April/May 2012 Chemo hang out

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

    Sandik- Hey Twin--- looking good as ever!!!!!  Still losing the hair and my scalp is a little sore.  Those poor little hair follicles.... they tried to keep the hair alive .... but alas the chemo got them......  I get the feeling that the scalp is going to be sore no matter how long or short the hair is.  So for now, I'm just seeing how much is left on next Tuesday's infusion.  After that, it may be time for the crew cut.  Hope your side effects are minimal!!!!! 

    Everyone- Have a wonderful Mom's Day weekend!!!!  Rest and have minimal side effects for all!!!!

  • Melrosemelrose
    Melrosemelrose Member Posts: 3,018
    edited May 2012
    IndigoMont11 - YAY!!!!  Second treatment done for you!!!!!  Yahoo for the Power Port--- now you can do anything!!!!  Hope you have a wonderful weekend and feel well enough to enjoy  Mother's Day with your boys!!!
  • Melrosemelrose
    Melrosemelrose Member Posts: 3,018
    edited May 2012
    IndigoMont11 - YAY!!!!  Second treatment done for you!!!!!  Yahoo for the Power Port--- now you can do anything!!!!  Hope you have a wonderful weekend and feel well enough to enjoy  Mother's Day with your boys!!!
  • IndigoMont11
    IndigoMont11 Member Posts: 1,095
    edited May 2012

    My scalp felt pretty tender before I buzzed my hair down.  We used a clipper with no guard so the stubble that's left probably isn't even 1/8th of an inch long.  It doesn't really hurt now. I'm wondering if all of it will come out before tx#3.  

    I was just reflecting a bit on Mother's Day.  I've had to spend a lot of Mother's Days away from my mom, since she lived in Missouri and now in East Texas, and I've lived in Colorado since 1982.  She's told me before that since she's loved being a mom, every day is Mother's Day.  During my hockey mom days, my son's team had to play a lot of games on Sundays, and therefore that also usually meant Mother's Day.  Well, I didn't think twice about it - that was part of being a mom for me, and I wouldn't have missed a minute of it.  This year, I've asked DS#1 to make us a steak dinner using his famous marinade.  The breakfast in bed idea is kind of appealing too, though, lol!  No matter what, I will enjoy the day somehow, and wish the same for you, Melrose - and all of us moms out there, and the moms who love us. 

  • Stacie
    Stacie Member Posts: 607
    edited May 2012

    LOL Dennis the Menace. I loved that show.

  • mb1024
    mb1024 Member Posts: 49
    edited May 2012

    Just getting back after a long day.  I spent a lot of time catching up with everyone, and reading all the posts I missed since this morning.  Sandik, I love your new picture.  I think you, and everyone else shaving your heads, are so brave.  I asked my husband about shaving mine in a week or so, and he said sure, but I don't know if I can go through with it.  I had it cut short, like a pixie cut, but I don't know if I can go down to stubble.  I may feel differently if my scalp starts hurting.  In my hippie days, I had hair down to my waist. Today was day 3 of first tx, and I woke up totally wired and with a bright red face.  My temp was only 98.3, so I knew it wasn't an emergency.  When I got to the office, I called the nurse, and she said it's a classic reaction to the steroids.  She said I should still take them tomorrow, which would be the last day for them.  I got a lot done in the office, because I couldn't stop moving and working.  Now I'm tired.  Still no reaction to the Neulasta shot yesterday.  I took Claritin before, and today.  How many days after the shot do we take it? If I still feel OK tomorrow I'll go see my mom, who's 94 in an Alzheimer's Home.  I don't know how I'll feel on Sunday, so at least I'll get to see her close to Mother's Day.  She knows me, but she never knows what day it is.  If I miss this weekend, she won't know the difference, but I'll feel guilty. 

  • ladybug1
    ladybug1 Member Posts: 21
    edited May 2012

    I buzzed my hair today.  I wore a wig home but I ended up taking it off and just going bald at home, it is so much more comfortable.  Even though I had been preparing for this moment it was still sad.  My wig is nice but I feel it and it just reminds me I am bald now.  I look like a chemo patient... but then again that is what I am.  

     I have to say it was empowering to shave it.  I was getting tired of loosing hair everywhere, it was gross.  I wonder if I will ever be bold enough to go out in public like this... I hope so. 

  • vballmom
    vballmom Member Posts: 426
    edited May 2012

    Kim, I bought my wig today.  I felt like a chemo patient when I put them on - some more than others.  I decided to have fun with it, though and went blonde. I think I will be bald at home. I bought a nice soft hat, too. I am more into comfort than style. I also work for myself, so I don't have to worry about looking good for other people.

  • Maghery721
    Maghery721 Member Posts: 68
    edited May 2012

    Hi ladies, just popping in to say hello and send my support and good wishes to you all as you go through chemo. I know it's tough. No other way around it. But believe me, if this big baby (that would be me!) can get through it, anyone can. Definitely had some rough days but I gotta say I thought it would be a lot worse (probably from all the stories over the years, prior to anti-nausea meds I believe).



