Starting Chemo May 2008

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  • sueper13
    sueper13 Member Posts: 1,224
    edited October 2008

    RanD,

    Sorry I didn't tell you this last night, but I'll be thinking of you today as well.  Hope your surgery is effortless for you.

    Love,

    Sue 

  • sueper13
    sueper13 Member Posts: 1,224
    edited October 2008

    And can I just add that I kind of miss when we were all in chemo, and that was our job, and we talked and got support from each other every day and every night, sometimes?  Yeah.  I kind of miss that.

  • kerry_lamb
    kerry_lamb Member Posts: 778
    edited October 2008

    What time of day is it where you are, Sue? What day?

  • ellenoire
    ellenoire Member Posts: 674
    edited October 2008

    K- Sue is in Texas. Today is Friday, we are 1/2  day behind you I think. 

    Looks like I am 12 hours behind you, which would put Sue 11 hours behind you and the west coast girls RanD, Eddie, Cris etc 9 hours behind. 

     I think I did this right. 

  • rock
    rock Member Posts: 1,486
    edited October 2008

    Getting ready to go into rads so this will be quick.

    Cris -- HURRAAAAAAAYYYYYYYYYY!!!!!!!

    RanD -- I am typing this from the building where I had my not-much-of-anything lumpectomy-which-I-recovered-from-in-ridiculously-short-time -- that has got to be a good omen, right?!  Will devote today's rads to you.  And I mean that in a good way.

    Tamox metab -- I've got to remember to ask about that.  Though Fridays are notoriously horrid days for getting info out of my med onco. Half an Ambien (+ half bottle of wine imbibed in during the debates, goshdarngoldangitshuckydarnkitchentable) worked last night. I slept for 6 hours straight! (Though there were teeth marks on the refrigerator door...)  I think sleep is going to help A LOT.  Also, I've learned that as soon as I wake up int he middle of the night, I throw the covers off and that usually lets me avoid the impending hot flash or keep it to a Bic lighter (vs. blow torch or blacksmith shop) level.(Kerry -- working my way to S Africa on a Fulbright in January.  Going through medical clearance for the State Department now. Fingers crossed.)

    There is another page of posts and I have only skimmed what is posted here. But I have to get going so suffice it to say... Yes.  To everything. 

    ;oX

  • ellenoire
    ellenoire Member Posts: 674
    edited October 2008

    Here is an interesting vid on a her2 "survivor" I wonder if they are talking about Herceptin.

     http://www.abcnews.go.com/Video/playerIndex?id=5738692

    If the link works, click on the vid about Stage 4 BC. 

     I HAVE to get my shit together today. 

     

  • ellenoire
    ellenoire Member Posts: 674
    edited October 2008

    30 min until RanD goes in.

    I hope you are doing ok!!! 

  • Sable
    Sable Member Posts: 738
    edited October 2008

    Randie~ I'm sending you prayers and good vibes right now as I type. You should be out of surgery at this moment providing they got you in on time. I hope you are resting comfortably sweetie.

  • drcrisc
    drcrisc Member Posts: 836
    edited October 2008

    Randie - It's 2 PM here and I hope you're out of surgery now and that it went swimmingly well.  (Get it?!  I know you did!). 

    I am feeling much better today, but that's probably only today (I had hydration this morning, so that helps).  The really crappy day should be tomorrow and then I'll be on the upswing.  Love all the shout outs!  And, Sue, I kinda miss that, too.  I like that we're all hanging in with each other still, even if it's not as often.

  • drcrisc
    drcrisc Member Posts: 836
    edited October 2008

    Okay, so here goes with the photo.  It's not nearly as exciting as some of yours because I had just woken up and we were in a hurry to get out and take my daughter her gym bag!  But you take what you get...and I know there's a way to make it smaller, but dang if I know how to do that.  I'm just glad it posted and didn't take the page way out!  Now I wish I had been more interesting...boo hoo.

  • ellenoire
    ellenoire Member Posts: 674
    edited October 2008

    Yay! Cris! Glad you made it! 

  • kerry_lamb
    kerry_lamb Member Posts: 778
    edited October 2008

    Christine! look at you! You are awesome. Now I wish I had taken one..I just wanted to GET OUT OF THERE.   Maybe I can fake one when I go in to get my port flushed. How do I post photos? Help! Usually I can work it out but I am a bit thick at the moment.

