February 2011 chemo pals

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  • charlottesmama
    charlottesmama Member Posts: 250
    edited June 2011

    Good afternoon! Thank you GG for the advice (all systems go, now!) and compliments on my profile. Funny, I just snapped that picture from my computer. PhotoBooth always shows the pictures like I would see myself in a mirror. I never bother to flip them. Seems like my eyes, ears and nose are all huge, but a friend told me that's because my hair is so little. It hasn't grown much in length, but it's filling in nicely. Just in time to lose it again! Oh joy!

    I still haven't "back-read" yet. I think the diet and exercise thread is a great idea. Maybe someone should start a new thread for something like "Diet and exercise Summer 2011". I could stand to lose about 10-15 lbs.

    Here's a funny story: After my surgery I had a check up with PS. Taking vitals, I asked the nurse about how much weight I'd gained (eating like no tomorrow) and she informed me that I'd LOST 6 lbs. I paused for a moment, then said, "Well, I guess we know where THAT went." (thinking of my former breast)

    Over and out for now, ladies. Have a great weekend! 

  • dogeyed
    dogeyed Member Posts: 884
    edited June 2011

    That's hilarious, Michelle.  I'll try to keep that in mind when they take mine off, too.  I think it's the Taxol that dries us out, spinach helps me, but it's still kind of a pain a lot of the time.  GG

  • pejkug3
    pejkug3 Member Posts: 902
    edited June 2011

    Ok, my chemo sisters...

    I'm packing up a box of items to send to my MIL who is doing Taxol/Carboplatin for stage IV lung cancer.  I want to put in some fun things to lift her spirits a bit.  She was only diagnosed a month ago and the poor thing has sure been on a wild ride.

    I have several headcovering scarves, some lemon drops (to kill the taste of the chemo, some encouragement cards, some things from the kids (letters and pictures, etc) and a coffee cup with a bible verse on it.  What else can I add?  Nothing that will melt - so chocolate is out.  :)

  • jenn_h
    jenn_h Member Posts: 149
    edited June 2011

    pejkug: I got a couple nice little inspirational books, my aunt made me a really nice relaxation box that had lavender soaps and sprays and relaxation tea and relaxation cd's in it...that was a fun gift. Willow tree angels are very nice too, some of the smaller ones are entitled healing and things like that...

    I gained about 13 lbs, can't get motivated to start working it off either! Nerves over upcoming appts and surgery...Also I am stuck 2 hrs away from home with son in hospital in Erie...the wound from his surgery when he broke his leg got infected. We are here until Wed and I have to leave here and go to Buffalo tomorrow fro MRI and mammo...I am nervous bc it is a closed MRI...i am claustrophobic and cant get medication bc I have to drive myself since I am going from here...feeling very misplaced right now!

    Have a head a grey fuzzy hair growing...missing the blonde, but I guess that why they make loreal...didnt miss the underarm hair though, that could have stayed away! :)

  • SpecialK
    SpecialK Member Posts: 16,486
    edited June 2011

    pejkug - Maybe some nice lotion, I used cocoa butter lotion.  I also used Aquafor on my hands and feet because the Taxotere made them so dry.

    Jenn - Sorry you are nervous about the closed MRI - have you had one before?  I had one before my first surgery and even though it was closed there was a mirror in front of me that let light in and I could kind of look out from my face down position.  I did some Lamaze breathing, in through the nose out through the mouth, to relax and they also played music for me.  When I wasn't looking at the mirror I just closed my eyes and imagined myself somewhere else, like on the beach with a pina colada!

  • christina1961
    christina1961 Member Posts: 736
    edited June 2011

    Done!  Last TAC yesterday. Just got to crawl back in and get my Neulasta shot this afternoon and then I can hit the bed.

  • SpecialK
    SpecialK Member Posts: 16,486
    edited June 2011

    christina - yay!!!

  • pejkug3
    pejkug3 Member Posts: 902
    edited June 2011

    Gah...unexpected news at the RO today.  I posted about it here:  http://community.breastcancer.org/forum/70/topic/770333 

    I'm trying to cram summer into three weeks.  If I go get to do rads, I'll start July 5.  SO we're off to the pool tomorrow.  :)

    Doing good with SE on this last round, dropping a bit of weight from the Big D but I'll expect that to return in a couple weeks.  ;)  Man, I'll be glad to be done with chemo SE!

