June 2010 Rads

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  • NotAgain2015
    NotAgain2015 Member Posts: 223
    edited July 2010

    Hi everyone, hope you are enjoying your weekend!  I'm almost half-way - 14 out of 30 treatments and as of last night my breast hurts.  It's feels like where I envision the lumpectomy took place.  I've got to take 4 advil every 6 hours or so to keep it at bay and I have to wear a sports bra as I feel I need support, like I want to hold it up.  Riding in the car, I feel every bump.  Has anyone else experienced anything like this?  I see others mention pain at times, and I've felt those sharp shooting pains, but those are fleeting - this is constant.  Just wondered if this is part of it or if I might have something going on. 

    Welcome marita, glad you have joined us - we'll get through this together.  I'm sorry that this experience has you so down.  It is different for each of us - where we are in life when it touches us.  It sounds as though you have been through alot and then this on top of everything.  Does your hospital system offer any counseling?  I know at first I felt like a deer in the headlights, immobilized by it, but then I thought shoot, I'm going to live and do the things I love.  I hope I beat this completely, but just in case it is lurking and plans to surprise me later, darn if i'm not going to make the most of everything while I can.  That's my pledge to myself for now anyway.

  • Blarney1828
    Blarney1828 Member Posts: 17
    edited July 2010

    Has anyone experienced increased peripheral neuropathy during radiation? Got it from Taxol; it was decreasing and seems back with a vengeance the last couple of days.

  • samsue
    samsue Member Posts: 757
    edited July 2010

    Kickon2it - I used the sports bra because it help hold my breast tight. It always felt the bumps of even walking. The strangest part was the "empty" feeling it had, not sure it it was because the numbness where the scar and tissue was removed or what. It is definitely a strange feeling!

    Glad to report that my pink has turned to a "tan" look. Doubt it the girls will match any time soon and I'm not about to hang one out to get some sunshine by itself. Would like to have been able to use the emu oil during the rads because it would have helped with the dry skin.

    It's raining tonight, it sounds so peaceful. If I could turn the AC down about 20 degrees (I'm flashing) I would make a cup of chocolate and curl up with a book. More important though is to thank all of you for sharring - I think talking to you ladies on this forum has been very helpful - you all understand the gambit of emotions that occur. Laughting one minute, crying the next.  And eating chocolate!

  • rayofsun
    rayofsun Member Posts: 204
    edited July 2010

    blarney, i am having increased periods of my hands falling asleep when i sleep, my PT says it is from positioning with radiation and the tightness.

    ray

  • BarbaraA
    BarbaraA Member Posts: 7,378
    edited July 2010

    Ladies, I am now 10 days post tx and the nipple is very tan and the red dots are fading. The skin above the breast and over the sternum is also tan and starting to peel. It's like a sunburn-type peel, no break in the skin. I still use emu oil 3xday.

    You will be happy to know that I have not had a fatigue attack in three days. YAY! I may be past that. I still get these twinges of pain deep in the breast but they pass pretty quickly. The armpit stopped hurting during tx and still is OK.

    Anyway, feeling pretty good.

    So there is a semblance of normality after rads, ladies!

  • Access2010
    Access2010 Member Posts: 33
    edited July 2010

    Hi ho June-posse! 

    I enjoyed the Lilith Fair concert in Indianapolis yesterday-- that was some good medicine!

    Am back on rads after Friday break and a long weekend; surgical scar is still opening and oozing. Doc says that radiation is harsher on "folds" or creases and the skin breaks down more easily there. My scar is quite a deep fold. So, we're covering it with a "second skin" type of dressing, trying to keep it dry and not wiping off new cell layers.  I only have 6 more treatments to go so I'm going to hang in there. Doc has prescribed some pain meds so that'll help me sleep at night. 

    Soon, Soon, Soon! 

  • eileenr56
    eileenr56 Member Posts: 135
    edited July 2010

    So how is everyone doing.  I  had number 9 today out of 23 whole breast and some boosts after that.  I think I'm a little puffy, but not  pink or red yet.  I imagine that's coming soon.  I to am trying to keep the area cool and dry.  I moisturize and have some gel packs in the freezer that i wrap up and put on top of my shirt. 

    So far so good.   

  • Ana1973
    Ana1973 Member Posts: 88
    edited July 2010

    Hello ladies...Had my SIM today for boosts that start on Friday...the end of rads is getting closer! I'm so happy because my skin is screaming for the rads to stop. My breast is red, itchy, achy and down right uncomfortable.

