Sept 2012 chemo

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  • Mariposa123
    Mariposa123 Member Posts: 267
    edited March 2013

    OMG- that is too funny!!!  Thanks ladies for something to laugh at tonight!

     

  • Mariposa123
    Mariposa123 Member Posts: 267
    edited March 2013

    I forgot to say welcome Jem!  I am glad that you posted and that we will get to know you on the FB page:-)  Sorry you are going through this with all of us, but I am happy that we have each other to lean on, ask questions, and sometimes make each other laugh. 

    I am counting down the minutes until I can take my next Valium.  I swear, this last fill is killing me.  I wanted to be a big buxom beauty... but I may not be able to handle too many more of these. 

     


  • Jem3
    Jem3 Member Posts: 7
    edited March 2013

    Thank you so much for your warm welcomes, everyone.  I look forward to being part of the conversation, here and on Facebook.  Hang in there, Mariposa.  I am thinking of you and it will get better.

  • jojo2373
    jojo2373 Member Posts: 662
    edited March 2013

    Welcome Jem! this a wonderful place to be.

  • kelleyb
    kelleyb Member Posts: 94
    edited March 2013

    Welcome, Jem!  You'll find a warm and supportive community here (or on FB).  

    Kelley

  • Amy4978
    Amy4978 Member Posts: 473
    edited March 2013

    Mariposa your verbage kills me I to want so melons lol im at 460 cc right now and think I wouls need at least 700 to e bigger than I was... All I want are D's is that to much to ask for? I think not lmao

  • Amy4978
    Amy4978 Member Posts: 473
    edited March 2013

    We have 13 ladies in our fb group so far and loving it!

    but I have an update just to make sure it is as private as possible some ladies want to be discreate and I completely respect that so when you PM me or jojo to get an invite please send both the following

    Your email address along with your FB Name

    This way we can be completely sure you are a sept2012 lady

    Much Love!

  • Cherioo
    Cherioo Member Posts: 305
    edited March 2013
  • Cocobean
    Cocobean Member Posts: 135
    edited March 2013

    Hey Ladies!

    Today was my last radiation treatment, yes! So happy! Also so weird to think I don't have to go there everyday anymore. There is a little part of me that feels unsettled, but mostly I am really really happy to be done and moving forward. For the other rad gals, hang in there, the finish line is getting closer!

    Also, got my period. It really light and at first I wasn't really sure it was happening, but it's back. I am just going to try to take it as a sign my body is continueing to recovery and bounce back from chemo and I will look forward to experienceing menopause all over again in 20 years. 

    I'm going back to work on 4/8, so I am trying to squeeze in my dr appts before then...really I am sick of dr appts, but I have the time off now so... Going to my ob/gyn for a check up, the last time I was there, he told me I had cancer, so I have a lot of emotions around that, but I know I need to take care of myself. I am also getting set up with a gerneral practictioner, I never have a reg dr, just saw my ob, but I know I need one. And going to dentist. yeah, so much fun. 

    And going to see my PS next week, very curious to see what he has to say about how my skin held up during rads and kinda getting ready to think about my exchange surgery, been doing a little daydreaming about getting these TES out and getting some squishies in. 

    We are going to FL in a 1.5 weeks, so excited! Ready for some sunshine, warmth, and some celebrating!

    Jojo- Your hair looks great! 

    Toastie-I'm sorry to hear about the situation with your mom, I hope you can get her to see a dr. '

    Amy- I'll looking forward to joinging the fb group, thanks for setting it up....love the name. 

    Jem- welcome! 

    Hope everyone is doing well! 

  • Foreverchanged72612
    Foreverchanged72612 Member Posts: 223
    edited March 2013

    Oh my goodness!! Never ceases to amaze me how much you miss when you don't log in for a day or two!!

    I'm so in on the FB page!! So Amy, I can pm you my FB name?

