Starting Chemo in December 2013

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  • OneTexasDay
    OneTexasDay Member Posts: 162
    edited December 2013


    Hang in there Lorreymom.  Hope your rash clears up!!!

  • KLI
    KLI Member Posts: 52
    edited December 2013


    I will try heating pad. Felt a little better in the afternoon but then started more cramps and diarrhea. Trying to get some rice down.


    Lorreymom do you take those meds at home or at chemo why do you have to order doesn't your onc do that?

  • atlbraves
    atlbraves Member Posts: 50
    edited December 2013


    Hi, I hope everyone's managing well. You are all in my thoughts.


    I would like to share this website: http://www.goodwishesscarves.org


    I found out about them through a blog called "But Doctor, I Hate Pink." I had completely forgotten that I put in a request for a scarf, but today I got an email telling me that one was on the way for me.


    :)

  • momat927
    momat927 Member Posts: 173
    edited December 2013


    Hi Ladies. With all the steroids, I couldn't sleep last night and felt pretty scared, like a kid wishing my own parents were still alive. The steroids have diminished and yesterday 's Neulasta shot kicked in. (TC Wed). Just feel weak and flu like, but hardest part is waiting to see what might happen next. My skin feels almost like it is burning, especially face. Is that normal? It is hard not to become hypervigiliant. My legs feel like jello. Will this resolve in a few days? Second TC is Dec 27. Thank you so much , Amy

  • lorreymom
    lorreymom Member Posts: 149
    edited December 2013


    KLI - my onc prescribed 3 rounds of meds for me. I pick them up at the pharmacy prior to each chemo. My 3 rounds of dex & stemetil were dispensed all at once to cut down on my co-pay costs. But the aloxi, emend & neulasta are all individually packaged and dispensed a few days before my chemo. Co-oay would be the same regardless of when I get them. Basically, I just call in a renewal on my original script. Does that make sense?


    For my first chemo, I brought all my meds with me. Blood was taken, and when the reults came back good & chemo was a go, I was instructed by the nurse when to take them. For my next round, I have bloodwork & see my onc on Tuesday. Chemo is tentatively scheduled for Friday. If all is good with my results, 2nd chemo will go ahead. Since I will know in advance if chemo is a go on Friday, I will take my meds at home one hour prior to going to the Cancer Centre. This way the nurses won't have to wait & chemo can start ASAP. Does this make sense too?


    They never want you to take your meds if they are not sure if chemo is a go. It would waste the meds & put drugs into you that you don't need. They always want to confirm chemo before you take the meds...it depends on whether you have bloodwork the same day or in the days prior.


    Neulasta is always given 24 hours after chemo. I have a community care nurse come to my house to do the injection because it will be Saturday & Cancer Centre is closed.

  • kjfromca
    kjfromca Member Posts: 283
    edited December 2013


    Lorreymom - I was wondering why you had to pick up your prescriptions too. It makes since. I guess every Infusion center does things differently. Where I go, they administer the anti-nausea meds in an IV right before the chemo. It would be nice to have a nurse come to the house to administer the neulasta inject. I have to go back to the center the following day. I hope your rash clears up. This is such a stressful time for all of us, not having control over how our bodies are reacting to these chemicals is so frustrating.


    Moma927 - I recommend that you call your doctor regarding your side effects. I have Norco for a backup just in case I have a lot of pain with the neulasta shot. I heard the first shot is the worst. My sister-in-law gets weird side effects when she takes compazine, I don't know if you are taking this drug. I can tolerate it, I don't like the zofran, I get headaches and it doesn't feel like it helps much. I hope you feel better soon.


    Kim

  • lorreymom
    lorreymom Member Posts: 149
    edited December 2013


    rash is getting worse, now about 4 -5 "(doubled since this morning). Still no fever, but very itchy. Trying not to scratch it. I just took an antihistamine & had an oatmeal bath. Smeared all the red areas with antibiotic & antifungal cream . Put on freshly laundered PJs. If that doesn't work...off to emerg I go. Worried!

  • momat927
    momat927 Member Posts: 173
    edited December 2013


    lorreymom, let us know if you need ER. My nurse gave me a list of symptoms I had forgotten I have. If a rash worsens, it seems you need to call your doctor- should be informed. Good luck.

  • momat927
    momat927 Member Posts: 173
    edited December 2013


    kim, i hope i am not repeating myself, but my nurse told me to try Claritin for bone pain with Neulasta. Thanks for your feedback. I am learning so much from these discussions. Just a bit of whining today! Good night. Amy

  • RobinLK
    RobinLK Member Posts: 840
    edited December 2013


    I am using the Claritin but needed to add Percocet for the neulasta pain. I don't think it would have subsided to a manageable level with either one alone. The med combo above was Dr. approved in advance of the shot.