    I'm happy to hear we are all making head way through this part of treatment. Hang in there ladies we are almost done!

    Hugs, Ana

  • allisontom911
    allisontom911 Member Posts: 425
    edited July 2010

    Hi Everyone, I have 8 treatments left. My underarm is horrible. skin is breaking down. It had turned purple but now the skin is peeling and it is raw and red under that. YUCK. I have a nice rash on my chest so I have cream for that. I also have cream for my underarm.

    Trying Emu Oil but I guess this just happens sometimes. Anyone else? I had a MX so no breast to get involved. I am doing delayed recon also

  • mixin
    mixin Member Posts: 48
    edited July 2010

    I have 3 more boosts to go but hit a bit of a snag today. The plastic stickers they put on to keep the field marks intact have caused a skin reaction. They started getting itchy the day after they put them on; she looked at them today and said they needed to come off.

    So off they came... all 5 of them, along with my skin, down to blood on one. It's really uncomfortable to have even the softest material touch them. My armpits are sensitive and one is slightly swollen and partly numb. I'm thankful I'm almost done and that I made it this far with no real discomfort..

    I saw a young woman yesterday; she had lost her hair, tubes were hanging, she had radiation burns and was in a wheel chair. She gave me such a wonderful smile when I spoke to her.. she touched my heart. I hate cancer; I hope we live long enough to dance on its grave.

  • allisontom911
    allisontom911 Member Posts: 425
    edited July 2010

    I have seen others talk about the tape they put over the marks. I dont have that. They redo the marks every day. And over the weekends they come off totally and never has seemed to be a problem. I am allergic to the tape...

    mixin - hope you heal up ok!!!

  • mixin
    mixin Member Posts: 48
    edited July 2010

    allisontom911: Thanks! I think they will be ok by tomorrow. I have silver sulfadiazine and that did a good job on the small raw spot in my armpit.

    Boy, these treatments are pretty tough on our poor bodies; I always thought breasts were beautiful... but I'm sure re-thinking that as I look at mine. And my armpit.. gah!!! Everything turns such an odd color/texture for some strange reason.

    My techs used body paint on me, along with sharpie markers..those colors are pretty. I have green, blue, purple and black. Xs, lines, squigglies, dots... LOL, some day, this all will be but a faint memory.

    Ana1973: Can you take some ibuprofin to help with the pain and discomfort? It helps me a lot.
  • Dilly
    Dilly Member Posts: 655
    edited July 2010

    Hi Ladies, well my count is 25 down 8 to go.  In about the same condition as others, pretty darn uncomfortable (and really tired of lukewarm-cool showers!)  But - 8 to go is encouraging, there's light at the end of this tunnel.  I've peeled a couple of times, gotten swollen, ultra-sensitive, red and bumpy, itchy, very grumpy, fatigued at times, and so on. 

    For the skin, Miaderm and emu oil, and exposure to the air, is what I've settled on as the most helpful.  Cool cloths and aspirin or equivalent helps some.   Rad Onc is doing 19 zaps, break with the 8 boosts, finish up with 6 zaps.  He thinks it gives the skin a break during treatment, and is helpful in minimizing problems.  Tomorrow will be boost 7.  I am looking forward to, and steeling myself for, the last 6 zaps.  At least there will be two weekends included in this last 8 tx...

    Best wishes to all, and hang in (or out) there gals, we're almost done!

  • faithfulc
    faithfulc Member Posts: 284
    edited July 2010

    22 down now.  6 more regular to go and then 5 boosts.  There is a visible tan, but skin is intact.  A bit of discomfort under the armpit but other than that, no thickening, itching, peeling, etc.  I hope I can pull through without any complications.  

    Did lab again today.  WBC went from 2.7 back to 3.2.  Good news.

    I put on emu oil right after treatment (4pm), again around 7 pm, and then right before bed.  The next morning I put it on first thing in the morning and then around lunch I put on 100% aloe vera (Fruit of the earth).  I don't put anything else on. 

    At home, I go topless as much as possible, pretty much from 9pm through the next morning. I do wear a bra during the day (I work full time) but leave it unhooked most of the time.  The bra helps protect the nipple from rubbing on clothing.

    Yes, the end is in sight. I hope we all go through this and regain our health.  Cheers.

  • ginadmc
    ginadmc Member Posts: 263
    edited July 2010

    17 down and 17 to go. So far, my skin is holding up. I'm tan and get a liitle redder by the end of the week but the weekend helps. I don't know if I'm having any boosts. I meet with Rad Onc tomorrow so I will ask him then.

