Starting Radiation August 2017

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  • Castigame
    Castigame Member Posts: 752
    edited September 2017

    hello sisters.

    I have three a lot older sisters but none of them had issue like I did. So I feel a lot close to my sisters here at times.

    I am still hot and more tired than ever. It must be my body expressing relief from zapping or it could be Irma stress related. Going to enjoy this weekend. Only 3 drs appointment and support group meeting next week!!!

    Mimi

  • DodgersGirl
    DodgersGirl Member Posts: 2,382
    edited September 2017

    rebamacfan123- sending you a hug and hoping you have a great weekend!!

  • TWills
    TWills Member Posts: 679
    edited September 2017

    Update-todays treatment was uneventful! Yay

    Thinking of you MamaOz:)

    Congrats to everyone finishing!!



  • VLH
    VLH Member Posts: 1,258
    edited September 2017

    Ohmigosh, TWills, I would have been screaming at the top of my lungs and clawing my way out. I hope things smooth out for you for the rest of your treatment.

    Lyn

  • MamaOz
    MamaOz Member Posts: 432
    edited September 2017

    Twills good grief! My hats off to you machine stopped once on me and I finally did yell what was going on!

    And the room didnt black out!! Im a weeny

    And illimae what pray tell is on your head? Thats bolted down???

  • illimae
    illimae Member Posts: 5,710
    edited September 2017

    Mamaoz, the rads folks call it a mask but I call it a face cage. I had a positive supraclavicular node, so my treatment includes part of my neck, the face cage makes sure I don't move, in fact, I only have the ability to mumble :(

    image

  • ShockedAt48
    ShockedAt48 Member Posts: 138
    edited September 2017

    illimae - That looks like a form of medieval torture! I wouldn't like that at all! I'm very claustrophobic

  • Goofycat
    Goofycat Member Posts: 39
    edited September 2017

    TWills - that sounded scary. I probably would have cussed out loud! I sure hope that doesn't happen again.

    illimae - You are a brave soul. I sure hope you will be done with radiation soon. Prayers for you!

  • TWills
    TWills Member Posts: 679
    edited September 2017

    Lol Goofycat, I was cussing in my head for sure. I felt bad for the techs, I stayed calm so they could do there job and get me out of there faster. That's what I was telling myself anyway. Fun times.

  • Landri
    Landri Member Posts: 9
    edited September 2017

    reading through posts here. So grateful for these sites. More info here than almost anywhere I look! I'm 19 of 28 rads done. Had to pause it for a week due to rash. Holy itchy!!!! I see that no one here is on tamoxifen yet! I was put on it July 10. Looks like my dr isn't concerned about cross over of SE

  • illimae
    illimae Member Posts: 5,710
    edited September 2017

    Landri, I'm on tamoxifen. I started it a couple weeks before rads and my RO said to continue but some do want you to wait until rads are complete. For now I'm only having stiff finger joints in the morning from tamoxifen and some redness & skin tenderness from rads. I keep a bottle of fruit of the earth 100% aloe gel in the fridge for my warm neck, it really helps.

  • Mimie
    Mimie Member Posts: 42
    edited September 2017

    feeling a bit better with my cocktail of Tylenol and Motrin. Thankful my RO came up with a solution to ease both the pain and swelling. MamaOz- so glad you are coming back. I ring the bell on Wednesday at MCI after my final treatment, then meet my oncologist. Will be glad to get the last three treatments done!!

  • inccmd
    inccmd Member Posts: 69
    edited September 2017

    illimae, I agree with your face cage comment. What a contraption.

  • MamaOz
    MamaOz Member Posts: 432
    edited September 2017

    oh my goodness illimae hope your done soon! Im heading back to restart Wed.. need to finish 8 more then ill starton aromatase( arimidex)

  • Castigame
    Castigame Member Posts: 752
    edited September 2017

    illimae, hope you feel better soon

    Mamaoz, yes get the radiations over with. be careful driving. Will you be taking brand name AI? I decided on brand name, brand name or generic arrrrgggh AI👹

    I am counting down days for both of you, You will feel like you just unloaded ton of bricks you carried for about 100 miles.

    Mimi


  • ShockedAt48
    ShockedAt48 Member Posts: 138
    edited September 2017

    Landry: I've beenon tamoxifen for about 9 days now, two weeks after finishing radiation. No side effects yet.

  • Landri
    Landri Member Posts: 9
    edited September 2017

    think I had some hot flashes, my RO gave me light dose of Effexor to decrease them. Think it helped. Hydrocortisone for itchiness

  • Legomaster225
    Legomaster225 Member Posts: 672
    edited September 2017

    Illimae, that kinda reminds me of Hannibal Lector. That would be hilarious if one of your tech's names was Clarise. You could have fun with that -or at least a would. Lol. Last week of yourrads my friend. Hope it goes quickly!!

  • Mandycat
    Mandycat Member Posts: 52
    edited September 2017

    congratulations to those of you who finished and to those continuing forw

  • MamaOz
    MamaOz Member Posts: 432
    edited September 2017

    thanks reba( mimi)

    I think she is starting me on anastrazole which is generic I asked for the real deal but she said she has to prescribe generic first. I have heard the geneeics cause problem

  • illimae
    illimae Member Posts: 5,710
    edited September 2017

    Lego, I sent that pic to DH after my 1st session and he did call me Hannibal, lol

    Today sucked, it was the 1st day of the 5 boost sessions, I was confined to that contraption for about an hour while the techs, marked me, moved me, took images, got RO approval, etc. I got very claustrophobic and the plastic headrest began to hurt but I brought myself back from the verge of nausea and tears. Hopefully tomorrow is better.

