December 2011 Surgeries - want to wait together?

Options
1313234363773

Comments

  • Kaara
    Kaara Member Posts: 3,647
    edited January 2012

    Blessings:  Hospital never found my clothes and never offered reimbursement!  I guess I could pitch a fit, but I'm so over it at this point.

  • goldlining
    goldlining Member Posts: 1,178
    edited January 2012

    I went for physio and a massage on Thursday and realized I had not tried lying on my front yet. She suggested we could try with me lying on my side but it wasn't that comfortable so eventually I put a pillow under my ribs and head and lied on my front that way and it was just fine. I have been sleeping on my side (both) for about a week. By far more comfortable than on my back. Yesterday I bought a long sleeve compression shirt for running and I slept in it last night and it really did enhance my comfort because there was less feeling of things possibly flopping around. I was on the treadmill for nearly 90 minutes yesterday and even ran slowly (4.5mph) for 3 minutes at about the one hour point. Coming along well. I was in the office 4 days last week. Some days I was just sitting there reading the news online, but I did get some work done. I took the subway on Friday to get to an offsite meeting, and fortunately it wasn't crowded. Physically I could drive but cognitively I don't think so. I don't think my reaction time and capacity for complex decision making is completely under my control yet. This week, I do have a work function to attend, but I will be spending more time on me with two physio appointments and the dentist in the schedule, and I fly to Disneyland on Friday (^:3

    Happy Lunar New Year to all. 

  • Moonflwr912
    Moonflwr912 Member Posts: 6,856
    edited January 2012

    Home from the hospital. Wow, what a mess. I looked at my surgical scar and, no, just no. Ugh. Now I don't know if I should fill the right one all the way when this mess is over and I am healed from the surgery, or just leave it alone. And, Kam, just because of what happened to m, I would NOT let anyone but my ps at them. Still sleeping in my magic chair because of my new drain.

  • Moonflwr912
    Moonflwr912 Member Posts: 6,856
    edited January 2012

    GOLD AND MYBODY, WELCOME, sorry I meant to say that before ranting. LOL KAARA, I NET YOUR HOSPITAL has a care coordinator she can help you get help to get your stuff.

  • Bogie
    Bogie Member Posts: 286
    edited January 2012

    Anyone else have sore ribs after bilateralMX with expanders, 4 wks post op.



    I've come to realize the waiting is worse than treatment ...waiting on results still.

  • Hindsfeet
    Hindsfeet Member Posts: 2,456
    edited January 2012

    Blessings...I woke up from surgery with a mastectomy wrap. It's very sweet, or pretty. It's a flowerly band (pink) with velcro holding it together. It might be compared to a waste or back support bands that you put around your waist to support your back when you exercise....except this one goes over your breast.

    It keep the swelling down. Tonight I put it in the wash and laid down only with a soft cami. I began having pain so I put on a mastectomy bra which is also slightly tight. I hate it and I love it. I'm getting used to wearing in 24/7. I don't have swelling or pain when wearing the wrap. And as I said, I easily sleep on my side without pain...and few times I rolled on my tummy and with the wrap it didn't really hurt too much...after a few minutes after rolling back to my side the minor pain was gone.

    My p.s. also used botox which also eliminates chest spasm. My p.s knows alot about pmps so he does everything to eliminate pain. He is also a master in reconstruction. I don't like the process, but I know with my pain syndrome problem I would be in such pain that the TE's would be out by now if I was not under his care. He takes very good care of his ladies...he says. His bc patients I heard in the hospital are given the best care. They are given special milkshakes with all kinds of vitamins, a soft cami, the wrap, and he'll keep you in the hospital until he knows your pain is under control and fluid from the drain. I stayed an extra day over a minor concern...not my choice.

    So make sure you are under the best plastic surgeon...although it does frustrate me he wants to take off the other breast. I'm not going through this again if I don't need to.

  • Janie-bug
    Janie-bug Member Posts: 181
    edited January 2012

    Ok after reading everyones post about there PS visits I got a little worried. I have not seen my PS since the day of surgery Dec-9th and really I didn't even see him then I was in OR he seen me!. I have had a 60 cc fill in each week that is done my his PA she says everything looks good. I have not had any major plbs but have wondered if that was normal procedure. Should I ask to see him?

