Summer 2015 Rads

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  • rosiesgirl
    rosiesgirl Member Posts: 89
    edited July 2015

    Thanks for the input regarding the waiting room. Maybe there is something more that they didn't show me. I don't think so however. I do not plan to strip from the waist up and put on a gown that ties shut with a small string and then go sit amongst the public. We'll see what happens on Wednesday. I appreciate the input. I wanted to make sure that I wasn't being overly sensitive (I figured I wasn't!)

  • Darumama
    Darumama Member Posts: 135
    edited July 2015

    You tell 'em Rosiesgirl! I don't mind sitting in a gown with other ladies in gowns in a patient-only setting, but I think it's really weird to have a gowned patient sit in the main area. Don't they care about patient dignity? I'm not sure why your story bothers me so much, maybe it's because we have to suffer enough indignities as it is with this damn disease!

    It's so interesting hearing how different our experiences " on the table" are. No mold for me. I never look at the ceiling at all. My entire treatment my head is turned facing left. I get to see the green laser guides in the wall that are used to line me up. During treatment, the machine does three different positions and I get about a 30 second (or shorter) dose from each side. My place plays music on satellite radio which I enjoy. No blankets because the temperature is perfect. I could fall asleep on the table if only the techs would stop fussing with me. My changing room is right next to the rads room. It's the size of a large closet, but private with a door. They do an excellent job of scheduling. I go in at 9 am and the only other patient I see is the the lady who goes in after me. I've had the same techs the entire time(male and female). I like them. They make small talk with me which is a nice distraction from the reason I'm there.

  • Hopeful82014
    Hopeful82014 Member Posts: 3,480
    edited July 2015

    Some of the positioning depends on the fields being treated, of course. I have 4. I NEVER look to the left but do see the ceiling while being positioned and part of the right side of the room during treatment. I do think it's unusual not to have a mold, however.

    I'm with everyone else - having to sit in a gown amidst the general public would bother me and I don't think it's at all appropriate. Someone needs to have a talk with management - or maybe start with the social worker or patient advocate...

  • Colleen73
    Colleen73 Member Posts: 11
    edited July 2015

    Thank you Diana! I will try ANYTHING at this point!! :)

  • movingsoccermom
    movingsoccermom Member Posts: 225
    edited July 2015

    Thank you everyone! Was too tired to post yesterday. Under my breast and under arm are quite sore and have to use Mepilex to wear the bra I need for the non treated side. More tired today than at any time through treatment, just the accumulation of tx, and many long drives (4 hours total every day). Overall I was lucky to have almost no fatigue during rads, but also no chemo prior either (onco type 3).

    There was a separate waiting area for those of us in gowns, and I too would be really uncomfortable waiting with everyone in those crazy gowns, because I was always holding the girls just to be comfortable! If there is no alternative what about 2 gowns, one tying in back, another tying in front for more coverage? This disease does stink, and treatment shouldn't make it worse!

    Hang in there everyone!

  • movingsoccermom
    movingsoccermom Member Posts: 225
    edited July 2015

    Colleen, take a look at your fluid intake. I tripled mine during rads and even with that had a couple of dizzy moments. I always had one of my sons liter sized soccer water bottles with me and made sure to drink at least 3 liters every day. Maybe that would help? Hope you find an answer!

  • ksusan
    ksusan Member Posts: 4,505
    edited July 2015

    The machine was fixed so I got to start this morning. The techs (2 female, 1 male) were kind and took time to explain what they were doing. 6 tattoos--enough to make a constellation! The only noticeable redness is where I had contact dermatitis from having stickers on for over a week--they pinked up enough that it looks like I fought off an octopus. Since my answer to "What happened to your breasts?" is "Shark attack," an octopus fits into my story well.

  • Hopeful82014
    Hopeful82014 Member Posts: 3,480
    edited July 2015
    Good one, ksusan. :)
  • SweetHope
    SweetHope Member Posts: 439
    edited July 2015

    I never wore one of those ugly gowns. When I entered the Rad Room, I would take off my button front shirt, drop the spaghetti straps on my $1.65 Walmart t-shirt and lower it to my belly and slip back on one sleeve of my shirt. It took all of two seconds, and I was ready before the techs had the bed ready for me. And I could pull up the T before I stood up. (If you need more support, put on a bra afterwards in the dressing room.)

