Is There A September 2011 Chemo Group?

Options
1151618202178

Comments

  • -RC-
    -RC- Member Posts: 287
    edited September 2011

    SStayton - Yes----it's gets better-----really!!!!!  Hydrate-hydrate-hydrate to move the chemo out of your body.  I bought straws which makes it a little easier to keep drinking.  Rest if you can, remember this drug is on a search & destroy mission and needs to do it's work!  I felt totally back to normal on day 6 after tx.  I have had 1 of 4 tx's with my 2nd one next Monday.  How many tx's do you have to do?

    belleeast - So sorry to hear about your maddening wait!  I can't imagine!  Your regimen sounds exactly like mine / same drugs.  I used the Ativan at night before I went to bed not because I really needed it but I didn't want to wake up in a few hours and then HAVE to take it.  My chemo nurse said to use the meds AS SOON AS YOU THINK you need them, don't wait otherwise you get behind the symptom and have to play catch up.  I am NOT a drug person so as tough as that concept was for me to accept, it makes total sense and I know there is an end to it all.  Are you taking the Claritin for the Neulasta?  I use Alavert (same as Claritin but cheaper) the day before and 3 days after tx and I had NO bone pain whatsoever.  I had what felt like a mild allergy congested head & ears for a few days.  Hope you feel better soon.

  • belleeast
    belleeast Member Posts: 653
    edited September 2011

    cjrt, i had steroids in my iv,too. i took my zofran sp? and 2 tylenol for the aches. thanks for well wishes.

  • Kelliregi
    Kelliregi Member Posts: 138
    edited September 2011

    Belleeast -  I was told the steroids were to avoid an allergic reaction. I take Decadron the day before, the day of, and the day after chemo as well as getting more steroids in my pre-med infusion. I get Benadryl as well. I guess this chemo stuff is pretty toxic =). Stay hydrated and I hope you feel better soon!!

    SStayton - Like RC said - hydrate like crazy! Also have you tried the Biotene mouthwash, toothpaste/spray for dry mouth? They really do seem to help. 

  • belleeast
    belleeast Member Posts: 653
    edited September 2011

    rhea,i mentioned it to my mo, she said to wait to see if i had that side effect before taking it.

    maggie,thanks,hope u are doing well.

    sstayton, are u using biotene mouthwash if not that might help.

  • Jerseylicious
    Jerseylicious Member Posts: 44
    edited September 2011

    Hi all, haven't read thru all of the posts yet but I wanted to post an update before I get too tired.  First of all, we are the coolest bunch of CHEMO-SABIS ever.....you are all so funny!  And you all make it so much easier to be positive and upbeatCool!

    I feel sooooooooooooo much beter this week than last. Except the hair started falling out today.....I was saying to  a co-worker, "Look, they say when it's ready to fall out u can just pull like this..." and then I pull and a big chunk comes out and we just both stare at it with our mouths open.  Kind of creepy, but now I feel compelled to keep pulling, is that OCD? Anyway I have to leave it alone til Friday night which is head shaving night.  

     Also, here's another sucky part....I lost 7 lbs last week because of being sick, and then have been eating nonstop for the past two days cause I feel better and gained every one of those dumb 7 lbs back.  I know we are not supposed to want to lose weight, but honestly, I have to lose 30 lbs sooner or later anyway, so I was kinda happy to say byebye to 7 lbs.  But I guess it was fake weight....boooooo.

    Kept feeling like chemo round 2 was a million days away then husband reminded me it's next Thursday, what a GEM he is.  Hope everyone is feeling good, or at least feeling humanSmile

  • -RC-
    -RC- Member Posts: 287
    edited September 2011

    belleeast - I hope you don't have any SE's!  My MO at Dana Farber said she heard they are just beginning to do studies on why Claritin works.  I don't care why, as long as it does!  Good luck!

  • -RC-
    -RC- Member Posts: 287
    edited September 2011

    Jersey - how weird about being able to pull your hair out!  I can imagine both of your faces!!!  I think the anticipation of losing my hair is worse than actually losing it.  I'm having my hair buzzed on Thursday.  I don't have a wig yet but only 1 scarf and 1 sleep cap.  I hope to get a wig next Monday.  I don't think you have OCD about wanting to pull it out - I would do the same thing, in fact, NOW I find myself pulling on my hair....sheesh...

  • belleeast
    belleeast Member Posts: 653
    edited September 2011

    rhea, the way i feel now, i think i'll take a clariton in the morning.

