January 2011 Rads

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  • Omaz
    Omaz Member Posts: 5,497
    edited February 2011
    michcon - Do you have three zaps for your boost?  I have three, one from the left at an angle, one overhead to the right, and then one from the far right down that enters just under the armpit area.  My tumor scar is upper quadrant near the armpit on right side.
  • walker2222
    walker2222 Member Posts: 558
    edited February 2011

    Luvmylab - the total treatment for boost takes less that a min.  The techs bearly walk out the room then they are back in. 

    My next RO sighting is tomorrow, bring DH with to talk about what next.  I am already on Femara for treatment, no bad SE's yet.

    End is in sight and I feel like I can start planning something.  Only have one additional surgery but that wont be until May at the earliest.  They are going to take my TE in Left side out, tone up the skin on both sides, no more recon for me.  Cann't handle it.

  • oakley
    oakley Member Posts: 206
    edited February 2011

    Thanks Victoria!  Thanks Sherry!  Feels GREAT!

  • suzieq60
    suzieq60 Member Posts: 6,059
    edited February 2011

    Congratulations Oakley!!!!

  • Eloise
    Eloise Member Posts: 137
    edited February 2011

    Re bloodwork -- I haven't had any before or during rads, nor did I have any before my surgery; but I had had a routine CBC panel in June of this year, which may have been enough.  Also, it may be that bloodwork is not so important for DCIS and/or people not having chemo. 

    As far as doctor and staff communications, I have to say that my team has been fantastic.  I have Kaiser, which is a "closed" HMO with its own staff and facilities.  I think they've made a great effort to train their people to ask at least once during every appointment "Do you have any questions? Is there anything else I can do for you?".  They have a health library where I could check out books and videos, and online education before the biopsy and surgery. As I think I mentioned earlier in the thread, they had a Radiation 101 session before treatment started; I got a tour of the facilities, explanations of how the machine worked, what the different techs did, etc. and got introduced to everyone who would be on my team.  Kaiser has an online component that allows me to make or change my own appointments and email any of my doctors, and I've always had replies by the next day.  There've been a couple of small things -- my surgeon didn't offer me a copy of my pathology report, I had to ask for it; the medical oncology nurse-practitioner who gave me the pitch for tamoxifen didn't have statistics about how much risk it would reduce, and it took her a couple of weeks to get back to me -- but overall I've been really pleased.  And my out-of-pocket costs for all of my treatment are going to total about $200. 

  • michcon
    michcon Member Posts: 145
    edited February 2011

    Yep Omaz - It's the one down low entering from the right that's zapping my armpit. Such a bummer.

  • oakley
    oakley Member Posts: 206
    edited February 2011

    Thank you Sue!  You're almost there!

  • suzieq60
    suzieq60 Member Posts: 6,059
    edited February 2011

    Yes - 11 to go!!! Doesn't feel like almost being there though. Had to wait ages yesterday - boy that pisses me off. They've got students doing pracs and it slows them down a lot - I waited nearly half an hour - usually they are right on time. My appt is earlier today, so I hope they haven't got too far behind by then.

  • rachel5738
    rachel5738 Member Posts: 920
    edited February 2011

    Omaz--I have three zaps for my boost also--for some reason, I had imagined it being only one zap but they told me that it zapped from different angles. I'm going to ask if it is hitting my armpit. In talking to the techs today, they said that it is just at your incision area. The area underneath my armpit is a little sore---MUCH better than Friday. I am using some 100% aloe on it and it feels better.

  • suzieq60
    suzieq60 Member Posts: 6,059
    edited February 2011

    No waiting today!!! 3 regular and 7 boosts to go :)

  • lrr4993
    lrr4993 Member Posts: 937
    edited February 2011

    1 boost down, 4 to go.  This is my last week!  Yeah!

    Good thing the boost started this week because my breast has rapidly deteriorated over the weekend. I don't get it because I had very few problems and the doc was just commenting l last week how great my skin had held up.  But it started peeling on friday then got really gross over the weekend.  My skin under the breast is blistered and raw and oozing.  Doc gave me silvadene today. Have to keep in on the raw area all day.  It does not really hurt, but it looks horrible.  

