February 2010 radiation starts anyone?

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  • MaryNY
    MaryNY Member Posts: 1,584
    edited March 2010

    Yes, the gray area. The oncologist who requested the test gave me the option of chemo/no chemo. I felt I didn't have enough info to make that decision so went to see another oncologist who said I should definitely have chemo. Unlike you, I had two positive lymph nodes, so I think the chemo decision was the right one for me. But at least the score of 18 showed me that the cancer wasn't as agressive as I thought it was.

  • YramAL
    YramAL Member Posts: 1,651
    edited March 2010

    MaryNY-

    I think the 2 positive nodes would have made the decision for me in favor of chemo as well. 

  • Karen09
    Karen09 Member Posts: 320
    edited March 2010

    20 down, only one left to go on Monday!!!!!   I'm excited!

  • YramAL
    YramAL Member Posts: 1,651
    edited March 2010

    Karen09-

    That is wonderful!

    Mary

  • chinablue
    chinablue Member Posts: 545
    edited March 2010

    Karen 09 - Please tell us how it feels to walk out of your last rad?  I think it must be great and somehow a little disconcerting.  Did your onc lay out a plan as to what is next?  Are you done...done?  I mean now do you just go for check ups once a year?  Oh, the thought of having long stretches without seeing a doctor's office sounds heavenly.

  • DiDiT
    DiDiT Member Posts: 135
    edited March 2010

    Congrats Karen!!  Do they have a bell to ring at your center?  For the ceremonious last treatment?!  Celebrate!!!

  • Karen09
    Karen09 Member Posts: 320
    edited March 2010

    Thanks ladies!  I'm quite excited about tomorrow!  I'm not sure if they have a bell or not.  I haven't heard of that. 

    I'm pretty much done now.  I can't do hormones because I'm triple negative but I'm taking Zometa to hopefully keep the bone mets away.  I had my first dose the other week and didn't have any side effects and I'll get it every six months for 3 years. 

    You're right Chinablue - no appointments for awhile sounds so nice!  I have a couple doctor's appointments coming up in the next couple months but that's such a change from so many for so long! 

    Hang in there everyone! 

  • jacee
    jacee Member Posts: 1,384
    edited March 2010

    Karen...big congrats to you. Enjoy this Spring weather with no treatment appts.

    I'm right behind you in a week or so. Finish 4 field radiation this Friday, then have 5 boosts to my scar line next week. Then DONE!

    My skin is really starting to breakdown. Very itchy and red. Changed drastically over the weekend. Went braless the whole weekend. Using biafine and calendula.

    Scheduled for routine colonoscopy in the a.m., then mammogram on Apr 2, and port removal on Apr 14. THEN hopefully things will slow down. It's been a long year of surgeries, chemo & rads. Working on scheduling recon in the fall.

    Hope all you ladies are tolerating this well. I'm hurting pretty bad, but I know relief is around the corner.

    Joni

  • thriceblessed
    thriceblessed Member Posts: 39
    edited March 2010

    Lieberman1,

    Encourage your mom that what's 'normal' varies by the individual.  I too was very tired even at 3 treatments out and I'm in my early 50's, if that helps.  Now at 12 / 28, I'm still tired just about the same (not really any more).  I try to get out and walk daily for 1/2 hour and that seems to help (yep, I rest before and after the walk...).  Encourage your mom to hang in there...soon we'll all be like Karen...celebrating being done!

  • YramAL
    YramAL Member Posts: 1,651
    edited March 2010

    Yesterday was lucky #13. 20 more to go. I am starting to have a radiation reaction under my breast-a red patch. So far, it doesn't itch or hurt, but I'm guessing it's only a matter of time. The nurse said to stop putting aloe under my breast and keep the area as dry as possible. I don't know why, but some small part of me is saying that if I had been keeping the area dry, she would have said to start using the aloe! 

    Mary 

  • chinablue
    chinablue Member Posts: 545
    edited March 2010

    Hang in there Jacee! I am so sorry to hear that you are hurting.  Don't feel guilty about taking a pain reliever (advil, motrin, whatever your doc advises).  Try to treat yourself to quiet moments of mindless TV, meditation, or stupid magazines.  

    Geez .. mammo, colonscopy, port removal...you really know how to live it up!  

    You have been through so much.  Do something you love (after 4/14/10).  We will celebrate with you online. 

  • msmpatty
    msmpatty Member Posts: 818
    edited March 2010

    Mary - LOL!   The radiation people seem to be all over the place with skin care recommendations.   The tech admitted to me this morning that they all recommend all kinds of different things, it just depends on who you go to.   So...I'm using stuff that ladies on BCO have found useful, even though my rad office doesn't specifically recommend them.   My little secret....

