Chemo May 2011

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  • Cyborg
    Cyborg Member Posts: 848
    edited May 2011

    Robyn- onc said it wouldn't hurt ne. He is at a research school of med - UCLA and has an open mind. So, if I start feeling like crud, I will eat but I am going to give it a shot even if it will be less than 48 hours prior to chemo. So far, humming on the steroids!



    Drove with the window rolled down and I know why dogs like it.

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

    Happy Sunday Everyone!

    GOODLUCK to those who will be in the chemo chair again or for the first time next week.  Ready or not, I will be going again tomorrow for my #2AC.

    Take care,

    Laureen 

  • neecee
    neecee Member Posts: 663
    edited May 2011

    Laureen - doing my first treatment tomorrow.  Good luck to you too!

  • Robyn_S
    Robyn_S Member Posts: 197
    edited May 2011

    Hi marybe! Keeping up your strength is important and doing a fast ONLY with the knowledge and ok from your MO is vital. The research found that while patients lost weight over the fast, they gained it back very quickly, more importantly blood counts in the patients recorded were much better with fasting which of course is protective against disease. Protecting healthy cells is my motivation as at 46yo I need to use them for a long time! That is why trials are being done now as pilot data is very promising- as a scientist I appreciate seeing theory and solid research being translated to something practical! Too often good research does not get used unless there is money to be made by a drug company!

    You have to keep up liquids so dry heaves are not a problem! The nausea was awful for me last time without fasting and lasted 10 days with meds to keep everything down and then the anti nausea cause constipation and headaches so I take more meds for those SEs..... Ugh! I was ill and rattling!

    First day at work in a scarf to cover the poor sore scalp- feel quite shy but I am sure will get used to it over the next 6 months!

    ((((hugs))))) to all those in the chair this week!

  • Sue53
    Sue53 Member Posts: 63
    edited May 2011

    Marybe, that's my issue.   I need to keep my strength up.  I lost weight after diagnosis due to stress so I really have to be careful.

    My daughter's hs graduation went beautifully...am so thankful that I finally felt good and could enjoyit.

    Tonight I'm getting my haircut cut since I'm at 12 days.  This is going to be scary nd liberating at the same time...

    Sue 

  • Cyborg
    Cyborg Member Posts: 848
    edited May 2011

    Good luck to the first timers in the chair this week. Wishes fir no side effects to all! Enjoying my day on steroids.

  • Beaglesgirl
    Beaglesgirl Member Posts: 287
    edited May 2011

    This is my "off" week from a/c just got my self back together and the constipation has kicked in. I think I can handle it over the nausea and pain from last week... I hope. :)

  • Cyborg
    Cyborg Member Posts: 848
    edited May 2011

    So

    Wine on a thread suggested Prunes soaked in lemon juice. That sounds really good 'bout now.

  • lisa1000
    lisa1000 Member Posts: 1
    edited May 2011

    First chemo was on 5/12/11 and I'm feeling lucky (almost like cheating) that I really only had two bad days. Second is this coming Thursday. I hear it gets worse, but I'm hoping that years of exercise and eating right will help at least a little bit. My biggest problem right now seems to be constant fatigue and some pretty significant muscle aches. Hope all goes well for everyone this week.

  • 40-years-old-now
    40-years-old-now Member Posts: 309
    edited May 2011
    Ok cant figure out how to put both long and short hair picture on. So here is me with the shorter hair. Same day as other picture. lolLaughing
  • bak94
    bak94 Member Posts: 1,846
    edited May 2011

    Marybe, my total white blood count 6 days after my first chemo was .8 but one part of white blood count was .1! So before my 2nd chemo my total white counts were 10. They took my blood counts while I was in the middle of chemo and they went up to 16. How weird is that? The nurse that was giving me my neulasta shot today seemed a bit worried that they were that high, she took my temp to make sure I did not have an infection and kept telling me to continue to take my temp, which is fine. Was you doc worried about your counts being 39? Maybe the shots just took awhile to kick in for me, but she sure was concerned.

