March 2012 chemo

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  • QuinnCat
    QuinnCat Member Posts: 3,456
    edited March 2012

    Brax - thanks for the tip on the Compazine and Zofran. I wasn't sure what to do with the Zofra!

  • Sissydi
    Sissydi Member Posts: 516
    edited March 2012

    Welcome Kerri and Katy! Feel free to TMI, and post any and all experiences and questions!

  • Sissydi
    Sissydi Member Posts: 516
    edited March 2012

    If your taking Zofran, watch for constipation...try to stay hydrated!

  • tc9876
    tc9876 Member Posts: 136
    edited March 2012
    Katy, Welcome to the group! I have a 9 year old.  I have not told him anything at all.  I just don't think he will understand it enough.  Brax, it looks like you and I are walking lockstep through this (joining arms).
  • galena_79
    galena_79 Member Posts: 107
    edited March 2012

    Hi all. I have taken two lots of anti-nausea meds now, and feeling a lot better. I'd been eating really well and hadn't needed the meds for a couple days, but I will now continue to take them preventatively.

    I spent the last few hours on the couch as I didn't feel like being horizontal. Snoozed a little, and took lots of sips of water. My cat decided to keep me company. I'll try to attach a picture below... my apologies if it is bung.

    5am here, and I think I might try getting some sleep. Thanks for 'listening' to me vent. xoxo

     

  • kltb04
    kltb04 Member Posts: 1,051
    edited March 2012

    Galena - Sweet kitty!  I have three but only one is a snuggler - that was a concern for me too w/chemo - is it ok for her to be walking all over me (she likes to sleep on my head)...I just remember my pregnancy days and concern with toxoplasmosis. I am borrowing trouble I guess.

     To all...to add insult to injury, my dad has just been called in for testing on his liver...worst case scenario right now would be hep C...which we cannot figure for the life of us where that would have come from...they are hoping for "fatty liver" or just an elevated level from his medications.  So now he is scared to stay here or come in the house (my parents are staying in their RV at our house) "just in case".  Intellectually we all know that hepatitis can't be spread casually but he has been doing a lot of the cooking.  I think he is just thinking that with chemo, my immune system will be compromised.  Thoughts?

  • KCB
    KCB Member Posts: 365
    edited March 2012

    Karri: I find worry about the kids very hard as well( though talk to me next week after I start chemo and I may have a different story!) Mine are 8 and 9 (almost 10) we have talked with them about cancer; they have seen our neighbor go through it, and a teacher at their school, so we felt they would figure it out soon enough: can't sugar coat the chemo and hairloss. Anyway we kept it simple and tried not to lie. I hate that their lives are affected. My daughter turns 10 ten days after my first chemo, and I am desperately hoping my hair won't be falling out in clumps on that very day... Any thoughts?

  • tc9876
    tc9876 Member Posts: 136
    edited March 2012

    Galena, how did you attach the picture????

  • kltb04
    kltb04 Member Posts: 1,051
    edited March 2012

    Katy, my oldest is about to be 12.  We told her everything, emphasizing the positive, getting through it, etc...she knows I am about to go through chemo as well and knows the basics.  She broke down at first (of course) and then brought it up again last week saying she had a friend at school that's aunt has had cancer and has had a recurrance so she was worrying "what if it goes away and comes back?" I just told her that we can't know what the future holds (i.e. one could get in a car accident, etc...) and we would just deal with it day by day.

    My youngest is 8 1/2.  We haven't specifically used the word cancer with her but I think we should/need to.  She just knows I am having "boobie" issues and had a little surgery, am going to have some medicine for awhile, and then will have more surgery later.  I really think we should have been more honest with her from the get-go but I kind of feel like it is what it is right now.  

    On the hair loss, everything I have heard about chemo says about 2 weeks from the first treatment but I am sure the more experienced chemo ladies could tell you better.

    My daughter's birthday is coming up too - the 28th - and I just know I am going to be right in the thick of things by then.  My mom will take care of planning things though, just like she had to get my youngest a Dr. Suess costume together at the last minute last week when I couldn't deal with it. ;)  I feel bad right now because my oldest wanted her two friends to come over to spend the night Friday and I just can't deal with that right now so I told her no.

    Ok, I feel bad about dominating this chemo thread with my issues so I'll shut up now!

  • Kadia
    Kadia Member Posts: 314
    edited March 2012

    Welcome, new ladies. Glad to meet you, but sorry you have to be here.



    Galena, sissydi and everyone feeling lousy, I hope things look up for you soon.



    I sure hope pets aren't a problem with chemo, since I have 5 cats and a dog, all indoors and all snugglers!



    Katy, I have an almost 9 year old son. We've told him what's been going on in broad strokes, and been very optimistic about how this treatment is temporary and will make me all better. We figured he doesn't need to know about the chance of recurrence or mets or anything like that...he'll probably wonder about that on his own when he's older.