    Patty

  • jacee
    jacee Member Posts: 1,384
    edited March 2010

    Colonoscopy done!! Everything normal. I love good news. The best thing was, I got a report the minute I woke up. Every test should be that way.

    They had to use my port to access a vein after blowing out 2 in my left arm. Now I'm wondering if I should keep my port???? But my recon surgeon wants it out by surgery time.

    Had my first haircut since chemo last night. Hair is only about an inch long, but cut some of the white "down" stuff off that grew first. It's so nice to have some progress.

    Patty...you are right about all the skin recommendations. My techs finally told me, there isn't really one thing that works better than another..just to use whatever feels good to me. I use oils on weekends when I don't have a treatment and they can stay on the skin longer. And Calendula feels the best to me, otherwise. But my skin is so red and bumpy..I dare say, nothing is really working. Knowing I'm almost through makes it all bearable. 22/30 done.

    Joni

  • jerseyjean
    jerseyjean Member Posts: 3
    edited March 2010

    i am in third week of rads, so far so good, aloe should be applied 4 hrs. before radiation and anytime after. my next step is aromocin... i have early stage 1, no node involvement, and an oncotype test score of 3,  no chemo.... i dont know if i want to take aromocin ....any advice. thanks jean

  • MaryNY
    MaryNY Member Posts: 1,584
    edited March 2010

    jerseyjean: That's a beautifully low Onco score. You must have been so happy when that result came back! I don't know anything about aromasin. Maybe someone else will chime in on that.

  • msmpatty
    msmpatty Member Posts: 818
    edited March 2010

    Jerseyjean - I'm pretty confused about all the hormone therapy options...Aromasin being one.  I googled the name and found their website, which has some good information.   Aromasin apparently works differently than Tamoxifen in that it actually inhibits the body's production of estrogen while Tamox works by preventing estrogen from "feeding" any cancer cells that are hanging around.  The only thing I am sure of is that if your cancer is hormone receptor positive,  doing hormone therapy is really important to prevent recurrence.  As to which one...guess we have to rely on our Oncs!

    Patty

  • precioustime
    precioustime Member Posts: 233
    edited March 2010

    SoCalDawn- I also am on the TOMO machine and I agree with the sound it makes.  I count 21 times going around me and my treatment for the day is done!!  I was told by the RAD Oncologist that she doesn't use the TOMO machine on other breast cancer patients.  Because of having a lymph node positive in the mediastinal node is the reason.  They also use a Bolus on me that is suppose to direct the radiation closer to the skin area-- she said they treat it like they do skin cancer.....

    Only 3 more to go after today!  I will celebrate St. Patricks Day this year for sure!!  I am usually the last patient they have at 6pm -- so I am going to Ring that bell really really good!! 

    My DH also said that I have little red dots on my back -- I guess the radiation beams go right through you?  

    Even using Silvadene Cream and a Petrolatum mesh applied at night-- I still find my upper chest itchy!!!  Maybe I should still use Hydrocortizone 10?

    Happy Weekend Everyone!!

    Loretta

  • micheleboots
    micheleboots Member Posts: 1,993
    edited March 2010

    I had my rads canceled for the day today.  I can't decide if i am happy or sad...after all it gave me a long weekend, but that means that I am done a day later...oh well..I think my chest could use the break...

  • YramAL
    YramAL Member Posts: 1,651
    edited March 2010

    1/2 way done as of yesterday! Woo hoo! 9 more full breast treatments and 7 "boosts" at the end. My doctor says people always hear boosts and think more powerful, but it's actually a narrowing down of the field of radiation to just the area of my tumor and a little bit around it. 

    I have a pretty red painful area directly under my breast where skin contacts skin when I'm not wearing a bra. I've been told to keep the area as dry as possible, which seems to help a bit. Otherwise, no complaints.

    Mary 

  • Anonymous
    Anonymous Member Posts: 1,376
    edited March 2010

    HI,

    I have had 18 out of 36 rads skin is darker but not red  yet. so I am doing pretty good so far. Was a little fatigued last night but it passed after I ate. Can't wait to be finished!!

  • SoCalDawn
    SoCalDawn Member Posts: 51
    edited March 2010

    YramAL,

    That area below is also a hot spot for me. Forgive me if I have already suggested as I am posted in 2 areas on this subject. My dr recommended cutting up an old soft t-shirt and placing the fabric underneath to prevent skin to skin contact. That has helped me a lot.

    I am 20 down out of 34. Itchy...very appreciative of cortizone.Tender. Ready for that to go away.

    Have a beautiful Sunday, ladies!

  • msmpatty
    msmpatty Member Posts: 818
    edited March 2010

    15 down, 13 to go!   Woke up this morning with a small bumpy itchy area on my chest, my first reaction so I count myself lucky.   We are getting there ladies!