  • bak94
    bak94 Member Posts: 1,846
    edited May 2011

    Day after chemo and my hair is coming out in handfuls, but I still have hair which is a surprise with how much is coming out! Had it cut even shorter today, thought about bringing out the clippers, but decided to wait a bit longer, as I have no bald spots yet. This is about day 16 after first chemo. Put on my free wig at my friends house and her daughter laughed at me! Well, I still need to find another wig, that one is not a very good one and I appreciate a younsters honesty!

  • Plils
    Plils Member Posts: 146
    edited May 2011

    Hello all you beautiful ladies,

    I also will be starting Chemo (TC x4) this coming Thursday, feeling a little scared of the SE and hoping there are very little.  Good luck to all of you and I hope we can all  get though this together.

    Lots of hugs to all.

    Pam 

  • twistedsteel
    twistedsteel Member Posts: 156
    edited May 2011

    I am having first chemo tomorrow, May 23rd.

    I am embarking on weekly Taxol for 12 weeks. Then 15 weekly AC.

    I meet with the BS tomorrow morning and then chemo in the afternoon. My sister is coming into town to drive me. I will need to be driven home after each of the first 12 weekly infusions bc of the Benedryl.

     I am nervous... and I never get nervous. I called Friday at the last minute to ask for anxiety Rx and nausea Rx so I have it in advance.

    I'd love to hear more about the fasting thing. I don't have time to go back through the zillions of posts here to track down the genesis. What's it about?

    thanks

    ps-

    I have a Port-A-Cath... anyone else here get one of these babies installed? 

  • SheriBell
    SheriBell Member Posts: 393
    edited May 2011

    I start my Taxotere/Cytoxan on Tuesday the 24th - I have 4 rounds at 3 weeks apart.  I had last Thursday a Power InJectable Port installed called a "Smart Port"  - is that a port a cath?

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

    My port is a Power Port. I still dont know when I will start chemo. I thought it would have been this past week latest, but atlast no, it is delayed until they know what my hot spots are.

    I dont like having the short hair. My hair is dirty looking 12 hours after I wash it. Hubby says it is because the natural oils are use to being brushed down the long hair.

    One of my hot spots are in my right leg, right by the groin. I have been having serious pain in it sence lump (april 21). I want that pain to go away. Like I dont have enough stuff I also have this stupid pain. It feels like I have dislocated my leg several times a day. The pain is actually worse then the surgery, port and biopsy.

    Sorry for the complaining.

    Candice

  • bak94
    bak94 Member Posts: 1,846
    edited May 2011

    Oh Candice, I wish I could take the pain away. Are you sleeping ok? Your short hair is cute! I used to have long hair also. Today had to get it cut even shorter, as it was coming out by the handful. I am surprised I don't have any bald spots yet, just getting thin. I must find a wig soon that doesn't make people laugh! I may just wind up being a hat person at this rate, although I only have one hat. Why is it the hairsuch a big deal? It is and I just don't really consider myself a vain person, pretty natural, not much makeup and such, low maintenance some would call me. I found myself trying to put in earrings, but one of my holes closed up!

  • bak94
    bak94 Member Posts: 1,846
    edited May 2011

    twistedsteel, the 15 ac sounds interesting. I am having ac first, but mine is every 2 weeks with a 24 hour drip t be safer on my heart, I wonder if the 15 ac is because of the same thought?

    I have a power port, it has been interesting, but makes it much easier!

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

    I made hubby force the ear ring in, because I knew I would want to wear earrings when I lost the hair. I dont wear makeup. I was a wash hair at night air dry and braid and brush. no curling, rarely blow dry. But the hair loss was one of my biggest issues.

    If you still have your starters you may want to try to put that in and repearce the hole. Have someone help.

    Have you looked at the TLC catalog for hair, not bad prices and they have some things for under hats too.

