Chemo May 2011

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  • Beaglesgirl
    Beaglesgirl Member Posts: 287
    edited May 2011

    Got home this afternoon from my first a/c tx I feel like junk. Bad sinus like headache. Hungry but eating sounds awful. Nuelasta shot tomorrow. One day at a time... And this scary 'first' is done!



  • MamaV
    MamaV Member Posts: 907
    edited May 2011

    Beaglesgirl - sorry you feel like junk.  Try some soup maybe?  Good luck!

  • ---
    --- Member Posts: 197
    edited May 2011

    Beaglesgirl,

    Hang in there!  Rest a lot.

    Laureen

  • ---
    --- Member Posts: 197
    edited May 2011

    Sunshinyday and Ruthii-

    I'm glad to hear both of you felt well after yout infusions today.  You gals are lucky to not have SEs immediately after tx.  My SEs kicked in only 2 hours after!

    Keep it up.  Be well.

    Laureen

  • 40-years-old-now
    40-years-old-now Member Posts: 309
    edited May 2011

    I got my hair cut short (or shorter). Had 13" cut off (set for donateing). I have biopsy on lung tomarrow at 7am. I should go to bed.

    I wont have results on biopsy until next Tuesday mostlikely.

    I still dont know when I will be starting my chemo. Things keep getting delayed.

    Take care everyone.

    Candice

  • MargieC
    MargieC Member Posts: 394
    edited May 2011

    HI Maybe....

    I got my  Neulasta shot last Sat and took my clartin as I was suppose to.  I did have some of the achy side effects, but I went to Pilates class Mon night and the gentle moving around made me feel soooo much better.  My Dr recommend light exercise to help with the side effects.  Which I know some days can stink because all you want to do is stay in bed, but I have found gentle yoga, walking and pilates has helped me so far stay mostly symptom free from the shot.

    Welcome to everyone new.  I consider myself still a newbie too.  I had my first TCH on Fri May 13.  I am thankful for the Dr I have.  They believe in meds for the side effects so I have had very few - just the above from the Neulasta shot.  

  • Anonymous
    Anonymous Member Posts: 1,376
    edited May 2011

    Margie, Well for sure I am taking the claritin BEFORE my next nuelasta.....I read that only 52% even get SEs with it and my friend got it the day after each chemo and she did not have any problems with it at all and she didn't even do claritin.  With any any of my chemos if I get any sort of SE it is at least two days after and with any of them it is a cummulative drug and as you get further into it you may start feeling things you did not in the beginning, fatigue, etc.  I was fine the lst three months on Abraxane, and then started dragging after that.  Wish you all the best. 

  • Cyborg
    Cyborg Member Posts: 848
    edited May 2011

    Good luck, Candice!

    Marybe, even with the Claritin I felt bone ache in the lower back and hip area. I am going to definately take it the day before and then for five to seven days after.

  • Cyborg
    Cyborg Member Posts: 848
    edited May 2011

    I am going to get a lint roller--- just have to.

  • justme1
    justme1 Member Posts: 223
    edited May 2011

    u can count me in starting friday May 20th .I am scared so scared when i got my call to begin friday I didnt even ask what i was getting he did say every 3 weeks total of 9 then  once every 12 weeks . So I am wondering about a port sould i get one or not? I hate blood drawn I hate IV"S .I guess we all do but  i got a feeling i am about to face a lot of blood being drawed .Plus the Chemo . Would it be easier getting a port and since i start friday . Can i get one between chemo's ? Another question do yall work with this chemo? I want to watch my grandbabies again 2 and 3 year olds . Can i do that still ? I hate my life right now all the uncertian things i am dealing with .

  • MargieC
    MargieC Member Posts: 394
    edited May 2011

    Hi Justme1

    We have all been there.  I currently do not have a port but will end up with one down the road.  We are doing my chemo prior to surgery so we are going to work with my arms/wrist for now and then we will do the port.  I hate needles and use to panic when I needed blood drawn.  they had to give me aniouxty meds for my biopsy, but as you go down this path the needles seem to become 2nd natural.  I still do not like them and don't look, but as long as the nurse is good it's not too bad.  