    My surgery (and Patricia's!!) is next Thursday. I have to go in Wed to get my node dye. My husband and I received gift cards to a beautiful spa in my town (hey Neta, do you know the Nordik Spa?) and so I thought why not book a relaxing couples massage and then use the spa baths/saunas/steam rooms on Tuesday evening? Nice way to relax and say bye-bye to my boobies and lymph nodes. Well, I call to make a booking and the guy says that before he makes the booking there are few questions he must ask..are both my husband and I over 16? Check! Do either of us have cancer or are in remission? Check! Uh oh, he says, I'm not allowed to have a massage. wah, wah, wah. Apparently the massage therapists there categorically refuse massages for people who have cancer or are in remission. Blah. Feeling sorry for myself now.

  • Mariposa123
    Mariposa123 Member Posts: 267
    edited March 2013

    Forever:  I don't understand?  Why won't he do massage if you have had cancer?  That seems odd to me.  Sorry about that.  I would be disappointed too.

    Cocobean:  I think if I wasn't ER positive, I would have been happy with my period coming back... but for now, I  just got my first shot to hibernate my ovaries.  Been having some horrific hot flashes all day.  Not good on top of the stupid surgery pain.  Sorry I am irritable today.  My surgeon won't do my exchange surgery until six months after I finish rads.  Is anyone else on this kind of timeline? 

    Since I went into my surgery, my son has regressed and decided he is no longer pooping in the potty.  Cleaning up with expander pain and arm pit pain has been excruciating.  Uggh.  Feeling sorry for my self today. 

     


  • jojo2373
    jojo2373 Member Posts: 662
    edited March 2013

    Forever, thats crap! Massages are so therapeutic and I have had several since cancer. You can pm me or Amy for fb.



    Cocobean, yeah no more rads! I am so looking forward to my last one next week. I fear I have not faired as well as some of you skin wise. Blisters and peeling now.



    Mariposa, hang in there!

  • Foreverchanged72612
    Foreverchanged72612 Member Posts: 223
    edited March 2013

    I actually have had a couple of massages since diagnosis but just not at this particular spa. I even have a prescription from my family doctor for massage to relieve stress since my diagnosis. The guy said sorry, it's a decision of the massage therapists at the spa. It sounds like they all jointly decided NOT to give massages to people with cancer.

  • damiana9
    damiana9 Member Posts: 389
    edited March 2013

    Hey guys!  I feel like I am always soooo tired that I have a hard time checking in here, but I think of you guys often.  I finished my last radiation treatment yesterday- wooohoooo!  So glad that is done.  I ended up burning pretty damn bad, and cried a bit over the weekend because it hurt so much but now I am done so I hope to feel better soon.  I had my herceptin today, so now I will finally get a break from my cancer center for 3 weeks!    Oh- and as for hair- I finally have hair on top of my head, so no more male pattern baldness!  It is still pretty darn short so I don't really go out without a scarf but soon!  I also think I am going to buy some hair chalk- it comes in a case with about 20 colors and the color only stays for 2-3 days.  I am gonna have some fun with my hair- it will be a rainbow of colors just because I can!  hehehe!

    Now  I need to figure out how to get on the fb group....

  • jojo2373
    jojo2373 Member Posts: 662
    edited March 2013

    Damiana, just pm me or amy with your email address! glad your finished

  • damiana9
    damiana9 Member Posts: 389
    edited March 2013

    I just pmd Amy :)

  • PatinMN
    PatinMN Member Posts: 920
    edited March 2013

    Forever changed, I had a couple of appointments shortly after surgery with a PT who specializes in lymphedema prevention and treatment. I was told to avoid massage on the affected arm and the chest. I wonder if the massage therapists are trying to avoid being accused of causing lymphedema (and being sued). I know there is special training for massage therapists who work with cancer patients - a woman here who runs a school brings her students (once they have learned enough) to my infusion center once a week to give free massages. I was a lucky recipient one day - it was awesome.



    I haven't signed up for Facebook - call me a dinosaur... if I ever decide to take the plunge I'll join in.

  • Foreverchanged72612
    Foreverchanged72612 Member Posts: 223
    edited March 2013

    Good points, PatinMN. But I haven't had surgery yet. I was thinking this would be my last chance at a stress-free massage before I had to worry about things like lymphedema. Oh well, I do know a massage therapist that will work with me but she is not at this particular spa...which of course would be the one that is closest to me.

