January Mastectomy

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  • ariesrottie
    ariesrottie Member Posts: 260
    edited February 2010
    Just stopped by before the benadrly take its full effect. I am on keflex for a boil that I have on my stomach, this too shall pass. I am 52. Been with my husband Bob since 1977. This September we will be married  the big 25. We have 3 children. Anthony is 23 working with my husband, Bianca (20) is a junior at Suny Corland, and Vincent (17) is a senior in high school. I am a big fan of Bon Jovi.  When I found out I had breast cancer I said I need to be better fast. I have a prom, graduation, 25th anniversary and too many Bon Jovi concerts that I paid for already. (Concerts are in March ,May and July). I do plan to go in March. This isn't going to stop me. I have to be positive.. I enjoy the concerts and my Jovi friends too much. Well I need to head off to bed the pill is starting to work.Good Night My BS. I will pray for all of us for Strength and Courage. Sleep well . Talk to you in the morning.Tomorrow is another day.
    (Hugs)
    Donna
  • neversurrender
    neversurrender Member Posts: 508
    edited February 2010

    It is waaay to early for me to be up, but tonight has not been a good one for sleep for me.  Due to my mom staying with us for my recovery time, my girls are all sleeping in one bedroom.  Well, one was not feeling well last night and I ended up with one (non sick one) in my bed with me.  She is like sleeping with a circus, arms and legs everywhere, mumbling.....I put a large body pillow between us at one point, as she kept hitting me on my drain area.  Then the arms were flying and she whacked me in the boob...I was so paranoid of getting whacked that I couldn't get comfy.  When I finally seemed ready to sleep, my phone buzzed and school is cancelled today for them........

    Debbie - you sure picked the right time to get out of town.  We have about 10 inches on the ground now, and they are saying up to 8 more today!  I don't know if Columbus can handle it :)

    My sternum was very sore the first few days, but is about normal now.  

    I'm sure you will all get a kick out this, but the first thing I complained about after coming out of the recovery room were my big toes.  They hurt so bad!!!   Like someone had been jamming the nails down into the nail beds.  My mom checked and kept telling me, they're fine.  The next morning after surgery, each toe ended up with a large blister on it.  Now 14 days out, I still have a dark, nasty bruise on the one and a smaller on the other.  Any ideas??  Everytime I saw my surgeon after, I had to many questions about my breasts and would forget to ask about my toes.  Maybe because of the long surgery and being both breasts, they had to put monitors on my toes???   I had two IV's on my left arm and an arterial line in my left wrist, so I can't imagine what else they would have needed my poor toes for.   They don't hurt anymore (only lasted a day or two), but never expected toe pain after a mastectomy ..... LOL

  • KatRNagain92
    KatRNagain92 Member Posts: 522
    edited February 2010

    Good Morning All.

    No school here today.  My daughter would be doing the happy dance if she were awake.  I'm awake at 0430 because the bendryl only lasts so long. I'm no able to lay almost flat on my back with my head resting on a side pillow...kind of gives the illusion of sleeping on my side when I'm not. Also gives a stiff neck in the morning.  gads.

    I was supposed to see the BS today but am not going to risk going into a ditch or even a minor fender bender with this condition.  All she is going to do is poke and prodd anyway...I can skip it I think.  My incisions look ok but the swell underneath has this orange peel look about it.  PS said that was normal last week so I'll stick with that.  My right armpit is ok...still sore.  No lumps or swelling just tight. 

    Robin, be careful with frequent aspirations of your drainage...the body is an amazing thing and will keep producing more and more if it sees the aspiration as a 'shortage' and you will run in to a viscious cycle.  Try drinking lots and lots of water and see if it will start cancelling each other out.  Sometime empyting the drains to frequently (enticing the vacuum process) will produce more drainage too.  Of course you don't want them heavy and pulling either so take this with a grain of salt.

    And yes to the rocks under your chest!  Although I always thought they were more like small flat cans.  I've got these dimples at the top of my 'breast' where it comes in line with the armpit.  I'm not sure if that's because the TE isn't inflated or if it's because I was so large breasted before this happened and now I'm not and I have too much skin.  I'm just so surprised he was able to give me an initial fill of 250cc....this leads me to believe that they didn't take as much skin as they probably should have.  Now I've got this imaginary fear of having breast tissue on the underside of the said skin when I probably don't have a clue of what I'm talking about.  At least my husband can see me now in my Cami and my A cup size.  baby steps. 