    I am so over this.  I hope it heals quickly. 

  • beacher4209
    beacher4209 Member Posts: 540
    edited February 2011

    im on 17 rads!!!!!Glad everyone sounds so good!! but im at my toughest place painwise right now. I got a blister the size of a dime on tpof breast plus little ones around and i itch,when i went in today the dr saw me first and canelled todays rad and said see how i feel tomorrow plus a new rx for percoset. i have pain from inside like the expander is squeezing me!!!!! ouchhhh!!!! help im scared againhow will i ever get through this i wany the expander to delate but she says its going to look so good when im done uggg,im not that vain,idony think?? 

     Did you all have lumpectomies,? Do you have your breast still? do you have a scar where they took the cancer out then sewed u back up? i just do not know how that works? they scooped all my inners out of my breast and then put expander in and sewed me up so i still have this thing in me stretching and pulling... i hate cancer i feel so alone now

  • Gingerbrew
    Gingerbrew Member Posts: 2,859
    edited February 2011

    Beacher, I am sorry you are feeling alone. We are all here standing with you and sharing lots of your experience.Rads sound simple but somehow it is just hard to do.

    I have a lumpectomy and have a scar where the tumor and some surrounding tissue were removed. I am not symetrical but I am beyond even noticing at this point in my life. 

    Hugs

    Ginger

  • Omaz
    Omaz Member Posts: 5,497
    edited February 2011

    ((((HUGS beacher!!)))))) 

    Maybe you would like to get a second opinion on your surgery for peace of mind.

  • beacher4209
    beacher4209 Member Posts: 540
    edited February 2011

      2nd opinion on what part?

  • Omaz
    Omaz Member Posts: 5,497
    edited February 2011
    beacher - I don't know very much about the process but I am wondering if another surgeon would have a thought on the expander. It really seems like it has been hurting you during rads - I don't know if it is supposed to do that or not.
  • beacher4209
    beacher4209 Member Posts: 540
    edited February 2011

    yea they would not have put the expander in if they thought i was going to need rads, but they did not ya know early noninvasive cancer...but there wasalot of it once thet got in there and was 1mila meter from my chest wall sssoooo that meant rads and i quess shecould have not put it but i planned on the expander but if i was awake i would have said skip it. some women do have this siuation not alot though i quess 

  • walker2222
    walker2222 Member Posts: 558
    edited February 2011

    Beacher - I had to have my right expander removed prior to rads due to infection and a hole in it. So it would not heal. PS said it had to come out. I was so depressed during that time but I reached out here and have been able to work it out. I feel for you and pray for you to get through this. God bless you.

  • suzieq60
    suzieq60 Member Posts: 6,059
    edited February 2011

    Beacher - (((((((((((((HUGS)))))))))))) sorry you're in pain.

    Sue

  • Victoria67
    Victoria67 Member Posts: 44
    edited February 2011

    One more boost tomorrow and then I'm done!  Very excited but a bit anxious too. Got my prescription for tamoxifen filled but I want to find out if I can wait 4 months before starting it as I have a big trip planned in June with some high altitude hiking. Guess I'll see what the BS and Onc say about that, I imagine they will want me to start straight away.

    Beacher, I'm so sorry you are in so much pain, I hope the doctors can give you some relief soon as it sounds so painful.  Am sending you lots of hugs.

    I had partial mx, scar goes across aerola right up to my armpit as the location of my tumors and the SNB meant it had to be one long scar. Like Gingerbrew, not too bothered about it ... I only was bothered when one of the techs said it was one of the largest he'd ever seen!! Not helpful.

  • suzieq60
    suzieq60 Member Posts: 6,059
    edited February 2011

    Victoria - I started Arimidex 1 month after rads last time. Congratulations on finishing tomorrow!!!!

