Spring 2016 Rads

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  • Grazy
    Grazy Member Posts: 373
    edited May 2016

    Jill - I'm in KW, so the other side of Toronto, about an hour away - my entire family is either downtown or north of the city (Newmarket area or further up on Lake Simcoe), so I schlepp up via the 407/404 when necessary to see them - I hate trying to get through the city these days via the 401!!

  • iammags
    iammags Member Posts: 216
    edited May 2016

    Jill- I think that rads are underwhelming. I drive 45 minutes to get to the cancer center, change my clothes, get on the table, have a 5 minute treatment, then drive 45 minutes back.The techs adjust my position on the table to exactly the same measurements every time. While the treatment is happening I don't feel a thing. The machine just kind of rotates around me. Then I get up and get dressed. On Tuesdays I see my RO who ask how I'm doing then checks my skin. Taaa daaaa....that's it.

    I do have a few SE's. My skin is red and hot and I'm super tender all over my breast, clavicle, and down through my rib cage. Sometimes I joke that if it weren't for those SE's I would think that this radiation business is all a scam. That is why I think that it's underwhelming. I don't know what I thought would happen.

    You were strong enough to make it through chemo (although I seem to remember some pretty bad SE's for you?) and you will, for sure, be able to do this.

    #cancersucks #happymonday



  • Autumn121
    Autumn121 Member Posts: 29
    edited May 2016

    Hi All!

    I start my Rads today, and will go until June 23. I'm nervous, but anxious to get started. I have been reading this thread thoroughly and feel I am ready for whatever may come. Seems like there is such a variety of machines, doctors, and side effects! If something unusual happens today, I know where to come to get some answers!

    Hope you all have a good week!

  • Grazy
    Grazy Member Posts: 373
    edited May 2016

    I'm with you, Iammags! "Underwhelming" is exactly the word I used to describe my first treatment. The machine is so quiet, I didn't even realize treatment had started under the thing swung overhead two and a half minutes into the five minute treatment - I kept waiting for it begin. I thought there would be noise, flashing lights, zapping sounds, "something".

    Good luck, Autumn! Let us know how you made out.

    Just took a 30 minute nap because I thought I should do that each day (?). Off to garden now.

  • Sheri64
    Sheri64 Member Posts: 113
    edited May 2016

    Hi Jill,  I am large breasted also and have had #15 of 36 rads today and so far I have been able to wear my regular bra. I am just a little pink. So far I am only using Aloe on it.  I am with you I am so ready to be done with TE.  I did chemo that ended the end of March.

  • DisneyGirl16
    DisneyGirl16 Member Posts: 121
    edited May 2016

    LTF, I completed 26 of 36 treatments today. The outer quadrant and under my breast are getting red but I don't have a rash or itchiness. The biggest problem I have had so far is that they use markers and stickers to help them line me up in the correct position and they keep getting rubbed off or moved. The machine does make some buzzing noise but they always have the radio on so that helps. I did buy some men's undershirts and I wear those between my skin and bra on days that my skin feels irritated. It does seem to help reduce the rubbing. Good luck!

  • peculiargirl
    peculiargirl Member Posts: 68
    edited May 2016

    Our local Sam's Club has shelf bra camis - 2 in a package for $12, sizes xs (4-6) to xxl (20). I'm on the high end of that scale, and while *I* can tell I'm not wearing a "real" bra, my husband says I look fine, and it sure feels better than wearing a sports bra. My Rad techs suggested them, and I'm so glad they did.

    Today was #25 of 33, and I'm one of those people who haven't posted because things are going well. My skin is really red and starting to peel, and I don't do much in the evenings after radiology and working all day, but it's manageable - and NOTHING like chemo fatigue. Probably the "worst" side effect I've experienced is trouble swallowing - when I'm eating or drinking, it feels like I've taken too big a bite/drink. So it takes me twice as long to eat as anyone else at the table, but again, it's not that big a deal. My RO says it's because the rads are hitting my esophagus due to the location of the (removed) lump.

    This journey is getting old, but I try to focus on the end goal - radiation is lessening my chances of recurrence.

    Good luck to everyone-

    Kathy

  • LovesToFly
    LovesToFly Member Posts: 1,133
    edited May 2016

    thanks all. I do have some loose cami type bras from after surgery. I think they probably don't look as awful as I think they do!! I usually wear hardcore underwire.

  • Kkubsky
    Kkubsky Member Posts: 231
    edited May 2016

    I was using Avo Cream that I got from the nurse at radiation. The last week or so of rads my skin got irritated and yucky in the inner upper area and underneath my boob was red and peeling. Radiation nurse switched me to Aquaphor and Silvadene cream along with a cortisone cream for the incessant itching. I have to say that things are pretty much back to normal now....

