Chemo starting in December 2010

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  • nolaa
    nolaa Member Posts: 76
    edited February 2011

    Went today for Taxol 4 of 12 and all counts are really low.  Will have 2 neupogen shots later this week and they want to do a blood transfusion tomorrow to help with my red blood cells.  Anyone else had the transfusion?  know what to expect?

  • hopefortomorrow
    hopefortomorrow Member Posts: 193
    edited February 2011

    Hi Joann, I have gotten brown spots and I swear my hands now look tan! My daughter even noticed how dark my hands are! I hope the rads go well. I talked to my cousin who had rads and she said compared to chemo they were a breeze... she said the only downside was at the end of them she started to burn, but she added there are lotions for that. It made me feel a little less nervous about it at least.

    Angel, sorry to hear that you have to be a shut in for a week! The only thing about Walmart- my older sister who is totally healthy gets freaked out about using the pen for the charge cards that EVERYONE touches! She is always like, "Can you imagine all the germs on that thing?" I always smile to myself when I am there and think of her saying that.

    Lisa, the cake decorating class sounds fun! Good for you!

    Ugh, massive headache tonight. feels like sinus, but with the nosebleed stuff who knows. The roof of my mouth is so sore, and the biotene doesn't help much. I have a night gel by biotene which helps the dryness at night, but the soreness is still there. Well I am off to bed, right about now that is the best place for me.

    Wishing everyone sweet dreams! Cathy

  • LisaMomOfFour
    LisaMomOfFour Member Posts: 465
    edited February 2011

    I have the same issue -- spots on hands and the back of my hands are totally darekened, looks like a tan.  My 14 yr old daughter suggested I go to get a spray tan for the rest of my body to even it out.  Too funny.....

  • hdangelbaby
    hdangelbaby Member Posts: 731
    edited February 2011

    sorry guys to unload this

    i had taxol today and my counts were down. my husband went out and got really and i mean really drunk tonight. didn't come home till after 2 am... i am soooooo upset and we got into a huge huge fight. i don't know if he will remember most of it. i know he is going through alot too but sometimes i don't think he understands just quite what i am going through. plus i am a shut in for the next week cause of my counts!

    it was a really bad fight. i finally got him into bed around 3:30, went outside in my car and called my mom and talked it out with her.

    i just hope when he gets up we can talk about it, :( bad night here sistas

  • karebear76
    karebear76 Member Posts: 288
    edited February 2011

    (((HUGS))) Angel. I hope you guys can talk it out. I hope your counts go up too and that things will settle down for you. You can vent anytime. that is what we are here for.

  • hopefortomorrow
    hopefortomorrow Member Posts: 193
    edited February 2011

    Hugs from me too Angel. Life happens. I hope you both can make it up to each other. My husband and I have had our fights too. Marriage takes work, you know? Hang in there! 

  • msjag
    msjag Member Posts: 416
    edited February 2011

     Ang, hope all will be ok, I totally understand how your feeling. its not like we can just go about our lives normally. Ya, know, its funny you mention the hubbies, mine has been great...but as of late when I get weepy over nothing, river of tears just comes on ..well I shouldn't say over nothing..geez we are going through so much, anyway, he says things like..come on, you've been so positive.  well yeah, I've been in shock since sept 29th!!!  I'm just waking up like my incisions are!!  I'm not complaining but, I think people forget this is a 24 round the clock thing for us, nothing stops us thinking.  People around me think I should be thrilled I'm "done" after rads, and be so grateful to be done with chemo, and I am...but then what? They think its over, including my husband.  But for us, especially Triple negative with no pills to take, the first few years are gonna be hell.  Sorry, wasn't planning on this venting but just had to get it out. Love and peace to all and appreciate you all so much.

    Cathy, do you have brown spots on your feet too? I just noticed those.

    Take care all,

    JoAnn

    JoAnn

  • hopefortomorrow
    hopefortomorrow Member Posts: 193
    edited February 2011

    Oh my gosh JoAnn, You are expressing exactly how I have been feeling lately. Suddenly I am waking up and questioning everything that I basically accepted with the diagnosis out of shock. I get frustrated that people expect you to pop right back because 'so and so' did (but maybe had a totally different diagnosis). I was reading that it takes about a year to get the chemo and rads out of your system and that you can still not feel like yourself for awhile. In the meantime I know everyone around me will be wondering what is wrong with me if I don't go right back to the person I was before. In fact, my husband and kids are used to things now and aren't help out as much as they did at first.

     I think more about those first 5 years out, and what if it does come back....My cousin who had breast cancer thrity years ago now told me it was an adjustment going from all the doctor's treatment to just being on your own... and feeling worried something might be brewing inside.... She didn't tell me to worry me, it was just how she said she felt.

    Yes I have noticed my feet are darker too- for some reason around the base of my ankles and sides of my feet.