    Sue

  • oakley
    oakley Member Posts: 206
    edited February 2011

    Beacher - so sorry you are feeling so low right now.  YOU ARE NOT ALONE that is for sure.  I had a lumpectomy and I have a pretty big scar (3 inches about) but my tumor was not large - 8mm.  Speak to the doctor about all of your feelings (your surgeon I suppose) and see what they can do for you.  Hang in there.  (HUGS).

    Victoria - yay for you one day early!  So happy for you - it feels wonderful not going this morning, and I don't miss that.  I am starting Tamox 2 weeks after rads because of a vacation.  I bet also since yours is four months away, maybe you start on the lower dose and then increase after you get back?  Ask your MO - I bet it's probably ok to start it after.  Where are you going?

    Sue - glad you didn't have to wait yesterday.  GO GO GO!!! 

  • bher
    bher Member Posts: 86
    edited February 2011

    beacher - You are not alone. I was not suppose to have rads either but my margins were close. Rads was hard on me too with an expander.  I finished about a month ago and even though it is still very tight, it is better.  My skin developed blisters too and the RO gave me Silvadene which helped.  I do not know much about what you can do about the tightness now unless you have your PS take a small amount of  fluid out.  They did this for me in the end (during my boosts) because I could not stand it and wanted to quit.  It helped to get me thru the rads but it got tight again.  The plan is to put the fluid back in but I just dont think I can do it now because I am still very uncomfortable. So sorry you have to go through this.

  • Teklya
    Teklya Member Posts: 435
    edited February 2011

    awwwhhhh, Breast Cancer it just keeps on giving and giving. . . 

    Teklya

  • rachel5738
    rachel5738 Member Posts: 920
    edited February 2011

    Beacher--sorry to hear about your probs through rads. I had lumpectomy so cannot help you with regards to expanders etc. I hope you can get some resolution.

    Boost #2 for me today--3 more to go. I feel energized to know that it is almost done!

    For those starting Tamox, I started Tamox about 1 month after chemo so I have been on it for approx. 2 months. I haven't had any problems -- had some hot flashes but other than that, I seem to be OK. Hopefully you have similar experience.

  • walker2222
    walker2222 Member Posts: 558
    edited February 2011

    Beacher - I deleted my earlier post because it was not beneifical to you.  Do what bher recomends with your PS, I know that is what I would do.  Hugs and prayers to you, you are not alone.

  • Mariposa109
    Mariposa109 Member Posts: 61
    edited February 2011

    I started my fourth week today and this weekend the skin of my areola started to peel. Under my boob its extremely red and painful and lets not even mention my underarm! It's dark red and brown. I am still in the calendula v/s biafine study but I am thinking of quitting because I cant use anything else (such as the aloe and miaderm I had bought). I also have itching and was told to try tylenol pm because it has some benadryl in it, but for the day time all the nurse said was "dont scratch it"...??? I'm worried about the condition of my skin since I still have about 11 rads to go, but all the nurse keeps saying is that everything looks very "normal" for the stage of treatment I'm at. 

  • lrr4993
    lrr4993 Member Posts: 937
    edited February 2011

    mariposa - I don't mean to scare you, but the red brown color and itching is where I was just before my skin fell apart.  Keep an eye on it and get some burn cream (I just got silvadene) as soon as it starts to blister/peel (assuming it does . . . hopefully not).  

    Thankfully mine fell apart only after the last whole breast treatment.  It is still raw, but looks better as I finish up the boosts this week.

    3 more!!!

  • suzieq60
    suzieq60 Member Posts: 6,059
    edited February 2011

    Irr - see if you can find Medi Honey over there - very small tube. You can't use it during rads but after rads my raw skin healed up really quickly using it.

    Mariposa - We can be doing SO well and then all of a sudden - the skin breaks down. I remember being VERY upset last time. Have they given you anything to dress the area with? Solosite was good too.

    I know I'm not out of the woods yet - could happen any day now. I keep checking under there, just in case.

    Sue

  • walker2222
    walker2222 Member Posts: 558
    edited February 2011

    Mariposa Have your RO check the skin. My skin fell apart between the 4th and 5th week. The dr gave me the silver cream. My RO stopped my bolus treatments on my last week of regular treatments because of it.

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