  • rjbaby69
    rjbaby69 Member Posts: 349
    edited September 2011

    Jersey:  I did the same thing when my hair started falling out.  I would say well my hair is starting to fall out and people would say it doesn't look like it.  Then I would rake my hand through my hair and helllllooooo bunch of hair in the hand!  Made believers out of them wide-eyed southern girls!  At any rate, I am adjusting to the wig very well and I kinda like it now.

    So this morning I get up at 5:00 a.m. to let my dogs out.  Decide to lay back down a minute or two and guess what?  You're right.  The next thing I know my boss is calling me wanting to know if I'm okay.  I told him I'd be there in a minute.  Called him right back and said I didn't have time to get there and to put the mechanic on my bus route.  Duh!  Can't just jump in my clothes anymore.  Now I have my hair to put on too!  Didn't get to work until 10:00 am.  I have just GOT TO STAY UP when I let the dogs out.  If I lay back down.....sleep just feels too good right now!

    Getting ready to begin the big hydration tomorrow for the chemo on Thursday. Hope all goes well.

    Hope all of you are doing as well as can be expected. You all are always in my heart.

    Til later!

    HUGS!

  • Sheypres
    Sheypres Member Posts: 35
    edited September 2011

    I still have my hair hanging on.  The MO today told me it will be Friday or Sat at the latest.  Just waiting for it to start coming out so I can just shave it off.  I just find myself grabbing a bunch and pulling all day to see if it has started yet. The MO told me he just had a girl who would not cut her long blond hair and when it came out in the shower she had a major panic attack and there was hair everywhere and they had to call 911.  Then an EMT fainted because of all the hair. It made me feel a bit better as I am thinking at least I'm not that bad. Gearing up for round 2 on Thursday! Wish I had a Sonic nearby.  I'm thinking a slurpee would be good too! 

  • Sheypres
    Sheypres Member Posts: 35
    edited September 2011

    Oh and BTW I am so impressed with all of you that are working through this.  I ran a couple of errands today and was out for 2-3 hours and literally felt sick when I got home. 

  • rjbaby69
    rjbaby69 Member Posts: 349
    edited September 2011

    Sheypres:  When mine starting going, I told my girls it was time.  I didn't want to wake up one morning and have nothing!  I wanted to be ready so I had my head shaved and wigs styled at the same time.  Been wearing my wig since Saturday and everybody is loving it.  Most of the people I work with knew my hair was going to fall out so they were prepared.  Those that don't know have complimented me on my new look!   ;)

    I am like you, at least I didn't have a panic attack!  I have 'em, but not THAT bad!

    Hugs!

  • RaeBob
    RaeBob Member Posts: 79
    edited September 2011

    I just love all of you on here and come here when I want friends who really get it. In fact I have this titled Breast Friends so I can find it quickly. I know corny but I am now on the,I feel better so my heart is gushing over side of my crazy mood swings it is better than crying and the grumpies. Tomorrow I feel I may swing back to the center and my family will be so thankful.

    Thinking of all of you.

    Jersey: would have loved to seen the expressions on your faces but it's an easy visual! I shaved my head before my first chemo because I knew I would be like the girl in the shower. It started growing back in and I was on my IPad and kept brushing away all these tiny annoying grey hairs and finally exasperated looked at my husband and said where are these hairs coming from he pointed to my head, and I said no mine are long brown and .... GONE!

  • lwarstler
    lwarstler Member Posts: 341
    edited September 2011

    OK, I slept most of the day and I am awake with a really bad cramp in my leg...ouch! So I wanted to share what happened before they started chemo.

     Nurse practicioner saw me before hand and tells me she thinks maybe we might want to wait a week because they like to do chemo 4 weeks post-surgery, not 3 and where the drain was isn't fully healed. Also 3rd Her2 isn't back and even though the doc is pretty sure it is negative and ok with starting TAC, she thought lets wait cause "cancer is gone." What???!!! You can't know that! So I told her that and said I didn't like her not taking this as serious as I feel it is. So I explained, "Well, first this mass grew 3mm in three weeks, then MRI showed no lymph involvement, followed by CT scan about a week later, which showed one somewhat enlarged internal lymph node under breastplate and CT almost a week later recorded it as 2 lymphs nodes because it was now 2.2cm (.5 is about avg.) So, I am thinking that if there is just one little cell in my lymph system I want to kill it quick because these little buggers are multiplying fast!! She asked me how I plan to view and deal with the cancer then if I didn't plan to just decide it was gone, so (refraining from hitting her) I explained that I would do that like any who agrees to chemo based on the cancer possibly still being present. She said we could do it today if I need it for peace of mind and I told her I would take the peace of mind. 