    You must be an incredibly strong woman Maria!  The wound vac sounds like the perfect solution after they debride the area.  Prayers for healing!

    Sally, your toes sound like my lips.  I woke up with a fat lip after surgery and they could only account for them ripping the tape off the intubation when I was done.  When I went in for round 2 a week later I said 'Hey, easy on the lips ok?'  They were all sheepish.  My bottom lip is still numb in the center.  Kind of pisses me off you know?   

    Also, my sternum is very tender and it's very difficult to tolerate even the lightest of fabrics over my chest.  I sit on the couch holding out what ever top I'm wearing so it doesn't graze.  Extremely sensitive. 

    Well, maybe it will be back to bed for me....have a great day everyone!  Stay Safe!

    Kat

  • pbebow
    pbebow Member Posts: 575
    edited February 2010

    Robin,  I would say that the TE's are hard, but not hard as rocks.  and they are not permanent!  That's what you have to remember, these are the just temperary.  I'm not going to lie to you and tell you that you don't notice them.  I seem to be aware of them all the time, but since my diagnosis I have been constantly aware of my breasts anyway, even before the surgery.  I would say that I am aware of them and there is some discomfort, but I wouldn't say that I am in constant "pain", but after what we have all gone through, pain is a relative term now.  I can't say that the TE's look lovely, but they're not bad if you aren't expecting perfection.  My right side kind of bumps out a little more on the side so that can be a little annoying, but I'm getting used to it, and again, this doesn't mean that this is how I'm going to look after the exchange.  that is what I tell myself all the time and this makes it better for me to except the hard TE's and the discomfort.  I would not let a couple months of being uncomfortable deter me from reconstruction if that is what you want.  And if you aren't looking to go really big, it wouldn't take that long.  Anyway, that's just my experience, hope it helps.

    Bless & Release!

    Paula

  • KatRNagain92
    KatRNagain92 Member Posts: 522
    edited February 2010

    Oh and Marianne (and our foursome), we watched some golf on TV last night...The Biggest Break..Anyone seen this? America's Next Top Model goes Realty Golf:)...and I can't even imagine swinging a club.  It hurts to watch.   I think my golf this season is going to be limited to Swingers (hit and giggles girls...get your minds out of there!)  Where you can ride around in the golf cart for 9 holes socializing and then have a nice meal <margarita> afterwards. 

    This is a good image warm inside with 6" of snow outside!
    Kat 

  • cleo100
    cleo100 Member Posts: 104
    edited February 2010

    Hi, all. It's Cleo-Linda here. I believe i was originally inflated to 250 cc per breast at initial surgery. Due to the hematoma a week later which required more surgery, my fills have been delayed by a week. Yesterday he injected 90 cc's into the right and 70 into the left. They look about equal. I really haven't needed any meds although i took 500 mg of tylenol 1 hour before and then again at bedtime. As to the rock hardness, I don't believe it is an issue. i have read that the implants to come are 100% different and better than these things. I will have silicone gel implants but don't know when because i am going slow. i need to be able to drive and play piano. I will go back in 2 weeks for my next fill. Other than the "tightness" I'm really not obsessing over the tissue expanders. As to sleeping, i left the recliner about 2 weeks ago for a bed in the guest room which has a wedge pillow for behind my head and many other pillows set up for my arms and behind my head. As i said before, the absolute best purchase i made before this process was a "travel" neck pillow which has really helped me avoid neck pain. All in all, i am glad i decided on reconstruction; certainly more difficult up front but next year this will all be behind me!

