Sept 2012 chemo

Options
12627293132165

Comments

  • patriciahurtado
    patriciahurtado Member Posts: 489
    edited September 2012

    Good morning Cindy74...thank you for all the support ...i been so tired from chemo that i havent event had time to be here ...i miss you my sisters...i had my neulasta shot and my bone have been hurting not as much but i can complain cause had just small side effects!!!

  • patriciahurtado
    patriciahurtado Member Posts: 489
    edited September 2012

    Good morning Cindy74...thank you for all the support ...i been so tired from chemo that i havent event had time to be here ...i miss you my sisters...i had my neulasta shot and my bone have been hurting not as much but i can complain cause had just small side effects!!!

  • patriciahurtado
    patriciahurtado Member Posts: 489
    edited September 2012

    Good morning Cindy74...thank you for all the support ...i been so tired from chemo that i havent event had time to be here ...i miss you my sisters...i had my neulasta shot and my bone have been hurting not as much but i can complain cause had just small side effects!!!

  • patriciahurtado
    patriciahurtado Member Posts: 489
    edited September 2012

    Good morning Cindy74...thank you for all the support ...i been so tired from chemo that i havent event had time to be here ...i miss you my sisters...i had my neulasta shot and my bone have been hurting not as much but i can complain cause had just small side effects!!!

  • patriciahurtado
    patriciahurtado Member Posts: 489
    edited September 2012

    Good morning Cindy74...thank you for all the support ...i been so tired from chemo that i havent event had time to be here ...i miss you my sisters...i had my neulasta shot and my bone have been hurting not as much but i can complain cause had just small side effects!!!

  • patriciahurtado
    patriciahurtado Member Posts: 489
    edited September 2012

    Good morning Cindy74...thank you for all the support ...i been so tired from chemo that i havent event had time to be here ...i miss you my sisters...i had my neulasta shot and my bone have been hurting not as much but i can complain cause had just small side effects!!!

  • patriciahurtado
    patriciahurtado Member Posts: 489
    edited September 2012

    Good morning Cindy74...thank you for all the support ...i been so tired from chemo that i havent event had time to be here ...i miss you my sisters...i had my neulasta shot and my bone have been hurting not as much but i can complain cause had just small side effects!!!

  • patriciahurtado
    patriciahurtado Member Posts: 489
    edited September 2012

    Good morning Cindy74...thank you for all the support ...i been so tired from chemo that i havent event had time to be here ...i miss you my sisters...i had my neulasta shot and my bone have been hurting not as much but i can complain cause had just small side effects!!!

  • patriciahurtado
    patriciahurtado Member Posts: 489
    edited September 2012

    Good morning Cindy74...thank you for all the support ...i been so tired from chemo that i havent event had time to be here ...i miss you my sisters...i had my neulasta shot and my bone have been hurting not as much but i can complain cause had just small side effects!!!

  • patriciahurtado
    patriciahurtado Member Posts: 489
    edited September 2012

    Good morning Cindy74...thank you for all the support ...i been so tired from chemo that i havent event had time to be here ...i miss you my sisters...i had my neulasta shot and my bone have been hurting not as much but i can complain cause had just small side effects!!!

  • patriciahurtado
    patriciahurtado Member Posts: 489
    edited September 2012

    Good morning Cindy74...thank you for all the support ...i been so tired from chemo that i havent event had time to be here ...i miss you my sisters...i had my neulasta shot and my bone have been hurting not as much but i can complain cause had just small side effects!!!

  • patriciahurtado
    patriciahurtado Member Posts: 489
    edited September 2012

    Amy does your onco prescribe melotonie for pain?

  • patriciahurtado
    patriciahurtado Member Posts: 489
    edited September 2012

    OMG...this site has gonna while!!!!....

    I am 39  and my baby girl is 18 she started college and also got herself a part time job which im real thank full keeps her busy and not trying to get depress about all this....she is my only child....so you already know how shes been feeling....but she is strong as her mom is...and i am strong....My aunts on my mom side both had breast cancer and i knew some how i could of being more on top of this...every year i would i asked my gyno that i need  a mamagram do to the family history and every year he would say no that i was too young and that its not heretary...well it was because i accidently found it....i checked my self every day just because i knew some thing might come up...i was at the gyno on wednesday nothing was there..Thursday nothing...Friday there it was......got my mammagram...said it was some type of mass...did the biopsy ...there it was!!!!!!!!! i whish that i had a different gyno who really paid attention instead telling me to wait till i was 40 so here i am almost 40 and now i find this out!!!!!!! why wait till 40...???!!!!

