Starting Chemo in December 2013

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  • jbokland
    jbokland Member Posts: 890
    edited June 2014

    char- I was living in Redington Beach before I moved to Sydney, Australia.  Now in Orlando but vacationing this weekend back in Redington. 

    We are celebrating our 10 yr anniversary and my last chemo treatment!  I plan to burn my little fucking chemo blanket on the beach!!

  • Leealice
    Leealice Member Posts: 87
    edited June 2014

    I have been able to exercise during rads. I do mostly zumba, some yoga. I go in the morning cause I get tired in the afternoon and don't feel like doing  a lot afternoon/evening. My treated area is very red with some peeling but I'm still wearing my same bras with no problem

  • Lisaj514
    Lisaj514 Member Posts: 719
    edited June 2014

    Have to share with my dec chemo girls! look, look!! I didn't realize I had so much hair in the back and sides until I took a picture with my phone after a shower when it was sticking up and "fluffy". I'm so exited! The front/top needs lots of growing but it's something. It's also sooo white and soft I barely feel it sometimes but I once said I'd take anything, green, blue or I guess white! There's hope for those of you like me that are late in the hair regrowth dept. (this is 6 wks PFC btw)

    image

    image

  • kjfromca
    kjfromca Member Posts: 283
    edited June 2014

    'My keyboard is on the blink.  I need to take in into Apple this week.  So if  you see weird characters''' it's not that I can't type.  

    Lisa - My hair came in white, then it started turning dark.  I am a slow grower too.  My hair looked like that around weeks 6 & 7.  You're getting there.... doing the happy dance for you.

    Kim

  • RobinLK
    RobinLK Member Posts: 840
    edited June 2014

    Congrats Lisa! Joining in the dance! for some reason a visual of Betty White/Sandra Bullock (The Proposal) popped into my head!!

    Found the video clip! Dance scene in The Proposal <----link!

  • oranje_mama
    oranje_mama Member Posts: 260
    edited June 2014

    Jodi, Sorry I somehow skipped over your post earlier.  So sorry to hear about your Dad.  2014 sucks! 

    I eat a half grapefruit for breakfast every day.  Several years ago, while on WW, I cut out OJ from my diet and replaced with the grapefruit (it had no points).  That was years ago, and while I long gave up on WW, I became addicted to my morning grapefruit.  Please tell me that cancer is not going to make me give it up! (Starting Tamoxifen after rads).

    I will post a picture later.  My hair on my head is really coming in now even as my eyebrows continue to go.  I'm almost 9 weeks PFC.  My hubby says that at this point he notices a difference daily.  I'm not to the point of going out and about bald but I am going bald around the house.  I was dying to take off my buff & dive in the pool this weekend but I kept it on & kept my head above water.  At this point, I don't really care so much . . . but my tween girl does . . .

  • Lisaj514
    Lisaj514 Member Posts: 719
    edited June 2014

    robin, loved the you tube clip! Had to watch it twice it was so funny. Never saw the movie. I'll have that visual everytime we say we are doing the happy dance. Thanks, that made my day

  • Amazonwarrior
    Amazonwarrior Member Posts: 485
    edited June 2014

    jbokland: Would you mind posting the same drug info for Tamoxifen?

  • jbokland
    jbokland Member Posts: 890
    edited June 2014

    There are NO food interactions known for tamoxifen....eat your grapefruit!

    There are about 60 drugs that can cause interactions (most of them will decrease the effectiveness of Tamoxifen).   There is actually a free web site  (we provide the data) called Drugs.com. There is lots of information there and you will see a tab that says Interactions Checker....this will allow you to list drugs that you take and look for any interactions.   If you see something labeled as MAJOR, that is a serious risk.

  • Crazywabbit
    Crazywabbit Member Posts: 563
    edited June 2014

    LISA, YEAH Definitely qualifies as more then peach fuzz. MY back and side grew in fastest.still pretty sparse on the top. Not ready for going topless until the front and top hair grows fuller.  mime still has a lot f pure white areas, but the back has a lot more gray in it now. there is even a round spot on the left side in the front that looks grayer, actually looks like a dirty spot in the white. 

    BTW love your shower curtain.

    I was very chilly in the RT room today and the techs got me out some nice warm blankets to wrap my arms and over my stomach. 3 down ONLY 30 to go.

  • keepthefaith
    keepthefaith Member Posts: 2,156
    edited June 2014

    jbokland, thanks for all of the helpful info! Congrats on your anniv and last chemo! When is your last TX? 

    Leealice, when is your last rads?

    Jodi, thinking of you~

    Lisa, I remember getting the peach fuzz, too! Good for you! 

    My 5 yo grandson spent the night with me last night. As always, he lifted my spirits! Kids are the best medicine!

    I noticed a ton of peach fuzz on my face! It's white, but annoying. How do I get rid of it? I feel like the "Bearded Lady"!!! 

  • Leealice
    Leealice Member Posts: 87
    edited June 2014

    My last rads is next Wednesday! I'm doing boost right now.