  • pbebow
    pbebow Member Posts: 575
    edited February 2010

    Kat:  I know, I can't imagine trying to swing a golf club right now, but that is a few months away!  A lot can change by then.  I guess we just have to except that we'll have to basically learn how to swing a club all over again.  My husband says that I'll probably be better than before with my new girls.  haha!  It wouldn't take much for me to get better, I wasn't very good to start with!  haha!  Anyway, guess we just have to keep doing our exercises (which I haven't done since my fill, need to get back to that, today would be a good day for that).  I have a really good dvd that I ordered that is made especially for us, the BC sisters!  It's call Strenght & Courage (sound familiar!?), exercises for Breast Cancer Survivors.  It is broken down into different sections.  The first section is for the day after your surgery, just a few light stretches and then the next one is for after your drains come out basically,  it has the walking your hands up the walls and some other good moves.  Then after that comes the flexibility training, and then weight training and then to aerobic exericise.  but they encourage you to master one before moving on to another.  I orderd it off the internet before my surgery.  I am sad to say that I didn't start it right away like I planned, but I figure at least if I do it some, it's better than nothing.  I think it was about $20 and part of that goes towards cancer research.  One of the ladies that helped create it was an avid golfer and used the exercises to help her golf again, so bonus!!!  Here is the website if anyone is interested...  www.strengthandcourage.net 

    Bless & Release!

    Paula

  • KatRNagain92
    KatRNagain92 Member Posts: 522
    edited February 2010

    I would love to start excerising Paula, thanks for the link.

    Linda, I'm encouraged by your progress...you're a few weeks ahead of me but I'm excited to think of switching out the TE.  No, they don't look horrible and I'm getting used to them but they are uncomfortable.  I want silicone implants in the worst way but my husband says its like buying a brand new car with no warranty.  I'm not going to be able to get an MRI every year to ensure their integrity so I guess it's saline for me.  I wonder if you can switch those out down the road....like if my saline one goes flat one day if I could just have them replaced with the silicone and throw caution to the wind?

  • pbebow
    pbebow Member Posts: 575
    edited February 2010

    I am definitely going with silicone.  They are softer and more realistic.  I guess I'm not sure I understand your husbands thinking...  I don't think there are any guarentees on either kind is there?  I know that I have read and my PS said that the new silicone are much better than they used to be.  Someone posted a youtube link to show a demo of the silicone implants, showing how when you try to cut them open they all stay together instead of oozing out all over.  I can't remember if it was on here or in another thread.  I'll see if I can find it.  Either way, you know that the implants will be better than the TE's.  I'm sure that you would be able to to switch them out later if you wanted to though... Here is the link...   www.youtube.com/watch?v9vFyAEggJSw (hope it works, it wouldn't let me copy and paste so I had to type it)... if it doesn't just go to youtube and do a search for silicone implants, it's durability between saline and silicone implants, a dr. is doing the demo.

  • TNgolfer
    TNgolfer Member Posts: 253
    edited February 2010

    Brenda,

    It's Marianne....I just loved the phrase "vampire bites" to describe the drain remembrances!!  It is perfect!  Today, is 12 days out from surgery.  Last night only took the antibiotic and 800mg Ibuprofen.  Slept for more comfortably than ever.  Slept about 6 hours straight, woke for a while and then fell back asleep.  Now that all the drains are out, I actually was able to sleep in my bed and almost be on my side.  What a relief! 

    Robin - your question about the TE's (re hard as rocks).  My right TE was filled at the time of placement and it does not feel hard as a rock.  It feels firm, but pliable (if that's an accurate description for you).  The left TE was filled at the time of placement, but then deflated the next day in a subsequent surgery.  It has been deflated since then.  I can feel the ridge of the TE and it, indeed, is hard.  But that will be filled on Thursday.  I would be anxious to see what others are feeling.  It has been my impression that the TE's filled with saline will be harder feeling than our natural breasts, but that the silicone implants will not be as hard. 

    I think so much of this is adapting to new feelings.  When we go to the beach/pool, the water feels cold when we first get in, but after a little while it becomes comfortable and feels normal.  That's what I am hoping will happen!

    Marianne 

  • robinlbe
    robinlbe Member Posts: 585
    edited February 2010

    Snowing here, too.....6" on the ground, and it's still coming down!  Kids are out of school, and nearly everything is shut down.  I only work part-time, but Tuesdays are one of my days to teach....so this "sick" day is now a "snow" day, to be made up at the end of the year.  This is the 3rd of my "sick" days that will not be taken as a sick day....I guess that's a good thing - maybe this is one of those silver lining things....I might need them later.  I had more than enough to cover these weeks off, but maybe God knows I'm going to need more for later - who knows?

    Thanks for all the feedback on the TE's. 

    Go figure on your toes, Sally...that is wild!  Kind of funny, though....but not the pain, of course!

    I've given up on the benedryl.....after taking it for so long, it stops being effective for me.  But at least it helped a great deal when I first really needed it!  It was a true life saver.

