Starting Chemo May 2015

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  • CatsRus
    CatsRus Member Posts: 310
    edited July 2015

    tjh, high five on reaching the last chemo! ✋ I too am looking forward to Thursday and the last one for me... I'm hoping recovery is helped along by the knowledge it's done.
  • StefLove
    StefLove Member Posts: 322
    edited July 2015

    So I officially started taxol and carbo friday so 1 down, 11 to go! I was so scared about having a reaction but luckily nothing happened. Crappy part was that they came back after my blood test and told me my hemoglobins were 7.9 which is insanely low. Only option for a quick fix was a blood transfusion and they wouldn't do chemo unless I agreed to getting the transfusion within the next few days. I asked about getting it the same day right after chemo and they were hesitant but then my onc called back and said that as long as I had no reaction to chemo then to go ahead with everything. Who the heck knew a blood transfusion takes so damn long? Two bags took 4.5 hours and then they made me sit there for 30 mins after to make sure I didn't have a reaction!

    Glad it's over though and I'm looking forward to feeling better. The nurse was amazed I didn't feel crappier bc of my hemoglobins. She kept asking "you're ok walking? Breathing?? You're not gasping for air???" Ummmm no? I'm tired as crap but you all said that was from chemo!! Lol


    Hope everyone had a great weekend!

  • lman
    lman Member Posts: 22
    edited July 2015

    I also go for last TC tomorrow! So excited to get this behind me. Went last week for markings and start radiation in August. Good luck to all heading for treatment this week...may the side effects be manageable!

  • dunesleeper
    dunesleeper Member Posts: 2,060
    edited July 2015

    Congratulations Iman!!!

  • mysunshine48
    mysunshine48 Member Posts: 1,480
    edited July 2015


    Wow, my PS said I need to wait 6-8 weeks after final treatment to make sure my body is healthy enough and I hsve to be released from my MO to heve my exchange. If you don't mind me saying, but I would think you need to do some research on implants. There are many kinds. Have you discussed options with your PS? I will be getting silicone and small waiting for the new Natrelle Inspira implants in September - works with timing too. There are several threads on this site it may be good for you to look at. Ypu need to be very informed and not just leave this up to your PS. Search for Implants 101 and Exchange City.

  • mysunshine48
    mysunshine48 Member Posts: 1,480
    edited July 2015

    Oh, just checked.....Thread is Breast Implant Sizing. Whippet mom is amazing and can be a lot of help. The forum is Reconstruction, I think. Good luck

  • tjh
    tjh Member Posts: 469
    edited July 2015

    Appointment with PS is July 22. I wanted info before that appointment. She said 4 weeks after last chemo as long as my blood counts are good...I am trying to start the school year. I have very limited sick days left.

  • mysunshine48
    mysunshine48 Member Posts: 1,480
    edited July 2015


    tjh, You must be superwoman. I was a teacher of young Special Needs children up until my surgery. I decided to retire as I was thinking about it anyway. You must be young! I could not imagine going back to school. Do you not have side effects and fatigue from chemo? I have been told and have read a lot about the tiredness and fatigue lasting for months. I hope you can do it, but, again, you are amazing to consider going back into the classroom

  • tjh
    tjh Member Posts: 469
    edited July 2015

    I am 57...this is my last year, mostly because I want to quit on my terms, not because I am sick. I am tired, I am hoping with 6 weeks to recover I will be able to do it...I'd not I will use sick days to do 4 day weeks for awhile. I am not doing anything extra this year.

  • mysunshine48
    mysunshine48 Member Posts: 1,480
    edited July 2015

    I am 66, so it is time anyway! Good luck

  • lman
    lman Member Posts: 22
    edited July 2015

    tjh - Good luck tomorrow. I am also a teacher, but not planning to go back to the classroom for a while yet. I am fortunate to have over a year of sick days so I can take my time. Since I do radiation in August, I will take another couple of months at least and I'm also thinking about doing it gradually, 3 or 4 days a week. I am 50 and plan to retire at 55.

  • tjh
    tjh Member Posts: 469
    edited July 2015

    I had almost 100 and then when Walker passed Act 10 in Wisconsin the districts wrote handbooks instead of contracts and 1 of the things they did was limit sick days to 65. Anyone over lost them and in the 4 years since I lost 10 each year up until last year. I was out 1/3 of last year. Luckily I had a good sub who likes "my kids". So going into this year I only have 11 1/2 sick days and lots of appointments.

  • lizannee
    lizannee Member Posts: 16
    edited July 2015

    My second TC is tomorrow. Hoping for a week that I can handle!

  • dunesleeper
    dunesleeper Member Posts: 2,060
    edited July 2015

    I wish the same for you lizannee. I have my 2nd treatment tomorrow too. This past week has not been good. This next week will be, though. Right?

  • tjh
    tjh Member Posts: 469
    edited July 2015

    Good luck and cyber hugs for all doing chemo this week. ..We shall triumph!

  • lman
    lman Member Posts: 22
    edited July 2015

    dunesleeper - here's hoping this week goes better for you...sending positive healing thoughts your way


  • tjh
    tjh Member Posts: 469
    edited July 2015

    Last TC is done. Seems to be hitting me harder then the other 3. Just really foggy and achy.