    After that, everything went great but I can tell she doesn't exactly care for me right now. I almost never stick up for myself with the doctors because I am afraid of making them mad, so I am kind of proud of my handling of the situation. The rest of chemo went fine and I am just awake now for a little.

  • lwarstler
    lwarstler Member Posts: 341
    edited September 2011

    Belleeast: So sorry for your rough day, I sure hope it gets better tomorrow. I understand the hotflash issue...That was certainly mega weird today.  Everything I read said lots of fluids so I think I have drunk about a gallon or more of water today. It has even flush the adriamycin out of my urine (no more red) at least for now. I hope you are able to get the meds and stay on top of those rough SE's. It does take a long time to get all the meds. 4 and half hours for me (after they got things ready) for all the IV's and pushes to finish up. Lots of meds they are pumping in...my poor liver.

    Sandy,My chemo experience went about like yours today with the Benaful and then I got the sandpaper thing but the Biotene did seem to help as did drinking tons of water.

     Rae: whatever you are taking I want some...sounds so much better than grumpySmile

    Jersey:: haha Chemo_Sabis...made me laugh!! 

  • Rockym
    Rockym Member Posts: 1,261
    edited September 2011

    lwarstler, Congratulations on getting though the chemo AND telling the NP what was on your mind.  I can't stand an Nurse, NP or anyone who thinks they're the doctor.  If the cancer was gone... why the heck would any of us being doing chemo!  Is she crazy??  None of us know if it's gone and that is why we are subjecting ourselves to this.  Chemo is an insurance policy and as we all know insurance policies NEVER come cheep.

    BTW, how you deal with your cancer or how any of us deal with it is of no concern to the NPs or even the doctors (unless we are asking for their counseling).  We have to choose our best method to keep us sane.  Whether it's worry, planning or just hanging on this newsgroup... that is for us to decide.  Tell her that next time she has a mass in her breast she should let you know her favorite coping mechanism, but until then...

    Okay I'm done ranting ;-).  Good for you for calling your shots!

  • SStayton
    SStayton Member Posts: 15
    edited September 2011

    RC... I have 4 cycles of AC, every 2 weeks followed by 12 weekly cycles of Taxol, then 33 rads. I did try the Biotene tonight and it helped some. I am having a hard time with water even with lemon, it just tastes funny. The only thing that tastes good going down is Diet Snapple, probably not the best choice but I guess at least it is something. Now I have a massive headache, Percocet isn't even helping and it keeping me from sleeping. I will ask the mo when I get my Nuelasta inj tomorrow. Thanks for all the advice reading everyone posts helps me to know it will get better.

    Thanks again ladies for being so supportive.

    Sandy

  • Kimberly1961
    Kimberly1961 Member Posts: 407
    edited September 2011

    Jersey - I gained the weight back too somewhere between the shrimp dip and potato chips and the can of cashews after my taste buds came back. 

    Sandy, Lee Ann, and Belle - Congratulations on beginning your counterattack on the cancer.  I have to hold myself back from getting too pushy.  Drink that water.  Take those steroids,  Eat lots of fiber.  Brush that sugar out of your mouth.  Take your nausea meds.  Get your rest.  Ha ha.  I have been through chemo once and now I am some expert, right?  What I mean to say is take care of yourselves the best you can and we are all here for you.

    Rae - Mood swings....I think we are all having them.  Sometimes I feel strong and sometimes I feel pretty weak.  Being sick and in pain can make a witch out of anyone.  For those of you who are premenopausal, the shutting down of the ovaries and hormones isn't helping any either.  About bone pain, you might try Glucosamine and Chondroitin, Fish Oil, or Flaxseed oil if it is ok with your MO.  Those are just some things people with arthritis do.  I know when I start the Arimidex in January I am going to try extra calcium, vitamin D, and the above G and C because I have heard the aromatase-inhibitors cause bone loss and bone pain too.  When all else fails, I take a pain pill.  I took a Percocet a day on day 4 and 5 and a Vicodin day 6 for my first round of chemo because I could barely move and there were a few things needing doing around here.  I wasn't drugged around the clock but getting a break from the pain made it easier to endure when it came back, and allowed me to get the bare essentials done.

    RJ - Bummer about being late, but I think our bodies need a lot more sleep to recover and rebuild, even in the in-between when we are not feeling major SE.  I think your body must have needed that little sleep-in.  I fell asleep really early tonight and now I am up in the middle of the night. 

  • Kimberly1961
    Kimberly1961 Member Posts: 407
    edited September 2011

    Bluejay - Congratulations on round 2 under your belt.