    As for my fluid build-up, I'm finding it's my right arm that's building up the most - I've read some other gals have been told to limit their movement because of this.  I'm right handed, and tend to use my right arm more.  I also have less motion in my right arm, so I've been trying to exercise it more - which is really wild, since I had only ONE node (as opposed to four in the left arm) taken, and the right side was my GOOD side!!  argh...  It's almost like a punishment for going extreme to being preventive....(and to avoid tamoxifen)....sigh.

    Everyone, have a great day....stay safe, continue to heal, recover, praying for all....blessings...robin

  • pbebow
    pbebow Member Posts: 575
    edited February 2010

    Robin:  Don't ever think that you are being punished for going extreme!  I had DCIS on my right side, they took most of it out in the biopsy (there was less than 1 mm left when they did the BMX) and that was it and I did both sides and SNB on right.  I feel that I have taken every precaution that I can, and I have no regrets!  Instead of feeling like you went to extremes feel that you have done everything in your power!  And I didn't want the tamox either!  Did the happy dance when they told me I didn't have to take it!  This too shall pass!

    Bless & Release!

    Paula

  • neversurrender
    neversurrender Member Posts: 508
    edited February 2010

    Kat - even though it wasn't directed at me, thanks for the heads up about the antibiotic and drains. (Never occured to me)  I finished my Keflex yesterday morning, and still have my ab drain and probably will for a while (still over 90 per 24hrs).  I called my BS office and they said I def. need to be taking antibiotic as long as I have my drain.........would have been nice if they had mentioned that at my appointment.  So off we ran to the pharmacy this morning through the snow storm to get me my new rx.    :) 

  • Lynbob
    Lynbob Member Posts: 140
    edited February 2010

    Thought maybe this would easier alphabetically:

    ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

    aces () - bilateral mastectomy, immediate TE 01/26/2010

    angicpa () - total right mastectomy 01/04/2010

    ariesrottie (Donna) - mastectomy, immediate TE 01/25/2010

    binga (Becky) - bilateral mastectomy, immediate TE 01/27/2010

    boromom (Melissa) - bilateral mastectomy, immediate TE 01/22/2010

    cat60 (Cathy) - right mastectomy, immediate TE 01/12/2010

    CinD (Cindy) - left mastectomy, node removal, immediate TE 01/07/2010

    CindiS (Cindi) - mastectomy moved to February

    cleo100 (Linda) - bilateral mastectomy, TE 01/05/2010

    Daler () - right mastectomy, immediate reconstruction 01/12/2010

    faithandfifty (Debbie) - bilateral mastectomy, no reconstruction 01/15/2010

    formykids (Cathy) - bilateral mastectomy, SNB, no reconstruction or delayed DIEP 01/12/2010

    frosty1 (Brenda) - bilateral mastectomy, delayed DIEP 01/11/2010

    grdnslve (Lola) - right mastectomy, delay reconstruction 01/27/2010

    iamgiggles1 (Kelly) - bilateral mastectomy, delayed recontstruction 01/12/2010

    jakhope () - partial mastectomy, SNB 01/12/2010

    Jill1965 (Jill) - left mastectomy, SNB, immediate TE 01/14/2010

    judgejaclyn (Jaclyn) - bilateral mastectomy, SNB, immediate TE 01/12/2010

    KatRNagain92 (Kat)- bilateral mastectomy, SNB, immediate TE 01/25/2010

    KELL414240 () - bilateral mastectomy, SNB, immediate TE 01/26/2010

    Leah58 (Leah) - bilateral mastectomy 01/07/2010

    lexislove () - right TE removed,implant placed, left breast lift 01/28/2010

    Lynbob (Lyn) - bilateral mastectomy, SNB, immediate TE 01/13/2010

    Lynh (Lyn) - bilateral mastectomy, immediate TE 01/07/2010

    MelissaD (Melissa) - bilateral mastectomy, nipple sparing, SNB, immediate TE 01/14/2010

    mom2mms (Maria) - left mastectomy, SNB, immediate TE 01/13/2010

    Neversurrender (Sally) - bilateral mastectomy, immediate DIEP 01/25/2010

    pbebow (Paula) - bilateral mastectomy, SNB, expanders 01/08/2010

    puddingirl84 () - bilateral mastectomy, no reconstruction 01/25/2010

    robinlbe (Robin) - bilateral mastectomy, no reconstruction 01/06/2010

    Shelly328 (Shelly) - bilateral mastectomy, reconstruction 01/19/2010

    SherryAF (Sherry) - bilateral mastectomy, immediate Free Tram 01/05/2010

    Sunsnow (Maura) - bilateral mastectomy, SNB, expanders 01/08/2010

    Susie123 (Susie) - bilateral mastectomy, immediate TE 01/21/2010

    taraleec () - bilateral mastectomy, delay surgery, TRAM reconstruction 01/18/2010