    I've been using L'Occitane ultra rich body cream but am running out. I'm going to start using my emu oil next.

    Has anyone heard of Calmoseptine? An acquaintance (BC sister) told my husband about it. It's not prescription but it's behind the pharmacy counter. I read about it and it looks like it's for burns. This woman did have radiation burns at the end of her treatment and used this stuff and it worked remarkably well to heal the burns. She was kind enough to order some for me so I'll pick it up today, just in case.

    Good luck to everyone with their treatments!  Gina

  • Blarney1828
    Blarney1828 Member Posts: 17
    edited July 2010

    Makes sense I wondered about that. Thanks!

  • chita
    chita Member Posts: 48
    edited July 2010

    I finished my last of 33 treatments today!  I baked brownies for the staff, they were great.  I'm counting the days till I can wear a regular bra again!  My doc says my skin will get worse before it gets better, about a week more and then it will start healing.  I'm so looking forward to that!  Hang in there everyone!

  • Access2010
    Access2010 Member Posts: 33
    edited July 2010

    Yay Chita! You did it!  After today I'll just have 3 more to go!  Good to know that things dip down for a bit before it gets better. I'll be on the first flight out to Aspen, Colorado as soon as I'm done!

    Have a restful weekend June-petals!

  • Ana1973
    Ana1973 Member Posts: 88
    edited July 2010

    Regular rads are OVER! Just 7 boosts left! I don't think my skin could take another day of radiation and now that I have learned (thanks to Chita) that the skin will get worse before it gets better, I will be babying my skin a little longer.

    Congrats to all those who have finished, I'm right behind you. Then I hop on the Tamoxifen train..I hope that's a smooth ride.

    Enjoy your weekend!

  • Iamstronger
    Iamstronger Member Posts: 378
    edited July 2010

    Woo hoo!   I finished 33 zaps yesterday!  So ready for a day without zapage!!!  I didn't post too much here, but you ladies really helped keep me going.

    I will start tamoxifen in a couple of weeks.  So, Imaybe  will see some of you there.

    V

  • eileenr56
    eileenr56 Member Posts: 135
    edited July 2010

    Well, today I had number 11 (out of 23 whole breast, boosts after).  So far so good. not red, maybe a little puffy, i'm not even sure about that. I do sit in my house topless. It is 100 degrees here so I'm trying to stay cool and dry.   So half way (kindof) through the whole breast.

  • mixin
    mixin Member Posts: 48
    edited July 2010

    Keeping cool and dry is tough when it's a hundred degrees with high humidity. Topless is good!!

    I have 1 more boost left; I feel like a whole new woman today. 

    Hang in there June ladies... and have a great weekend. 

  • chita
    chita Member Posts: 48
    edited July 2010

    Now that I'm done I feel more fatigue than ever.  Has anyone experienced this? 

    Ana1973, vmarie : I start Tamoxifen August 1.  Which blog will you be on?  Shall we start an August 2010 tamoxifen thread?

  • Ana1973
    Ana1973 Member Posts: 88
    edited July 2010

    Chita- I think that's a great idea...since we have to be on it for 5 years, sharing info would be so helpful. I start Tamoxifen on Aug 9th. My Onc said to start taking it 1 week after I finish rads. So far I have heard a lot of women are tolerating it well...I hope we do too. Let me know if you do start an Aug. 2010 thread...I'll be there :)

    Ana

  • Access2010
    Access2010 Member Posts: 33
    edited July 2010

    Good morning June-clan!

    I also like the idea of August Tamoxifen-Starters! I'm wondering about the variation in suggested start times for Tamoxifen? One says "in a few weeks" while another says 1 week later.  My doc said that I could start it the next day if I wanted.  Hmmmm, what was the reasoning?

    3 more to go! 

  • redsoxfan
    redsoxfan Member Posts: 162
    edited July 2010

    Hi, Junies.

    The countdown continues:  8 left.  3 regular and 5 boosts.  Breast still holding up.  Kinda pink, kinda swollen.  A few bumps and an occasional itch.  (Extra aloe dollops for those.)  Continuing regimen:  water, emu oil, aloe.  Thanks so much to the sisters here for introducing me to emu and aloe.  And a special thank you to the person somewhere on this website who said to "drink water like your life depends on it."  Glad I read the label and didn't use the recommended aquafor.  I'm allergic to the lanolin in it and the skin irritation could have made this a nightmare. (The other day I checked out a tube of biafine.  The fragrance in that would have been a problem for me even if I weren't being zapped!)  The rad team who were not familiar with emu know about it now.  Thanks again to everyone here for suggestions and support.

