Fall 2013 Rads

1313234363756

Comments

  • hobbesla4
    hobbesla4 Member Posts: 72
    edited November 2013


    Wishing everyone a wonderful day. Hope you treatment goes smoother today, Summergal. Still waiting for my rads schedule and rads to start in about a week.

  • summergal
    summergal Member Posts: 208
    edited November 2013


    Thanks, ladies, for your encouragement. I did a lot of yoga last night and I think I'll go for a run this morning to loosen things up - it can't get much worse than yesterday, right? McKatherine - I love your song!


    Even in the short time I've been going, I know what you mean about the moments when the techs are a little "vague" - yesterday I noticed they were so precise in getting me lined up and then all of a sudden one of them kind of looked at the other one and they both shrugged their shoulders, and nodded, and then they left. ??? Shoulder shrugging is not good in radiation!!

  • honeybair
    honeybair Member Posts: 746
    edited November 2013


    JB, my heart is with you on the loss of your mother. You are to be commended for taking care of her in your home which I know was no walk in the park for you. My 89 year old mother currently lives in a nursing home and has suffered from Alzheimers for well over a decade. When our parents live to be really old, there are few people to attend services or memorials for them, it is true after they pass. Whenever I visit my mother, I always leave crying because it is so painful to see her as she is as I remember who she was.


    summergal, so sorry that your sessions are so difficult. I take a tranquilizer 2 hours before my 5 pm appointments which has helped me tremendously. In fact the RO suggested it and wrote the script for them. I have three sessions to go including today's. Will jump for joy, energy permitting.


    Wishing everyone a good week-end.

  • FierceBluebird
    FierceBluebird Member Posts: 758
    edited November 2013

    I love the McKatherine song!  I have so much to say and no time, gotta run to my appointment! But feeling f'ing (for Bounce) cheerful today thanks to you ladies! Radiance all around!!

  • peacestrength
    peacestrength Member Posts: 690
    edited April 2015

    I'm done with radiation treatments!   Yea!

  • summergal
    summergal Member Posts: 208
    edited November 2013


    Yay, peacestrength!! Just YAY!!!!

  • McKatherine
    McKatherine Member Posts: 300
    edited November 2013


    happy dance for peacestrength! :)


    Bounce - during my first week they used a measuring device that they taped to my skin (or my gown - cant remember) that measured the dose as it was being delivered. I don't remember them doing it after that, though.


    Because of the way my head was turned, I could see the display screen in the room which showed the planned / actual measures for alignment and it would briefly show the doses just after each zap. The computer keeps track of all that. I know the machine itself has two "filters" just behind the collimator that ensure a consistent dose coming out. It's hard to trust all that technology we can't see - but the system (the machine itself, the computers, the software, and the techs) have so many redundant safeties built in, I think you would have to work very hard to get the wrong dose.

  • MsPharoah
    MsPharoah Member Posts: 1,034
    edited November 2013


    Good morning radiant ones!


    Peacestrength, congratulations are in order. You fired up your radiator and the job is done. You have only one task left....exude as much joy, love and good health as possible. Happy healing, sweetie.


    Bluebird, your machine name was the best. Bounce, I agree...gotta love the trash-talkin' truck mammas! (Not that I have ever said a naughty word, for fear of getting a case of the vapors....teehee)


    Kruise, I wanted to tell you that I love your hair. (And you are so pretty). This morning, I actually had to blow dry my bird's nest and I worked like hell to have it look like yours. Not yet, but I am still working on it.


    Summergal, good luck today!


    Shine on, dear friends and have a restful, healing weekend.

  • denilynne
    denilynne Member Posts: 102
    edited November 2013

    Thank you all for the great amount of information and the support. Radiant hugs and more hugs to all of you! I am 3 weeks down and 3 more weeks to go. I will shine this weekend as I hope you all do.


     

  • summergal
    summergal Member Posts: 208
    edited November 2013


    Here's my dispatch from the radiation front: today went even worse than yesterday, if that's possible (I'm sorry to be such a Debbie Downer! It can't get much worse, so it has to get better soon!). I took some Ibuprofen ahead of time to calm down the pain in my left shoulder, did some stretching, etc., went in with a good attitude. After a few practice breaths I could actually hit the level, so they started the treatments, but I could not hold my breath at that level for long enough. The machine went on and off. On and off each time I couldn't hold my breath.


