MAY 2009 Rads

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  • americanpinay
    americanpinay Member Posts: 338
    edited May 2009

    hello all..hope everyone is doing well...

     Princess...I was also very sleepy yesterday before my 11th rad and did not think to associate it with rad fatigue...but I wasn't sleepy this morning for my 12th rad...hmmnnn...I guess, it comes and goes...

     The rad tech told me that there will be no treatment for Monday, Memorial Day...I guess it's ok to do rads less than five times a week...

     take care y'all

  • americanpinay
    americanpinay Member Posts: 338
    edited May 2009

    what is bolus?

  • lisalisa
    lisalisa Member Posts: 824
    edited May 2009

    Congrats Idaho!  woohoo!!!

    Today was day 7 for me....only 29 to go LOL!  (I have 36 total including boosts).  So far so good.  I'm also "off" for Memorial Day!!!

    Today was hard as a little boy was being radiated in the room next to me.  He was not sedated and was crying and screaming that he wanted to go home.  He broke my heart.

  • kt57
    kt57 Member Posts: 425
    edited May 2009

    chevlev;  My onc told me the taxotere is metabolized 21 days after the last dose and that i would pretty much feel like I did pre-chemo at 4 weeks out.  i am 5 weeks out and feel really good- still have a little neuropathy in feet and hands ( he said that would take a while to resolve) an overall fluid retiention (due to the steroids).  He gave my a diuretic to help the fluid retiention - it is working.  Other than waiting for hair, I do feel pretty much back to normal.

    11 done 19 to go.  I am a little pink in the evening, but it is more tan by morning time - using aloe and vaseline intensive care.     Have drivers yesterday, today and tomorrow --- yack yack yack --- time is going by quickly.  It is a little hectic to try and accomplish 8 hours of work in 6 hours before I dash out the door..... busy is good!    And everyone at work is helpful and supportive.

    Had my chest x-ray and labs yesterday to get my port out tomorrow... YEEHAA!!!   And for the first time in months my labwork is 100% normal!!!!

    Hope you are all doing well... 

  • Cruise4life
    Cruise4life Member Posts: 394
    edited May 2009

    Afternoon Ladies...

    KT57...yeah on getting your port out.

    Pringles...See its really quick and easy...

    Princess...yes we seem to be on the same schedule...and they are closed on Monday - Holiday...

    Had #6 this morning....nothing sore, hot, red or otherwise...just tired from going everyday...we will get a three day repreive after tomorrow...YEAH!!!

    6 DOWN AND 27 TO GO!!!!

  • PrincessKauai59
    PrincessKauai59 Member Posts: 288
    edited May 2009

    #6 Down and #24 to go, last five will include the "boost" to high risk areas. 

    americanpin - I sent you a PM about Bolus, I asked the same question of my Rad Techs.

    Guess being sleepy may have been more related to staying up late and watching Sex and the City re-runs.  I'm off to a healing flower ceremony with one of our fellow posters!  Best to all!

  • Bold
    Bold Member Posts: 692
    edited May 2009

    Greetings Rad sisters. I left my Sims kinda sad and mad. Everything went well the tumor board said to only radiate the breast and not and nodes. So that was good. What got me going was she said no swimming at all. Well I ask how about after Rads. She said take the summer off for sun and the pool. I have to tell you that is my life in the summer. I garden and swim entertain BBQ. Its hot so I jump in cool off and then get back to work or fun. I have been known to jump in right before bed to cool down and make it easier to sleep. I was a life guard when I was young and on the swim teams through out school. I just hate that it is taken away from me. It seems like the winter was very hard with chemo and now no summer either. I know that I am making sure that I am here next summer. But still it just bummed me out. I think I should be able to jump in real quick and get out right away if I have aquafor on it water proof. How about a waterproof wet suit.?