  • hdangelbaby
    hdangelbaby Member Posts: 731
    edited February 2011

    thank you ladies!

     i appreciate it. when he woke up this morning he told me he didn't remember any of the drunken stupor fight. we talked and i got at the root of what was wrong. he is just so super stressed himself he just gets sick over it. he actually cried a little today while we talked. it was nice that he not only apologized the heck outta me but he told me what was going on in his head

  • karebear76
    karebear76 Member Posts: 288
    edited February 2011

    I am so glad you talked it out Angel. I know my hubby gets super stressed about this whole thing and the financial end of it all. He has been amazing through all this though!!

  • ShelMel
    ShelMel Member Posts: 207
    edited February 2011

    Angel - I'm so glad you and your husband are doing okay today. I think it's so incredibly stressful for our spouses and they tend to get left out in the wind, wondering which way is up. My husband has been so wonderful through this, but he went last month and talked to the doctor and got put on some "happy pills". I think that has helped him tremendously.

    No one understands what we're going through except those of us going through this. Likewise, we don't understand what our husbands are going through. It's not easy... Sending you - and everyone else - special hugs for your marriages. 

    I'm sick. Been running fever, up to 100.5, which my oncologist originally told me to not come in unless it shot up to 101 or I couldn't control it. I went in to see him yesterday and they did a chest x-ray. It came back as questionable pneumonia. They're also running blood cultures. They threw me on some meds (inhalers, antibiotics) and I go back for a follow-up on Monday. I just took my last chemo treatment last Thursday.... I'm still running fever off and on... *sigh*  

    Just ready to feel "normal" again. I guess it's gonna be a long-while before any of us feel normal again. I talked to a 9-year survivor not to long ago and she told me, "Welcome to your NEW normal." :) 

    Love you all!

  • sammolisa
    sammolisa Member Posts: 180
    edited February 2011

    Praying for all tonite in your distress.....

    Glad to hear you are doing better with the hubby angel.  I know you said he doesn't remember it - but you do and will for awhile,  sending big hugs to get you thru.

    Had my 3rd Taxol today - so far so good.  Counts came back normal again and the dr is continually amazed that (on paper) I don't even look like I am having chemo.   He says quote.... "You look good on paper!"

    I don't have any brown spots.  Nails are fine.  I wish I could take some of everyone's problems away so you all have less side effects...

    Hope - ask your onc for some magic mouthwash.  Your RX should pick it up --(might be a rather hefty copay for mouthwash tho)   helped me when my mouth was bothering me alot.  

    Waiting now for the side effects that are sure to come on friday - today I feel ok - not normal - not even the "new normal"  just ok.   A little nauseated, a little apprehensive of the coming SE's.  I slept most of the day away due to the Benadryl.    I  have my first consult with the rad onc tomorrow morning at 10.   Anybody hear how much time the plastic surgeons usually wait until they do the final reconstruction?  I'm not sure about any of you, but on me they only worked on the left breast and left the right one alone - so I am lopsided.   The left one looks like I am 20 years old  - lol - all perky and beautiful.  The right one needs some serious help, as it's lookin at the floor.   I am hoping he doesn't want to wait too long.  I'm getting tired of being lopsided.

    Love and blessings to all.

    Lisa

  • nolaa
    nolaa Member Posts: 76
    edited February 2011

    I actually had a huge fight with my husband last night and he wasn't even drunk!  It's true, they are stressed too, in their own way with their own different world of troubles.  Just important to both stay on the same page throughout this mess and support each other.  Sometimes you really need to yell it out so that it all comes out and then everyone feels better.

    I had a blood transfusion today.  My red blood cells were so low they decided it was the only thing they could do.  I was constantly short of breath and sleeping like 20 hours a day.  They gave me benadryl with the blood to help reduce any rejection so I slept all morning (infusion took 6 hours!) but I really am feeling better!  It's such a relief.  I've really not been doing great on Taxol.  Well, sort of.  I think that's what our fight was about last night.  I look better.  I can get out of bed and not puke.  And no evil side effect meds that make you unable to drive and think clearly.  So because of that it "looks" like I'm fine when really there is so much death inside my veins I need someone else's blood to survive!  

    I've also been thinking about life "after" this is all done.  When I was first diagnosed I thought, okay a year of yucky treatment then back to normal.  And it feels like every week I discover something that has changed or will change so that my life will definitely never ever be the same again.  Like ShelMel said, it's definitely the new normal.

    Hang in there everyone.  We're getting closer.  And it's making us stronger.

  • karebear76
    karebear76 Member Posts: 288
    edited February 2011

    Hey girls!

    I had my blood counts done today and my white cells are good. Unfortunately my red cells are bad. I have to have a transfusion tomorrow. I am a little freaked out about it but I know I will be fine and will prob feel better too. Hopefully the next chemo doesn't take me down again.  

