January 2012 rads

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  • bgirl
    bgirl Member Posts: 538
    edited February 2012

    Lucky #13 down today.  Getting itchy - saw RO today and got some cream.  In the shower this morning all the hair fell out in treated area( doing lower node area).  So now half my underarm is hair free!  It just made me laugh.  Always something new on this journey.

  • NWArtLady
    NWArtLady Member Posts: 360
    edited February 2012

    Ann, you're right: it's for cleaning up. I used the wrong term. Can I still claim chemo brain? :p

  • Ossa
    Ossa Member Posts: 919
    edited February 2012

    Annalive.

    Have never gotten a stage officially but on MO raport it states T2N1M0, when I googled it, it came up as stage IIB

  • lifechanging2011
    lifechanging2011 Member Posts: 48
    edited February 2012

    #9 today. Very red. I'm exhausted. Fatigue has definitely set in, however, many factors; 3 arthritis flairs in two weeks, report card week last week, fighting off a cold, and #9 rad treatment. I feel like I have led feet. I took off tomorrow in hopes of feeling better.

  • AnnAlive
    AnnAlive Member Posts: 450
    edited February 2012

    Ralston - I'm glad the blue bump is just a blood vessel! Come to think of it, my RO may have mentioned rads to prevent local recurrence as well as kill residual cells post-MX. I asked him in one of my first appointments whether radiation would be effective for me since it had been 3 1/2 months since surgery, and he explained that the timing is near the outer edge of how long he would prefer to wait, but that the treatment is still a benefit to me. You're right -- it's easier to say not to worry than to do.

  • AnnAlive
    AnnAlive Member Posts: 450
    edited February 2012

    NWArtLady - I guess you could say rads prevent local recurrence by cleaning up. Wink  We can claim chemo brain for a while yet. I have evidence of it every day!

    Bgirl - funny about the free half-shave. I didn't get hair back in my armpits since chemo and it's been 5 months. But I am losing my eyebrows and eyelashes for the 2nd time!

    Ossa - IIB is what it shows for T2N1M0 on the chart my BS gave me. It has the "5-Year Relative Survival" percentages too, but what does the "relative" mean? Do the stats assume our current treatments were done? My MO told me initially that my prognosis was "not good." But with presumably clear pathology, I guess it has improved??? I don't recall stats comparing before/after various treatments for a given stage.

    Lifechanging - Are you taking tomorrow off of work or rads? I hope a break with good rest will renew your energy and let you push on! I haven't hit that fatigue wall yet after today's #14, but dealing with Taxol side effects -- seeing a dermatologist tomorrow about my sore fingertips and messed-up nails.

  • Ralsper
    Ralsper Member Posts: 352
    edited February 2012

    "Not good"... Seriously? It's the first time that I heard something like that. Normally they give you a percentage of probably recurrence in 5 years depending your stage. I like that way much better than "not good". Well, this come from the woman that it is still trying to make peace with the meaning of Grade 3 (Aggressive) Wink

  • tnhelen
    tnhelen Member Posts: 63
    edited February 2012

    Booster 1 today!  4 more to go!  Sore as hell and have some blisters but will be glad to get it over.  I am religiously using my rads cream.  They told me I probably don't believe it but my skin looks good.  The doctor also gave me some percocets.  I may be digging into those next week.

  • chef127
    chef127 Member Posts: 891
    edited February 2012

    Time to put away my sports bra. I have a rash under my breast where the bra rubs but without the bra I'm hanging low( not a prettysight.) so the moisture does not evaporate.  I'll try the cornstartch. I hate the chalky feeling of it.

    My breast is covered with freckles. Now I have to watch for skin CA. No one told me that was a possibility........UGH.

    #20 today. Not  bad so far.

  • rjbaby69
    rjbaby69 Member Posts: 349
    edited February 2012

    Hi ladies!  Hope you are all doing well.