    My daughter giggled but said it was very cute. She cried when I got it cut. I managed not too.

    How many days has it been sence your first chemo?  And what type is it?

    Candice

  • Barb_in_BR
    Barb_in_BR Member Posts: 4
    edited May 2011

    Hi all,

    Newbie here. I start chemo this Tuesday...so, a little nervous. My main concern is how my body will react, since I also have fibromyalgia. I'm doing the chemo first, then surgery, followed by radiation for 6 weeks.

    I'm so glad to have some new team mates that understand. ((((Hugs to all))))

  • Robyn_S
    Robyn_S Member Posts: 197
    edited May 2011

    Candice- you poor thing! I hope that you get some relief from the pain in your sore spots soon!

    Welcome to Barb in BR! You have lots of company in the chair on Tuesday! (Mental image of lots if strange women holding hands around the world!!!!)

    Cyborg- I think that the steroids are the best part of the chemo- it cures the asthma problem I have, the respiratory specialist will only prescribe a short term course on special occasions to get my sense of smell working! unfortunately the chemo means everything will smell like mouldy chemical oranges for 10 days!!! Win some lose some! I am glad you have a positive MO - it gives confidence when the people looking after you are research receptive! My doctors are all involved in clinical research st the centre here- I am starting a clinical trial and will get an extra injection tomorrow which is part of the D-CARE trial into denosumab. It is a double blind RCT which means that neither me or the doctors will know if I receive the antibody or the placebo. The upside is that I will have bone scans and CT for the next 5 years which will hopefully give peace of mind. As a researcher and patient I appreciate that every treatment we have has been tested in one study or another on

    brave women long ago.

    Best wishes everyone! Robyn

  • neecee
    neecee Member Posts: 663
    edited May 2011

    Getting ready to head to the chair for the first time today.  I am as prepared as I can be.  Time to get on this train and see where it takes me.  Good luck to all who are having treatment today!

  • MamaV
    MamaV Member Posts: 907
    edited May 2011

    Welcome to those of you joining us.  Sorry to welcome you to the club no one wants to join.  Good luck to everyone in the chair this week - sounds like today and tomorrow are the big days.  I'm in for Taxol #6 on Thursday. 

    Hugs to all - together we can do this - one day at a time!  (Sometimes, it's one minute at a time - but we WILL get through this!)

  • MargieC
    MargieC Member Posts: 394
    edited May 2011

    Good luck everyone this week.....  Everyone here is thinking about you and hoping you have a side effect free week.

  • jrh1953
    jrh1953 Member Posts: 56
    edited May 2011

    Neecee,

    I hope it all goes well for you today. I know it is a scary time but you will get through it.  I have my second of 4 on thursday.  Keep us posted.

  • Beaglesgirl
    Beaglesgirl Member Posts: 287
    edited May 2011

    Barb I too suffering from fibro and was scared to death what all of this would do to me. So far, I have only one treatment under my belt (a/c) I also had the nuelasta shot. Both gave me extra pain, but what is really holding me back is my BMX pain, the fibro has really done a number on post surgery. :( keep in touch

  • sunshinyday
    sunshinyday Member Posts: 13
    edited May 2011

    RANDOM THOUGHTS ONE WEEK AFTER FIRST CHEMO:

    1.  I feel like an alien.  Things feel strange. 

    2.  I plan on working for the first month of this regimen and then I am going to take a leave of absence.   But I realize it is going to be essential that I have a task.  Work is one way to take my mind off of this, but I think I deserve to do something more enjoyable.  I am going to break out my paintbrushes and produce at leat three masterpieces this summer!

    3.  This is my last week with hair. 

  • bak94
    bak94 Member Posts: 1,846
    edited May 2011

    I'm about ready to shave my hair. Had it cut short yesterday, but it is feeling weird and soming out like crazy. Thought I could just let it shed until I got bald spots, but no bald spots yet, just thinning, just can't handle the shedding....this is day 16 after first treatment of ac and 2 days after second treatment. Still don't have a good wig, don't feel like looking for one today.