    Then I noticed that when I did reach the level and hold my breath for more than a few seconds, I started to black out. My ears closed, my vision was going black, and once I swear I "left the room" - I felt like I was moving in waves, because I was passing out. After a long time of me struggling to hold my breath at that level, they completed the treatment and came in the room. We all agreed that this was just undoable and unsustainable, and that my adrenaline had allowed me to breathe to a level, during my original CT sim, that was just way above what I could do on a daily basis without passing out (and I want to add that I am in pretty good physical condition, ran 3 miles this morning, and other than BC, have no other health issues).


    We then decided that I would try to do it at a much lower level of hold...and that necessitated another CT sim. I was feeling pretty light-headed (and they did offer that I come in on Monday for the additional CT, but nooooooo, Ms. "I may have breast cancer, but I can take on the world" decides to go through with it today), so I sat in the waiting room for a while and the tech brought me crackers and water. Sounds like the story gets better? Wait, it gets worse.


    So, I'm feeling pretty okay and we go into the CT sim room. They finally get me all lined up and I start working on breathing to a much lower level (but still one that would have an added benefit), and then they start the scan. All's going well, I have my eyes closed for the whole thing and then.....then I feel myself starting to spin. Literally, like I was spinning. I'm trying to hold on til the end of the scan, but I'm getting sweaty and I know what's coming, "Guys? You have to get me out. Please get me out. I'm going to throw up!" And they pull me out and throw up I did. My bp was at an all-time low. That officially ended today's 2 1/2 hour session. I think my body just went through so many extremes today that it finally couldn't take any more.


    So now I'm nauseated and thank God my husband will be coming home late today, so a frozen pizza will be dinner for our little one tonight. I am going to give it one more chance in the CT sim on Monday and if that doesn't work, regular radiation for me. It was funny, here I had been worried about my skin, "was I going to burn? Was my skin going to break down?" and, not that I'm minimizing the skin changes, but it turns out that would be the least of my worries compared to these past few days. While I sat in the waiting room trying to get my legs back under me, three different patients came and went for their regular radiation. I know I signed up for the gated breathing, but I'm beginning to think that the regular way would have been just fine!!!


    Wishing you all a great, restful weekend! Hugs.

  • MsPharoah
    MsPharoah Member Posts: 1,034
    edited November 2013


    Holy guacamole, Summergal! Just don't know what to say except that your tale of today had me on pins and needles. I think my jaw dropped several times and "oh no!" came out.


    I sure hope Monday is better. You definitely had on your big girl panties today.


    Have a restful weekend. I'm pretty sure your boys will like pizza!


    MsP

  • JanerT
    JanerT Member Posts: 8
    edited November 2013


    I just finished my first week of rads and am reading posts here and I am confused. I don't have to do any breathing, I just lay there and the machine moves around me and sometimes the table moves me. What is the difference?

  • Sandymomto3
    Sandymomto3 Member Posts: 37
    edited November 2013


    whoa summergal, what a day. Today was 16/33 for me, I am also doing gated breathing. I have noticed a few things....at my hospital they take new X-rays twice weekly that they use I believe to be sure we are breathing within the range. I'm having whole breast radiation traditional 33 treatments with the last 8 being boosts to the surgical tumor site only. So, the "machine" has 3 positions for my treatments. With each one it requires moving the table, the machines etc. Some days the breathing part is just harder than others, which I've noticed results in more but shorter beeps. If I get the breath hold right the first try it's a longer beep. The machine is designed to cut off the rads when your breathing falls out of range. I hope for you that Monday will be better. Have a good weekend.

  • Sandymomto3
    Sandymomto3 Member Posts: 37
    edited November 2013


    JanerT....breath hold or also called gated breathing is sometimes used for left sided breast radiation. Helps to protect the heart from rads.

  • JanerT
    JanerT Member Posts: 8
    edited November 2013


    Thanks I will ask about that because I am having rads on the left side. I appreciate all the advise I am getting here. Thanks to everyone.

  • Bounce
    Bounce Member Posts: 574
    edited November 2013


    Hi summergal


    Sorry its a hard start. I wanted to ask if you ever got the special goggles to help you see where you hit the mark? I think you said they were "sold out"!!!!