    TexasPeaches (Susan) - right mastectomy 01/21/2010

    TNgolfer (Marianne) - bilateral masectomy, immediate TE 01/28/2010

  • Lynbob
    Lynbob Member Posts: 140
    edited February 2010

    I woke up Sunday morning with pain and swelling in my right arm (the lymph node removal side) I placed calls to my PS who was concerned it may be a blood clot (but it wasn't really hot or red) He said I should call my BS or go into the emergency room. I called the BS and the on call doctor was also concerned about blod clot but told me to take aspirin, ibuprofen, elevate the arm and use low temp heating pad. And if it got significantly worse to go to the ER. Honestly my concern was for lymphedema. It feels like someone squeezing the muscle in my upper arm too tight. And there are very tender spots where if I just touch it - it hurts. It feels thick and tight. Monday I get a call from the BS's office telling me to come into the office asap. Sit there for 2 hours before being seen. He decides to get an ultrasound to rule out blood clot. But the ultrasound is the office across town so I have to race across town to that office and quess what... I sit for 2 hours :D  Finally have the ultrasound - no blood clot. And thats it. I guess if it is lymphedema they would have realized that? I feel like I have been jerked around and still have the pain and tenderness in my arm. It doesn't seem to be be as swollen. Ugh.  I have never been giving exercises nor has anyone talked to me about what to watch out for regarding lymphedema.

  • pbebow
    pbebow Member Posts: 575
    edited February 2010

    Lyn:  I am definitely not an expert, but did you have a SNB or AND?  I'm sure it doens't matter a lot, but seems more likely to be an issue if it was AND...  I think that I would call your BS and specifically ask if it could be Lymph. and what you should watch for in the future and if there are any excercises that will help you.  I am so sorry that you are having togo through this on top of everything else!  As if we don't have anough on our plates with just recovery, now to have to worry about this, too much!  Bless & Release!  and breath....  Keep us posted and definitely call and ask specific questions.

  • faithandfifty
    faithandfifty Member Posts: 10,007
    edited February 2010

    Hugs & hugs & prayers & prayers & hugs.

    It does indeed seem that at times we are each "inventing-the-wheel" for our own case. Which just shows we must educate ourselves and be our own best advocates -- whatever the issue: from lymphodema, to prescriptions, to necrosis,  to pathology, to treatment, to sleep, to emotional side effects, to range-of-motion etc etc etc.

    Much easier said than done.

    Here's a reading by author Carolyn Larsen, called "Comfort When you Hurt."

    "Physical pain usually triumphs over whatever you are trying to do. When your body hurts it is difficult to think about anything else. Pain is all-consuming. It's hard to care about others and it's hard to concentrate. Ongoing physical pain wears down your endurance and your attitude. Hope becomes a mere memory. Where do you turn? How do you combat the hopelessness of pain?

    You must be open to receiving comfort. You cannot be comforted if you put a wall around your heart. Ask God to fill your heart with reminders of His care and concern for you. Accept comfort and help from those around you. Your body will tell you what it needs: rest or medication. Pay attention to it.

    Remember that God loves you, especially in your pain. He wants you to focus your thoughts on His love and care for you. Remember that you are not alone."  

    I guess I have been fortunate in my 53 years not to have ever experienced the need for physical recovery. I must confess that the unrelenting nature of the tightness and the vampire bites and the impact to my range of motion etc has all come to bear on my 'spirit' over the last 24 hours.

    This little snipit acknowledged how I feel. The 'ongoing' nature of all of this has worn down my reserves of endurance. The monsoon rains outside the windows parallel my feelings today. Enough already. Enough. Our thread here, reminds me of the final line: "Remember that you are not alone" as you have been my life raft. It's so encouraging to see that some are up to the challenges of re-integrating & returning to work and responsibilities.  There in lies hope.

    xx00xx00xx00xx00xx

    Strength and courage.