    But the people in the waiting room would not have noticed what I was wearing. They were struggling just to keep it together, as they were so ill with lung cancer and brain cancer and would share with me their poor prognosis. They couldn't care less what I looked like.

  • InStitches
    InStitches Member Posts: 80
    edited July 2015

    Good morning sisters!

    I had my sim yesterday and everything went well. I am scheduled to have my radiation treatments after 5:00pm, beginning Monday. The two techs who worked with me were wonderful. Being that it was after 5:00 I was able to park right by the door. I am having my treatment at Mary Bird Perkins in Baton Rouge. The dressing area is right in the treatment room with a curtain. I like that I can have my clothes and purse right there and not have to worry about a locker and key and walking through a hall with a gown.

    I just want to thank you all for the great information you have provided. I feel so prepared going into this.

    As hard as this is I am just thankful to live in a time where there is this kind of treatment available to reduce the chances of this ever coming back!

    Peace and healing,

    Nancy

  • rosiesgirl
    rosiesgirl Member Posts: 89
    edited July 2015

    Thanks, Darumama and others. I am going to call on Monday and express my concerns over the waiting room situation. It's not that I am overly modest, it just doesn't seem right to me. I think that patient privacy and dignity should be respected in some way. Some of the people in the waiting are not having treatment, but waiting for people having treatment. I was particularly bothered because I did not see a single other person in the room in a gown. It's not like I go to my family doctor and they have me dress in a gown and then go and sit in the waiting room with everyone else. Just seems odd to me.

  • live_deliciously
    live_deliciously Member Posts: 346
    edited July 2015

    i agree the dizziness is likely dehydration. A friend who went thru rads said you need to hydrate as much as we did in chemo. I had one dizzy spell the first day and then started hydrating more and no more episodes since I hope it stays that way. And remember diet effects hydration levels too. Drinking fluids is good for you anyway so doesn't hurt to try and see if it helps.

  • lman
    lman Member Posts: 22
    edited July 2015

    Looks like I'll be starting rads in August. Last chemo is Monday and went for my markings this week. I have sat in waiting rooms with a gown on for every procedure that I've had, from mammogram to cat scan to wire insertion for lumpectomy to radiation markings. They always give me two gowns, the inside one closes in back and the outside one closes in front. It hasn't bothered me as there is usually someone else wearing one as well.

    I appreciate you all sharing your experiences, it helps to lessen anxiety. I will only have 16 sessions so I feel fortunate that side effects may not be too bad. My tech recommended Glaxal Base cream from costco. Has anyone used it?

  • DianaNM
    DianaNM Member Posts: 281
    edited July 2015

    Sweethope, I like your idea. Is the Walmart spaghetti strap just a tank? Did it give any support at all? I hate struggling with the shelf bra ones, with a healing lumpectomy on one side and swelling on the other side from a mastectomy three years ago.

    My consultation for brachytherapy is in 9 days, and I get the tubes in 10 days. Still no call from the nurse or the insurance person. I did quit taking one supplement, since I read not to take it with radiotherapy. Hope it was soon enough. Guess I will start calling them tomorrow. Would really like to know what this will cost me, I have BCBS basic and there are a lot of copays.

  • ksusan
    ksusan Member Posts: 4,505
    edited July 2015

    I asked the rad tech why radiation causes fatigue and she reminded me that the body wants to rest when it's healing, and that radiation kills cells. This reminded me to keep up hydration, protein, rest, and gentle exercise to support that healing.

  • SweetHope
    SweetHope Member Posts: 439
    edited July 2015

    Thanks, ksusan.

    DianeNM, the t-top is snug so it gives a little support and definitely stops the jiggle. It has a long torso which helps you tuck some of it under the fold which stops skin-to-skin contact there and absorbs the moisture that wants to accumulate.