    Lisa-Congrats on the hair! I'm noticing some peach fuzz on my head half white/half brown

  • jbokland
    jbokland Member Posts: 890
    edited June 2014

    my last chemo is Thursday.   Working in my poster now!  

  • charusa
    charusa Member Posts: 107
    edited June 2014

    DJJ- You look terrific...go girl!!!

    Went to surgeon today good news pathology report read clean margins and out of 15 nodes that were removed 15 were  clean!!! Still dragging my drain he says he wants to wait a bit longer until it is draining less fluid but likes that the fluid is clear. Walked home from his office, only about a 5 block walk, then went to the grocery store with a little help. I did forget to tell him that the neoropathy is a lot worse in my arm on operated side. Actually it is the numbing feeling like asleep in my elbow area and upper arm and also in my lower thumb joint. When I touch it or rub it hurts and tingles more. Not sure if this is  common or a SE still from chemo or something new from surgery. In the morning it isn't there comes on suddenly when I start using my computer...this is the same arm I ripped/hurt something while stretching a few weeks ago and that was resolving. Any ideas?

  • chicopeach57
    chicopeach57 Member Posts: 166
    edited June 2014

    Charusa, I am still numb in my arm pit and under my upper arm. When they go in the arm pit to get nodes they can do nerve damage.  It gets less noticeable with time, hoping it will get even better. Congrats on having clear nodes!  I had the drain for about a week over the Thanksgiving holidays. We safety pinned it up on my inside shirt so it wouldn't show.

    Dancing for everyone finishing their phase of treatment - WooHoo!  My last rads is June 30th, almost there :)

    Started Femara this week, guess that is a common drug for us menopausal women. Will see how it goes.

  • RHGSR
    RHGSR Member Posts: 774
    edited June 2014

    DJJ- great picture. You look beautiful. 

    Jbokland - thanks for all the med info. Post a pic of your poster. So happy for you. 

    Char- so happy for your clear nodes and margins!! I am numb under the arm where they took nodes. What is so strange to me is that I can't feel temperature under that arm either. 

    I followed up with my MO today. Still haven't started on the hormonal therapy yet. Looks like he may not be putting me in Tamoxifen but instead in Aromasine and Lupron shots. Anyone familiar with this? 

    I asked when I was considered cancer free and he said now. But then he added that now the waiting begins to see if it comes back.  That hit me pretty hard. Cried all the way home. 

  • RobinLK
    RobinLK Member Posts: 840
    edited June 2014

    Ugh...sorry Holly. What a "Debbie Downer," you have for an MO. I asked my MO about Switching to an AI with either an ooph or suppression(Lupron.) Supposedly ILC and Tamox are not always an effective match. My MO said there is not enough data to support the switch, and he felt the benefits of the switch did not outweigh the potential SEs from AIs. Did your MO explain why he wants to change direction?

  • RHGSR
    RHGSR Member Posts: 774
    edited June 2014

    He said he had just come back from a conference where studies were showing that the AI and Lupron had better results with premenopausal women. But he did mention that the SEs could be worse. Although he didn't go into them much. 

    I had an ILC along with my IDC and in situs.

    He doesn't sugar coat much. But I've been really happy with him. 

    I go back to see him in 6 weeks and should start the Lupron then. Supposed to get BRCA results back next week. 

  • Jodi040812
    Jodi040812 Member Posts: 383
    edited June 2014

    Hi ladies!  Just read up and stopping by for a quick report.  My family decided to have my dad's service Friday so I could keep my port removal and rads simulation appointments today in Houston.  Nothing was planned for my dad's passing, so this Monday we had to do everything from picking out land to deciding on clothes.  Rough day and very exhausting. I then jumped in the car to drive to MDA. After that, got checked into the apartment I'll be living in this summer.  About to go back to MDA for all the stuff today. Tomorrow drive back to BR and go to the wake.  Friday - funeral.  Home on Sunday then drive to Houston again and for good on Monday.  

    My mom has decided to come and stay with me this summer.  She will help with the three girls and won't be alone.  We will be helping her as much as she is helping us.  Praying I can run on fumes until Monday when I get back here to the apartment.  Rads officially start Tuesday.  

    I am doing good, but I get sad thinking that he won't see me get better. I did get to tell him I finished chemo and the doctor reports last week when he was in ICU.  I wasn't suppose to go to the hospital since I had just had chemo the week before, BUT- I am so happy I did!!!!  That visit has given me a lot of peace.  I am keeping it together for the family.  Reminding them that he is no longer sick and is with us. Now that I am in Houston, I hope their spirits haven't dropped.  Forever a cheerleader I guess, but that seems to be a gift I have- port out today, meeting with RO, chest X-ray.  No scans:(. I'm going to ask RO wth!  I want to know if and how much the AC worked after Taxol!  Grrrrrr!  Thank you all for the kind words.  I'm still swimming;). Just keep swimming, just keep swimming...

  • Lisaj514
    Lisaj514 Member Posts: 719
    edited June 2014

    Jodi, the posts about your dad have been beautiful, heartfelt and inspirational. What a beautiful gift he gave you in so many ways.  Good luck to you this week and next. So much for you to do and take in, I think you are running on autopilot now. My heart feels for you, we are all here with you and for you. Keep us updated.