    Anyway just bitching. I thought that this weekend I would swim to my hearts content. And right before I left she told me to stay out of the water because they want there blue pen to stay on til Tuesday. I am going in anyway and if it looks like it is fading I will have my DH rewrite with a stupid sharpie. Now you all can tell I have a problem with authority figures. Spent grammar school in the hall way. Learned to behave in high school. A master by the time I got my masters. I think I am reverting. I just hate that we have to go through this and there is nothing that can be done except to capitulate.

    I was told to drink 8 to 10 glasses of water a day. And eat a lot of protein. I have my dry run on Tuesday. They said if it goes fast and well enough they may actually start rads that day. We will see.

    I am glad I am with such great woman that are going with the flow and not stressing. I will be ok after I morn the loss of my favorite hobby.Cry

  • ddlatt
    ddlatt Member Posts: 448
    edited May 2009

    ivorymom - we never get gowns at the hospital here in reno (renown). we get pillow cases! there are hundreds of them stacked up in the changing room. since i have a bilateral mastectomy and i'm not shy, i don't care. but if i still had my large breasts, this would annoy me!!

    bold - i'm also totally bummed out about no swimming. it's my very favorite sport and i usually swim for hours every day in the summer. but it makes sense to me - think about how tender our skin will be during radiation and susceptible to infection. my onc said the chlorine would be especially bad for the skin.

    4 down! 

  • Genia
    Genia Member Posts: 1,335
    edited May 2009

    Today made number 14 for me.....and I am hurting. 

    My underarm and that side of my breast is very tender and sore.  I have been totally wiped out today......just don't feel good!!!  If I'm hurting this bad...this early in the ballgame....what wonderful things do I have to look forward to!

    Genia

  • Anonymous
    Anonymous Member Posts: 1,376
    edited May 2009

    Kathy - I agree with you - I am 5 weeks out from last chemo, and with the exception of a little numbness in my fingertips, I pretty much feel great (especially now that the scalp infection is clearing up and I don't look like a mutant).  I think I look a little swollen from the steroids, or maybe it's just that my face is rounder than I thought and all of my hair made it look not as round.

    8 down, 17 to go!  Been just feeling a little swollen in the evenings at the treatment site, not too bad, and a little warm.  Aloe is working great.  The onc nurse who examined me yesterday said that because I'm not very large breasted (I always thought I was, but I guess from what she sees, I'm not, she called me "tiny" - something that usually isn't associated with my boobs!), I may not see the really radical side effects (I hope not!), just like Meg mentioned.  I too am free of treatment on Monday, the hospital is open, but they closed the rad onc department and some of the other treatment centers, I guess it's not a "critical" area to remain open.  Was wondering about that.  Oh well, pushes treatments back by a day, but it's okay.

    Have the day off today (it's my official paid Memorial Day holiday, because next week is my furlough week and I can't claim unemployment if I am getting paid), so my best friend is picking me up in a bit and we're off to the outlet mall, some lunch and she is insisting on driving me to treatment, since we'll be out and about and there's no reason to rush me back.  She is such a wonderful friend, took me to my last chemo, calls frequently to check on me (her mother died of bc over 20 years ago after a long fight, so it's something that is really close to her heart), and I couldn't ask for a better friend.  She's getting a very nice lunch today on me!

    Have a wonderful day, everyone!

  • Texas357
    Texas357 Member Posts: 1,552
    edited May 2009

    Americanpinay: A bolus is a thin rubbery thing they slide over the area to keep the radiation close to the skin. They use one on me every other day.

  • ddlatt
    ddlatt Member Posts: 448
    edited May 2009

    chelev - our radiation dept is also closed for memorial day. i'd much rather have it on holidays and get it over with! 

    i have treatment #5 today. so far no reddening of the skin. i'm applying aquaphor after treatment and again at night. 