  • SpecialK
    SpecialK Member Posts: 16,486
    edited December 2013

    momat927 - Decadron will cause a red face and flushing - this is a normal SE and will dissipate within 24-48 hours usually.  It happened to me every time.

    Those who don't want to take Zofran, there is nothing wrong with eliminating it and just using another anti-nausea drug, such as Compazine. I had Zofran, Compazine and Ativan as take-home anti-nausea meds - I could use whichever one worked.  Zofran was totally useless for me and I got a wicked headache.

    goldie - Sancuso patches are usually the anti-nausea drug of last resort (most likely due to cost - about $1500) and usually are used only for intractable nausea and vomiting.

    For those receiving Neulasta, the first injection is usually the worst as it is the first expansion of the bone marrow to produce extra white cells.  Subsequent injections function a bit like a new pair of shoes - they get more comfortable each time you wear them because they are broken in - as is your bone marrow!  For those receiving Neulasta after a taxane drug (Taxotere or Taxol) bone and joint pain are also SEs of those drugs so it can be difficult to determine what is causing the pain.

  • lorreymom
    lorreymom Member Posts: 149
    edited December 2013


    Update - woke up at 5 am due to itchiness. Looked in mirror - rash is still there but receding. Whatever I am doing is working!! Woot. Smeared it with more antibiotic & anti-fungal cream. I will take an antihistamine every 24 hrs until it completely goes away. So relieved!!! Going back to bed now!! ER here I DON'T come! I took pictures to tell my onc.

  • KLI
    KLI Member Posts: 52
    edited December 2013


    lorreymom sounds like a rough night maybe you can get it checked during the day so you don't have to worry again about ER. Glad it is getting better. I guess taking your premeds at home gets you out faster they do mine through IV before chemo drugs so long day of infusions.


    Momat I have not been sleeping since steroids started either know what you mean just laying there wondering what your body is doing. My onc said I could take a Benadryl but I did not feel like putting more in me.


    Woke up sweating soaked anyone going through that?


    Taking my first zofran now will see how it goes.


    Nice to share our troubles .... Hopefully easier days ahead.

  • emq2
    emq2 Member Posts: 60
    edited December 2013


    KLI:


    The Zofran caused a slight headache with me yesterday. Just a heads up. Pay attention to the side effects.


    Lorreymom: So glad for you the rash is subsiding.


    Liz

  • IamNancy
    IamNancy Member Posts: 1,158
    edited December 2013

    Here is a site that will send you free hats - I remember when I received mine - I was so touched and it really made me feel better.. I just wanted to share it with you ladies..

    http://www.heavenlyhats.com/heavenlyhats/request+a+hat+package/default.asp


  • keepthefaith
    keepthefaith Member Posts: 2,156
    edited December 2013

    Thanks ladies, for the links to the hats! My first TX was the 3rd. I, too, had a hard time sleeping for the first 3 nights. Got a RX for Ambien yesterday; took 2 last night and slept for 11 hrs! Boy, that felt good! Woke up this morning to the start of a yeast infection, but all else is good;  well, the big C, which I am still working on. Someone mentioned molasses...may have to try it; a few aches and pains, but not enough to take anything for. I told my DD that my body feels like a pinball machine, with the ball going around and hitting a different part randomly...then, stops. Crazy! I'm glad it's cold outside today. Will write some Christmas cards and take it easy! I hope you all have an easy week-end. Hang in there! We've got this!!

    ((HUGS))

  • nmcd
    nmcd Member Posts: 28
    edited December 2013


    Hi Ladies!


    Just wanted to stop in and offer support. I had chemo three years ago and had a difficult time. However, whenever a SE hit I would focus on the out come ~ cure! You can handle whatever you need to handle. Try not to focus on the negative, but focus on how good things will be when this part of the journey is over. Nothing that happens during this time is permanent. Your life will get back to normal, this is just a side trip. My oncologist prescribed ativan for me which helped in many ways, but mostly helped me sleep. I wish I had found this forum during my chemo time, but I am glad to help anyone through their personal journey. Believe, and remember, this is not how you will spend the rest of your life.

  • momat927
    momat927 Member Posts: 173
    edited December 2013


    KLI- i know what you mean- Didn't want to take Ambien or Benadryl as already so medicated. If not sleeping continues, I will reconsider.


    lorreymom- Yay, No ER!!!


    Liz, thanks for Zofran headache info- so far I am not nauseous at all. Let's see what day brings


    Are you all kind of resting or trying to tackle daily activities?


    Hope today easier for all. Amy

  • emq2
    emq2 Member Posts: 60
    edited December 2013


    Hi All:


    Well, I had my first bout of nausea late this AM. Most likely the banana I ate before taking the Cytoxen was not enough. I took a Compazine at 11:30AM and feel better...just a little weak. No headache..not even slight, so I will assume the headache yesterday was from the Zofran.


