April/May 2012 Chemo hang out

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

    ladybug1- Yep those port placements hurt!!!  I was warned by my BS and his asst. that would happen and the patients complain that it hurts more than the post op surgery areas!!!  It should feel better in a week, less sore..

  • ladybug1
    ladybug1 Member Posts: 21
    edited April 2012

    Thank you ladies for posting so quickly.  I was so afraid the port hurt and now I am getting chemo and then my brain starts spinning into all sorts of scary scenarios.  I knew you all would have the answers and I feel better already.  I am so grateful I found you.

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

    You may want to tell them at the chemo infusion that the port placement is really new and ask if they can spray it with something to numb it before the infusion starts.  Mine was placed the middle of March and had healed really well.  I got a prescription for EMLA cream from my MO  which numbs the port that you apply an hour before you go to your chemo appt.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited April 2012

    Ladies,

    I read all your posts and am simply astounded at your bravery. Your fear was evident when you started this thread and now you're moving through chemo, gritting your teeth and getting it done.

    Some say it doesn't take courage to save your life, but your ability to make jokes about this speaks volumes about your grace and power to take charge of your txs as best as you can.  I'm honored!

    (BTW, I used peri-colace caps for occasional slow movement-you know--and it worked great. Tried milk of magnesia when things were really slow, and had to be careful although it worked when I was more needy as well).

    Hugs

    Claire

  • dancetrancer
    dancetrancer Member Posts: 4,039
    edited April 2012

    Yep, my nurses spray mine with that fluoromethane spray really good prior to accessing it each time.  That stuff is great.  Numbs it right up.  Plus, my one nurse holds the port really tight with one hand while putting the needle in with the other.  He's says keeping the port from moving at all is the trick.  I barely feel a thing at all when he does it.  He's got the magic touch!  

  • sandik
    sandik Member Posts: 482
    edited April 2012

    Welcome to the new people!

    My port was sore for a good two weeks. Hurt more than the incision did for the lumpectomy.

    day 2 was uneventful so far. Had toast this morning, then a few crackers a couple hrs later. Lunch was chick n rice soup, fries n a blt. Ate the soup, picked at the fries and the smell of the mayo scared me away from the sandwich. Haha that went in the fridge for tomorrow. Going to have some grapes then lay down til dinner. So far so good.

    Went for my shot. Drank about 40 oz so far + the soup. My cheeks are really really red. Is that the chemo or the shot?

    how are the rest of you making out?

  • SadeSurvivor25
    SadeSurvivor25 Member Posts: 119
    edited April 2012

    Chapter 4,I'm feeling horrible!!! I'm nauseated and I keep vomiting. I took the nausea meds a few hours ago but they don't seem to be working. I'm not sure if it's too early to tell.



    I pray the rest of you are doing well. Hugs for everyone.

  • sandik
    sandik Member Posts: 482
    edited April 2012

    Sade that sucks. Try some ice pops or gatorade. Keep getting fluids down. They told me if the pill doesnt work in 4 hrs to try the other one. See which one is better. How long have you been puking? Let the drs know if it continues!

    I can totally take pain, like back pain, stitches, dentist stuff, but the nausea I can not do. That is the worst!

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

    Hey Sandik! The redness so I hear is from the steroid (decadron). I know my face was bright red for the first three days but faded after I stopped the decadron. I have mild rosacea and that really lit it up.

  • sandik
    sandik Member Posts: 482
    edited April 2012

    Ok thanks! I feel fine but its beet red like when I get mad! Haha

  • lsharvey822
    lsharvey822 Member Posts: 257
    edited April 2012

    SadeSurvivor - I hope you feel better fast.

  • dancetrancer
    dancetrancer Member Posts: 4,039
    edited April 2012

    sandik - it might be the dex! 

    sadesurvivor - Oh no!!!!  Perhaps call your onc and get something else called in.  The meds should work really quickly - my Zofran (kind that melts under the tongue) did.  Once the n/v starts they say it is harder to control - you may need a different med.  Don't suffer - call!   