    Regarding wigs and cutting/buzzing hair, I'm all about comfort like vballmom says. I only wear my wig to work. All other times I have a head scarf on (except at home where I wear nothing). I wear my head scarves everywhere - I love them. Even saved me from a speeding ticket one day (I was in such a rush to get to chemo - ha, ha - not - but seriously, I definitely shouldn't have been speeding).



    So ladies, I wish you well. Feel free to ask me questions if you have any, or PM if you prefer.



    Best wishes, Cathy

  • Fierro6
    Fierro6 Member Posts: 224
    edited May 2012

    Pauletta, I have never been much of a "girlie" girl, and I have always seen crying as a sign of weakness in myself (never in others...I'm weird like that.)  Anyway, I've cried more since this diagnosis than I can ever remember crying in my life.  I'm buying stock in Puffs.  Wink

    You don't sound like a baby.  You sound like someone going through a difficult time.  I haven't even started chemo yet, but I sure could complain a lot about the back of my arm on the mx side.  I hear it's from the lymph nodes being removed, but it is like a bad sunburn feeling, and it's annoying as hell.

     I've been so happy to find the support here.  Lots of excellent advice.  I hope you all have an amazing weekend.  (I get to see my son and grandbabies later today!)

  • dancetrancer
    dancetrancer Member Posts: 4,039
    edited May 2012
    mb1024 - the clinical trial protocol is to take Claritin for 7 days after a Neulasta shot (b/c neulasta is long acting).  I get Neupogen, which is short acting, so I just take it on a daily basis whenever I am getting those injections.  
  • Husker123
    Husker123 Member Posts: 101
    edited May 2012

    I don't know if it was in this thread that I read about the apple cider vinegar for mouth sores or not. I have to tell you it WORKS!! I took some on a qtip and dabbed the sore. It is GONE this morning.

    I haven't lost my hair yet. Still a few days from that but a couple of friends that have been thru this gave me a tip for sore scalp. They said to use leave in conditioner on your scalp. Said it really helps!

    I think this is the first time I've posted on this thread. I'm a week past my first treatment. Doing ok. Have had pretty minimal SE's. I'm knocking on wood that it continues. Being tired has been the worst of it.I have been drinking a ton of water and maybe that really does help.

  • mb1024
    mb1024 Member Posts: 49
    edited May 2012

    Thanks, Dancetrancer, I'll take the Claritin until next Thursday.  Husker 123, so far my SE's are minimal, and I've been drinking lots of water.  Maybe that does help. Today was the last day for steroids, so the fatigue hasn't hit yet.  I'll keep the tip for sore scalp in mind if it happens.  I have learned more information on this forum than from the doctor and nurses.  

  • lsharvey822
    lsharvey822 Member Posts: 257
    edited May 2012

    @Maureen - totally agree with you on learning more here!  Hope you continue to have minimum side effects.

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

    FYI I have declined Procrit (too risky).  I will do a transfusion if my hemoglobin drops below 8.  It climbed a bit from Thursday to Friday (9.1 to 9.7), so I'm hoping it continues to climb on it's own.

     My ANC (absolute neutrophil count) has moved from Gr IV neutropenia to Gr III.  Do a self neupogen tomorrow and will retest Monday.  

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

    Just snipped snipped snipped my hair off and it feels so good!!!!  I made little ponytails before cutting my hair and got those scissors and no more bob!!!  Got tired of the handfuls of hair coming out  and the amount of hair that coming out was starting to "wig" me out.  My DH buzzed my head to clean up my snip job!!!!  Took control of that hair before it controlled me!!!  Just love it short!!!! So liberating!!!!

  • lsharvey822
    lsharvey822 Member Posts: 257
    edited May 2012

    @ Dancetrancer - I'm SO GLAD you're ahead of me!  I have no idea what half of that means but know I'll be coming to you for explanations when I need it!

    @Melrose - You go girl!  I'm with you!  I'll tell cancer when my hair's going not the other way around!

  • Melrosemelrose
    Melrosemelrose Member Posts: 3,018
    edited May 2012
    Isharvey822- That's right.... you decide when the hair goes!!!!  No tears here because I made the choice to snip and when to snip.  Hair or no hair.... we are all beautiful!!!!!!
  • dancetrancer
    dancetrancer Member Posts: 4,039
    edited May 2012
    Thanks lsharvey822!  I'm learning through the school of hard, er, chemo knocks.  LOL  When something happens, I do lots of research and ask lots of questions.  The girls on the TCH board and in particular one girl who knows A LOT about transfusions helped me SO much when my hemoglobin (iron levels - anemia) dropped this week.  I have a medical background, so if I use technical language which doesn't make sense, feel free to ask away.  
  • lsharvey822
    lsharvey822 Member Posts: 257
    edited May 2012

    I have docs that don't explain much and just tell me (or half tell me) what they're going to do so I could see them telling me I was getting a Procrit shot.  Now I'll have to make sure I have all my facts before that.  Having worked for the local Blood Bank for 10 years I have no fear of a transfusion if need be.