  • Melanie_Ann
    Melanie_Ann Member Posts: 414
    edited June 2011

    Congratulations Christina! =)

  • MamaV
    MamaV Member Posts: 907
    edited June 2011

    pejkug3 - I couldn't get your link to work, but from your comments, I suspect you need RADS when you didn't expect it.  I will be having rads after chemo too.   

    Taxol #9 for me tomorrow - also final got insurance approval for the BRCA test.  No relatives on either side of my huge (really) family with BC or OC so MO didn't think it was necessary b/c I have little to no risk.  Really?  Why wouldn't I want to make sure?  No, I'd rather not have more surgery if necessary, but I was only 40 at DX so let's just make sure for crying out loud!  B/c my anxiety isn't already off the charts  ... UG!

  • charlottesmama
    charlottesmama Member Posts: 250
    edited June 2011

    For the face-down BC MRI (I too was anxious and am claustrophobic), may I recommend music, specifically Green Day. LOL! Tha machine is REALLY loud and the "soothing" music they recommended was fiercely irritating. I had seen Green Day (I'm a fan) on the list, and during a break I begged for a change of music. Green Day. LOUD!!!!

  • Melanie_Ann
    Melanie_Ann Member Posts: 414
    edited June 2011

    I didn;t get music with my MRI. I started counting. I counted to 1000. I thought, it surely can't last that long. I made it all the way there. When I told the tech that I did that, she laughed and said, no one had ever done that before.

    I for sure, would have loved some Greed Day!

    Happy Birthday to me! I'm 27 today. It feels good to have a birthday. I hope for many  more. 

    I hope your chemo goes well tomorrow MamaV!

  • MamaV
    MamaV Member Posts: 907
    edited June 2011

    Happy birthday Mel!!!!!! Here's to many many more!

  • charlottesmama
    charlottesmama Member Posts: 250
    edited June 2011

    Happy Birthday Mel. And here's to many many more!

  • M1nn1e
    M1nn1e Member Posts: 33
    edited June 2011

    Happy Birthday Melanie!!! 

    Congrats on finishing Chemo Christine!!!

    Pejkug; I'm smack in the middle of Rads and it's really not bad. It's every day but I'm in and out of the office in half an hour. No side effects yet, just a little tan at the rad site. Good luck! 

  • pejkug3
    pejkug3 Member Posts: 902
    edited June 2011

    Happy Birthday, Melanie!!

    About my rads - I knew I'd need rads.  But when I saw the RO yesterday, he told me that the usual kind of rads they use, he couldn't use for me due to me being large breasted and the location of my scars.  My heart is in the way.  He said that he may be able to use IMRT, but he wasn't sure.  And if he couldn't miss most of my heart, I may have to skip rads.  HUH?!  I certainly didn't see this coming.

    My tumor was officially sized at 0.5cm, 3 o'clock position, 15cm from the nipple.  Certainly others have had similar placement and had rads. 

    Now, I have been thinking this over - he much have some hope for me since he has me going for a mammo on Tuesday and returning to his office.  So maybe I'm overreacting?

    Anyone else already have another mammo?  The fateful mammo that changed my life was on January 5.  The MO said annual mammos were fine.  The RO said he wanted them every 6 months to monitor changes, not really look for cancer.

  • alison0415
    alison0415 Member Posts: 35
    edited June 2011

    pejkug3 - My lump was in the exact same spot and yours, and I fit everything else you described, other than mine was a bit larger.  I am going to my first appt with the Rad tomorrow so I will be curious to see if I hear anything similar.

    Right after my surgery, I received a wonderful care package from my friends which had a Kindle which I never thought I'd love so much ( I like holding books:)  But there was also the book "Chicken Soup for the Surviving Soul."  My hubby has given me several Chicken Soup books and I've never enjoyed them (and never had the heart to tell him).  I loved that book.  It was filled with stories of people going through much for challenging cancer treatments and it was so uplifting to read about their journeys and how much they had overcome.  