    On to t-town.  The oncologist mad my husband promise I'd start the day after rads, 8/5.  The radiation oncologist said I could wait a couple of weeks....Hmmmm.   Kind of surprised about that and looking back, wish I didn't have a biopsy.  The lesion was so large and suspicious it would have had to be excised anyway. I wonder if cells have been spread during biopsy.  Or duing the surgery.  Could they have found their way out?  Does anyone else worry about this? Maybe it's a more of a fear because I didn't have chemo. (Don't mean to be a downer here.  Forgive me, please.  Just fearful.  Hard for me to relax with this whole experience.)  So, I'm submitting my name for membership in the August Tamoxiphen Club beginning August 5th.  

    Here's hoping and praying that we'll all be here and healthy at the end of the adjuvent therapy in August 2015. 

  • chita
    chita Member Posts: 48
    edited July 2010

    I started a thread over in the Hormone therapy section for August 2010 Tamoxifen starters.  My med. onc. wanted me to start one week after rads were over.  I decided to go a few more days and start August 1 so that I'll remember when to stop.  July 31 2015 here we come!

  • eileenr56
    eileenr56 Member Posts: 135
    edited July 2010

    Hi Redsoxfan,  I'm glad you are doing well.  Here, the heat index is 107 so far and it's only 12:55 pm (est).  I have been  using aquafor (but I'm not allergic) at night only and Udderly smooth during the day.  My question has to do with the water.  I have a hard time drinking lots of water.  I wonder what that is doing for you.  I think I'm going to try that this weekend and see what happens.  I have noticed that my skin everywhere is much dryer then it used to be.  It is ichy in places where I didnt have radiation.  hmmm.  Of course, I had to change everything, the soap for my body and cloths.  I have to start moisturizing my whole body more than I had to do  before.

    I have 12 more full breast to go. so far so good.

    I'm going to take tamoxifen also, probably in september.  ( a month after I am completed rads).

  • Dilly
    Dilly Member Posts: 655
    edited July 2010

    Hi ladies, I'm glad to hear how you're doing.  Congratulations, cheers, and best wishes to all.

    I'd guess the water has to do with hydrating, plus flushing toxins.  I'm drinking more than ever myself and have been drinking a pint before and after tx plus lots of additional, and a lot of fresh fruit.  Also, extra protein to help rebuild tissue. 

    This is no walk in the park and I'm taking a couple of days' break, but have finished 19 regular, 8 boosts, and have 6 more full-breast to finish out, then will begin AI, Arimidex in August.   Talked with Rad Onc & we will do my last 6 tx over the course of two weeks (3 this wk & 3 next) and give my tissue a few extra hours healing time between.  The couple of days delay will not make an overall difference except to give my skin some relief. They gave me some Biafine and it seems to be helping; I'd been using Miaderm and emu but was still way too dry and cracking.  All my skin is dryer than usual and am using much more lotion overall, in fact my hands are softer than in years, hah!   Even my eyes are dryer, but drops help.  Have a pleasant weekend, all...

  • redsoxfan
    redsoxfan Member Posts: 162
    edited July 2010

    Hi, Eileen.  Wow! 107!!! Just checked and here the HI is 94.  It's the humidity that I can't stand and I'm so grateful for AC.  Right now, I'm inside trying to do some housekeeping that I've neglected. (Taking time out to post,Smile, of course.)  Company tonight thru Monday....

    Anyway, about the water.  I did a lot of reading here before beginning radiation, and the advice about water made sense,  After all, radiation is a burn and hydration is extremely important in treating burn victims, along with good nutrition, to help healing.  So, as I've written before, I drink a lot of water, with ice and lemon because for some reason it's easier to get it down that way.  It's been so hot, that if I'm outside at all, I add a bottle of something like (chilled) lo cal gatorade for the electrolyes. I think the fluids have helped a lot in preventing a real burn during this and I've had no trouble with dry skin. 

    Here's a Univ of Wisconsin info-site on radiation treatment.  They suggest 8-12 glasses a day.  http://www.uwhealth.org/healthfacts/B_EXTRANET_HEALTH_INFORMATION-FlexMember-Show_Public_HFFY_1126651042681.html

    By the way, did you ever get my personal message response to your message?

    Hang in there.

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