  • sandik
    sandik Member Posts: 482
    edited May 2012

    Yay twin! Feels good to do it, didn't it? Today should be my bad day. It doesn't seem as bad as the last round. Im tired, but Im not so tired that I can't function like last time.

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

    That is great to hear about your experience at the blood blank lsharvey.  My docs don't explain that much to me either.  I'm just a really inquistive patient, so I do lots of research on my own.  It makes me feel more in control and comforts me! 

    What I found out about Procrit is that it is not clinically indicated for cancer patients who have a high cure rate, because it can actually cause any lingering cancer cells to grow.  I read this straight from the prescribing pamphlet which can be found on line.  Eeeeks!  No way was I going to take that risk and negate the benefits of my treatment!  My nurse had mentioned it to me as an option (and did say it had some cancer risks I'd want to read about, so she was aware and wanted me to make an informed decision).  I don't think she had consulted with the onc yet (and of course she didn't know my particular case like he does).  Still, lesson learned for me.  No Procrit. 

  • Melrosemelrose
    Melrosemelrose Member Posts: 3,018
    edited May 2012
    Sandik- Yep Twin--So glad that I cut that hair!  Hope your SE's are minimal.... time for you to nap and rest!!!! Have a good Mother's Day!!!! 
  • Pauletta
    Pauletta Member Posts: 54
    edited May 2012

    Thank you so much for the advise of the salt\baking soda and water rinse. It has really helped!!! Amazing!!! I got up this morning feeling very nauseated and not wanting to eat anything at all. : 0 (  I made a cup of hot tea and that was delicous! Tried to eat a piece of toast and it seemed like forever for me to chew up one little bite of toast to make myself swallow it. That toast got thrown away and I made a chocolate protein shake. That seemed to be okay with my nausea. Been laying on the couch all day drinking 4 bottles of water since this morning and using the bathrom every little bit (YAY!). About 30 minutes ago I was able to eat 6 chicken wings (they are not big at all) and a couple of bites of macaroni salad!! YAY!!!!! I wonder if it was the water that helped and going to the bathroom alot? 

    I hope everyone has a great day and a wonderful mother's day tomorrow!!! Smile 

  • lsharvey822
    lsharvey822 Member Posts: 257
    edited May 2012

    @Pauletta - Yay!!  sounds like things are getting better!  I'm so glad for you!  I noticed that hot tea helped me too.  Even when I felt really bad the hot tea tasted pretty good!

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

    Hi all, since some of you have mentioned the Zofran headaches, just wanted to share what works for me. After tx#1 those headaches bothered me the worst. It was suggested to try Tramadol when tylenol didn't work and I didn't want to use percocet since that made the constipation worse. Tramadol is a non-narcotic prescription pain reliever, doesn't make me feel loopy at all. It worked great. This time I took it after my tx yesterday right when I felt the headache starting. So far, no nasty headache.



    I was able to take it in combination with ibuprofen for my port soreness, and that is much better too.



    Hope the Tramadol helps you; no bigger deal precribing that than the percocet.



    Hugs and wishing us all minimal SEs today.

  • chapter4
    chapter4 Member Posts: 155
    edited May 2012

    Day 4 after treatment number 3 for me.....a lot of burping, tired and slight sick feeling that seems to hang around.



    Claritin does work for me after the nulesta shot. It's so important to stay on top of nausea meds.....as for the crash after steroids....my oc advised instead of 2,2,2. Take them 2, 2,1,1 so I'm taking them an extra day but less on the last two days....hopefully this will lighten the crash days.



    I hope everyone enjoys mothers day tomorrow :)

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

    chapter4 - thanks for that tip.  I think I'll ask my onc if I can try that. 

  • sandik
    sandik Member Posts: 482
    edited May 2012

    Hmm. I don't take steroids. They are given via port during infusion along with everything else.

    Tired today but not as bad as last time. I need to shave my head shorter. It was coming out in the shower.

    Hope you all have a great Mother's Day! So glad I have all of you to whine to! Haha

  • rgina
    rgina Member Posts: 100
    edited May 2012

    Evening Ladies - Looks like this is my spot for the near future.  I've been hanging around for a couple of months since I was diagnosed in March (had my lumpectomy and SNB last month), get my port on Tuesday the 15th and first chemo on 5/24 - TCH regimen with the "H" until May 2013 - gonna be a long year.  Quick question - those of you that got a port - did you have down time at all?  The reason I ask is that I need to do some major barn, yard, horse stall, misc., next weekend after port and before chemo - can't do it this weekend because we've been blessed with 4 inches of rain this week - but this is part of my catch up/get ahead before chemo mode.

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