  • JenH2015
    JenH2015 Member Posts: 31
    edited July 2015
    I started radiation on Wed - the 4 week course, so I am now 3/20ths through the treatment. I am amazed at how quickly they can get me in and out - the first two days I was walking out of the office within 15 minutes of the time I entered the waiting room, and the third day was only 20 minutes despite the fact that one of the two machines was down so they were having to treat everyone with a single machine. As for gowns, I am taken to a dressing room where I remove everything on top, put a robe on, and then leave the door open a crack. They then get me from that room and take me straight to the treatment room across the hall. I was very tired but that was because my 16 yo daughter and I were doing massive sight-seeing before each appointment (we live about 100 miles from Seattle, so this was a fun chance for her to hit all of the museums and attractions that we have not been to in years.) Next week will be more relaxing as it will be just me in Seattle.
  • RV6gal
    RV6gal Member Posts: 331
    edited July 2015

    Iman - I used the Glaxal base cream once I was done radiation. It is quite thick but sure helped soothe the area. During radiation I only used Eucerin and only on the weekend. Not sure why my RO gave me such a different protocol. Other then an area that got bad because of friction, I didn't think radiation was too intolerable.


  • PatRN10
    PatRN10 Member Posts: 332
    edited July 2015

    rosiesgirl, I think you are right to say something. It is one thing to sit in a private patient only area with other patients in gowns or awaiting treatments but quite another to wait in a general waiting area with family members etc. This just doesn't seem right.

  • sailorbev
    sailorbev Member Posts: 75
    edited July 2015

    Midgie--yesterday was much, much better. The treatment took less than 15 minutes. I also asked if I could keep my left arm bent so the shoulder didn't hurt so much.  One of the techs was different so maybe that is why it was quicker. 

    My skin also feels a little warm and prickly after the treatment for the rest of the day. By the next morning it is better. 

    I asked if I could swim and the tech said I couldn't. Bummer. 

  • InStitches
    InStitches Member Posts: 80
    edited July 2015

    DianaNM, the WalMart $1.68 tank tops are surprisingly wonderful. I really like the fact they are long and they are very soft. They come in a ton of colors. I had to ask the sales clerk to help me find them.

    There is a lot of conflicting information on supplements. I am taking a lot right now and plan to take Taurine to help with radiation fatigue.

    Peace and healing,

    Nancy

  • Hopeful82014
    Hopeful82014 Member Posts: 3,480
    edited July 2015
    Nancy, can you provide any package info or other detail that would help me find them on line (or ask for them in the store)? If so, many thanks.

    I did find the Playtex bras that a couple of members liked and thet are, indeed, VERY soft. Unfortunately, the cups are way too big for me - really disappointing.

    I do have some of Jockey's Elance supersoft camisoles which are marvelous (and were very inexpensive on sale but they don't support the scar area as it needs to be. I HIGHLY recommend them otherwise and will definitely wear them over a bra in the winter as an extra layer of warmth.
  • Darumama
    Darumama Member Posts: 135
    edited July 2015

    image

    Re: Walmart cami Look in the juniors section. In my store they were on a table right in front of juniors. They were running out a few weeks ago when I got mine. If you don't see them try by the sale or clearance stuff. Or better yet, ask

  • queenmomcat
    queenmomcat Member Posts: 3,039
    edited July 2015

    (shyly) What were the Playtex bras others recommended? The Playtex 18Hours are my favorites now, and I really wasn't looking forward to a) going out and buying bras just for radiation and b) relinquishing that tie to normalcy and my pre-breast cancer diagnosis days. My future treatment's still somewhat up in the air---waiting for verdict on clear margins for lumpectomy #2---but if all is good, I will be having rads later in August/early September.

  • Hopeful82014
    Hopeful82014 Member Posts: 3,480
    edited July 2015
    Super, Darumama. Thanks a ton.

    QueenMomCat, the Playtex P844 have no undersides and are very soft. They were fairly inexpensive, too. You will want.something without wires (causes friction) and SOFT. Also something you won't mind ruining with lotions and cream.

    There was another one suggested, too, earlier in this thread. You might check back a ways and see if you can find it.
  • queenmomcat
    queenmomcat Member Posts: 3,039
    edited July 2015

    Thank you! off to check One Hanes Place online.....but not buy them until I know I'm actually having rads. And thank you for mentioning the "something I don't mind wrecking with lotions".