  • chrissera
    chrissera Member Posts: 79
    edited April 2012

    Hello ladies.  I will be joining you as I haved my port placement scheduled for next Wednesday 5/2 and then my first chemo next Friday 5/4.  I will be getting neoadjuvant chemo of  Herceptin/Abraxane every week and  then Herceptin/Abraxane aand CArboplatin every 3 weeks. I don't think I have ever been so scared of anything before!   I have read so much that I don't know what to expect.  Any suggestions would be appreciated!  and does anyone have experience with working during this type of chemo?  HUGS to all!

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

    Sade, definitely call, but I was wondering what meds they gave you? They told me to take emend and zofran whether I felt sick or not for the first 3 days and if that didn't work, they gave me compazine as a fallback to take as needed. The compazine is supposed to work pretty well.



    I sure hope you feel better soon!

  • Denise-G
    Denise-G Member Posts: 1,777
    edited April 2012

    Ladies, just stopping by to give you some encouragement, too.  I started A/C in December, then 12 weekly Taxols - 3 more to go.  You swear you will never make it through.  It seems so far away.  But one day at a time, you get through it.  YOU WILL TOO!  

    My port hurt like heck for a week after it was put in, mostly because it was on my BIG BOOB side and bouncing big boob made it hurt.  But it has been a great blessing to have.  I need Herceptin for quite some time, so my port will be with me awhile.

    Be encouraged.  You will make it through! 

  • lsharvey822
    lsharvey822 Member Posts: 257
    edited April 2012

    Welcome Chrissera.  Sorry you have to join us but you're in good hands here.  I totally understand this being scary as H#LL!

  • 7donatela81
    7donatela81 Member Posts: 16
    edited April 2012

    Chrissera, welcome.  I was scared before chemo.  It was the UNKNOWN that bothered me.  Now that I have had 1 chemo and 1 herceptin treatment I'm not as nervous.  I get the herceptin weekly too.  It didn't bother me too much Monday when I got it alone for the first time.  In fact today I felt pretty good and ate whatever I wanted with no problems.

    Let us all know how you are doing.

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

    Good Morning everyone!!!!  Wishing for minimal SE's for all!!!!

    Since there seems to be a laundry list of possible SE's and I couldn't figure out what the heck I should be feeling, I called my onco's office this morning to chat.  Started feeling a little funky and weird yeaterday afternoon (48 hours since 1st infusion) and by the evening, I was moving really slow.  Drinking water like crazy and also burping a lot.  I'm trying to keep up with the eating so I don't have an empty stomach.  Last night was a "white" meal-- everything was white in color---- fish, mashed potatos, mac n cheese, tampioca pudding.  Sounds lieka lot of food but when you have a only a few bites of each, it really isn't.  Thank goodness the anti nausea meds are working and no plumbing issues.  Still thinking that stupid period of mine is coming.... it's due anytime.  I can feel those ovaries tightening up and wondering what the heck is happening around here.  Have been a little weepy too.....hormones, chemo.... who knows why but absolutely necessary!!!

    Rest everyone and drink, drink, drink!!!!

  • dancetrancer
    dancetrancer Member Posts: 4,039
    edited April 2012

    melrose you are moving into 3 days post chemo...steroid "crash" time...sx starting time. Frown  I had terrible indigestion.  Keep up the drinking water, maybe ask your onc about pepcid and/or a proton pump inhibitor like Protonix, etc.  Smart to keep up with the eating and in small doses.  The small meals help quite a bit.  Be careful not to eat too much at one time...I suffered for doing that!!!  

    I just read a little bit about the B-47 trial you are doing.  Fascinating.  Do you know if you are getting the Herceptin or not?   

  • SadeSurvivor25
    SadeSurvivor25 Member Posts: 119
    edited April 2012

    Good morning ladies. I'm feeling much better today. I couldn't keep water, ginger ale or the popsicle down. After puking and the big D for hours and after Decadron and Ativan didn't work my hubby (DH??) called the after hour hotline. I had two other prescriptions for Zofran and Emend but it was for day two and three after chemo and it said to take as directed. The nurse called my onc who said to take a Zofran and Imodium for diarrhea. She also said she would call back in two hours to see how I was doing because they would want me to go to the er if nothing had changed. But the Zofran (and prayer) did the trick. Before he could come back with the Imodium I was knocked out. I'm feeling good so far. My stomach is feeling a little funny...I'm not sure if it's from hunger or if the nausea is trying to creep but. I'm scared to eat or drink, fear of yesterdays episodes.