  • Mariposa123
    Mariposa123 Member Posts: 267
    edited September 2012

    Hi everyone,

      Spent most of the night in the Emergency Room.  Lots of pokes, blood tests, and a chest x-ray.  I was there for four hours before they let me go home  My blood counts were okay.  They did give me a full bag of IV fluids, which helped a ton with my constipation (now I am on the opposite side of the spectrum!)  

    Mostly today I am feeling weak, tired, and depressed.  It is my six year old's birthday and I want her to have such a special day- but I have no energy and feel like a science experiment that has gone terribly wrong.  I have promised her a small party in a couple of weeks, but she is little and doesn't quite understand.  

      Cancer sucks.

  • allurbaddayswillend
    allurbaddayswillend Member Posts: 355
    edited September 2012
    whenlifegivesyoulemons, the clock is ticking on those buggers.

    Mariposa, Taxol (the older sister of taxotere) has given me constipation too. My MO and I worked it out for me. First I was trying Milk of Magnesia at night but then by the time that worked it would give me diarrhea which is also not good and can cause potassium deficiency. So then we tried that I should eat prunes after every meal. I already eat tons of veggies  and have plenty of fiber in my diet. :/ That helped but not perfect and was a little gassy. So then a couple days I was constipated and gassy and I got pretty uncomfortable. This time around, I have been taking a pro-biotic with every meal, MO approved, drinking a homemade gatorade that uses erythritol which can be a little laxative-ish for sweetener, and prunes usually once a day. That is keeping me regular, no diarrhea, a little gas. So I will stick with this plan for next week too. My Taxol chemo is on Tuesdays and I was constipated Weds, Thurs, Fri and then Sun and Monday on the first round, the next round was a bit better with prunes and this past round has been ok with probiotic.

    oh Justine, 23 yrs old...  AC was difficult for me for the 5 days after infusion but then I would bounce back and be ready for the next one. Best of luck!  So glad you caught it this early.
  • Cindi74
    Cindi74 Member Posts: 363
    edited September 2012

    The website is not working correctly.  When you push the submit button, nothing happens, so you think the message has not gone through.  If you keep pushing, it will print multiple times.  Just push once and go back to beginng and your message has gone through.  If it is a long message, copy and paste into an e-mail to save it so you don't lose it.  This pbm is why the multiple messages.  If someone will flag this message I am sending, maybe the moderators will pick up and get tech people to fix it. Seems to me there was some message about a time they would be working on the system.  Sometimes, in trying to fix something, they mess up something elso. 

  • Waitingforthenextstep
    Waitingforthenextstep Member Posts: 251
    edited September 2012

    Hey friends

    Tuesday is coming fast and it is the day of my first chemo. I wish I could say I wasn't apprehensive.  I know this question will prob. cause an avalanche but here goes...what do you guys do to pass the time?  Will it be three hours? four?  Won't know if I don't ask I guess.  As always appreciate all of you.

  • Waitingforthenextstep
    Waitingforthenextstep Member Posts: 251
    edited September 2012

    Hey friends

    Tuesday is coming fast and it is the day of my first chemo. I wish I could say I wasn't apprehensive.  I know this question will prob. cause an avalanche but here goes...what do you guys do to pass the time?  Will it be three hours? four?  Won't know if I don't ask I guess.  As always appreciate all of you.

  • Waitingforthenextstep
    Waitingforthenextstep Member Posts: 251
    edited September 2012

    That's right, Cindy.  Same thing just happened to me.

  • Mariposa123
    Mariposa123 Member Posts: 267
    edited September 2012

    Thanks allurbaddayswillend!

      I was taking a pro-biotic, but my doctor asked me to stop. I will talk to him again.  I also will try the prunes and the gatorade.  The constipation cramps were unbelievable!!!  That mixed with the vomiting made for a very unpleasant evening.  Feeling much better today.  I just ate a blueberry bagel- which is the first thing I have eaten in over a day.  My stomach just felt empty.  I usually eat tons of veggies, but lately have felt so ill I haven't eaten anything.  I will try to have a huge dinner of broccoli tonight!