    Hair just got shaved 20 minutes ago. I am now Mr. Potato Head again, only Mr. Potato Head didn't come with 3 zits on the back of his head from night sweats. I'm with Shawna on this one, I won't be making a living as a barber anytime soon. So long hair. Bye bye now. Y'all come back soon, ya hear?

  • swarna
    swarna Member Posts: 3
    edited September 2011

    Hello, my mom is diagnosed with Stage IIA. So far, she has had the first chemo cycle, and there has been no major hair loss but we are expecting it at any time. It is Day 17 today after the chemo cycle. Some one told me that it does not always happen in the first chemo cycle - is it so?

    The next chemo is scheduled for Oct 3 and she is feeling tired and having leg pain as well, including nausea.

  • Kimberly1961
    Kimberly1961 Member Posts: 407
    edited September 2011

    PinkShirt - I envy all your testing in that I sure wish I could get a PET/CT to be sure nothing else is going on that I am not aware of, but I don't understand why you are having so many biopsies.  What's up with that?

    Cooka - Keep safe.  Stay home.  Spray your husband with Lysol.  Whatever it takes.

  • Kimberly1961
    Kimberly1961 Member Posts: 407
    edited September 2011

    Hi Swarna - Sorry to hear about your mother.  What chemotherapy did she have so far?

  • Kimberly1961
    Kimberly1961 Member Posts: 407
    edited September 2011
  • Kimberly1961
    Kimberly1961 Member Posts: 407
    edited September 2011

    My halloween costume.  All I need is some jammies and a nipple.

  • Kelliregi
    Kelliregi Member Posts: 138
    edited September 2011
    Kimberly -  I'm laughing so hard, tears are rolling down my face!!! I LOVE IT!!! I decided I would be Uncle Fester this year. All I need is one of those lightbulbs that will light up in my mouth.
  • PinkShirtNow
    PinkShirtNow Member Posts: 134
    edited September 2011

    Kimberly - love your Halloween costume.  Technically, I only see one nipple in the picture so it just might work if you use a little doublesided tape. 

     Regarding my high number of tests - I am on the ISPY2 trial to test a PARP inhibitor in addition to regular chemotherapy.  I had my initial biopsy to diagnose the breast cancer, then I had another biopsy to get a mammaprint score to decide which study drug I would get.  The biopsy yesterday was part of the study and was done after 3 rounds of chemo.  I don't know if I will get the results from that one.  The 3 MRIs are for the same thing.  No more biopsies until surgery but I will have a few more MRIs.  I just hope they show that the tumor is shrinking.  I'm getting good at holding very still while lying on my stomach with my tiny breasts in huge holes and my arms overy my head at uncomfortable angles.

     I'm sorry that you didn't get a PET or CT scan.  I needed one to make sure that I didn't have cancer anywhere else (also a requirement for the study).  I guess I am "lucky" to be  a lab rat.

     Take care, everyone.  My round 4 of weekly taxol is this morning.  Praying for uneventful...

  • mags20487
    mags20487 Member Posts: 1,591
    edited September 2011

    I love the costume kimberly...his boobs are bigger than mine now!

    Maggie

  • RaeBob
    RaeBob Member Posts: 79
    edited September 2011

    Kimberly: when the picture first came up I thought whoa am I on the right site and then I burst out laughing. That was great!

    Kelli: maybe we can all come up with a character Uncle Fester is a good one. Many days lately I have not felt like anything more than a caricature of myself I am going to be the smiley face head grin and bear it no matter what.

    Pinkshirt: hope taxol goes easy on you today.

    I actually feel a tiny bit human today. Returning to normal if there is such a thing anymore but hey I will take what I can get these days.

  • Kayrem
    Kayrem Member Posts: 164
    edited September 2011

    Thanks for the laugh Kimberly!



    I am feeling a bit out of sorts today. Day 9 out from treatment and my 7 year old son desperately wants me to do the Terry Fox Walk with him at school today. Apparently I am the only parent invited from his class because "you have to have cancer".



    Nobody thinks I should do it (probably not the best place to be around a whole crowd of other people's children - especially when both my 5 and 7 year old are already sick with colds!)



    But then I think it is outside ...



    It is tough to know what to do. I want to be there for him but not put my ability to be there for him in the future at stake.



    Anyways, I really laughed hard at your picture Kimberly! Have not decided on my Halloween costume maybe the Tin man from the wizard of oz (he was bald but had such a "shiny" personality!).

  • PinkShirtNow
    PinkShirtNow Member Posts: 134
    edited September 2011
    Kayrem - can you make a poster with your picture that your son could carry on the walk?  Or maybe your face on a stick kind of thing?  Tell him you have a date to walk with him next year when you can be around all the kids again.

Categories