    Gonna try and head out and do a little shopping in a few hours - After I eat. LOL


    How is everyone feeling?

  • Siennasugar
    Siennasugar Member Posts: 5
    edited December 2013


    Hi Ladies, I started Chemo on 12/05/13. I have 4 cycles of Cytoxan/Taxotere with Herceptin. Then Herceptin will continue for a year. So far , so good. One bad bout of nausea yesterday. Today is the second day, and I am just really tired. Forcing myself to eat , and drink water. So I feel pretty good .


    Bought 2 wigs, brow stencils & powder, 2 hats, and a non slip scarf. I had a fully packed chemo bag, and I was glad . It was cold and uncomfortable. I'm glad I had my pillow, and throw.


    I am scheduled for a Look Good, Feel Better session on Dec 19th. Just trying to prep for whatever comes.

  • gia444
    gia444 Member Posts: 68
    edited December 2013

    Hi ladies,

    I had my #3 chemo on Dec 4 and so far I feel better then I did for the first two.     I take Emend, Zofran and Dexamethasone 1 hour before starting chemo and then for a couple of days after.    I take Metoclopramide if I need it for a day after that and so far no nausea at all.     Sometimes on day 4 & 5 I get a queasy stomach.     I take Biotene mouth wash and brush my teeth after eating with Biotene tooth paste and so far no mouth sores.    Colace & Senokot controls the big C. 

    These boards have helped so much and I am very thankful for all the info I have received.

    Hang in there everyone.     

  • OneTexasDay
    OneTexasDay Member Posts: 162
    edited December 2013


    First chemo was Thursday,.... I have been pretty good on SEs so far, knock on wood. I have been napping and resting all day. I really don't know if I am that worn out or just taking advantage of the opp to be lazy. Husband is in other room working on Christmas tree and my DS has been entertained by all of the neighbors and it's nasty outside, so no walking for me.... Mom is being mom to all of us, which is a wonderful thing in our case. :)


    I am all snuggled up in bed, sipping water, watching football and trying to figure out if I might be milking this a bit. Don't want to be the boy who cried wolf, especially when I have a long road ahead of me yet....


    Cheers!


    Steph

  • emq2
    emq2 Member Posts: 60
    edited December 2013


    Steph:


    You deserve to be pampered. Take advantage of it. I am sure your family is glad to pitch in.

  • OneTexasDay
    OneTexasDay Member Posts: 162
    edited December 2013


    Emq,


    How are you doing today?

  • atlbraves
    atlbraves Member Posts: 50
    edited December 2013


    Everybody sounds as though they are doing pretty darn well. Woot, woot!


    Anybody else having scalp discomfort? Lorrey, you mentioned something the other day, I thought. My scalp is driving me nuts...itchy and sore...I'm blaming it on the AC, but as Amy said, I'm quick to blame everything on the chemo. ;)

  • lorreymom
    lorreymom Member Posts: 149
    edited December 2013


    atlbraves - my scalp is very very tender to touch now...started around day 14 post-chemo. No hair loss yet. It only hurts to touch my head. Washing my hair is no fun. I have started to wear my hats in public now. My hair just looks ... well...dead, for lack of a better word. It has turned an ugly greyish dirty blonde from auburn-brown & is dull. I am having other skin issues too (stomach area), but it is getting better with oral antihistamines and topical antibiotics & antifungal. I suspect hair loss isn't long to come. I am ready though...got my wigs, hats & tons of scarves.


    So glad to hear of all the minimal side effects! Woot!! :). Rock it, ladies!!

  • nctrout
    nctrout Member Posts: 2
    edited December 2013


    had first TCHtreatmentThursday. Felt ok untl earlyafternoon yesterday. Then tired and nauseated. Took care of that by s,eepin if off,


    Today not so lucky. Diabetes going nuts- glucose readings all over the scale! Finwlly have gktten some control over them.


    Dr concerned about this and heart history. I just don't feel too good right now!!


    This too shall pass!

  • nctrout
    nctrout Member Posts: 2
    edited December 2013


    had first TCHtreatmentThursday. Felt ok untl earlyafternoon yesterday. Then tired and nauseated. Took care of that by s,eepin if off,


    Today not so lucky. Diabetes going nuts- glucose readings all over the scale! Finwlly have gktten some control over them.


    Dr concerned about diabetes w/chemo, but no radiation due to heart issues.


    Feeling puny but glad to have started on this journey to get rid of the evil growing inside!

  • OneTexasDay
    OneTexasDay Member Posts: 162
    edited December 2013


    Nctrout, sending hugs and prayers your way. Hope your sugar counts stabilize and the nausea stays away.


    Hugs!

  • SpecialK
    SpecialK Member Posts: 16,486
    edited December 2013

    nctrout - are you being given Decadron as a pre-med? It will mess with your sugar readings.

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