    Waiting for the next step:  I know it can be so anxiety provoking before you begin!  I try to stay connected to friends, draw, play with my kids, imagine what I want for my world- I also started a blog. I am a board certified art therapist/licensed marriage family therapist- so I am kind of using my blog as a way of being my own therapist. 

    http://breastcancerartandme.blogspot.com/

    I am also organizing cabinets when I am at home.  When I am there, I read, write, talk to my husband, play sudoko, and just do nothing.   And just try to give myself a break as much as possible.  Of course we are anxious!  But we will get through this.  It is only temporary.. and we will be back to our regular life only stronger and with more insight.

  • butterfly14
    butterfly14 Member Posts: 253
    edited September 2012

    Hi Waiting - we are starting chemo on the same day. I am bringing my smart phone, tablet, book and husband. Like you very nervous.

    Have a great wekend.

    Carla 

  • damiana9
    damiana9 Member Posts: 389
    edited September 2012

    Waiting- your first treatment will probably be the longest because they watch for any reactions. Are you on the TCH combo? I am doing that plus a study drug, and I was there about 7 hours total the first time :-( it gets shorter the next time though! Bring a laptop and a book and some snacks.

  • jojo2373
    jojo2373 Member Posts: 662
    edited September 2012

    Mariposa, I loved your blog! Thanks for sharing with us. Day 3 my diarrhea has stopped, but figure its just fooling me and setting me up for the constipation route now. Ahhhh just to be regular!

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

    FYI- The system has being going through some maintenance work and I'm guessing they aren't quite finished.   The system seems slow to posting. 

    Glad to hear you are back home, Mariposa!!  Easy does it on your tummy.  You may want to stick to a bland diet until things have settled down again.  Maybe some chicken broth, rice, chicken, plain noodles, mashed/baked potatoes.  I know you've been through a lot the last 24-48 hours. Rest, keep drinking the fluids, eat a little and keep taking your meds. 

    Waitingforthenextstep- What chemo regimen are you having?  The first round of chemo lasts longer than others because the infusion staff wants to be very careful and watchful of any immediate allergic reactions.  The chemo may be run a little slower but it is out of precaution to you.  While I was having chemo, I watched mindless TV, talked to my husband and the clinical trial research coordinator, flipped through magazines, napped and ate lunch.    I drank a lot of water/ate ice and sometimes asked the nurse to unplug my IV pole from the electrical plug so i could walk around.  I had Ativan (anti-anxiety med) plus benedryl in the pre-chemo IV so I was pretty chill and couldn't focus on much.   If you are anxious the day of the chemo and don't have any meds for anxiety, ask your onco for some.  It's okay; it isn't unusual to get a med to help keep you calm.   I always tried to just go with the flow of things in the infusion center and didn't get upset when I had to wait for the chemo to arrive from the oncology pharmacy or how long each infusion took.  I just always knew I'd be there for a while and made sure I didn't have anything scheduled the same day. 

    Wishing a wonderful weekend for all with minimal side effects!!!!Cool

  • whenlifegivesyoulemons
    whenlifegivesyoulemons Member Posts: 184
    edited September 2012

    CNN is airing a segment on advancements in cancer treamtments (Sanjay Gupta is interviewing staff from the Anderson Cancer Center).  Someone else mentioned this in a post earlier this week so I'm letting you all know it's out there today at 3:30 central - I bet it'll be rebroadcast too.

  • JodiRocksthePink
    JodiRocksthePink Member Posts: 23
    edited September 2012

    I had my first round yesterday. I was there for 5.5 hours. It went fast really....I brought magazines and read a book. The anticipation is way worse than doing! I had a long night of steroid crazies. I took an ambien and still only slept 2 hours. I'm a little out of it and can feel the chemo lurking around the edges. Has anyone stopped taking the steroids? I hate not sleeping! My kids understand sick mom, but not tired.



    On a side note, when I got home yesterday my 5 year old said I need to go back....the meds didn't work. I still have hair. He had my wig out at the door ready for me. He calls it the "thing". I totally understand the feeling of missing out on the kids lives. I hauled myself to soccer this morning....I only made one of 2 games. But it was worth it, she scored her first goal!