    Good luck Fri.... 

    I do project management for a living so I have taken the approached to this as a project - my Dr laugh at me in a good way.  There is so much we can not control through this that being able to orginize myself with my meds, stuff to take to chemo (I actually worked part of the day), etc makes me feel like i have some control. 

  • ---
    --- Member Posts: 197
    edited May 2011

    Hi Everyone!

    I showered with some pain on my scalp today.  More painful when being brushed on.  Today is my 10th day.

    I hope everybody's well today.

    Question:  What kind of daily exercise do you guys do?  I have not been exercising since my Axillary Dissection in April.  Now that my energy is back, I'm thinking of going to the gym (24-Hour Fitness) to do just a bit of cardio on the treadmill.  I'm not sure though about being around so many sweaty people and my immune level.  Thought I'd get your opinion.

    Thank you,

    Laureen

  • neecee
    neecee Member Posts: 663
    edited May 2011

    I am back home after my port placement surgery.  Everything went well.  Now looking ahead to my first treatment on Monday.

  • MamaV
    MamaV Member Posts: 907
    edited May 2011

    justme1 - I meant to say this on the other thread, but to answer your question, I work full time.  I only missed 1/2 days on treatment days and the 1-2 days after with A/C.  With taxol I only miss 2 hours on Thursday afternoon for treatment.  You will have plenty of good days in between treatments to do anything you want!

    Laureen - I've lost 19 pounds since I started chemo so the doc told me I could only take short walks, but no real cardio.  Now that I'm done with A/C and onto taxol, the weight loss has stopped and I've been given the green light to up it a little.  HOWEVER, I was told to stay out of the germ infested gym b/c my counts are running low.

    neecee - glad it went well.  Shoulder will be just a little sore tomorrow, but you will be ok.  (I went to work the day after my port surgery).  Rest this weekend and try not to stress about Monday.  We will help you get through this!

  • Cyborg
    Cyborg Member Posts: 848
    edited May 2011

    I am encouraged to exercise without the gym. Laureen did your doctor or PA show u any exercises? Try getting range of motion- slowly at first in that arm. Please talk to the Inc nurse or someone about exercise or physical therapy.

  • neecee
    neecee Member Posts: 663
    edited May 2011

    MamaV, Iam working tomorrow, too.  I will limit my lifting and reaching, and should be fine,  I plan to work as much as I can during treatment.  It is good for me mentally, emotionally, and financially!

  • Ruthii
    Ruthii Member Posts: 17
    edited May 2011

    Hi Marybe, I didn't realize I resembled Florence Henderson until I started traveling for business and then it seemed like someone in every airport would insist I really was she.  So funny.

    I'm on my first day after chemo #1, and I think everyone should have a Benadryl drip once in their lives.  I was not in the least interested in my book, my Droid, or my lunch.  It was hard to stay awake enough to ice my fingers and toes.  I heard someone say Oh, Look there's water all under her chair; and for a moment I thought perhaps I had not awaked to get to the restroom--but it was just one of my ice bags leaking, thank goodness.  I'm still on Zofran for nausea until tomorrow; then Compazine for the same thing.  I forget what's causing the insomnia, but Ativan did nothing for it, but Sudafed finally worked.  I think it's the Zofran:  it makes me sleepy for 2 hours, then hyper.  Started crashing this afternoon with headace, body aches, trembling legs and arms, total weakness & flu-like feeling.  Good news:  Tylenol ES pulled me up again.  Was on the Onc's suggestion sheet.

    I loved my chemo #1--no pains, no scary moments, no side effects--well, except for the lovely Benadryl drip.  Even if it's downhill from here, I can at least always remember my wonderful first chemo treatmentSmile

    I can ony wish others such a happy first time.

  • 40-years-old-now
    40-years-old-now Member Posts: 309
    edited May 2011

    I had my biopsy today. Everything went well. Wont have results until next week.