    Melanie - Happy, Happy Birthday you young thing!!!

     Alison 

  • alison0415
    alison0415 Member Posts: 35
    edited June 2011

    OK, so I thought I would post separately about the exercise and weight loss discussion.  Should I go ahead and start a separate thread?  I lost almost 20 pounds at the end of last year and just about all of it is back, and there is no flippin way I am going to stay this way, cancer or no cancer.  I so get that during chemo we can't worry about the weight gain, and obviously I kept that in the back of my mind since I just about gained it all back.

     But post chemo and even during rads, I think most people can start working on a plan to lose any weight they gained.  You don't have to be a runner or start taking classes or starve yourself, but maybe we can put a group together than is committed to making small incremental changes each week.

    Example: everyone go get a pedometer.  Start with no changes and see what your average daily steps are.  Then set a goal of 10% improvement each week.  So if you typically take 3,000 steps a day, you now shoot for 3,300.  And if you're not there by the afternoon, then go walk around the block, take the long way back from the mailbox, whatever.  We could make similar commitments in terms of food.

    Let me know what you think!

    Alison 

  • mks16
    mks16 Member Posts: 415
    edited June 2011

    Melanie, wishing a very happy (belated?) birthday to you!

    May you celebrate many, many more in health and happiness!

    Pejkug, I start rads in July, although I had BMX - it turns out RO still recommended it so I went ahead with it. I started taking Tamoxifen yesterday and so far, I have a relentless headache but its not too strong, I can live with it for a couple more days. Hoping it will stop soon.

    Alison, I love your idea! I have been tracking my food intake through livestrong.com and its working out well for me. I never realized how much I really ate when I thought I was eating next to nothing, lol! I have a pedometer, but its a cheap dollar store thing, so I don't use it. I have found google pedometer online which I love and rely on heavily. I track my walking route online, and it tells me the distance then all I need to do is track the time it takes me to cover it and voila!

  • DivineMrsM
    DivineMrsM Member Posts: 9,620
    edited June 2011

    Happy Birthday, Melanie!!!!!  May it be your best ever!

    You have the cutest avatar; beautiful smile.

    I had a breast MRI on Tuesday but was advised to take Ativan prior to the procedure.  That's because the previous two MRIs  I'd had caused me severe panic attacks.  I am not the type person where I thought an MRI would ever bother me, but they really did.  I think one reason is I was in the  position of lying face-down.  Anyway, after taking Ativan this time I practically fell asleep and everything went much quicker.   

  • SpecialK
    SpecialK Member Posts: 16,486
    edited June 2011

    Melanie - Happy, Happy birthday!  You are young enough to be my child!  OMG!  Glad you made it through the MRI, even without Green Day!

    Alison - Your thoughts on the exercise thing sound excellent - we need to encourage each other just like we have been all along.  I think I have seen similar new threads from former chemo groups.

  • sukie10
    sukie10 Member Posts: 96
    edited June 2011

    Happy Birthday Mel! 

    Alison, please take the inititive. I will be joining, although I do still have surgery to go yet so I'll keep up with the things that I can. My legs aren't broken. This year started so badly I would really like to get a jump on next year.

    Taxotere #2 is behind me, it was so much better than the first one. The longest SE is the mouth/tastebud thing I've heard you all complain about. No neuropathy this time and much less pain. Still feeling pretty energized so I'm going to try and catch up on some dusting and weeding.

    Have a wonderful day chemo troopers! Smile

  • MamaV
    MamaV Member Posts: 907
    edited June 2011

    On my way to the chair today - I hate this so much!  I am so jealous of all of you who are done!  3 more weeks after today.  UGH - seems like forever sometimes!  I'm tired of being tired.

  • mks16
    mks16 Member Posts: 415
    edited June 2011

    Good luck today MamaV!

    I started Tamoxifen yesterday and the initial SE brought back memories of A/C after effects that are still so fresh in my memory... 

    Hoping for a good week for you with no side effects! 

  • dragonfly1
    dragonfly1 Member Posts: 766
    edited June 2011

    Melanie Happy Birthday

    MamaV Good for you re: pushing for the BRCA test and getting it approved. I did the same thing. In my case, I didn't know of any breast/ovarian cancer in my family but there was also a lot of family history missing in my case so I was worried. My BRCA 1/2 test was negative but I needed to know for sure so I could make the best surgery decision.