    Rock..omg the sleep. SAME. I slept so soundly I woke up with a concrete head. How cool is that?My family is going to be relieved..I feel they are a bit over the slow-moving bitch in the pyjamas... Drew and I had the big talk about the big T and the big AI and I am THIS close to naysaying. I've trawled the stats and those predictor things, and I THINK I'm going to put all my money on the horse called "Kerry's Family is Tough as All Feck." This flirtation with cancer has taught me that you can't plan, or predict so....Feck it! I THINK I'm going to live on the edge....(thought I was doing that already....)

    RanD, I'm sure the first thing you'll do is plug in that laptop....so...WELCOME BACK! How do you feel? I dedicated all the meltdowns during the night to you..maybe they were tracking your progress. There has to be SOME purpose for the feckers, surely.

    Today I am going to start packing my house for the move (brought forward to November) and I have no idea how to. Suggestions?  sigh 

  • sueper13
    sueper13 Member Posts: 1,224
    edited October 2008

    Kerry,

    Right now, in Texas, it is 5:10 p.m. on Friday afternoon.  You just posted 19 minutes ago, when I posted this.

    RanD, hope you are out of surgery and well and not in pain.

    Cris!  You look gorgeous, even in socks....

    Noelle, I forgot to tell you about the weekend away--it was great. Just quiet time, reading on the front porch, a bit of shopping, dinner out, walks by a creek--and lots and lots of girl talk.  It was a really good weekend.

    Today after I got home from work I was outside with the dogs, and I felt this weird sensation on the back of my head--and it was the wind in my hair!!! It almost scared me until Ifigured out what it was!!  For some reason it is growing wildy fast in the back and hardly at all on the top or sides.  I have about 3/4 inch in the back and 1/4 inch everywhere else!! 

    FIVE MORE RADS!!!

    (Radical.) 

    Sue 

  • rock
    rock Member Posts: 1,486
    edited October 2008

    Cris!!!!!!  I love this photo! I love seeing you! I love you being done with chemo! LOVE THIS PHOTO! LOVE YOU AND SO HAPPY!

    (And Randie -- ?? I wish I were Karin to find and post the photo that will make you smile. Hope you're well!)

    xoxox 

  • lewing
    lewing Member Posts: 1,288
    edited October 2008

    Cris, so glad you're done!!!  I hope the weekend treats you gently.  Great picture, too . . . it made me smile to see you smile.  (Even though the chemo room backdrop gave me the heebie jeebies.  It looked JUST LIKE mine, right down to the clock and the bulletin board.)

    And did you kick off your crocs in order to show off those sexy chemo socks?

    Randie, hope you're doing well, and are able to post soon.  I want to see what expletives you come up with to describe your drains!

    LInda

  • Sable
    Sable Member Posts: 738
    edited October 2008

    Cris~ you look mauvelous daulink! Man look at all that hair you still have. I'm jealous.. once again LOL.

    For the tamoxifin ladies~ I asked the onc yesterday about the blood test for tamoxifin you ladies had been talking about. He said that about 99% of the women metabolize the drug just fine. It is a rare occasion that one cames along that does not. (I'm sure I will be one of them) He was surprised at the questions I had this time around, I made him do research while we stood there. I'm such a meanie ;o)

  • ewesterman
    ewesterman Member Posts: 417
    edited October 2008

    Cris, yahoo and the socks MAKE the photo. You are beautiful. Congrats on your final chemo.

    Sue, what you say about our talk during chemo resonates with me. I would give anything even two ovaries and another breast for all of us to NEVER have to do chemo again (but we'll wait until we all finish up here) but you're right about the talk being different. I do feel we are all starting to regain our original selves and we didn't really know one another when we were our original selves. My sense of humor is just starting to come back. It's not that we didn't laugh (and I mean laugh hard) during our ordeal-- it's not that we weren't hilarious (charm bracelet, sharts, hair where, etc.) but we are going, now, to get to know one another as cancer is not our 24/7 job. I love that. That is why Kerry is slowly moving us off the breast cancer site and onto a Facebook page....Randie, I am sending my prayers that you are sleeping well right now and that all went well. Love you all. Here is another thought for Halloween before I sign off -- what about putting a nipple on the top of our heads and going as a boob full of brains? Those like Noelle with more hair would be a hairy boob with brains. Okay, this is getting bad. Goodnight all. 