  • neecee
    neecee Member Posts: 663
    edited May 2011

    38, For me the waiting is the worst part of the journey!  Glad the procedure went well.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited May 2011

    Hello ladies,

    I had my first chemo today Adriamycin and Cytoxan.  The nurse gave me the antinausea meds (pills) first, then started the cytoxan drip and after that one was done, she put adriamycin directly into my IV line from three different syringes.  The whole process took about 40 mins.  She told me about the meds I was to take home with me and when to take them.  I haven't had any side effects from the meds as of yet and the nurse told me to stay on top of the nausea as best I can  because" once you begin vomiting, you may as well come to the ER so they can run an IV because nothing will stay down at that point. 

    As a side note, I will share what my mom told me as well.  She said to just keep on moving and living your life as if nothing happened until something happpens and you will be fine.  It's not a good idea to sit around waiting for something to happen because it always will. 

    I will continue to pray for all of us and sincerely wish you all the best.  Keep living!! 

  • Ruthii
    Ruthii Member Posts: 17
    edited May 2011

    Welcome to fraidy cat city JustMe1--I was there all week last week waiting for my chemo #1 yesterday.  About the veins or the port:  you have 21 treatments total it looks like so I can see why you would be considering a port--I was too when I thought I might be in a Herceptin trial for a year.  I'm in the trial, but I'm in the control group not getting the Herceptin.

    As I think they can do a port and continue with chemo the same day, you might consider giving the veins a try first, with this warning:  at least 24 hours beforehand if not even two days, start hydrating.  You will not only have fewer side effects from your chemo, but you will have nice, big plump veins for the nurses to see and use easily.  When you are not hydrated, the veins are harder for them to find and they also roll around on them.  You want nice turgid veins.  When I had my surgery and could eat or drink nothing from 11 o'clock one night until I finally got into my (late) surgery the following evening at 6 o'clock, the nurse had a bad time because my poor limp veins were rolling all over the place.  I mentioned this to one of the nurses yesterday because I thought she did such a fantastic job and she said hydrated veins always made her look good.

    I don't know about taking care of your grandbabies; it might not be the best thing for them or you. I assume you are taking care of them on a regular basis, so that's what's bad about it--you won't know how you are going to feel on any one day as the side effects are erratic--they come and go at will and are different each week, some better, some worse--from what I hear tell anyway.  If you can take care of them only when you feel up to it, then go for it!  I sympathize with you.  I am older and have 3 dogs, and I haven't felt like taking care of them for the past two days as much as I love them.  They are much more self-sufficient, of course, but if they were children, I'd be feeling so guilt-ridden I'd make myself sicker.

    The waiting is so frustrating because until you know exactly how it's going to come down, you're in limbo land with insufficient knowledge.  Good luck with whatever decisions you make, and we will all be thinking of you on the 20th.

    Ruthii

  • Sue53
    Sue53 Member Posts: 63
    edited May 2011

    Everyone seems to be doing so well...I feel like a babyCry.  Had to go to ER last night with temp of 100.4.  Did labs, didn't see an infection but got hydrated.  Feel much better today.  Onc has me on 2 different antibiotics until they figure out what is going on.  Also got the ok to take something for the diarrhea, since antibiotics cause it, too.  My work won't allow me to go back until I get a release from doc and she won't do that until she see how I react to all of this.  Not that I feel like working anyway, but am lonely here at home.  Did get out today to go to my daughter's hs award assembly.  Glad I did because I could tell see was happy I could make it!

    Am I being too hopeful to hang on to my hair until May 22 (12 days post tx)?  That is her hs graduation.

    Stay strong...you all seem to be doing so wellSmile.

    Sue 

  • DebRox
    DebRox Member Posts: 437
    edited May 2011

    Hang in there 38.  My thoughts are with you.

    Marcya:  nice side note from your mom, thanks for sharing.  I'm sure we all know how hard it is at times to act as though nothing has happened.  But a year from now, this will all seem like a dream!  I look forward to that day.