    I had my final sim for rad yesterday and start officially today. They said I was "easy" and it only took 15 min. I'm all marked up with lines, circles, triangles, x's. You lay there all exposed with arms over head, they are drawing on you with markers, taking pictures ( with an actual camera). It feels so inhumane even though they are all so sweet. With my head turned to the side I started getting a little emotional and a few tears came, streaming across my face and into my ear. Of course I had to stay still. I got it together and was a good patient and did not move. I don't think anyone noticed as they all step out of the room to watch the computer or something. Glad they didn't because if so done had said " are you ok?" I probably would have lost it big time. Ok.., deep breaths I keep telling myself. The anticipation is worse than the actual treatment I know. But I'm just so done with this whole thing sometimes...but bring on the rays!

    The hair is coming as you saw. There is little eyelash stubble also and I see eyebrow growth on my brows (R more than L) but it is very pale like my head hair. This whole hair regrowth thing is really "fascinating" I think. Never know what I will see in the morning.

    Good luck to all of you with the post treatment hormone meds and decisions. There sounds like there are many options and opinions. There is no targeted treatment for TN as you all know but metformin has promise for us and my MO said she'd start me on it once I finish rads.

    Well... gonna catch me some ray's today! First of 33 starts today.

  • missy6758703
    missy6758703 Member Posts: 218
    edited June 2014

    I got the giggles on Monday when they were doing the xrays and whatever else it was that they were doing and they had to stop and come in and remeasure me! oops!.....the machine has these long arms that come out as you all know....well this one was just a big flat screen....I was watching it out of the corner of my eye and it just kept coming closer and closer and closer to me and all i could think of was that i felt like a panini sandwich and was about to get squished! It thankfully stopped about 12 inches from me! whew!

    I met with my MO yesterday.....all my labs were perfect! I don't have to see her again for 3 months!

    My skin is holding out well......This Califlora gel stinks but seems to be working, then i blow on it to get it nice and dry and then use a new big makeup brush and dust the area under my boob and under my arm with corn starch.  Today will be #6.

    Good Luck Lisa!

  • keepthefaith
    keepthefaith Member Posts: 2,156
    edited June 2014

    char, great news! You may want to ask your team about an LE specialist, if you haven't already, since you had several nodes removed. Hope you get your drains removed soon!

    jodi, good to hear from you. Nice that Mom decided to be with you! Take care of yourself while "swimming"...sounds like you will need some rest soon.

    missy, good for you!

    lisa, glad you got started. 

    Leealice, congrats on your LAST rads today! Happy Dance for you!!!

    jbokland, will be thinking of you tomorrow at your last chemo!!! Whoo-hoo! 

    It's been nice to follow everyone through their treatment. I never realized BC could have so many different stories!

  • RobinLK
    RobinLK Member Posts: 840
    edited June 2014

    What she ^^^ said! 

    Best to all of you and congrats on each person finishing another chapter! 

    Wow! Keepthefaith - I am in awe of how you kept track of that all! 

  • charusa
    charusa Member Posts: 107
    edited June 2014

    Keepthe faith- what exactly is a LE specialist?

  • RobinLK
    RobinLK Member Posts: 840
    edited June 2014

    Char - Lymphedema certified therapist. Finding LE therapist <----link

     
  • Lisaj514
    Lisaj514 Member Posts: 719
    edited June 2014

    I didn't realize I'd have to keep all these marker "drawings" on the whole time of rads. There are x's, circles, triangles, lines etc. I thought it was just for the sim and planning. They said they highlight them when they fade. I have 3 small tats also, one under my arm, one in cleavage and one about 2" below sternum. Everyone else have all these drawings that you have to keep on all treatment?  I thought that was what the tats were for. I have tiny dot tatoo and then a circle or triangle around it, I guess to make sure it's found correctly

  • Crazywabbit
    Crazywabbit Member Posts: 563
    edited June 2014

    Michelle,  the Rad Techs were laughing when I told them what you said about the panini machine. 

  • keepthefaith
    keepthefaith Member Posts: 2,156
    edited June 2014

    Lisa, I had two large X's for my rads after my sim/planning....no tattoos. Then, when they did the boosts, they drew a circle around that area. They put a bandage type plastic circle over my X's so they wouldn't come off so easilly. It will rub off on your clothes; I  put a kleenex between to keep my clothes from getting stained...it sounds like they got carried away on you! 

  • Crazywabbit
    Crazywabbit Member Posts: 563
    edited June 2014

    Lisa, maybe they were bored and were really playing tic tac toe.   LOL. 

  • DJJ
    DJJ Member Posts: 229
    edited June 2014

    Char, Congratulations.

    Lisa, I have 6 tattoos.  I don't know if you all remember a few months ago that I was planning on getting a tattoo when this was over.  NOT ANYMORE!!!! Those lil buggers hurt.  I have a marker X by each one and they redrew them today.  So yup! Markered up body for 6 weeks.

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