  • drcrisc
    drcrisc Member Posts: 836
    edited October 2008

    Thank you for your wonderful comments about my picture.  You all are the BEST!!!

    Eddie - You made me want to join the Facebook group now.  I've been putting it off because coming here and checking my email are about all I can handle, but I will join it eventually.

    Linda - You made me laugh - yep, kicked off my crocs - should've taken one with 'em on!  Now that would have been super sexy!   And I'm sorry I gave you the heebie jeebies!  Surprised

    Kerry - It's not hard to post at all.  Much easier than I expected.  Otter gave me the instructions a while ago, but she said she would be out of touch for a few days.  Maybe somebody else knows where they are...?

    Sable - Yours is coming, honey.  I promise.

    Rock - I love that you love my picture!!

    Sue - So glad you had a nice weekend!

    Noelle - Hey! 

    Randie - I'm with Linda.  Can't wait to hear you describe your experience.  Hope it went well.

  • Sable
    Sable Member Posts: 738
    edited October 2008

    Is anyone else in our group doing anything to prevent lymphodema???

    I just joined facebook.... who wants to point me in the right direction???????

  • sueper13
    sueper13 Member Posts: 1,224
    edited October 2008

    Jen,

    Quick! Tell me how to join Facebook! 

  • Sable
    Sable Member Posts: 738
    edited October 2008

    I went to facebook.com and signed up..... now I'm trying to find everyone LOL

    edit: so far I found rock, eddie, kerry and I think noelle.. I hope LOL. If not I have a stranger with noelle's name

  • Sable
    Sable Member Posts: 738
    edited October 2008

    fyi you all have been saved..... I tried to make a new avatar of my new hairs.. couldn't get one to turn out like what I wanted... you are saved for another day LOL

  • kerry_lamb
    kerry_lamb Member Posts: 778
    edited October 2008

    Hey girls!

    My men 'did' the back yard and I'm so happy I could cry. Aw....that's right.... I'm just being a bit neulastafied...NO! it's amazing. All ready for the Manchester terrier to arrive and destroy it all. The dog's name is Phoebe and I'm not sure an Australian farmer's daughter is allowed to have a dog called...Phoebe.  Quick! What sounds like Phoebe? My husband's only suggestion is 'Fleabag'.

    My Facebook idea (May O'Eight) was one of those good-ideas-at-the-time, but with the benefit of a small amount of hindsight, I think normal Facebook pages are much easier than a separate one (May). We'll see how we go. I like signing on here, and the cancer-connection is hardly one we can ignore.

    Jen, I am freaked out by the poss of Lymphodema. Y'all will probably NOT believe this but I am more freaked out by the possibility of developing IT than I am about recurrence. I think it's because there is no cure..there is no 'fight'. There is only a debilitating condition, and for someone like me who is a rural/feral lass and who likes physical, blokey activities, the thought of not being able to do ANYTHING I DAMNED WELL PLEASE freaks me. I'm not nursing my arm, but I am being aware and feck it! sensible. I tend to cuts (before bc my arm could rot off...I wouldn't notice..) and do a lot of gentle stretching and rotations. I'm getting good info off the L thread. One big worry is flying..although real research doesn't show it, there's a wealth of anecdotal evidence that a flight commonly kicks it off. It will make a 'catch up' in the US tricky..but hey! if I have to have lots of fancy stopovers...who can complain??

    Randy! Randy!

    XXX Kerry

    PS I think I may be a little too far along from dex now...I'm not getting the costume thing. Am I over-tired? 

  • sueper13
    sueper13 Member Posts: 1,224
    edited October 2008

    Kerry,

    That's right, you don't do Halloween there.  October 31st. Trick or Treat. Everyone dresses up in a costume and goes around to houses for treats. (The trick or treat part is if no treat, people can supposedly do a "trick" such as soaping windows, toilet papering trees, etc., but that hardly ever happens) People give away candy. It's from the auld "All Hallows Eve"  before "All Saints Day" on November 1st. 

    So the group on Facebook is "May" or "May O'Eight"?

    for the dog, how about "Heebie-Jeebie"?

    Sue 

  • kerry_lamb
    kerry_lamb Member Posts: 778
    edited October 2008

    Hey Sue! May O'Eight is the 'person', but I reckon it's easier just to add each other (provided we know the real names and we agree..this could be done through PMs on this thread). (Feel free to add me, anyone) Otherwise we have to log on to use our own FB and then again to use May O'Eight's. What was I thinking.......??