    I am so excited cause I only have 10 more to go!  Yeah!  I am so ready to get this over with.  I am now using the cream my RO gave me.  I have peeling skin under the fold of my breast and I noticed today that my nipple area was trying to peel too!  Ugh!  Went to wearing my sports bras cause they are lots more comfortable.  I usually go braless around the house.  Can't seem to find the time to lay down and put a fan on my boob.  The RO told me this would help dry out the area underneath my breast.  That may be true, but right now, I just can't find the time!!!

    Hope you all have a good day and treatment (if you are still having them) tomorrow!

    HUGS!

  • Ossa
    Ossa Member Posts: 919
    edited February 2012

    Finished # 10, staring to turn a bit red, not sore hope it stays that way...4 more weeks.. 

  • Susan726
    Susan726 Member Posts: 16
    edited February 2012

    Two more boosts this week and I'll be done. The itching and the rash cleared up and now my skin is just peeling. The boosts are hitting a smaller area, so the rest of the breast that was being treated is starting to heal. I'm more pink than red now. Just using the Aquafor. So much better than last week.

  • mags20487
    mags20487 Member Posts: 1,591
    edited February 2012

    9 down and only 26 to go.  Must say I kinda feel bad for you ladies that have to get the breast irradiated.  Mine are gone so just zapping the chest wall and lymphs.  5 last ones will be boosts to the scar line.  No signs of anything yet.  Started back at gym (Zumba classes) to help combat the oncoming fatigue.  Using aquaphor 2x a day --when I remember to put it on.  Also wearing my lymphedema sleeve everyday from treatment to bed to help keep the swelling beast away!

    Maggie

  • lifechanging2011
    lifechanging2011 Member Posts: 48
    edited February 2012

    Hi AnnAlive,

    I took off work today. I don't want the rads to take longer than they have to. # 10 today, only 23 more to go. Red today but not sore, thank goodness. The fatigue hit hard. Not necessarily all due to rads, but no matter how long I stay in bed I don't feel rested. I guess that's the definition of fatigue. I hope for a breather soon.

  • Ralsper
    Ralsper Member Posts: 352
    edited February 2012
    #13 done. My breast is barely tan and not sore, but my underarm is sore. It seems that I missed to apply Aloe Vera in that area  Undecided
  • Christyn37
    Christyn37 Member Posts: 12
    edited February 2012

    Had #25, my last whole breast tx today. I start boosts tomorrow. Talked to the RO today about the treatment plan and, as expected, they can't do the electron radiation on me. He explained that my tumor bed is too deep in my breast since the electron radiation shoots shallow. So it will be the 3D conformal photon radiation I've been getting all along but just to the surgery scar and tumor bed area and in a stronger dosage. The great news is that since it won't be electron they have cut me back from 8 boosts to 3 and I'm done on Monday!!! OMG! I can't believe they cut a whole week off my tx. I will end up with 28 total treatments. I'm still doing great on the skin. Dark pink under my arm and upper chest area close to the arm. I have a little pink under and on my breast and still have the rash on my upper chest. The doctor really didn't think I would do this well since I'm fair skinned and big breasted. Of course, he had also told me from the start that the worse week will be the week after it ends and I'm not there yet. He wrote me a prescription for Silvadene cream just in case I start to blister after I'm through. We said our goodbyes to each other today as I won't see him again. My MO also said he doesn't need to see me again as well as my BS. Guess I'm back to my nurse practioner at the GYN office. I have refused hormonal therapy and both my RO and MO support my decision. RO said I need a mammogram in 6 months and then yearly after that and my nurse practioner is going to do breast exams for me every 6 months. The fatigue has been okay. I take every Wednesday afternoon off and take a 2 hour nap and I take naps on weekends so that, along with a good dose of caffeine daily, has gotten me through my workdays. Thanks all you ladies for getting me through this in one mental piece. There were days I wasn't so sure I would make it. I'll continue to check in and let you know how the week after works out for me for any that are curious how it might be.