  • mybodymydecision
    mybodymydecision Member Posts: 19
    edited January 2012

    I am a triple negative so they think chemo is the best treatment.  I'm almost month out of surgery but still having pain mostly where they put the drain back in.I m really feeling like I need to get back to work but it just not happening tomm going to shoot for Tuesday.  The drain back in just feels like I have went backwords but doctor said it was just to be sure didnt get infection.  Anyone eles in a similar situation.  I feel like a big baby sometimes but the pain at times is terrible I'm still taking pain meds.  I tried to slow down on them I went from every 4 hours to more like every 6 hours, but at night I sleep for 8 hours.  I sleep in a recliner tried to sleep in my bed last night didnt work out very painful will be waiting until after drain out before I try that again.  Glad to see so many of you are doing well.

  • Kaara
    Kaara Member Posts: 3,647
    edited January 2012

    Janie-bug:  Every doctor works in a different manner...some want to have more control than others.  If you are happy with your results, and not in any pain, I wouldn't worry about not seeing you ps each time you go in.  The NP's are very good and have obviously been taught how to do the fills just fine.  If you felt a need to see the doctor he would respond accordingly.  

  • Ginger48
    Ginger48 Member Posts: 1,978
    edited January 2012

    Janiebug- I saw NP's when I had fills and only saw PS when she wanted to double check on incision where it was not healing properly. If you are comfortable and things are going fine then I would not worry about it, The NP's were way nicer to me than the PS ever was!

  • A_FIGHTER
    A_FIGHTER Member Posts: 109
    edited January 2012

    Hi Bogie-

    I was told 2 weeks for results...However, it will be a month waiting for my OncoType Dx due to it not being sent out when requested...My surgery was Dec. 28th (when it was supposed to be sent out)...When I found out it wasn't sent they assured me it now has and the results would be in Wed. Well, I personally called Genomic Health today (866-662-6897). They recieved my specimen Jan. 17th and she said my results would be in on Thurs. She was pleasant and very helpful. I also questioned whether there would be a problem due to specimen beng held back for so long . She told me it makes no difference as they take speicmens up to 5 years old :)

    Hope this helps you! I would call :)

    I was aggravated with myself for NOT calling sooner! As I am usually good about things like this :)

  • Bogie
    Bogie Member Posts: 286
    edited January 2012

    Fighter,



    Great tips, as I was about to call Genomic today, my Oncologist called me and had already made the call. He said the Oncotype test will be back by the end of this week. Other than initial diagnosis I think this is the second hardest test result to wait for. I also got blood drawn today (per my request) to see if I'm in menopause to determine which hormone therapy drug I will be given. I was scared to have a blood draw with double masectomy even on the side no lymph nodes were taken out. The lab nurse said to always have them draw blood without the turnicate, I think that is how it's spelled.



    Has anyone gotten a second opinion either from pathology slides or on treatment from your current path report? If so, was there any difference and was it a difficult process. I see MD Anderson and John Hopkins have online second opinions. I May look into Rush, any suggestions? I think my OC is very good just not sure QI need to go that rout or not.



    Someone helped me today outside my Oncologist office when I dropped a handful of things. This woman was so nice, she told me if people would just start caring about people again in this world, there would be no war. I thanked her, and told her how kind she was, that I had just been diagnosed with cancer. She said she just lost her husband , and I began to cry. I think hearing my own words telling a perfect stranger I hade cancer, and her kindness after her tremendous loss,it got me sobbing...geesh.



  • Hindsfeet
    Hindsfeet Member Posts: 2,456
    edited January 2012

    This is one of my supportive threads, and wanted to say thanks for your support while going through my surgery...recovery. I'm still recovering, but feeling much better. I'm moving on from bco for awhile. I hope and pray that you all recover and are able to move on too.

    With love, Evebarry

  • CookieMonster
    CookieMonster Member Posts: 1,035
    edited January 2012

    Best wishes to you for a continued recovery - hopefully it gets easier and easier.

    HUGS!!

    -Judy

  • A_FIGHTER
    A_FIGHTER Member Posts: 109
    edited January 2012

    Bogie -

    As far as second opinons on final pathology -  I've been seeing two Oncologist from the get go (before I had surgery). They both have recommended the same "cocktail" if Chemo is needed and five years Tamoxifen. However, one would also like to do Ovarian Suppression. 