    Strength and courage.

    Strength and courage.

  • neversurrender
    neversurrender Member Posts: 508
    edited February 2010

    Lola - Did you have your ct today?  I am sending some good thoughts your way.

  • TNgolfer
    TNgolfer Member Posts: 253
    edited February 2010

    Lyn,

    After my axillary node dissection and SNB, I was instructed to start raising that arm as soon as I could.  Stretch and stretch again.  The breast surgeon actually showed me how and showed my husband as well.  Make her do it, she said, even if it hurts a litle.  I did (and it did hurt) and I could even see a tendon stretch, but it feels fine now (AND on 12/10).  Use the internet to find out everything you can about Lymphodema (this website and others).  I am sorry you got the runaround! 

    Marianne

  • pbebow
    pbebow Member Posts: 575
    edited February 2010

    Is anyone going to physical therapy?  I have been reading some other threads about fills and exchanges and a lot of the ladies are going to PT and they it helps a ton and helps them get through the fills easier and just makes them feel better.  although they do stress about not strengthening the pectoral muscles, just stretching there and strengthening other muscles.  Not sure if any of us are ready for that yet or not, but I think I'll as my PS about it at my next fill.

  • grdnslve
    grdnslve Member Posts: 310
    edited November 2010

    counting the minutes to leave for my ct scan & terrified.  hubby says i have been --well lets just say grumpy - this morning.  plus he decided he wants to sell the 5th wheel--i am devastated.  want my arizona time!!!!!!!!!  i know he is panicking--he was a widower when i met him.

    lyn--ask about a referral to the lymph clinic--they are sending me to the physical therapy clinic for both--physical therapy & lymph issues.  the onc explained the pain to me as being caused by the irritation to the nerve when they took out the lymph nodes.  it's a syndrome girls...very real.

    off i go....sniff

  • sunsnow
    sunsnow Member Posts: 92
    edited February 2010

    Paula - I'm going to the PT tomorrow for my first of 2 sessions. My range of motion is fine, but my BS keeps a PT/OT on staff, and every surgical patient goes to at least 2 sessions in order to at least gain awareness and information. I am hoping it will help me with the fill I have scheduled on Thursday. I know the PS is planning to put another 100 cc in, so I'll be up to 500. Not sure if I'm stopping there or having one more.

     Lola - Thoughts and prayers are with you today.

    To everyone - It's amazing to see how far we've all come in 2010. So much strength and caring in this thread. Continued good wishes for us all.

     Maura 

  • faithandfifty
    faithandfifty Member Posts: 10,007
    edited February 2010

    I just got my referral for PT in the mail today. I have been on the phone to get into a PT clinic nearby. The earliest that I could be seen by their senior female therapist is next Wednesday, so I will have to be patient until then -- continuing with my own arm raising exercises and walking the wall etc. Eager to see what else can be added to the mix.

    xx00xx00xx00xx

  • pbebow
    pbebow Member Posts: 575
    edited February 2010

    Maura, I wish mine had that.  He hasn't mentioned anything about PT, but I've read that it's helping a lot of people, also massage sounds like a good thing.  My problem is I live in a very small town and although there are PTs and Massage Therapists I don't think that they specialize in BC and I don't want to go anywhere if they don't know what they're doing.  Have to be careful about what you do, don't want to make matters worse.  I drive an hour to PS so I'm sure there would be options there, but that would mean more driving.  Guess I'll talk to him when I go back on the 22nd for my next fill.  He said he'd take it easy on me for the next fill so don't know if that will be 100 cc's or less.  I know that I am at 400 ccs right now and he wants to overexpand to about 600 or 700 ccs, so don't know how many more I have in store.  good luck to all!!!

  • binga
    binga Member Posts: 140
    edited February 2010

    ariesrottie,

    I am a huge Bon Jovi fan too and really want to go to the two concerts close to my area (Nashville and Atlanta).  I haven't bought tickets yet because I usually do ebay and get the seats I want.  I have went to over 20 concerts and there is just nothing that can compare to it!  Last time On Lost HIghway I had second row center seats and loved loved loved it!.  I don't know if I will be up for it or able to really afford the seats I want but I hope so.  Good luck to you.  Nothing better than a little Bad Medicine!