  • chitown3
    chitown3 Member Posts: 8
    edited March 2013

    Jojo can you tell us what hair dye product you used.....I am totally grey and totally scared.........but don't think I can wait much longer to get rid of the grey.....i want to be young again!

    thanks

  • whenlifegivesyoulemons
    whenlifegivesyoulemons Member Posts: 184
    edited March 2013

    Cgesq - Too funny!  Especially since porn star is the last thing that springs to mind when I look in the mirror.  More like army recruit.

    Forever - Too bad about the massage. I had several during chemo/before surgery, and I loved every minute - even the part where I yanked the wig off to ensure I got an awesome head massage (gotta take advantage of the very few perks of being bald).  I understand a cautious approach but not at the expense of removing one of the few pleasures we can enjoy!

    Daminia - Many  months ago I think you posted something about hating your tissue expanders.  I'm sad to report that I finally know exactly what you meant.  

    Cocobean, Neta and Amy - I so envy you your vacations.  I'm desperate to get out of this icebox.  We still have giant piles of dirty snow everywhere, and there's more on the way.  Last week I went back to work after a month on leave so my vacation plans have to wait a bit.  :(

  • Jem3
    Jem3 Member Posts: 7
    edited March 2013

    Forever--so sorry about the massage, though the lymphadema risk makes sense.  My shoulder is hurting from rads--I feel like I could use a massage right now!

    Damiana--congrats on finishing rads!  Enjoy that 3 week break!

    Mariposa--so sorry about the potty training.  My 6 year old has been "holding" and is terribly constipated.  I am sure that one of the reasons for it is my being in active treatment again with rads.

    I met with my oncologist today and am trying to decide whether to go on Tamoxifen or Zoladex/oopehrectomy and an AI.  There's a little bit of research (from the San Antonio conference) that ER+ cancers with hi Ki67 (mine was very high) do a little better on an AI--but the research is on postmenopausal women.  I'm 46 but was premenopausal before cancer.  Although I'm not getting my period now, I feel some cramping and my hot flashes have diminished.  Anyone else trying to decide between ovarian suppression/AI and Tamox?

  • Cindi74
    Cindi74 Member Posts: 363
    edited March 2013

    Timbek, sounds like a good idea.  Will repost the list from our group soon.  It would be fun to have a place with pix.  Also, we should have an on line reunion each year.  I read every post to keep up with everyone. We are traveling for the month between chemo and rads,  Feel much better, but still no hair and little energy.  Must be crazy to leave warm Florida to go to cold, rainy TN in Feb., but change of pace is good.  Hugs and no pain or SE to all.

  • marianelizabeth
    marianelizabeth Member Posts: 1,735
    edited March 2013

    cocobean and damiana, yay for last rads but not yay for back to work! It has been a bit of a hiatus for appts. between chemo and surgery but next week they all start up again. Blood work is first on Monday and I am paranoid after having to be put to sleep with gas last week for the anesthetist to find a vein after the preop nurse could not. Now rethinking MO and PS advice to have port out!

    Forever, sorry about the massage too. Seems that the therapists don't want any possible "issues" in their court though none of us seem to have any idea of what those issues could be. I see my PT Friday and am looking forward to hearing what he thinks. One drain out this AM but second will be in a few more days I think.

    Mariposa, I think I will have my first fill on the 20th when I first see the PS post op. Not looking forward to it and glad I am still a few days away. My PS says 3-6 months minimum before exchange after rads and seemed to lean towards the 6 months. I guess that is to minimize chance of failure.

    cqesq, I too LOL about the porn group. Can you imagine a calendar with us? More LOL.

    cindy74, what I would do for some sun/warm! And you have left it! 

  • Faith-Focus-Finish
    Faith-Focus-Finish Member Posts: 124
    edited March 2013

    Someone mentioned about being a dinosaur when it comes to FB.  I too am in the dinosaur family!  I am not on FB.  So that means I can't join the Hottie page?