  • sammolisa
    sammolisa Member Posts: 180
    edited February 2011

    Wow!  so sorry to hear all the transfusions! 

    Day 2 of Taxol here and still hyped up on steroids and running on 2 hours sleep.  Wooohoo!!!

    I am gonna regret all the runnin around I did today, and my hubby agrees... 

  • LisaMomOfFour
    LisaMomOfFour Member Posts: 465
    edited February 2011

    Sorry to those of you having tough weeks personally.  Hope things brighten soon.  I am feeling tons better emotionally after throwing in the towel on the whole antidepressant thing, and starting effexor about a month ago.   Working much better than Xanax, I can actually think about things other than cancer for awhile, and I didn't have the miserable three day crying jag after the steroids wore off last cycle either. 

    First Taxol yesterday, after 4 DD A/C.  So far feeling ok... definitely better than how I felt after A/C.  I just felt noticeably different after each A/C treatment, not so much specific side effects as my whole body chemistry seemed different, I could just feel the chemicals.  That's weird, I  know.   But I don't feel that different with Taxol, hopefully it will stay that way.   Only three treatments left now, feels like the end is in sight, even if I have to do rads after this is over. 

    However, my fingertips hurt, hurt, hurt!  Getting much worse, can't even pull a credit card out of my wallet... which could be a good thing for household budget, I guess!  Typing is painful.  Hope this wears off a bit.   I know others have complained about this one, anyone find a remedy that helped? 

    Hope everyone is having a good day. 

  • hdangelbaby
    hdangelbaby Member Posts: 731
    edited February 2011

    i gave myself my weekly manicure last night, to try to cheer up a bit and when i took off the old polish from last week, all my nails are turning black! like they are bruised!!! weird. my fingertips are sensitive and the skin is super brittle. weird.. but my nails are like a firey red/pink, and that makes me smile when i look at them!

    hope everyone is having a better day today! with minimal to no SE's!

    ((((((HUGS))))))

  • hopefortomorrow
    hopefortomorrow Member Posts: 193
    edited February 2011

    Hugs to you all that have had to get transfusions! I know it would make me nervous too!

    I just had my 3rd taxotere yesterday. I am glad I only have to sit in the chair about 2-2.5 hours instead of 4 hours for treatment.  I think it is a little easier than the AC... but  not alot. Today I woke up and felt like my insides were burning. Hot flashes are constant!!!  My toe tips and fingertips hurt. I haven't found a cure yet either.

    Don't mean to sound whiny, because I am getting accustomed to what I can do and can't, and really utilize my up days. Before I had a hard time doing that. So that is a positive!

    Wishing everyone a good day! The sun is trying to breakout here- makes it a little bit more cheerful!

  • hdangelbaby
    hdangelbaby Member Posts: 731
    edited February 2011

    ugh, just got over a "down below" infection, now i woke up with symptoms of a sinus infection  or a cold! just called docs, waiting to find out what they will do with me since my counts were down this week! ugh i wonder if i will be on anti biotics AGAIN!

  • karebear76
    karebear76 Member Posts: 288
    edited February 2011

    Feel Better Angel.

    Transfusion went well. I did get a little sick to my stomach but not terrible. It was prob just nerves! My nurse said that I should feel better tomorrow.  

  • msjag
    msjag Member Posts: 416
    edited February 2011

    Geez, Angel, your not catching a break here,  Hope things work out soon. I know it sounds so strange, but ever since my blue cross, blue shield nurse told me to eat a yogurt everyday, I have been so healthy and no infections, and my mouth always ffelt great too. don't know if that is the reason why, or if I was just lucky. Hope you're feeling better soon.

    Hope,  your not whiny, I don't think anyone here could be.  I hope some of your s/e disappear soon.   I cried at work today, never do that, just sometimes this whole thing is so overwhelming, I am moving on to rads next week, and I just can't believe this is all happening. I'm sure we all feel like that.

    Another nasty snow/freezing rain day didn't help either, I so want spring!!!   Do something nice for yourself this weekend.

    JoAnn

  • hdangelbaby
    hdangelbaby Member Posts: 731
    edited February 2011

    well the doc called back. wants me to use a humidifier and some afrin and advil this weekend and see how i do. don't want to throw antibiotics on me yet. so that's good. and i'm not running a fever. ready for this week to be over! this week really was the pits, but next week has got to be better!

  • ShelMel
    ShelMel Member Posts: 207
    edited February 2011

    I just back from an extensive testing day, poked about 7 times, a chest xray, chest CT (to check for pulmonary embolism - I was clear - YAY), a shot and more meds. I've got pneumonia.

     They gave me a shot of rocephin (heavy duty antibiotic) and will wait to see how I do over the weekend. Go back Monday morning. If I'm not better by then, they're probably going to put me in the hospital. 

