald, did your docs explain the prohibition on Vit C?  I can understand why they don't want us to take it during chemo or rads, 'cause it's an antioxidant and those treatments work their magic by creating oxygen radicals.  But, why would it be bad to take a regular, FDA-recommended dose of Vit C (not a megadose) once we're through with treatment?

    Just curious.  I've actually heard that same thing from other women on this board, but I've never heard an explanation.

    otter 

  • robink
    robink Member Posts: 336
    edited May 2008

    Hello All.  I'm writing this while in the chair poolside.  Please forgive me if the posting gets a bit wordy.

    Tina - too bad we can't see who is on-line when we are.  I was up in the wee hours of the morning also, thinking Decadron to be the culprit.  Wishing you well across the miles for a smooth treatment #1 today, and that all the SE you are fearful of are nonexistent. 

    Angels - my scalp started itching day 10 then a few days later my scalp became very tender.  I have always had short hair so I don't know the tight pony tail feeling.  Day 17 a number of hairs began to drop and by day 19 I had my dh buzz cut my hair to 1/2 inch.  Yes, I cried but in the privacy of my home.  Doing the buzz cut helped me come to accept the inevitable.  Now it's day 22, I have just a little stubble and I am OK.  Much better than I thought I'd be.  And getting ready is so much quicker!  No hair to dry and style.  You will manage this and come to accept your new look - in your own way.  I think each of us come to grips with this individually, just like how our SE are unique to each of us.

    rock - my onco said no vit C 7 days before and 7 days after chemo.  Never heard about the never ever.  I use mega doses when I am getting a cold and would hate to give that up (after chemo is a has been)

    Leeayn - Welcome!  Sorry you are on this journey but hope you find this thread, and the website to be helpful and a lifeline.

    Craftygal - It was good to read that you liked the way your wig was styled.  Currently I have two wigs, one human hair and I can style that one myself.  It looks very similar to my pre-chemo hair (without the gray).  The Raquel Welch wig I purchased is attractive bu seems a little ratty.  The is a salon in town that cleans and styles wigs for free so I may take advantage of their service before I banish it back to the box.  Yesterday I tried on a Noriko wig and loved the silky feel, the cap felt secure without being too tight.

    Your wig should not slip as much or at all when your hair is gone.  The wig hugger sounds like a good idea!  Is your wig adjustable?  That will help if it is.

    Cristine - I am glad you now have a game plan!  I understand the need to get it underway, we all do.

    Well, I'll close for now.  I have about 2 more hours here so I may be back before they boot me out of the pool.

    Robin

  • rock
    rock Member Posts: 1,486
    edited May 2008

    I posted a clarification below based on a conversation with a dietician.

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