  • Faith-Focus-Finish
    Faith-Focus-Finish Member Posts: 124
    edited March 2013

    Welcome Jem!  You are not alone. 

    Congrats Cocobean on the last rads!!!  Woooo Woooo Yippeee Yippeee!!!  Enjoy your trip down here.  The weather is gorgeous!

    Damiana - Congrats to you too!!  Yeah!!!  Enjoy your 3-week 'vacation.'  Hair chalk?  Sounds pretty cool.

    Forever-I did a lot of research on this too and I found most massage therapists won't work on cancer patients (after surgery though) due to the potential exposure to lymphedema.  I plan to search for someone local that has experience in this area.  It's a shame they won't do it before your surgery.

    Mariposa-Keep the meds coming!  Hang in there!  I know the expanders suck.  Mine have been in since last July.  So tired of being in pain / being uncomfortable.

    Jojo-I am so sorry you are having such difficulty with the blisters and peeling.  Sending you a big hug ... only one more to go!

    Whenlife-I agree with you.  I look like I am ready to join the army too!  I don't have any time available to me either.  I used it all up - and I have to be out again for the exchange surgery.  I can't wait to plan a real vacation!

    All of us in a calendar?  How grand would that be!!

    Hugs to all! : )))

  • Cindi74
    Cindi74 Member Posts: 363
    edited March 2013

    These are the Members of the Exclusive September Club No One Wants to JOIN.
    If I've left you off, please let me know. This was updated the week before Thanksgiving.

    If you send me updates--chemo survived, what is left to go, anyone left out, will add it. Remember the 5 year reunion on line. This board has been a life and sanity support. Thank all of you. Hugs.

    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

    Faith 45. Self, no children
    Firestorm531------- 1 C. Texas 41
    florbo------- Dallas, Texas
    Foreverchanged------- 72612 Self Chelsea, Quebec 3 C. 38
    Frannygirl------- Louisiana

    Hopex3 Vancouver.WA Self 52
    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
    Kathec----------Los Angeles, CA

    KelleyB

    Kidsandlabs
    Kstillie
    Laura_g

    Linn65 Indiana
    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

    QueenKong
    RSDavid------- 3 C. 4G. 58
    Runnergirl71------- Fort Collins, Colorado
    SandeeAR------- Conway, ARm, M, 2DD, 53
    Sheerbab Dallas------- , Texas Self Diagnosed M, NO C, 43

    Shock2bhere--------------RI--M. radiologist 48
    Sjayne2u Ohio
    Sparkysbrat------- East Tennessee Mountains
    SugarlandlDC------- Houston 3 C. 43
    Tara88
    Terri07-11
    Timbek2-------Peoria, IL., radiologist, 3 C. 40
    Toastiecat
    Twinsplus1 3 C. 44
    Usmcblondie 25
    Waitingforthenextstep
    Whenlifegivesyou lemons------- Minneapolis M radiologist 46
    Wendy49------- Michigan 2C M self 49

    That's 60. 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

  • Faith-Focus-Finish
    Faith-Focus-Finish Member Posts: 124
    edited March 2013

    Cindi - Thanks for keeping the list updated.  I totally agree - This board has been a life and sanity support.

    I admire everyone here!  We are awesome!

  • marianelizabeth
    marianelizabeth Member Posts: 1,735
    edited March 2013

    cindi, M, 3C, self (mammorgam 7 months before missed it), 64

    Thanks! I am in the Facbeook group.

  • whenlifegivesyoulemons
    whenlifegivesyoulemons Member Posts: 184
    edited March 2013

    Faithfocus - You'll need a facebook account to be able to view and update the "hotties" group page.  

    Here's a thought.  If you're not ready for your own personal facebook page you could opt to create a facebook account based on another name.  All you need is a valid email address to join.  If you use a different name and an email that you don't normally use then no one else will be able to easily find your page.  That'll get you into facebook without committing you to friending everyone else in your life who's already on facebook.  

  • cgesq
    cgesq Member Posts: 319
    edited March 2013

    Faith, or, your kids can make a facebook page in your dog's name!!

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