    Becky

  • binga
    binga Member Posts: 140
    edited February 2010

    So happy that I got 2 drains out today and the other 2 should come out Friday! Woo hoo!

    Bad news is the  PS filled each side with 100cc and I am in quite a bit of pain.  I will not let that happen again.  The only thing that helps in 10mg Valium and a Percocet.  When I go for the next fills on Tuesday I will insist on a smaller amount.  This is way too uncomfortable and what is the hurry anyway?  I am pretty pleased with the way they are looking but not feeling.

    Becky 

  • TNgolfer
    TNgolfer Member Posts: 253
    edited February 2010

    Becky,

    Glad you are getting drains out.  My PS said he would try to fill the one TE that he had to deflate in surgery.  He suggested 100cc......Should I beg for less?  I am in no hurry either.  Is there a reason for the amount?  Do they have a timeline?  Guess I'll ask.

    I, too, can't believe how well we are all doing, despite a few more setbacks for some.  I never thought I would feel this well.  Actually put make up on and went out to buy "thank you" notes today.  Feeling almost human again!

    Marianne 

  • ariesrottie
    ariesrottie Member Posts: 260
    edited February 2010

    Hope everyone is feeling good today. Right now I a tired, still filling these drains its killing me. Everyday call th PS and they want me to be 30cc or less. Will that day ever come? I can't wait to take a shower. These sponge bath are not working anymore. Is it okay for us to use deodorant? 

    Becky, good for you on your drains. Hopefully by the end of this week for me to be drain free. Thats great that you too are a  Bon Jovi fan.., No one knows what its like until you go to one of his concerts and get your Jovi fix. I'm glad your doing well.

    How are the rest of my sisters Kat, Sally, Debbie, Marianne, Lyn, Paula, Kelly, etc????? Hope everyone is having a good week. Getting  a lot of snow. Just got the call that school is closed tomorrow. That means i can sleep late. ( yea right. Can't get more then 4 hours straight) Well enjoy the snow, if you are getting it. I hate it. Its pretty and all but hate driving in it. Not that I'm driving lately. But the family and friends are. Anyway enjoy the night sleep well and most important feel well.

    Hugs,

    Donna

  • robinlbe
    robinlbe Member Posts: 585
    edited February 2010

    Well, when I asked my BS about PT, he didn't seem to think it was necessary - maybe because I didn't have reconstruction.  But I probably don't need it, though.  I didn't start my exercises until the drains came out and my ROM is back to normal, as near as I can tell.  I can feel my skin pulling under both arms (mostly my right arm - my "good" side), but all I did were the exercises in the Reach to Recovery book the ACS sent out.  Of course, I only had four nodes taken from the left side, and one node taken from the right, so I have it made easier than most.  But my chest is cut from under one armpit all the way to the other, with only about an inch (at the sternum) that isn't. 

    Debbie, I think the emotions, pain, etc. all come and go as ocean waves and roller coaster hills.  There are the good and the bad, the sad and the happy....and I think it's OKAY that we allow ourselves to experience them all.  No matter where our diagnosis has taken us - we each have had our lives turned upside down the past few months.  And we've gone places, and have had to do things we never dreamed of last year this time.  Who knew we'd all be chatting together like this right now February, 2009??  Last year this time, I was nagging my then, 17y.o. son to complete scholarship applications as he was completing his senior year of high school - wondering how in the world I was going to handle it when he actually DID graduate.  My mom and I were counting down the days to go on an 8 day cruise together (just the two of us - she's a widow) for an early celebration of my 50th birthday.....WOW.  Little did I know what was lurking in MY future.....glad I didn't.

    So, you know what?  We let ourselves grieve....we let ourselves cry....we let ourselves be down....then, we pick ourselves right back up, and keep on going....onward and upward.  It might be cancer, but as those sappy little things all say, it might take our breasts, or our hair, or whatever, but it can't take away our spirit, our spunk, our fight, our right to live, our enjoyment of life, and everything else!!!  And it certainly can't take away our love for our families, our love for God, and our newfound friends!!!  (for which I thank God for AND pray for daily!!!)

    blessings.....robin

  • neversurrender
    neversurrender Member Posts: 508
    edited February 2010

    Very well said Robin.

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