    Patty

  • DiDiT
    DiDiT Member Posts: 135
    edited March 2010

    First - thank you all for sharing updates on side effects...I'm of course, hoping I don't get skin breakdown as I'm anxious to get that tissue expander replaced (the proph side removed d/t infection) But ps will not do surgery if any significant skin stuff for fear of acquiring another surgical infection - which I understand, just wanted to be sort of done by summer...

    As with many of you - it's been a looooooooonnnnggggg year!

    Patty - and others ?'s re: hormone suppressant  - I'm no expert and haven't done any research myself, but my onc is young, progressive, thorough, super intelligent, and very caring....

    In regards to Tamoxifin vs. Arimidex (or other names) That hormone levels should be checked prior to the start of the therapy and periodically throughout the duration if not yet menopausal - when menopause reached, should switch form tamoxifin - according to her, drug no longer effective AND risk for use continue ie endometrial cancer.

    Again, I don't understand all of this, but I do ask alot of questions - I was planning on possible hysterectomy with exchange surgery due to endometrial ca risk involved with Tamoxifin - she tested and said I'm currently high end menopausal range, will check again prior to starting med, but if menopausal - will not take tamoxifin.   And if I do start with it and have the hysterectomy, she would take me off at that time and switch to Arimidex.   I really wonder about this....I know many women who've been treated entire time with Tamoxifin and had hysterectomies either prior to being started or sometime during treatment....

    So many possibilities.........

  • YramAL
    YramAL Member Posts: 1,651
    edited March 2010

    I showed the nurse the painful red spot directly under my breast today. I had been keeping the area dry as possible with cornstarch powder as directed, but this morning, after my shower, the area started to peel. The nurse thinks I have a yeast infection in the fold beneath my breast. That makes sense to me because I frequently got them there before I even started radiation. So now, I'm using an antifungal cream under my breast, and I am hoping for some relief. The rest of my breast is a lovely light pink, but doesn't hurt at all, except for some allover breast tenderness.

    18 down-15 to go!

    Mary

  • chinablue
    chinablue Member Posts: 545
    edited March 2010

    16 down 12 to go!

    Has anyone noticed breast shrinkage?  My foob from diep reconstruction seems to be getting smaller. Ug!!  I have a d cup on my natural and now less than a b cup on my foob.  Heavy sigh. 

  • MaryNY
    MaryNY Member Posts: 1,584
    edited March 2010

    This group is going very quiet, the March group is almost passing us out in number of posts. Cry

    Chinablue, haven't noticed any breast shrinkage, but I didn't have reconstruction.

    Today was #15 for me. I'll soon be halfway there. But my arms hurt so much, now fingers too so it even hurts to type. Nurse said it may be due to holding my arms over my head, but I expected the achiness to go away after a couple of days instead of which it's just getting worse.

  • YramAL
    YramAL Member Posts: 1,651
    edited March 2010

    MaryNY-

    I have a cramp in my neck these days. I'm sure it's from holding my arms over my head and holding so still every day. My fingers don't hurt though....

    Today was #19 for me. I'm still having trouble with the sore spot under my breast, but the anti-fungal medication seems to be helping some. It is way more comfortable for me to wear a bra than not because it keeps my skin from touching skin. Overall, my breast is turning a lovely salmon color.

    Mary

  • micheleboots
    micheleboots Member Posts: 1,993
    edited March 2010

    It seems that the ladies with lumpectomies have a harder time with sores and blisters than us non breasted ladies...or is it my imagination?  18 down/7 to go...

  • msmpatty
    msmpatty Member Posts: 818
    edited March 2010

    Michele - Speaking as a lumpectomy lady, so far my skin is doing great.  (17 down, 11 to go)  My rad Onc said it is really difficult to predict who will have problems and who won't.   She said  it is sometimes related to how much breast tissue there is... the more tissue, the more reaction.   So that could support your theory that non-breasted (LOL) ladies get by a little easier?

    MaryNY - Sorry to hear about your arm pain.  Are you holding your arms/hands really tensely during the treatment (like isometric exercise)?   Are they using supports to help your arms stay in position without the muscles doing all the work?   It doesn't seem quite right to me that you are having this much achiness.

    Mary - I've also got a very nice pinky tan going.   Too bad no one can see it (without getting arrested that is!).

    Patty

  • SoCalDawn
    SoCalDawn Member Posts: 51
    edited March 2010

    I am 22 down of 34. My little irritating, itchy, bumpy rash turned angry and multiplied. I will leave it at that. Switched from cortizone to RX so am looking forward to a good night's sleep. Regretting not always using sunscreen on the decolletage. (sp?) The rest is dark pink. I am also itchy underneath. Looking forward to April 1. Best to all!

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