  • FACECRAFTER
    FACECRAFTER Member Posts: 1,092
    edited May 2009

    I went for my last "check" today and I start on Tuesday.  He said the treatment will take about a half hour. I think he includes the time to get dressed and undressed, I can't believe it actually takes that long.  We'll wait and see.  The rad ofc is only just down the road from my house, so no long drive, for which I am grateful.  Enjoy the weekend,  JUDY

  • lisalisa
    lisalisa Member Posts: 824
    edited May 2009

    pillowcases!  towels!?!?  i guess i should be happy that i get TWO gowns.  i put one on with the opening in the back.  then i put on another with the opening in the front.  i walk to my rads room.  take off the top gown, get on the table and then pull the sleeve down for the radiated side.

    when i'm done, i go back to the changing room, apply my aloe & aquafor and wipe my slimy hands on the gowns before putting my clothes back on.   works for me :)

    they have a HUGE cabinet filled with literally 500 gowns or more!

  • ddlatt
    ddlatt Member Posts: 448
    edited May 2009

    facecrafter - to make the most of the time, i wear jeans and a shirt with snaps. no bra, of course, because those days are over for me, thank god! it takes me less than 2 seconds to pop open the snaps, and i'm on the table, have a CT scan which takes about 4 minutes, then i have 4.5 minutes of tomotherapy radiation, then i'm off the table, snap up as i leave the room. no muss, no fuss. it takes me 10 minutes to drive to the hospital, so overall i'm spending about 45 minutes/day dealing with on radiation. sure beats the hours and hours of chemo.

  • BonnieK
    BonnieK Member Posts: 655
    edited May 2009

    Hi everyone,

    Today will be #18 for me, with just 10 more treatments to go.  So far, radiation has been much easier than chemo and I hope that all of you have minimal SEs too.  SEs for me so far -- a mild rash on my chest that is expected to go away after rads; fatigue that comes and goes; a mild sore throat from rads to subclavical and axillary nodes.  My skin is a little pink and is starting to feel tight, but it doesn't hurt at this point.  I also have mild lymphedema in my left arm and hand that started before rads, and am seeing an LE therapist every week and doing exercises every day. 

    No rads on Monday -- YEAH!!  The 3 day reprieve will be great! 

    Hugs to everyone,

    Bonnie

  • FACECRAFTER
    FACECRAFTER Member Posts: 1,092
    edited May 2009

    dd  maybe it takes more time if you wore a gown instead of a pillowcase !!  LOL...just kidding. 

    we'll see.  I think they said 15 min last time..30 min this time so who knows..we'll see on Tuesday.. Can't wait for this part to be over and I can start getting filled up again!

  • americanpinay
    americanpinay Member Posts: 338
    edited May 2009

    hi everyone..

    texas...thanks on the bolus info...

    genia...sorry to hear about your SEs...hang in there...

    facecrafter...good luck on Tuesday...hope the first TX will be easy for you as it was for me...

    bkokie...thanks for the post...it gives me hope that rads will really be a breeze compared to chemo...

    had 13 of 33 today and so far so good...keeping my fingers crossed that it stays this way...

    about gowns, towels and pillowcases...I put a gown on with opening to the front...after I lay down on the TX table, rad tech moves one side of the gown out of way to make sure the tattoos line up with the machine...the first time, I asked him if I needed to remove the gown sleeve as I am also supposed to get treatment on the nodes/armpit...he told me that there is no need to do that because the "rays" go through anything except for the metal that they use on the machine...hmmnn...

     have a great holiday weekend everyone...

  • Anonymous
    Anonymous Member Posts: 1,376
    edited May 2009

    Okay, just to clarify - I do wear a gown, open to the front, and when I remove my arms from the sleeves, they cover up the non-treated area with usually a towel, but sometimes they use a pillowcase.  Although since I am the last one of the day, I guess I could just wear a towel if it were big enough!!!  can you see trying to wear a pillowcase?? 

    Treatment #9 down, 17 more to go.  Met with the nutrionist today to see if I had any questions, and she reminded me about not taking any antioxidant vitamins, but a multivitamin is okay if I were used to taking one prior to diagnosis.  Otherwise, stay away from C & E, and soy, because of the ER/PR +.