  • PlanB58
    PlanB58 Member Posts: 157
    edited May 2016

    Hi All!

    I started my rads today as well Autum! One down 29 to go!

    I use the breathing apparatus and was nervous about that but it went fine. Have had terrible dreams about not holding my breath and zapping my heart!🙀 Good luck to everyone these posts really help me

  • Sunnyone22
    Sunnyone22 Member Posts: 191
    edited May 2016

    Just chiming in to say at 17 days post rads, I can barely even tell where the tan rectangle was. I had no skin problems at all, no itching, no open spots. I used Miaderm at least 2-3 times a day and Aquaphur at night. Fatigue yes, but it has passed and I feel fairly normal now.

    Warmest (no rad pun intended) wishes to all here who are just starting or are early in the process. You've got this!

  • Paxton29
    Paxton29 Member Posts: 221
    edited May 2016

    I finished 3 of 33 today. So far so good. I'm being really vigilant with the lotions because I don't want to have to wait a single second longer than I have to to get these ;)&$@!! tissue expanders exchanged for implants. (They tell me it will be six months' wait as it is.) I use emu oil after treatment 2 x a day then Aquaphor at bedtime. The emu oil cream absorbs quickly and hasn't stained any of my shirts. I hate having to wear separates all the time as I'm a dress girl, but I have no choice. I don't wear bras since the TEs are basically rocks. Zero movement.

    Does anyone else have the bolus used on them? They do it every other day. I'm wondering if it's mostly for BMX patients since we don't have breast tissue left?

  • Tinkerblond
    Tinkerblond Member Posts: 2
    edited May 2016

    Hello! Finished treatment 6 of 30 today and I'm wondering if any others are having same side effects as early. Every day (including the first) after a few hours the breast being treated feels much hotter than the rest of my body and on the "rest" day Saturday my entire body was feverish. After day 2 I spoke to the nurse who recommended aloe gel and ibuprofen and I was lucky enough to have been given Miaderm as a gift. It seems that every day my breast feels more and more inflamed even using all of the above. It's the same feeling as when I quit nursing my kids. Is this normal for anyone else?

  • Lovinggrouches
    Lovinggrouches Member Posts: 530
    edited May 2016

    Tinker, the same thing happened to me, but wasn't severe enough to worry too much. I figured it was normal. My breast felt hot the first day, and as time goes on, I can feel the rays now, but it isn't horrible. I guess because my cancer was so close to my nipple, it is taking the brunt of everything and makes me want to scream if it rubs on anything. It will all be ok. The feverish feeling comes and goes, but is never severe enough to worry about!

  • Tinkerblond
    Tinkerblond Member Posts: 2
    edited May 2016

    Thanks Lovinggrouch, my radiation team told me "that usually doesn't happen this soon", and it had me wondering... Hope your pain is not too awful. Hang in there

  • LifeOfBabbs
    LifeOfBabbs Member Posts: 28
    edited May 2016

    I have 15 more treatments left, with 36 all together (over half done). My armpit is really hurting. I see the doc on Mondays and she gave me Aquifer mixed with lidocaine. I have been using Aloe and Aloe mixed with Aquifer. It feels like someone peeled off the first few layers of skin and the nerves are exposed. It's waking me up at night when I move my arm. Something that does help is taking a piece of cotton cloth and placing it in my armpit so things don't rub on it. My RO is very helpful and compassionate. I get my RADS in Albany, NY. It's a 50 minute drive one way. My breast really is fine so far! It's just the armpit that's bad.

  • Autumn121
    Autumn121 Member Posts: 29
    edited May 2016

    First treatment of 33 yesterday! Only 32 to go!

    My machine was not quiet, but not too noisy either, so it didn't bother me. My doctor and the technicians were so nice, and explained everything, which was reassuring. I was surprised there were no actual "beams" of radiation! I guess I thought there would be so that I could actually see them work on me!

  • Grazy
    Grazy Member Posts: 373
    edited May 2016

    LifeofBabbs - that reminds me of how my armpit felt after surgery -- I pinned a soft square of polar fleece inside my shirt so that it covered the seam of the shirt's armpit (if you know what I mean) and it protected my armpit from rubbing on the fabric.

    I just got back from treatment #4 and feel as though I have a little lump in my throat when I swallow -- I've read that the esophagus can be affected around the two week mark with breast radiation but I'm obviously not at that stage of treatment quite yet.. Hoping it's coincidental, however, I have an appointment with my RO every Wednesday after treatment so I'll ask if this is a reasonable side effect at this early stage. My daughter has had a terrible virus that really affected her throat, and it could well be that I'm just coming down with her bug. Time will tell, I guess.