  • Midgiemoon
    Midgiemoon Member Posts: 174
    edited July 2015


    Hi, I bought a nice bra at Target that is really comfortable, for about $21. I am a 38D and wear a large. See The picture for the model.

    I had a great day with my beloved yesterday.... If you are ever in Maryland, after you visit me, you must go to Fort McHenry, home of the Star Spangled Banner!

    unfortunately , I am running a fever today. One of the women who works for me has been very sick, and I think she shared it, ugh.image




  • wpmoon
    wpmoon Member Posts: 270
    edited July 2015

    I'm only 3 treatments in of 30, and my breast is already tender. No color changes yet, and I'm putting calendula on 3 times a day. But it hurts to wear a bra, and also not to.


    Asked the doc on Friday about swimming. He said it's fine so long as I'm not uncomfortable and I wash off the chlorine right away. And as for exercising, he also said okay since sweat is a natural thing our body produces. I have the cornstarch baby powder though to soak up excess. I need to lose the 20 pounds chemo so graciously bestowed upon me.

  • april25
    april25 Member Posts: 772
    edited July 2015

    Well, last week was interesting because the radiation machine stopped working and I skipped two days! They said the battery died and they needed to re-load all the software, so it took longer than they expected. I actually didn't mind taking a few more days off, although I worried since I'd just had the Friday before the 4th off, too! But the techs told me that it was all OK because I was over half-way through my treatments. For some reason that makes a difference...

    So I just did #19 of 35. I just learned that the last week of treatments was for boosts--and I may or may not get a full week of them depending on what the RO thought. Hmmm...

    Waiting Room... I'm lucky, even though I'm being treated in Los Angeles, I'm at a little satellite of the Angeles Clinic that was just purchased by Cedars-Sinai. Cedars was a bit farther from my sister's house, where I'm staying, so I'm going to this little branch. There is only the one machine, so that's why I had to wait until it was fixed. But I also NEVER have to wait and never see any other patients there, except for maybe once or twice! I just run in, sign at the desk, run right back where they ask my birthdate, etc., then go to the changing room, run out and into the radiation room, like down, get tugged into position while lying on my back with arms up in little braces/rests... No form-thingie... just lying there with short gown over my top. Around 30 seconds from one side and the machine moves to the other side and another 30 seconds, then I'm up and out!

    I get to chat a bit to the cute, boppy girl tech about what we did over the long weekend and about a cool dessert place over on Sawtelle. And that's it. I actually kind of like it! It's so nice being able to get out of the house, unlike when I was doing chemo.

    I think I'd complain if I had to go out and sit in one of those big waiting rooms in a hospital gown, too! I hadn't had to do that before... For mammos, they'd call us back to change and we'd wait in a tiny area in the back with a couple of other women in gowns... Of course, that was in the Breast Center at Cedars, so it's all bc folk... Lots to chat about if we want to... or just sit and watch the tv or whatever...

    So far I've just been using Calendula cream and Aloe gel. They told me to use it 3x a day from the very beginning because rads can dry out the skin and make it itchy and irritated (and the first treatment did dry out my skin!). I haven't been doing it 3x a day... more once or twice... and there's a very slight pink-ness at this point and some little itchiness, but I'm still wearing my regular underwire bras (I'm an a/b cup, so it's not like they're holding up that much)... but might switch to something softer if things get a bit more sensitive.

    Fatigue--not bad. I sometimes feel the urge to nap, but not every day. Most of the time my energy is pretty good.

    Good luck, everyone! Fascinating hearing everyone's different experiences.

  • knittingPT
    knittingPT Member Posts: 156
    edited July 2015

    There must be something in the air! The week before last I only had one radiation appointment (our machine was down) and four extra days off. Last week, I had all five days and my skin is not happy! I've now done 28 of my sessions. The area around my armpit scar (from lymph node dissection) is VERY red and swollen. I have one little area about the size of a pencil eraser that looks a little bit white/blister like but isn't open. This came on suddenly and I hadn't had many problems leading up to this. Tomorrow I will see the RO and see what she recommends I do next. I am still supposed to do 5 boosts but I think those will only be on the breast so maybe we can move forward still. I was doing fabulous up until about Thursday of last week (so treatment 27 and 28). My skin has decided that it has had enough.

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