    So I have a new and annoying side effect--eczema. Never had it before in my life, now it's on my face and chest. Not real pretty, and feels dry/itchy. Anyone else develop this?

  • Kadia
    Kadia Member Posts: 314
    edited March 2012

    Also, lisacjc, my PS said the folds in the skin and the TE should smooth out with fills. Which of course I can't have while I am on chemo...sigh. I will just have to put up with the wrinkly boob for a while longer!

  • tc9876
    tc9876 Member Posts: 136
    edited March 2012

    Okay, I know this is TMI so forgive me in advance but I think I finally released my constipation.   Whew!  I feel like a new person.  Ladies, stay on top of your stool softeners and water.  I thought I was doing everything I should but I plan to do more.  I also take a super strength probiotic and digestive enzymes.  Never again do I want to feel like I was feeling.  That explains the FOG.

  • Msbelle
    Msbelle Member Posts: 235
    edited March 2012

    My chemo packet from onc says not to mess with animal feces especially liter boxes. I don't have cats just dogs. I just wash hands really well when I touch them.

    Kadia: I am getting fills while I'm on chemo. They are waiting to do my first one as soon as therapist works out this tightness. PS told me I just couldn't get fills if I were doing radiation. Are you also going to radiation?

  • Sissydi
    Sissydi Member Posts: 516
    edited March 2012

    I have a sweetheart golden retriever who is a snuggler, and he makes me feel so much better about things; I can't imagine not snuggling with her!



    how did you copy your picture to your message?

  • Love74
    Love74 Member Posts: 175
    edited March 2012

    Hey Girls...a quick note on the hair.  Mine started shedding on day 15...same day I shaved it.  Its still shedding today on day 19 with small 'clumps' that have about 10 stands each in them.  If I pull on the stubble it comes out a few strands at a time.  Its really itchy too so I put baby oil on my head when I get home from work.  I would say that my hair is thinning but I still have about 75% of it.

    Also...I'm still getting a headache every day and heartburn...but not quite as bad as the first week.

    Friday is my 2nd TCH...I'm hoping it goes the same or better than the first...it was definitely doable the first time around.

  • Sissydi
    Sissydi Member Posts: 516
    edited March 2012

    Oh well, that's my girl in my avatar!

  • Kadia
    Kadia Member Posts: 314
    edited March 2012

    Msbelle, fortunately, my DH handles the litter boxes! As for fills, my PS has a policy not to do them during chemo. Not sure why, but I had to postpone my fills till after chemo.

  • brax
    brax Member Posts: 98
    edited March 2012

    TC:  I got all warm and fuzzy after reading your post about us going through this arm in arm.  My youngest is ten, seems quite a few in 8 - 11 or 12.  We also have a birthday this month.  Maybe try senekot-s.  Have you gotten any headaches?  I should just throw the cold cap on-it might help.

    Sissydi:  I did try increasing water today for the headaches.  It is better today, but still there.  At least no jaw pain today.  What do you do for it?  I have just been taking ibuprofen and I have been taking an Aleve in the morning and evening (says to take every 12 hours) for the neulasta.   I guess I will stop taking the claritin and Aleve tomorrow, day 6.  No side effects so far from neulasta. 

    Kadia:  Is the eczema from the TC?  That's the one side effect I have not heard mentioned yet. 

    Love:  I don't understand (but believe me it wouldn't be the first time).  You shaved your head but you have 75% of your hair.  You shaved part of it?  Also, have you found anything that is helping with the headaches?

    Hope everyone is feeling better, even if taking babysteps!  The headaches I have are very annoying and the jaw pain makes it ten times worse but I have to say I expected far worse so I still consider myself lucky that this really is the only se I am dealing with.

  • journey4life
    journey4life Member Posts: 517
    edited March 2012

    Kadia - luckily, my PS will continue to do fills through chemo unless my WBC/RBCs get really low or unless I don't feel up to it. I'm sorry you have to wait. I can't imagine what it would be like to stop midway.

    Hello to the new Marchers!

  • journey4life
    journey4life Member Posts: 517
    edited March 2012

    Yay for tc !!!

  • KCB
    KCB Member Posts: 365
    edited March 2012

    Love74: good news about date of hairloss . I suppose it depends on type of chemo though? anyway just hoping not to be too freaky on my daughter's birthday.

    Trying to figure out what I need to get done before I start next Tuesday...(besides a haircut)...feeling a little stuck.

    Karri: so nice your mom is nearby. Mine is coming, she's the best to have around, was here for my surgery.
    Btw how do you add surgery and chemo details to your profile?
  • Love74
    Love74 Member Posts: 175
    edited March 2012

    Brax...I shaved all of it but its about 1/4" long...there is still about 75% of the stubbly stuff! left!  No bald patches...just getting thinner and thinner each day. 