  • iammags
    iammags Member Posts: 216
    edited May 2016

    Tinker- That happened to me my first week but by the 2nd I wasn't feeling feverish or super fatigued. Good luck!

    What doesn't kill us makes us stronger, right? Right, ladies? (I'm trying to be my own cheerleader!)

    It's RO day for me. That includes the scale, which I am trying to avoid at the moment. argggh.

    image



  • Paxton29
    Paxton29 Member Posts: 221
    edited May 2016

    Did anyone's RO tell you anything about weight? My mom's neighbor said they told her don't lose or gain weight during radiation. I don't remember anyone telling me that and we have the same RO.

  • Wenrisa
    Wenrisa Member Posts: 94
    edited May 2016

    hey Jill - I just finished my 4th week (of 6) of rads and my skin has barely reacted at all. I still wear a regular bra and use regular aveeno lotion. I just make sure that I use lotion 3 or 4 times a day and a little hydrocortisone creamfor the small rash I have in one spot. I too was very worried about skin reactions since I have very sensitive skin that burns easily. But all has been really good so far. So it's possible you'll make it through with minimal side effects. All my best to you.

  • Grazy
    Grazy Member Posts: 373
    edited May 2016

    Paxton - my rad therapist said they x-ray once a week to make sure we're still in the right position because things can shift if we lose or gain weight during treatment - they have to do some recalculating I would guess if there were changes. It would be interesting to know if that has happened to anybody who is further along in the treatment.

  • iammags
    iammags Member Posts: 216
    edited May 2016

    Isn't it amazing how many different pieces of advice we all get when we are all having more or less the same treatment? I was never told anything about weight and I don't think that I'm being xray'd once per week. It's interesting to hear all of the stories.

  • Lovinggrouches
    Lovinggrouches Member Posts: 530
    edited May 2016

    mags, you crack me up! I do get a "picture" every week, but no more, I'm done Thursday!!!!!

  • Deaconlady
    Deaconlady Member Posts: 158
    edited May 2016

    Very interesting stuff. Saw my RO today (and will each Tuesday) and her nurse gave me a packet telling me what to expect and what to get to take care of my skin.This was my 2nd treatment. I believe they said I get an xray each week? The next 2 days are going to be busy since I have rads before my echocardiogram tomorrow and my first Herceptin only Thursday morning. Between that and trying to make up time at work I'm tired already!


  • iammags
    iammags Member Posts: 216
    edited May 2016

    Wow, LG! Almost done? That's great! 2 more weeks for me.

  • Lovinggrouches
    Lovinggrouches Member Posts: 530
    edited May 2016

    Mags, it seems to take forever, yet seems like I just started yesterday lol!!! Hope you do well with your last two weeks! I am blessed to only do 20, but the boosts are rough, my nipple will never be the same again lol!!!!

  • Z317
    Z317 Member Posts: 3
    edited May 2016

    Hi....I have a few questions.....I had my mapping today and will start Monday......why do they mark my back?? And only one mark on the area near my incision? I'll be in a prone position. Anybody else lying face down?? And has your armpit been affected?? Thanks in advance,

    Ruthie

  • Sawyer
    Sawyer Member Posts: 43
    edited May 2016

    Hi all;

    I have my "dry run" tomorrow. I have 3 tattoos and they said they will place the 4th near the nodes area either tomorrow or on day 1 which is Monday.

    My place is nice, quiet, staff is very kind. The RO is young and beautiful Asian woman. I felt very comfortable with the male rad tech who made appropriate jokes on my first day for mapping and made me feel comfortable.

    I have to do the deep breathing kind so will have that device in my mouth during treatment which I am not happy about....

    I will have 30 treatments total starting Monday. They are down a machine so my appts are at 6:30 pm which will be tough for me...I live 35 min away and if I work my work gets out at 5;00 and is only minutes from the RO office....so I will have time to kill and with the thought of fatigue I just don't like the time frame. Oh well.

    I read through the previous posts; thanks for the great tips. I look forward to joining in more on the conversations!

    Sawyer

  • Grazy
    Grazy Member Posts: 373
    edited May 2016

    Sawyer, you might be able to get some earlier appointments in time as others finish their treatment schedules and spots open up - just ask regularly. I asked to move my early Monday morning appointments later this month to around 11 and it was absolutely no problem to reschedule. Doesn't hurt to ask. Good luck with your treatments!

    I have just completed #5 of 21 today - yesterday, immediately after treatment, I thought my throat felt funny and my voice was hoarse all day, but as I suspected, it was just a coincidence - my esophagus is not in the line of fire with my particular treatment and it turns out I'm just coming down with my daughter's virus. I have zero skin issues or fatigue so far - my RO is still adamant that nothing be applied to my skin at any point so I'm following her orders :) We shall see what happens.

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