    Maybe its time to demand (Bounce speak for ask very nicely but very firmly) they get you a pair INSTANTLY. Ask what exactly they are called and where you can obtain them. Volunteer to go fetch them if they are available somewhere a little ways away. When they see you seriously want them they may be motivated to get a pair. And if techies don't help ask RO.


    I think with some visual aid it will give you more control.


    I know that I have no sense of time in the treatment room. And my brain keeps trying to make sense and understand everything around me even though I have a severely limited range of vision because I have to lie still. So maybe the glasses will give you some control that will make things easier.


    Its worth a try and they won't only benefit you they will benefit everyone else too.


    Maybe some of the difficulty is also coming from the techies having to learn something new.

    Do you know how long you need to hold your breath for each time or do you have to wait for techies to tell you?


    Maybe some kind of song or mantra can help you keep track of time. Maybe playing a particular song/songs would help. I know on days when my techies have put music on its much easier than days when the room is just cold and silent.


    All you can do is try again on Monday and hope for the best. Use the weekend to practice breathe - hold - release. Drink a bit before the treatment to get your blood pressure up and remember we are with you.


    Hugs

  • denilynne
    denilynne Member Posts: 102
    edited November 2013

    Dear summergal and all the others that are going through gated, we are all with you. You may not hear from some of us very often but our hearts are still with you. God bless us all.

    JanerT, how are you doing after your first week?


     

  • LanaM
    LanaM Member Posts: 142
    edited November 2013


    Getting ansy and wish I could just get rads started! Have my rad consult next Thurs., then still have to do simulation, etc. Was hoping to be done by Christmas but guess we'll have to see - don't know how many I'll have. I'm 51 - do they always do fewer rads if over 50? I'd be interested in how anyone's skin did thru rads for those that had mastectomy and no reconstruction.

  • denilynne
    denilynne Member Posts: 102
    edited November 2013

    Hi LanaM, I know how you are feeling because I felt the same way. Now, I am 3 weeks into rads. I am 60 years old. I am getting 28 treatments with the last 5 being boosts to the surgical site.

  • Rainyday13
    Rainyday13 Member Posts: 29
    edited November 2013
    Hello summergirl,
    I am with Bounce and have a lot of questions regarding the breathing method they are using. I am doing the gated breathing with the goggles and it has worked well. Like Bounce said, it gives you some control and something to look at. It is hard enough to deal with breast cancer and then having the treatment being an ordeal like this.
  • Rainyday13
    Rainyday13 Member Posts: 29
    edited November 2013
    Questions to all you ladies - Has anyone notices an insomnia issue since starting rads? I go to sleep just fine, but I don't stay asleep. I know when I was first diagnosed, I had some sleepless night. But it was pretty good after surgery and all.
  • L2girl
    L2girl Member Posts: 113
    edited November 2013


    summergal,


    I was hanging on your every word in your last post. When you started out by saying it went even worse than the day before, I found myself shouting at my ipad, " no...noooooo!!" I felt like I was watching a movie or reading a book I was really involved in. Well, if it is too hard to be the guinea pig next week, just do the regular rads. Someone else can be the guinea pig. Unless it is safer for you to do the gated breathing. In my case I didn't have to do it, but maybe the machine is different, or the type of rads or field locations, etc. Everyone's case is different I'm sure. Remember, we will still be in your pocket no matter what.


    Rainyday,


    Funny you should ask about the sleeplessness. I too have been having a terrible time sleeping lately. I feel like I am in hyperdrive or something. I feel energetic and excited, when I should be tired. It is weird, because i have hypothyroidism, so if anything, my metabolism is usually sluggish. But now I am wondering if something has changed, or if it is just rads revving up my metabolism. I thought I read someplace that it does that. If so, I wish it would help me lose some weight! But nothing yet. One can hope! But seriously, I am afraid when I start Tamoxifan next month, the insomnia will get even worse. I hope not!

  • denilynne
    denilynne Member Posts: 102
    edited November 2013


    Rainyday, it was the same for me for about a week and a half then I was ok. I also had some very weird dreams.