    Venting here:  We had to cancel an annual family trip to be taken June 18.  My HB contacted AA 3 weeks ago  to request an extension on our airline tickets for a year without penalty out of reasons of compassion - we did book the tix a year in advance so they expire this July. We haven't heard ANYTHING to date which saddens me.  I would at least expect a response.

  • Cyborg
    Cyborg Member Posts: 848
    edited May 2011

    38 years old-- sending you positive thoughts re. your biopsy.

    sue53 -you are not a baby. The same things went on with me. Everyone has their moment. I don't know what to say about the hair. A pretty scarf to go around your head with a sun hat of sorts

    could be very pretty. I am pretty much bald at day 16.                                                                                                                                                                                                                                                                                                                                                                                                                                                                                     

  • ---
    --- Member Posts: 197
    edited May 2011

    Cyborg,

    I am doing Range of Motions exercises.  The surgeon will see me in two months for another assessment if I need PT referral or not.  As of now, i'm on my own.  I'm wondering if cardio exs will be too much for someone who's going through chemo. 

    How much hair are you losing now?  I saw your new picture.  I woke up this morning with sensitive scalp.  I might as well be ready for the impending hair loss.

    Take care and I hope you are feeling much better now.

     Laureen

  • Cyborg
    Cyborg Member Posts: 848
    edited May 2011

    Good then Laureen. I take walks.I have lost 80% of my hair since Monday. My scalp was sesntive more than a week before I started to lose hair.My scalp is not so sensitive now. The lint roller feels good and takes care of business with the bedding. Smile. It is very freeing. Nothing says " I don't give a F@#$%" than a bald head.

  • Katarina
    Katarina Member Posts: 386
    edited May 2011

    I just finished round 1 of TC.  My Infusion RN was funny, she said she's had a few patients tell her their hair fell out the very next day -""they woke up to find a head of hear on the pillow next to them""..L and it wasn't a strangers hair." 

    You have to just laugh about this stuff - not sure I believe her story but it made me laugh.  But definitely don't laugh about this disease. It's life changing and we're all heros! 

  • Anonymous
    Anonymous Member Posts: 1,376
    edited May 2011

        Well, as much as I hated the way the neulasta shot made me feel, I guess it really did the job it was supposed to do.  Last week I think my white count was something like 3.2 and today it was 39.9!!  The nurse said wow, be sure to point that out next time.  They might decrease the dosage to half from the way you responded.  My onco just rolled his eyes when I told him about the claritin and rolled them again when I said I got the info from the breast cancer message boards.  I felt downright good today and worked the afternoon with no problems.

    When I looked down at the keyboard this evening I noticed a lot of hairs and they are not from the cat or the dogs. I think I may put off shampooing in the morning.  Two weeks since lst treatment.  Last time I went longer than 3 weeks before it started.

    I talked to a woman in the treatment room today who had signed up for  the Look Good, Feel Better class on Monday and she gave me the number and I am now going also.  I have never been to one of those, but a good friend of mine went and she said they give you all sorts of great namebrand makeup, plus tips on how to draw on eyebrows, style you wigs and tricks to do with scarves and headcoverings.  I am looking forward to it. 

  • ---
    --- Member Posts: 197
    edited May 2011

    Hi Marybe,

    I just attended a Look Good Feel Better workshop this past Monday.  It was nice and i was glad i went.  I met new people at different stages of treatment, and got a bag full of brand name make-ups:-)  I always love freebies!  The thing is, I don't wear make-up on daily basis so I will give them to my mom!

    They taught us how to take care of skin during chemo, how to apply make-up, how to wear scarves, caps, hats, how to care for hair during and after chemo, and told us a bunch of stuff of what to expect.  They recommended use of Nioxin Scalp Treatment even during chemo.  I didn't know we have to wash out scalps with shampoo and conditioner even after losing out hair.  They said it helps in avoiding ingrowns and somehow helps clean the scalp from the chemo drugs.

    Have fun when you attend yours!

    Take care,

    Laureen

  • Anonymous
    Anonymous Member Posts: 1,376
    edited May 2011

    Thanks Laureen,  I did use Nioxin the last time and there was also another product I got from a beautician, but I can't recall the name now.

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