  • Scarlett152
    Scarlett152 Member Posts: 175
    edited July 2015
  • lizannee
    lizannee Member Posts: 16
    edited July 2015

    Same for you dunesleeper. My port had a clot in it so it took longer but I am ok for now.

  • Moderators
    Moderators Member Posts: 25,912
    edited July 2015

    We are thinking of all of you and wishing you much luck. Please continue to keep us posted!

  • rosesrx
    rosesrx Member Posts: 458
    edited July 2015

    way to go tjh!

  • lman
    lman Member Posts: 22
    edited July 2015

    I'm done chemo! Neutrophils were way down but my MO agreed to let me go ahead. Hopefully that won't mean infections this week.

  • rosesrx
    rosesrx Member Posts: 458
    edited July 2015

    congrats Iman!

  • tjh
    tjh Member Posts: 469
    edited July 2015

    Fantastic! How are you feeling? I am very foggy and achy. Looking forward to bed and bathrooM trips and neulasta tomorrow.

  • lman
    lman Member Posts: 22
    edited July 2015

    I'm in bed but can't sleep, feeling bleh and almost nauseous. Hope I sleep soon. I don't get neulasta until 48 hours post chemo. Hope you feel better tomorrow tjh.

  • MarlanaB
    MarlanaB Member Posts: 292
    edited July 2015

    Is anyone else making plans for "when this is done"?. I have all of October off but I'm not sure if that will be too soon.

    I think it's good to set goals to motivate us but right now, my goal is to get off the couch. We generally have cool summers here (72-75 degrees) but it's warming up in the next couple of days. I'm 4 days out from TC#3 but I swear I'm going to get my sand chair out and head to the beach this week even if I have to be completely covered up and I only end up 10 feet from the parking lot!

    I'm not as completely wiped out this round as the last. I think the bronchitis after round 2 really did me in!

  • mysunshine48
    mysunshine48 Member Posts: 1,480
    edited July 2015

    So good to hear many of you are done with chemo. Now, it's time to rest and recover. I hsve my last T/C on Thursday but feel Inhsve not recovered from the last one. They called me in for fluids today because of blood work. I had to have a friend drive me because Inwas weak and lightheaded. I guess I need to force myself to drink more water, although it seems like I drink a lot. Does anyone else get so weak for the weeks following treatment?

    Mariana, Inwas hoping for a visit to my son's in October, but am not making any plane reservations. Afraid to. I have exchange surgery between now and then and he has 3.children under 5, so am a little skeptical. My ticket may be more, last minute, but all this makes it difficult to plan much right now.

    IMan and tjh, YEA for finishing! I will join you soon! We will get through this!

  • Shanann
    Shanann Member Posts: 106
    edited July 2015

    I this posted on Facebook, and I thought of you all, and wanted to share it.

    Good morning!

    You never know how blessed you are until you see how cancer affects others.

    I experienced the bare minimal of aches, pains, nausea from chemo nd burning sensations from radiation.

    I thank God my mother in law was a survival and she told me what NOT to do.

    Her 1st words to mean in November 2011:

    1. Don't be mad, crap happens
    2. Stay positive
    3. Speak life filled words to your body
    4. Drink wheatgrass
    5. Drink ginger tea
    6. Drink a gallon of water
    7. In spite of your pain, don't stay in that bed. Move and let your body know you ain't quitting
    8. Pray
    9. Live, tomorrow ain't promised
    10. I am here

    I have been doing this since that day!

    In my world. The bilateral mastectomy cut it out. Chemotherapy cleaned me out. Radiation was the prevention. My way of thinking is my BOXING GLOVES!!!

    My joints ache, but I keep moving (slowly) and I get there.
    I cannot sleep, so I take mini naps.
    I don't remember well, so I take notes.

    But I AM STILL ALIVE!!!!!

    No pity party here, just a GIGGLING WIGGLING RASPBERRY freckled face diva giving life ALL she got.

    Praying for all of you, name by name, need by need.

    Hugs
    Giggles

  • Shanann
    Shanann Member Posts: 106
    edited July 2015

    image

    Marlanab- I was thinking the same thing- a goal for when this is done. I am like you and will probably head to the beach. I don't begin the second part of my treatment (Taxol) until July 29th, because I got 4 weeks between, so I won't get my last dose until September 9th, so I figure I'll need two weeks to recover from that before trying to plan anything. I hope to be at the beach by the end of September, and catch the tail end of the warm weather!! Also, my best friend made me a quilt. Surprisingly, she got it finished WAY before she thought she would. I am going to take it with me to my next four treatments, and cover up. It is beautiful.

    image


    And, call me vain, I can't wait for my hair to grow back- I'm wearing a wig to work, and I just wanna rip it off!! I carry heavy school books (packing), and yesterday I walked 7,700 steps in a warehouse and sweated like a pig. Our busy season has begun.

    image

  • rainnyc
    rainnyc Member Posts: 1,289
    edited July 2015

    Congratulations to all those who've finished chemo. I'm on Taxol/Herceptin/Perjeta for at least another two cycles, then either A/C or surgery. Waiting for the surgeon to get back from his vacation (what? how can they go on vacation?).

    Have the MO's okay to go camping for a few days later in the month. We stick to state parks with showers--I've never been much for seriously roughing it. But we have a teenage son, and DH is a former boy scout, so camping we will go. Glad to be feeling well enough to do it, and I have no problem sitting around the campsite with a book if I'm not energetic enough for heavy-duty hiking.

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