  • LeesaD
    LeesaD Member Posts: 383
    edited September 2017

    Mamaoz- I started generic anastrozole
    thr night I finished radiation. My pharmacy gave.me Teva. 12 days in and zero issues so far! Hoping that continues. From the Arimidez threads most people do better on the Teva than the other generic. I was so anxious about starting due to all I've read but it's really been fine even to the point where I'm like I hope it's doing it's job as I don't even know I'm on it. I understand some effects could be cumulative and others will need testing for like bone loss but so far so good.
  • macprer
    macprer Member Posts: 5
    edited September 2017

    I finished radiation in May (shorter course Canadian style treatment my RO called it.) My skin did well using Calendula cream for a topical treatment and I still use it twice daily. I say well because it has been several months, but I am sure I thought my skin was on fire then. I was super tired 2-weeks into treatment, and exercise was grueling but I continued as I was able (30-45 minutes daily.) I lost a good 10 pounds during radiation but I was super vigilant about self-care and my diet. Now my skin is tan and a bit thicker. My right breast is also larger than it was originally which was unexpected given the lumpectomy.

    I was not aware until now that stiffness increases 3-6 months after radiation and now my pectoral muscle is super tight. I can deal with this for now doing stretches, but also I have a vein like thread that runs along my middle-lower ribs in a vertical direction that is causing pain. I have been doing cross friction massage and stretching which is not yet working. Anyone heard about a similar situation? I found only a single comment on the web with no subsequent responses about it.

    My cording resolved with home stretching, massage and swimming (side stroke.) The repetitive lengthening in the water with side stroke really helped to relieve my symptoms.

    My biggest frustration about all the treatment is the lack of information my medical team has provided about side effects. I knew nothing about cording, sentinel node removal pain, pectoral stiffness and hormone medication side effects: all which seem to be very common. I was given great information about skin care following surgery and radiation though. FYI: I have elected not to take Tamoxifen after trying it twice over the last 6 months and hope my self-care will be sufficient to prevent another diagnosis.

    I am super thankful for all who have gone before and share their experiences. We all have a very different and personal yet common journey.

    Best all.


  • Castigame
    Castigame Member Posts: 752
    edited September 2017

    Illimae, Sorry about 1st boost being long and painful. If I remember correctly, pain and everything else peaked right after 1st boost. #27 to #30, boost 2 thru 5 were really breezy.

    Today is 5days after radiation. I felt my arm is a lot lighter when I got up this morning. Still just aloe gel dabbing only. Light scabbing in the area. Reddishness slowly fading along w nerve pain. The general heat disappeared quite a bit. Going to enjoy a peaceful day before the next round of drs appts start. Darg it I do have an appt come to think of it,

    Mimi

  • Legomaster225
    Legomaster225 Member Posts: 672
    edited September 2017

    Does anyone else have low blood counts? I did my standard testing before my MO appt today. My WBC count is down as well as platelets. RBC is still lower than normal but a little higher than right after chemo. I was surprised my counts dropped again. Hopefully just radiation effects. 11 more days!!!

    My breast was suddenly very red after yesterday's treatment. Like they changed the light bulbs in the tanning booth or something. 😜 Some parts are turning blackish. Thank goodness it doesn't really hurt -just itchy.

    Illimae/ they have me scheduled for a Boost simulation on thurs before treatment. I didn't realize it would take that long.

    Mimi-glad you're fine and starting to feel better

    Macprep - sorry you are having troubles. Cording is painful. Stretching and massage does help though. Have you talked to your dr about an AI instead of the tamox? Maybe you can tolerate that better. Everyone is different.

  • Goofycat
    Goofycat Member Posts: 39
    edited September 2017

    illimae - wow you have gone through a lot - prayers and best wishes for you

  • Mimie
    Mimie Member Posts: 42
    edited September 2017

    Rebamacfan1- I experienced my worst day after my first boost too, but after that have been better, might be the cocktail of Motrin and Tylenol RO put me on, but not complaining. I usually don't like taking meds with frequency as worry about the effects, but this time I blew caution to the wind. On another note a woman waiting for rad's yesterday told me I should be doing wheat grass and pomegranate as radiation is bad for the liver, and they will help to rid the toxins, anyone hear this too? And I finish tomorrow, and am traveling in 2 weeks, will I still be using aloe and emu oil, should I pack them??

  • Annbee
    Annbee Member Posts: 208
    edited September 2017

    wait a minute... there is more mapping before the boosts? I have number 26 of 32 today. My RO said that boosts were easier because they are shorter?

    Illimae- you have gone through a lot.

    So since being back to teaching in August, I called in today because I just couldn't do it. I feel completely worn out and tired, not to mention all the redness and pain. I did not want to but really no choice. I hate this feeling. Is it the radiation?

    I can't wait for radiation to be over. I go this Saturday and my last one should be a week from today. I get my port out on Thursday. I see my MO next week too. She canceled 2 weeks ago because of the storm. I wonder if my counts are low.


    Anne

  • Legomaster225
    Legomaster225 Member Posts: 672
    edited September 2017

    I didn't know about a second mapping either, Annbee. Maybe you don't need it or your RO dit i already. I would get tired with just one day of teaching! Rest if you need it. I'm sure it will get better.

    My RO explained that the boosts were the same amount of radiation but just in my tumor and scar area and will be quicker. That will be good because the middle of my chest is where it is the reddest and starting to peel. That area will start to heal while I'm getting the boosts.

    My MO wasn't concerned about my counts and did say that radiation could be causing the little dip. Just keep plugging along.

  • Annbee
    Annbee Member Posts: 208
    edited September 2017

    thank you legomaster2! You made me feel better. I will ask about mapping when I go today. It is my underarms that are peeling. I am resting today. Back to school tomorrow.

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