  • tnhelen
    tnhelen Member Posts: 63
    edited February 2012

    3 more boosts to go!  My skin has split in two areas, under my breast and under my arm and it is very hot.  The other doctor examined me today and gave me another medication Xero which has really helped the pain.  I want a whole barrel of it so I can just dive in!  I did great up until about the end of the 5th week and then wham........party over.  Something else I started doing on week 5 was taking vitamin D because my level had dropped so low.  I asked the RO and he said it was fine that he believed your body tries to heal itself and he supports vitamins,etc. and doesn't think it has any effect on your skin.  Then by the end of that week I was a mess.  But I know it's cumulative.  Needless to say, just in case...........no more vitamin D for me!

    Hugs to all of you.

    Helen

  • lifechanging2011
    lifechanging2011 Member Posts: 48
    edited February 2012

    Hi Christyn37,

    I was curious why the week after rads was going to be the worst? Also, why did you decide not to do hormonal therapy?

  • twistedsteel
    twistedsteel Member Posts: 156
    edited February 2012

    They say the damage to your skin from the rads you are getting today doesn't show up for 4 days to a week. I found thismto be true for me.

  • Christyn37
    Christyn37 Member Posts: 12
    edited February 2012

    Hi lifechanging2011,

      You know how you leave food in the microwave oven to continue cooking for a minute or two after the heat is off? It's the same with radiation. We keep on cooking even after the tx is done. My doctor and radiation tech both said about 1-2 weeks beyond the day you finish the rads before you are sure you're done burning.

      As for my decision not to do hormonal therapy my MO showed me statistics for my risk of recurrence if I did nothing more than a lumpectomy, if I added on radiation, and if I did hormonal therapy. I had to choose the number I was comfortable living with. Since there is such a large decrease in risk by doing radiation therapy I agreed to do it (though I actually also looked into the Van Nuys Prognostic Index, used for DCIS, to see if I was comfortable skipping it and I wasn't). Though I have non-invasive cancer, clear margins and a small tumor I had high grade cancer and at that point I quit fighting radiation.

       The statistics I've seen when tamoxifen is used in conjunction with radiation therapy cut your risks only a couple of percentage points more over 5 years. Besides the menopausal symptoms brought on by tamoxifen there are also the risks of blood clots, strokes, uterine cancer and cataracts. I've already been through menopause and would probably have to use AI which have less SE than tamoxifen but they have their own. They include possible heart attacks, broken bones and osteoporosis. I really didn't want the risks or the walk back through menopause hell and since I'm older I'm taking the chance to pass on the pills. I probably wouldn't make the same decision if I were a lot younger and had many more years ahead of me but I'm not so I'm going to take my chances.

  • Ossa
    Ossa Member Posts: 919
    edited February 2012
    !2 done - 16 to go.. Getting a bit red and sore. Got hydrocortizone cream today, hope it will slow the burning down. Was told they will most likely use my bolus one more week then take it off.. MO told me the bolus actually makes your skin hotter, but it is needed so rads it just millimeters below the skin as it could have been "contaminated" during surgery.. Countdown until treatment is on.. 24 days and I am done  (other than exchange surgery) Mammo on good side came back good YayLaughing Have a great weekend ladies
  • Rockym
    Rockym Member Posts: 1,261
    edited February 2012

    #27 down!  Monday will be the last regular tx and then I begin the 5 boosts.  I can't wait to finish.  I Have a MO appointment coming up and I'm sure he will hand me the tamoxifen script.  I think I'll wait until March 1st to begin.  I want to give my body a rest from treatments and medicine.  I also think I'll ask about testing my estrogen levels.  I was in peri-menopause before the dx of BC and I haven't had a period since October.  I have a feeling you have to be without a period for 12 months before they consider you post-menopause, but it's a good question for me to ask.

    Have a great treatment free weekend everyone!