    Hang in there everyone who is still going through chemo-you will get through it. I'm still having side effects from the Taxotere. My eyes are watering constantly with "taxotears" which makes me look like a real mess and I'm still retaining fluid but my taste is coming back finally and I can feel some stubble on my head-hooray! I had my radiation planning session today and will start rads next week...

  • LisaGH
    LisaGH Member Posts: 242
    edited June 2011

    Hang in there those finishing up. I am glad to be done w/ TCH. It's now over 2 wks out and gets better each day. Almost got my taste for food back- my legs are weak at times. It is getting better.

    Got my first 3 wk Herceptin yesterday. I was a little tired- but nothing like TCH.

    I need help on nutrition and exercise too. I did contact a nutrionist for help and information. Trying to build up my hemoglobin now to get my exchange surgery in 3 weeks. 

    Hope yall are having a good day! Hang in there fellow warriors!

    Lisa

  • MamaV
    MamaV Member Posts: 907
    edited June 2011

    dragonfly - good luck starting rads next week.  My last chemo is July 7 so I expect to start rads at the end of July. 

    mks16 - I will be right there with you for July rads i think.  Not looking forward to Tamoxefin either.  Hope the SEs subside soon! 

    Off the the chair again - 3 more after today.  Hating this more and more every week even though the light at the end of chemo tunnel is at least turned on now. 

    Vicky

  • Melanie_Ann
    Melanie_Ann Member Posts: 414
    edited June 2011

    Thanks for the birthday wishes!

    Start a new thread Alison! I'll join! I lost about 15 pounds after diagnosis but have gained it all back. =( So I'd like to lose it again. Sounds like a good plan.

    For now I'm getting a mammo every 6 months. I had one a few weeks ago and it came back as BI-RADS 2. It showed surgical changes and that was basically it. I did ask at my last follow up for a repeat PET or MRI sometine in the near future. My ONC was fine with it, but wants to wait at least 5 months if I'm not having any symptoms. He said radiation would just light up the whole screen. So I'm ok with that. I also go back in November for a repeat mammo.

    I'm 4 weeks out from chemo and starting to feel pretty good. My legs were so shot for about 3 weeks. I was so weak. But I'm starting to get back into the groove of everyday life. Now I'm just dealing with Lymphedema which is no picnic. And I start radiation next week, so back into the throes of cancer world. 

    Good luck today MamaV!  You can do it! I would say..only 3 more! But I hated when people said that to me, so just pretend I didn't say anything. =) It will be tough, but I believe you will make it through. Then we'll all be here to celebrate with you. 

    dragonfly- i still have taxotears too! Ugh...I always feel like people think I'm crying all the time. haha. Hopefully that dries up soon. 

    Oh and my radiation is on my right side, so he said we don't have to worry about the heart. And that's all that was said. He just told me about damage to the lung. I hope it works out for those facing that decision! 

  • MamaV
    MamaV Member Posts: 907
    edited June 2011

    Thank you for understanding Mel - and if one more person (not on here) who has no idea what I am going through tells me to hang in there, I might just punch them out!  Ha ha!

  • dragonfly1
    dragonfly1 Member Posts: 766
    edited June 2011

    MamaV and Mel I also find it annoying now that I've finished chemo that people at work all make comments implying that I should be absolutely fine now as if all the effects are gone the minute you finish chemo and you should be completely back to normal now! Hmmm, excuse me but I'm still having side effects from chemo (just look at the taxotears streaming down my anemic face:), I've been put into menopause at 41, I'm beginning radiation and soon I'll be put on Tamoxifen with another whole set of side effects that I don't even want to think about. Some days I feel like I'm just going to throttle someone!!! Honestly, it's a wonder we all stay in control through all of this. I was driving to work today in Long Island traffic and had images of Kathy Bates from "Fried Green Tomatos"...Remember when she reached her breaking point and starting ramming her car into another car after someone stole her parking space? Don't worry...I'm in control. In fact, I think this journey makes us superhuman when it comes to handling stress...

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