    I hope everyone has a blessed weekend with smiles and some laughter.

  • damiana9
    damiana9 Member Posts: 389
    edited September 2012

    Jodi- I HATED those steroids, and honestly with my 2nd treatment coming up it is the steriods that are making me anxious again, and the SE of the Neulasta shot- the chemo meds were a breeze, it's the stuff we have to take in addition to the chemo meds that I had a really hard time with!  Just know that you will be able to make up for your lack of sleep in a couple of days.

  • Cherioo
    Cherioo Member Posts: 305
    edited September 2012

    Day two in bed no appetite, the nausea is awful . I have thrown up three times and praying I am done . I can't wait to feel better

  • Cindi74
    Cindi74 Member Posts: 363
    edited September 2012


    These are the Members of the Exclusive September Club No One Wants To JOIN.
    If I've left you off, please let me know.  

    7312012   M   47

    301724    Vermont
    Aic 1 C. 35
    Aliasismo radiologist 56
    allurbaddayswillend M, 1 C. 48
    Amy4978       Howard City, MI     34
    AmylovesBubby
    Bearcub Prince George, British Columbia  M.,  3 C. 8 G radiologist    55
    Butterfly14 Self Clearwater, FL 3 C. 44
    Cgesq New Jersey radiologist 2 C, 50
    Cherioo Florida 4 C. 46
    Cindi74 Apopka, Florida radiologist 3 C 6 SC. 21GC M 75
    Damiana9 Burleson, Texas
    DonnaDo8 Self 2 C. 42
    Englishrose75 Self Diagnosed Milton Keynes United Kingdom 2 C. 37
    Ergirl
    EvaNJ
    Firestorm531 1 C. Texas 41
    florbo     Dallas, Texas
    Foreverchanged72612 Self Chelsea, Quebec 3 C. 38
    Frannygirl Louisiana
    Internutz1 Van Alstyne, TX USA
    JodiRocksthePink M, 2 C. 39
    Joemommy Portland, Oregon 1 C. 46
    Jojo2373 Maryland Self.....5C.     50 
    Justegan Wolcott/Kingston Dr. Diagnose, 23
    KelleyB
    Kstillie
    Laura_g
    Lokimax2 Siler City, NC
    Mariposa123 Bay Area, Californiz 2 C. 44
    Melrosemelrose (visitor from April) Houston, Texas
    Mindy703 M, 3 C 41
    Momto5children
    Movinonmom
    Mycancerjourney Illinois
    Neta69
    Nickythebean
    PatriciaHurtado Miami, FL
    RSDavid 3 C. 4G. 58
    Runnergirl71 Fort Collins, Colorado
    SandeeAR Conway, AR
    Sheerbab Dallas , Texas Self Diagnosed M, NO C, 43
    Sjayne2u Ohio
    Sparkysbrat East Tennessee Mountains
    SugarlandlDC Houston 3 C. 43
    Tara88
    Terri07-11
    Timbek2 radiologist, 3 C. 40
    Timbek2 Peoria, IL
    Toastiecat
    Twinsplus1 3 C. 44

    Usmcblondie     25

    Waitingforthenextstep
    Whenlifegivesyou lemons Minneapolis  M radiologist 46

    Wendy49      Michigan   2C  M  self  49

    That's 54. So many enduring together.
    Appointment now for reunion on this website in five years!
    Code: M=Married, C=children, GC= grandchildren, SC= Step Children "self" =self diagnosed, radiologist=how diagnosed

  • EnglishRose75
    EnglishRose75 Member Posts: 147
    edited September 2012

    I've had really bad problems with sleep for the first few days with all three of my treatments so far and have just resigned myself to the fact that nights one and two after chemo will not be good.  After the third night I find it gets much better.  I've tried taking prescription sleep meds and also tried taking some of the codeine that I had left from surgery which usually makes me pass out within 15 minutes but neither make any difference at all.  I don't think that skipping the steroids is an option unfortunately.

    Cute story about your son, Jodi.  I hope you get some better sleep soon!

    Cheerioo, sorry you feel so awful :( 

Categories