  • msmouse
    msmouse Member Posts: 60
    edited February 2012

    #20 of 33 in the can! Still no significant skin changes other than some really deep itching the other night. Took an Advil PM and was gone by the AM. Using Dove unscented body wash, Target brand aloe vera gel & generic aquaphor. Doing the range of motion exercises given to me by the RO and strength workouts 3-4 xaweek and daily cardio for 30 minutes 7 days a week. Some mild fatigue starting last Fri but gone by Sunday. Today was the worst in the fatigue dept; woke @ 5:30, fed the animals and was going to rest for a bit. I didn't wake up until 12:30p! The count to come are 8 full breast rads then 5 boosts. Can't wait to be done. Hang in there ladies; the  finish line is in sight!

  • chef127
    chef127 Member Posts: 891
    edited February 2012

    Rockeym,

    Good idea to rest for a couple of weeks before starting the tamox. It may be your last chance to rest from tx. for 5 years. I had my estro levels checked and they came back negative. Menopause all the way. So its most liklely arimidex for me????????? If i decide to give it a try.

    Only 3 more WBR and then I start the 10 boosts. burn baby burn.

    Enjoy your weekend off

  • treegirl
    treegirl Member Posts: 24
    edited February 2012

    Rockym:

    I think to be truly post menopause you not only have to be period-free for 1 year or more but all symptoms need to have stopped. I haven't had a period in 3-1/2 years and was done with hot flashes too until breast cancer diagnosis. I am not taking hormone therapy nor did I do chemo so all docs say it is a stress reaction that hot flashes have returned.

    Msmouse: I am at exactly the same point as you, 20 out of 33 done. My symptoms so far are manageable, a little itchiness, redness, soreness, not significantly worse than post surgery. I am praying they don't get worse. Just so glad it is Friday and two days off! Sounds like you are really lving healthy, may be an inspiration for me to get more focused on that. I was really good pre and post surgery but slipped into stress and fatigue induced snacking and blowing off exercise opportunities since. 

  • lifechanging2011
    lifechanging2011 Member Posts: 48
    edited February 2012

    Hi Christyn37,

    Thanks for the information.Great analogy with the microwave. Also, thanks for sharing your story. I'm not looking forward to the SE with the tamoxifen. I'm 48. I want to reduce the possibilities of a recurrence  as much as possible because if it comes back I lose my breast. It's all very stressful.

    #12 today. 21 to go. I'm very diligent about using the lotion 3x a day all over the irradiated area, but my side got so itchy today I thought I was going to scratch my skin off. It's a spot I didn't even think would be affected.  I'm trying to be proactive but sometimes I'm just frustrated.

  • lifechanging2011
    lifechanging2011 Member Posts: 48
    edited February 2012

    Is heartburn associated with radiation therapy? I thought I saw someone mention it in a post but didn't pay much attention to it because I had experienced it. I've had heartburn most of the evening and that is not usual for me. Any input?

  • Ossa
    Ossa Member Posts: 919
    edited February 2012

    Had heartburn for a few days during the first stage of rads

  • tnhelen
    tnhelen Member Posts: 63
    edited February 2012

    One more treatment to go!  I am so glad - then tamoxifin.  My MO told me it would help reduce the risk of occurrence in my other breast by 50 percent.  She made the comment that both breasts had been in the same place throughout my life and one developed cancer so the blueprint is there for the second breast.  That has stuck with me and I guess it's true.  She also said if the treatment was worse that the disease I could always quit taking it if I could not tolerate it.

    I have been through menopause also.  I was a little surprised that she didn't suggest the other medication since I am post menopausal.

    Have a good weekend.  Monday's the big day for me!

    Helen

  • Momine
    Momine Member Posts: 7,859
    edited February 2012

    Helen, why tamox if you have been through menopause? I really think you should ask about that.nI had an onc suggest the same strategy, but everything I have read saysbthatan AI is better. Better survival, less dangerous SEs.

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