  • GrammyR
    GrammyR Member Posts: 702
    edited November 2013

    70charger- some of us don't have the nipple part anymore so afraid am not chuckling :(

  • wyo
    wyo Member Posts: 541
    edited November 2013


    summergal- this is really like a reality show- and not in a good way. I think the stress of all this is significant and I am so concerned that you are having blood pressure changes, nausea & vomiting to say nothing of the time spent feeling like you are doing something "wrong"


    I don't know where your cancer is on the left but can't they develop a treatment plan for you with minimal cardiac exposure that does not require you to do all this special breathing?? I am sure you are dreading going to your treatments. We are with you in spirit and enjoy your weekend "off" from all this


    rainyday- interesting you ask about the insomnia- my RO and the nurses keep asking me if I am sleeping okay and now I think I know why.... I have felt more energy and active 8 treatments in but- I have been sleeping through the night and not liking that alarm going off for my 0730 zap


    Hope everyone enjoys their weekend off and congratulations to those who are finished with rads

  • Bounce
    Bounce Member Posts: 574
    edited November 2013


    Hi Ladies - about sleep issues -


    The day after my fourth treatment I got totally hyperactive and had energy to power a small city. But that soon left and the next week I had some pain which reduced my energy levels pronto. Now - (9 down) I get tired during the day (not the usual sleepy feeling - more like feeling that gravity got stronger and I can't move). I think at the beginning it is more the adrenalin that keeps you up and going than the actual effects of the radiation. I think its emotional not physical. But for anyone with health issues you should check with the doctor if its bothering you.


    With Tamoxifen the first week I hardly slept. As soon as I woke up for any reason I would start thinking about Tamoxifen and treatment etc.


    Then I made a deal with myself that if I woke at night I would only think about sleep related good feelings and that I would do my worrying during the day time. My sleep got much better.


    I went off Tamoxifen a few days before rads and will start again afterwards. It will be interesting to see how I react the second time.


    I can't imagine what it will be like to finish all treatment and stop thinking about myself and my boobies all the time. I know I'll be taking Tamoxifen but not waking up and rushing off to rads each day...... Not feeling like someone hit me in the chest ..... I can't wait.

  • wyo
    wyo Member Posts: 541
    edited November 2013


    Great post Bounce


    I have been jumping up and running to rad then working all day and telling people "please don't schedule anything for me before 0900" After all I have to grab a shower and get on a train after my treatment- crazy.


    Tonight I was at Yoga class and the random thought came over me- I actually felt kind of normal just going to yoga on my friday night like I always do and hardly thought about my breast- except during a few "key" poses where I was stretching the heck out of it haha

  • anne11595
    anne11595 Member Posts: 101
    edited November 2013

    Lanam I had a mastectomy and my skin is red but holding up pretty good. But underarm is a mess. But it took 22 treatments to start to peel. But done with underarm area now. Just the boost. Oh and I'm 58 years old and will have 30 treatments all together. I had a lot of enery at first. But this last week I lost it. So if anyone finds it give it back to me . I really need it!!!!

    Summergal I really wish there was a magic pill for you to take to make it all better. Just fell so bad for you.

    Hope everyone has a good healing weekend. So we can start all over again on Monday. Hugs to all.

  • Jo6202
    Jo6202 Member Posts: 372
    edited November 2013


    Hi LanaM, just a quick note I 'm 63 and having 33 treatments. The last five will be boosts to the tumor bed.

  • LisaSp
    LisaSp Member Posts: 253
    edited November 2013


    Hi radiant people!


    I'm 53 and having 33 treatments. My RO said because I had chemo she wouldn't do less as that course would involve higher doses. Also my tumor was on the left side but I am not doing gated breathing because they just began the treatment at my center the day I started and I did not want to be patient #2. I'd rather be patient #30 frankly, so I decided against it.


    Summergal, so sorry this has been happening to you! Don't worry if you have to go back to 'regular' rads, I'm sure they know what they're doing with that method. And if they can get you the googles that help, press them for them! And the best to you Monday.


    Dennilynn and Rainyday, we're all halfway am I right? Yay! My only effects are slight redness and a bit of soreness that just began this week. I see my RO every week and she just looks at my skin and asks if I have any questions.


    Hope everyone's weekend is great. McKatherine, great song! The Brownie song, am I right? :)

Categories