    Are you on a farm (ranch) in Texas, or are you in town?

    We get the Halloween thing..but it's not a big event..really just another excuse to dress up and get shickered..:)

    Anyone know how long this glass-shard gut is going to last?  It's been 5 days. That's long enough!  

  • ellenoire
    ellenoire Member Posts: 674
    edited October 2008

    Wake up RanD! we are all here with waffles and coffee!!!

    and lots of us are joining facebook too! 

  • Gracie713
    Gracie713 Member Posts: 302
    edited October 2008

    Randie-thinking of you this morning!

    I have signed up on Facebook, but haven't done anything there yet.  I'm computer challenged most of the time.  May have to try to do something with it today or tomorrow.

    The neulasta shot causes my neck and shoulders to ache.  I've had the first taxotere, and although the nausea hasn't been as bad, the body aches, especially in the hips & legs, is terrible.  Onc has me taking ibuprofen and benadryl together (Can we say space cadet?)  

    Cris--I love your pic--what a beautiful smile!

    Hope that everyone is having a wonderful day--loving this cooler weather!

  • Sable
    Sable Member Posts: 738
    edited October 2008

    Gracie~ I had bone pains in the same areas as you. My skull would even hurt in the back... that was kinda freaky in itself.

    Kerry~My surgeon sent me to a therapist for LD right after my surgery. He said he was for preventing anything before/if it happens. I had swelling right in the beginning and we got it to return to normal. I did good for awhile until taxol came along and then my chest area swelled up. So right now we are working on that area to get it down and hopefully it will stay down once all the chemicals are out of my system. I do a manual massage twice a day right now to help the body find new ways to send the fluid out. I guess with every surgery there is a chance to develop LD. Since I had the left mastectomy and then they had to take out more nodes, I have a higher risk of getting it. I am determined not to. We just have to see how things go over time. Therapist has conned me into ordering a sleeve for the days I do swell up from the heat or whatever. I have fought that battle this entire time.

    Randie~ Sending you good vibes again this morning sweetie. We love you and are thinking of you!!!!!

  • familyroks
    familyroks Member Posts: 575
    edited October 2008

    Hey Randie - I hope you are getting some much needed rest.  Thinking of you!

  • lewing
    lewing Member Posts: 1,288
    edited October 2008

    I just joined facebook, too . . . then got booted off the site (before I could try to find any of you) and can't reconnect.  I have no idea what is/isn't on my page at this point.  Or if my page is still there.  I'm good at some computer applications - if you have any Excel questions, I'm your gal! - but not uploads and web stuff.

    On the lymphedema discussion . . . Jen, I remember you casually mentioning something about LE before, but didn't fully realize what was going on with you.  I really, really hope it stays well under control.  I'm with Kerry: the prospect of lymphedema freaked me out right from the beginning.  Pre-surgery, I took comfort in the fact that the incidence is less with the sentinel node procedure - except, of course, my sentinel node turned out to be positive.  So I got the full dissection treatment anyhow.  Fourteen stinking nodes out, and the only one that was positive was the first: it makes me angry that there isn't a better way to assess our node status. 

    I try to be careful with my surgery-side arm, but it's a struggle, because I'm fundamentally not a careful person.  (I'm one of those who, during chemo, would forget and lick the cake batter, raw eggs and all.)  I'm reasonably good about not carrying bags and such with my left hand.  I'm not at all good about staying out of the dirt . . . I'll see a weed, yank it with my good hand, see another, yank that, see another . . . and so on, until 20 minutes later, I'm scrabbling around in the garden with two ungloved hands.  I did get an off-the-shelf sleeve that I've worn during the three short flights I've taken since my surgery (though I'm not anywhere close to 100% confident the thing even fits properly).  I have a referral to see a therapist for a baseline consultation, but haven't followed up on it yet. 

    Since my diagnosis, I've had only one BC nightmare that I remembered when I woke up, and that one was actually a lymphedema nightmare.  I dreamt I took off my watch, and there was a band of swollen tissue beneath it, that kept getting bigger and bigger and bigger . . .

    On a positive note: ran a 5K this morning, just a small race to benefit my daughter's high school's athletic programs (not that she's into athletics in the least: she slept in while I ran), broke 23 minutes handily, and won a 6-month gym membership for being the first grown-up female to cross the finish.  (A few of the cross country girls beat me, but not too many.)

    Linda

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