    I try to drink more water when I feel a headache coming on and I take Tylenol when it gets really bad but nothing really makes it stop completely.  Make sure you take your temp before taking tylenol and about 4 hours later because it will mask a fever.

  • KCB
    KCB Member Posts: 365
    edited March 2012

    Thanks for the warm welcome, and I love the term Marchers!!! So fierce, so brave....and proud.

  • brax
    brax Member Posts: 98
    edited March 2012

    Love thanks for explaining what I should have understood.  Thanks also for mentioning temperature taking, I did not think of that.

  • kltb04
    kltb04 Member Posts: 1,051
    edited March 2012

    Just a note, I deleted a post above talking about my dad because I didn't feel like that my was my news to share at this point (as if any of you know me from Adam, lol)

    I agree with Katy - thanks for the welcome - I have joined a couple of different sites and this one is by far the most responsive and also one of the easiest to navigate.

    On the earlier pet issue, thank goodness my DH does the litter box too.  So I am going to TRY not to obsess about that issue.

     On the hair, I am going to go to one of the programs at one of the hospitals tomorrow before my appt and check out their wig/head coverings program - its free so I don't know about the quality but at least I will have some sort of something to start with.  It's called A New Outlook...there is also a Look Good Feel Better at another hospital but they only meet once a month and it happens to be the first day of my chemo - blah.

    Ok, I hope everyone does ok the next little bit and I will be checking in after I get going next week.  My mom is trying to be positive and saying "everyone is different, you may handle this just fine" and I am like "uh huh...get ready"...I never thought I would be happy for my parents living in a camper in my yard but they have been lifesavers.  

    One more question for those more experienced at this - are there any "supplies" I need to have at the ready to have immediately on hand the first day (my "education" in chemo is on the same day as my first session)??  I know they called in anti nausea meds already and I need to pick those up.  But will they tell me what else I need to get - I have seen the stool softeners, people mentioning Biotene mouth products etc... thx in advance.

  • tellie_savalis
    tellie_savalis Member Posts: 121
    edited March 2012

    Galena_79 glad to read you were feeling a bit better.

     I start chemo March 13th T/C/A with a Neulasta chaser.  (Hope I posted that right).  Once every 3 weeks for 4 rounds.  Then surgery, most likely a full masectomy Doc said because of the size of my mass.  He calls it a mass because my tissue is to dense for it to really show on ultra or mammo but by feel they are calling it 10cm. Ct scan did not show spred to chest wall or anywhere else so that is good. I am going to cut my hair short and dye it either bright pink or green (St. Pattys) before it falls out.  Got my chemo supplies stocked, thank you everyone for posting your experiences, it makes me feel so much better to have an idea what I am in for and what to have on hand.  And very much not to feel alone in this!  Again thank you everyone. 

  • galena_79
    galena_79 Member Posts: 107
    edited March 2012

    Hi all. I'm feeling much better now. Managed to get a little sleep and drank water and some chicken soup. I will attempt a little solid food for lunch.

    Hope you are all doing well.

    ... ... ... 

    How to attach a picture.

    1. You need to upload your image to a hosting site. I uploaded mine to my facebook account, but you could use something like photobucket.com.
    2. Next you need to obtain the URL for that image. I right-clicked the image and then clicked 'Copy image URL' but your computer might have something slightly different.
    3. Back in the forum now, in the 'Post a Reply' area, you need to click on the button that looks like a tree. It is next to the smiley face button.
    4. Paste the image URL in the space. It seems to allow you to change the image dimensions but I don't know what size is optimum. Click 'Insert'. Voila! When you submit your reply, it should show up.
  • Kadia
    Kadia Member Posts: 314
    edited March 2012

    Brax, the doc says eczema is an unusual side effect. We're trying to determine what kind of rash it is.



    Karri, you might not need much that first day. I had hard candies (to counteract metal mouth) and also Gatorade (to hydrate). Also colace! I'd recommend starting the stool softener right away. Also something to occupy you during the infusion. I watched a movie.

  • kltb04
    kltb04 Member Posts: 1,051
    edited March 2012

    Thanks Kadia...ahh stool softener...sounds like fun. 

     I have my Kindle loaded up with books and I think they said someone could come in with you?  Is that common practice?  My husband will be there the first day and then my mom probably after that...I am either hyper/chatty/nervous or I am quiet/upset/nervous so it will just depend how I am feeling how much talking and/or reading I will be doing.

  • Kadia
    Kadia Member Posts: 314
    edited March 2012

    From what I observed, most people had someone with them. I decided to go alone. Didn't want to feel like I had to chat or entertain someone....

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