    I will choose which one I will be in the care of once I receive Oncoyype DX results (today or tomorrow, thank goodness) and having one more appointment with each of them. They both know each other and are aware I am seeing the other. My "Team" of Dr.'s meet every Thurs. to discuss their patients. Yes, BOTH oncologists are at the meeting. I told my Cancer Surgeon it must make for an interesting meeting...LOL

    I already have an idea of who I will probably see...This is based on how I feel with the Dr.'s office themselves...One is a VERY busy office and the other has a more homey feeling (office is on a much smaller level). I will choose my treatment based on their recommendations. I will also see which takes the time to look over my supplements in whether I can continue them. This is VERY important. I do not want to hear them just say no. I need to know exactly why I wouldn't be able to take them. This will take some time on their part and I hope at least one of them will be willing. 

    Also another bit of importance to me, my Recontruction Surgeon and Cancer Surgeon were wonderful! I had their email adresses and would email them as need be. I ALWAYS received an email back the same day or a phone call! They offered their emails from the get go. Yesterday, I somewhat put the Oncologists to the test. I called and asked for their email adresses. I received both of them. Boy, are they in trouble now...LOL...I kept forgetting to ask them myself cause, as you can imagine, a gazillion other questions were coming out of my mouth at office visits.

    On another note, received some of the best news yesterday! I am able to go back to working out...Wahoo! One day shy of a complete month of healing...I'm back in the saddle! I also was told to start removing the glue they used on incisions and to start using scarring ointment...As of last night, ALL glue has been removed and everything looks EVEN better Laughing

  • Kaara
    Kaara Member Posts: 3,647
    edited January 2012

    Fighter:  I was very disappointed when my first RO told me that I would not be able to take my antioxidants during rads treatment because it could interfear with the effectiveness of the treatment.  It doesn't make sense to me that a supplement that protects good cells would also protect bad cells as well...that just isn't the purpose of an antioxidant.  The RO said they don't know this for a fact..it's just a theory...hummmm.   I am going to discuss it further with my holistic doc and if he feels differently I am going to continue to take the antioxidants through the treatment to help protect my cells from the excess damage of the radiation.

    Glad you were able to heal so quickly from surgery and get back to what's important in life...living! 

  • Bogie
    Bogie Member Posts: 286
    edited January 2012

    Fighter, thanks for the info. I'm glad to hear they came to the same treatment plan. I am getting a second opinion before starting treatment and once the Oncotype dx score comes in.



    it's been so nice comparing notes here. Won't be getting fills for quite awhile since I'm healing very slowly from the bilateral mx, ps wants to wait and I'm in no hurry.



    Let me know when your Oncotype comes in.

  • CookieMonster
    CookieMonster Member Posts: 1,035
    edited January 2012

    Hi everyone,

    I hope you're all continuing to heal up and are feling better every day.

    I had an interesting experience last night. Our school newspaper is doing an article on me and a student who went through cancer treatment (she has a titanium femur for her trouble, I have the foob). The editor sent me some questions last night. Mostly they focused on when I was diagnosed and so I had to go back and think about that time. It brought back a lot of feelings. I really don't want to go back there, I'm glad to have it behind me. It did leave me a bit down at the end of typing up my answers to her questions. It was probalby good for me, but I'm gald to have it done.

    -Judy

  • CharB22
    CharB22 Member Posts: 310
    edited January 2012
    Fighter and Kaara - my RO said the same thing about antioxidants - not good to take during chemo/radiation. The theory is that the antioxidants are protecting all of your cells, including the cancer cells. Antioxidants can't distinguish between good and bad, they just protect. So, for me that makes sense. He said once chemo/rad was done, go back to using antioxidants because the bad should all be gone and now I'll just be protecting the good.
  • Bogie
    Bogie Member Posts: 286
    edited January 2012

    Cookie, think of it as therapeutic and remember its all about you now. If you don't feel comfortable sharing or talking about it that day then say it. I'm trying hard not to have to please everyone else all the time and now trying to take care of myself. Curious if you had an MRI or Ultrasound after your original DX of DCIS that showed the IDC? I am asking because the same thing happened to me and my tumor invasive did NOT show up in MRI and Ultrasound. That still bothers me! If an MRI can't find it then what can, geesh. QIm having an angry day today instead of an acceptance day.

  • fitzdc
    fitzdc Member Posts: 1,467
    edited January 2012

    Anger day here too.  DH traveling and I was just feeling tired and angry and sad. (Actually good he was travelling as he doesn't know how to cope with my meltdowns.)  Some days I seem like I am moving forward full steam and then it just hits all of the sudden.   Pulled out of the funk as having movers come tomorrow.  Decided to change up some things in the house and I need to move all the books from the shelves - fun! 