    You gals that keep working rock! I will go back part time, but only on the second week post chemo, just can't do it the first week and my work is very flexible. I don't know how you gals work full time going through this!

    Sunshinyday-yes, it is weird feeling! Good for you for doing something you enjoy, I bet you will create some beautiful, meaningful paintings during this time. And yes, I am about ready to get rid of my shedding hair! I can't take it anymore!

  • thinkpiece
    thinkpiece Member Posts: 7
    edited May 2011

    Hi all, today is one week after my first TC cycle (25% done).  I'm back in the office, and although I feel distracted and all over the place, it's kind of nice to get out of my cave and into the real world.

    Here's how things have gone!

    My kids pixied my hair last Sunday and I fedexed it to HipHatswithHair.com.  For like $300 they make a piece with your own hair that you wear with hats/scarves.  I'm in Manhattan and went to every fancy wig place in town but it's just not me, I actually found the wigs more upsetting than the idea of being bald. I unveiled my pixie cut today and am actually getting compliments.  They are just trying to be nice!

    Anyway, tx last Monday was uneventful, although really long. No port, which is great. I iced my fingers and toes, and my daughter fed me ice chips while we watched Real Housewives New Jersey re-runs. Very distracting!  She's 25, took the day off from work, and they gave us free sandwiches and candy -- after 2 hours she turned to me and said, "This is fun!" 

    The fun didn't last!  I was shaky but ok on Tuesday, and worked from home -- I had that glittery, alien/fragile feeling, like I would break if someone bumped me. I got my Neulasta shot on Wednesday (The nurse said, "No, it doesn't hurt!" OUCH) and spent Thursday and Friday feeling physically awful, I couldn't lie down, I couldnt stand up, I didn't know where to put myself, I couldn't even look at the computer screen, it hurt my eyes, so no work. I did the Claritin/Aleve run up to the shot, day of the shot, and day after and I have no clue if it helped -- if it did, thank god or I would have been taking myself to the ER.  I wasted tons of money on food I would take one bite of and then chuck because it tasted VILE. Anyone want 6 tubs of fancy greek yogurt!? I subsisted on ice pops, Corona, and the occasional potato chip.

    Friday night a friend came and took me to dinner just to get me out the door.  I ate spicy lemongrass soup from the Thai place near my apartment and it was delicious -- although they say spicy prompts thrush and sure enough, next morning, my tongue is white. The physical symptoms subsided and then the dark-darkos set in for Saturday and Sunday. Just. Completely. Depressed.  Crying, moping, hiding in the bed, non-stop television - very unlike me!  My poor dog looked traumatized. Walking a 100lb standard poodle is a trip under any circumstances, but sheesh.  He's a good boy, understands something, is taking it slooowww. I cancelled lunch with daughter and she insisted on coming up to see me -- I hate having her take care of me, especially with the emotional stuff.  It just seems like the wrong way around, very hard to accept. But she goofed around and bossed me around and ... voila!

    Today I feel better.  Again I'm at work and it's really hard to concentrate.  But I got over the hurdle of everyone seeing me without much hair, and I'm feeling ok, and it's nice to be distracted by anything other than ME.

    And that's my one-TC-down/three-to-go update!  Thank you all for your stories.  They make this bearable. 

    I forgot to add:  OPI Envy nail hardener plus Sally Hansen on fingers (I can't take color on my fingernails) and OPI Envy and Navy Blue on my toes -- can't hurt.

  • lifelover
    lifelover Member Posts: 553
    edited May 2011

    Uggghhhh.  My first chemo course was again delayed today.  I have an infection or possible thrombosis in my PICC line entry site.  I'm duly taking my umpteenth course of antibiotics and they will try again on Thursday to give me my treatment.

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