    I've been sick since my 3rd treatment. Supposed to go see my radiation oncologist next week, but I have a feeling that's going to be delayed. So sick of being sick. I feel like my life has been on complete hold. I've missed so many events, my son's choral contest, school meetings, taking the kids out. Sorry. I'm just having a pity party right now. 

    I've been having huge crying jags for about a week now. It just happens over the smallest things. 

    Angel - I'm praying for no fever for you this weekend. Hang in there sweetie. 

    Karebear -  I hope you wake up tomorrow with a ton of energy!! 

    Praying for a better weekend for all of us. Much love!!!

    Shelle

  • sammolisa
    sammolisa Member Posts: 180
    edited February 2011

    I think about all of you everyday, and pray that everyone has a good day and is on the road to recovery.   We all need some bright sunshine and lights at the ends of these damn dark tunnels!!

    Saw my rad onc yesterday.   He talks fast but is very thorough.   Last chemo is on March 9th so 2 weeks after that I will be having xrays and cat scans and the body cast to get things moving for  rads.  Sometime around then will also be the removal of the port .... yay!!!!  I can't wait for that part.   But the delay in the start of the rads means the rads will be running into my return to work on May 2.  I  am hoping the fatigue isn't bad to help the return.  

      This is day 3 of Taxol and that's when the SE's usually start.  So far so good.  Took a little nap today.  Feeling pretty tired today.

    Hugs to all,

    Lisa

  • hopefortomorrow
    hopefortomorrow Member Posts: 193
    edited February 2011

    Lisa, I miss being in sync with you- since I was switched to the 12 weeks of taxotere instead of taxol...and then you also got to do the DD. I can relate to the return to work time frame and the start of rads. I worry about the fatigue too. So far I am approved until April 23 which should have been around the end of my last chemo, but I missed one dut to getting the port put in, so already I am a week behind. 

    Shelle, please get better soon, I am keeping you in my prayers! 

    I want to mention you all by name because I read all of your posts and you are all in my thoughts. I really don't want anyone to feel left out! Big hugs girls! You are all so wonderful!

  • nolaa
    nolaa Member Posts: 76
    edited February 2011

    oh crap, ShelMel, so sorry to hear about the pnemonia.  I hope they can get on it fast and fix it.

    I still feel like total crap, even after my infusion.  Started running a temp and am back on antibiotics.   I still sleep about 17-18 hours a day.  I just can't wake up and have no energy.  They keep saying it's just the Taxol. But in some really awful dark corner of my brain I keep wondering what will happen if I just keep sleeping and sleeping and don't wake up.  I spend my few awake hours with the kids and then crawl straight back into bed.  This is miserable.

  • hdangelbaby
    hdangelbaby Member Posts: 731
    edited February 2011

    shel mel!! i hope you get to feeling better NOW!! you are in my thoughts!

    thank you to everyone who listened to my crappy week....it really was hellacious

    even though my counts are down, i have got to get out of this house. it has been since tuesday(chemo) when i have stepped foot. need to get some cat food and a prescription picked up. i could have hubby do it, but i just gotta get out. despite low blood counts.

    question on that.... am i over reacting to that? i mean, i have holed myself up in my house for the week, scared to go out in fear of infection. but , if i go out and wash my hands and make sure i don't contact anyone sick, it's ok, right?

    the sinus thing is improving, i think my sinuses were severly dried out. the humidifier is helping alot! i wake up, blow my nose, and feel better. still watching the temp. been running 98.2.

    well, that's all today. i do hope you ladies who needed transfusions are doing better! haven't needed one but i can only imagine!

    and to all who have the sniffles, hang in there, we are almost done!

  • karebear76
    karebear76 Member Posts: 288
    edited February 2011

    Shel Mel: I hope you feel better quickly.

     Angel: If you have been in all week and you make sure not to touch your face before you get your hands washed you should be ok to run out quick. I totally understand. I can't drive cuz of the meds. They are totally messing with my eyes so I don't want to risk driving. Staying in all the time is driving me nuts sometimes!! Glad you are feeling a little better.

    I am concerned cuz I really don't feel any better since the transfusion yesterday. My stomach is all upset on and off and I am still tired. Also I am freezing and it isn't any colder in the house than it normally is. I just hope I don't need more. I did have hot flashes again last night and I haven't had them in a wk or 2 so I guess that is good right?? LOL 

  • hdangelbaby
    hdangelbaby Member Posts: 731
    edited February 2011

    hot flashes are good for us ER/PR + gals. it's a signal our estrogen is low, which is good, but, keep taking your temp, cause it can also signal a fever, best wishes karebear!!

  • LisaMomOfFour
    LisaMomOfFour Member Posts: 465
    edited February 2011

    For those of you doing dose dense taxol....how many days do the bone pains last?    I'm on day 5, they started day 3 for me. Thanks.  Lisa

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