    Teresa

  • faithhopenluv
    faithhopenluv Member Posts: 323
    edited January 2012

    Cookie - I can relate, I am trying to gain control over my inbox at work and I'm deleting and filing emails.  Everything is anchored around BC milestones, those were the days leading up the the surgery, that was the day I came in late because I had the MRI....getting to the 'those are the days that I didn't know that I have breast cancer' creates a feeling that I just don't think there is a word to adequately capture.  We are so focused on moving forward with our strength as our amour, looking back does something to us.

  • Moonflwr912
    Moonflwr912 Member Posts: 6,856
    edited January 2012

    Bogie, I felt my ribs were broken with the TE's up until about 5 weeks, then they really didn't hurt much anymore.  Then of course I had to have one removed,. so please be extra careful the next few weeks?  I don['t want anyone to have to go through that.  Love to all on this board.

  • Bogie
    Bogie Member Posts: 286
    edited January 2012

    Fitzgerald and Faith- I'm reading a great book that a friend recommended "Life Over Cancer" by Andrew Weil and Keith Bloch, M.D. He talks about how we don't have to be strong every day and to hold it in can be hard on our system. I know what you mean about feeling so strong some days and other days someone is mean or overly caring and I get choked up, it comes out of no where! We are allowed to have melt downs and be angry. I then want to be strong again.



    Moon - how the heck did that happen? Did you break a rib and did the expanders cause it your saying?



    Karen

  • faithhopenluv
    faithhopenluv Member Posts: 323
    edited January 2012

    Bogie - you are so right, I need to have a few days where I just crack and break down. I absolutely agree that if someone is overly nice or is mean that very often is my catalyst.

  • CookieMonster
    CookieMonster Member Posts: 1,035
    edited January 2012

    Bogie - As far as I know, my pre-op MRI did not show the IDC, just a somewhat bigger area of DCIS (and another area that it turned out was not cancer - yet). Clearly it didn't show it all as I had 3 lumpectomies and didn't get clear margins so finally had the UMX. I only learned about the IDC after the first lumpectomy as it was small (a line of IDC about 1.1 cm long) and in the middle of the area of DCIS. I only had an ultrasound with my very first mammogram and they couldn't really see anything with it, then one with the wire placement on the OTHER area that the MRI found, but that was it.

    Let me know if you have further questions.

    -Judy

  • Bogie
    Bogie Member Posts: 286
    edited January 2012

    Cookie, Interesting and sounds all to familiar. I know MRI especially picks up a lot but seems as I learn it's also not a full proof test, and cancer cells are sneaky, at least mine was!

  • CookieMonster
    CookieMonster Member Posts: 1,035
    edited January 2012

    Bogie - my DCIS was, as my BS put it, pesky. Apparently DCIS likes to spread throughout the duct system, so wasn't continuous, but they kept finding bits of it in the margins. After the third lumpectomy the BS told me that even if we did another lumpectomy and got clear margins, she'd not be confident that we'd gotten all of the DCIS anyway, so strongly recommended the MX. I'd already, separately, come to the same conclusion. At least she and I were on the same page with this, too bad it had to get to this, but I did avoid radiation, at least.

    I don't know if I mentioned it previously, but you and I were diagnosed 1 day apart too. My mammo was on 7/28 and received the diagnosis on 8/2.

    Take care.

    -Judy

  • Janie-bug
    Janie-bug Member Posts: 181
    edited January 2012

    I have read through most of the thread and am glad that most are doing well for those that are having some set backs I am keeping you in my prays.

    I had my last fill in yesterday and am having quite abit of pain the foobs are so thight. My back hurts and I can not get comfortable.....whine whine whine..... feel a little better now. I have appt with PS nx Monday and hopfully we will set a date for the exchange...

  • Kaara
    Kaara Member Posts: 3,647
    edited January 2012

    I have healed so well from my surgery in December that my RO called yesterday and told me that she could not even find the surgical bed to plan the partial beam rads that I was looking for.  She said the only thing left is the clip the BS placed and the scar; otherwise, it is as though the surgery never happened.  My DS and DIL prayed for this exact thing...that it would be as though the tumor never existed.  Looks like our prayers were answered!

Categories