    I wanted to thank you all for your advice. I really appreciated it. I pray that you all minimal to no side effects.

  • dancetrancer
    dancetrancer Member Posts: 4,039
    edited April 2012

    Sade, thank goodness for Zofran!!!!  So glad you called.   My onc told me to take the Zofran every 6 hours, even if I didn't have symptoms - to keep it in check, b/c as you know...it's awful once it starts.  I tried to wean too early (6 or 7 days post chemo) and ended up with horrible indigestion, thought perhaps I was having a heart attack b/c it was so bad!  He had me go back on the zofran until day NINE!  I had no idea I would need to be on it that long, but that was the case for me.  So just a heads up in case you are similiar.  

  • SadeSurvivor25
    SadeSurvivor25 Member Posts: 119
    edited April 2012

    Thanks Dance. I'm going to call for another prescription because they only sent me home with 4 Zofran and 2 Emend...for two days after chemo. After my first treatment I was felt sick for 4 days straight which I made clear to him yesterday before chemo.

  • dancetrancer
    dancetrancer Member Posts: 4,039
    edited April 2012

    eeeks Sade, that sure isn't much!  My presciption is for 90 Zofran (8 mg)!  And 6 refills.  I think I'm set for the duration of my chemo.  LOL   I get Emend and Aloxi in my IV as well on chemo day. 

  • SadeSurvivor25
    SadeSurvivor25 Member Posts: 119
    edited April 2012

    Wow!!! I feel cheated lol! I get Emend on chemo day as well along with two to take for two days afterwards. They have got to give me more Zofran! He was also talking about possibly giving me a marijuana type of prescription for nausea but I'm not too sure about that one lol. So far it's trial and error hopefully it stops at the Zofran.

  • dancetrancer
    dancetrancer Member Posts: 4,039
    edited April 2012
    LOL SadeSurvivor...too funny!  I did not know medical marijuana is legal in Georgia...I don't keep up with these things.  That could be an interesting prescription to pick up!!! Wink
  • SadeSurvivor25
    SadeSurvivor25 Member Posts: 119
    edited April 2012

    Me either Dance! When the onc walked out my husband was like "did he just say marijuana"?!? I was just as shocked. If I end up needing it I'll let you know how it goes lol

  • SadeSurvivor25
    SadeSurvivor25 Member Posts: 119
    edited April 2012

    I'm googling it and it doesn't look legal here. So I'm not sure how that's going to work! We shall see.

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

    Just woke up from a nap--- feel a little better but now it's time to drink drink drink and find some nibbles to eat. and just rest. 

    I found out I was receiving the Herceptin after the clinical trial people randomized me.  It is one of those studies, either you receive ir or you don't---- no placebos.  My onco and her research coordinator are thrilled that I'm getting it since I'm the first patient to volunteer with them.  I can tell you I'm being very carefully monitered.

  • dancetrancer
    dancetrancer Member Posts: 4,039
    edited April 2012

    hmmmm.....sade...your onc sounds like he may have some interesting connnections!  JK!!! LOL

    That's very cool melrose.  Hoping for minimal SE as you move along post chemo!  

  • LisaG65
    LisaG65 Member Posts: 65
    edited April 2012

    if you can get a Rx for maryjane i "highly" recommend it!!  take your mind off the fact its maryjane, it will help you eat, and calm you. if your luckiy enough to have a cool dr who will give it to you, take it for those of us who wish we could get  it, i am fighting a battle royal trying to get marinol to stimulate my appitite, the insurance keeps kicking it and wants to subsitute an anti nausea med. i dont have nausea, i have no appitite. i have nausea meds already and they work fine for that, but they dont help me eat when food tastes, smells and sounds gross!!

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