    Had a nice day shopping with my best friend, who also took me to treatment because it was on the way home.  She's a great friend, and we were in and out in 10 minutes and on our way.

    Have a nice night, everyone!

  • jrgolomb
    jrgolomb Member Posts: 1,236
    edited May 2009

    Hello Rad sisters.  I will officially start Wednesday the 27th.  I was told if there is a nice fluffy gown available, I can use it, and if not, I will wear one of the classic hospital gowns.  I had the simulation done on wednesday and thought I might start today-Friday, but nope, gotta wait till next weds. 

  • americanpinay
    americanpinay Member Posts: 338
    edited May 2009

    Jess...I noticed that they schedule it in a way that you get three treatments for the first week...not sure if there's a special reason for that...anyway, good luck on Wednesday...hope it'll be easy for you as it was for me...take care...

  • jrgolomb
    jrgolomb Member Posts: 1,236
    edited May 2009

    yeah, I wondered about that, and asked.  They didn't seem so concerned about only three days.  and then a break.   i hope it will be easy too.  thanks, americanpinay

  • PrincessKauai59
    PrincessKauai59 Member Posts: 288
    edited May 2009

    Happy Friday everyone!  I'm grateful for the break and ability to go out of town for a few days.

    Completed #7 today, so far so good.  Am so sleepy, but that has to do more with being a working mom I think. Viva la Vida!  Cathlene

  • kt57
    kt57 Member Posts: 425
    edited May 2009

    Hi May Ladies:   12 down and 18 to go.... this is really going by quickly.   Got my port out today YIPEE!!!!  Another milestone.  I didn:t expect it to take as long as it did - 30 minutes or more.  I kept it... hope to find a large gemstone and have a jeweler make a pendant out of it.....one unique piece of jewelry!

    No SEs thus far - am a little tanned but that's about it.   I joked with the crew that I would have to go to a tanning bed to even it out -- whoa, I got the business about staying out of a tanning bed ---- I was only kidding...

    Meg: my experience is much like yours, right down to the special parking.   Must be "Minnesota nice" - I get my rads in Duluth.

    I get a three day break from rads.  Fine with me... I'm getting bench butt form all the time in the car.....Laughing.

    Have a great weekend everyone!

  • Cruise4life
    Cruise4life Member Posts: 394
    edited May 2009

    Evening Ladies...

    Got #7 done today...and only 26 more to go...Nothing noticeable...no pain, no redness, no hardness...no nothing...

    We have gowns too...small and large...of course...opened in the back for easy access to take the arm out.  My sessions last less than 10 minutes...and I am out the door.  It is way easier than CHEMO...just a pain to go in everyday...

    My doc said I can swim....as long as I wash off the chlorine...so glad as we have a pool in our backyard and it has been warm lately.

    I think we all get a three day break in Rads...YIPPEEE....

    Have a great and safe Memorial Holiday!!!!

  • AlohaGirl
    AlohaGirl Member Posts: 213
    edited May 2009

    Two down, twenty-three to go for me.  Yesterday took a lot longer than the first one.  Seems they were having trouble getting the right depth.  But I am glad they are being careful.  Also met with the doctor yesterday (apparently Fridays are my day to do so).  So far, all is well.  I do feel like the treated breast is more tender than it was before and I have a little pain in the top front of my armpit, but it is hard to tell if the pain is related to rads since my breast was still tender from the surgery (and now PMS).  But I figure if I am not sure whether I am having a SE it must not be too bad!  Definitely no fatigue or burning yet.

    I was disappointed that the doctor told me not to wear underwire bras at all during treatment (I'm a 36D or DD depending on the style of bra) -- I had thought that wouldn't start until I had skin issues, but apparently they want me to stop wearing one now to prevent chafing.  I ordered a couple of bras online last night from Title 9 and Jockey.com that look like they are shaped more like normal bras but have no underwire.  I don't mind sports bras but would rather not have my breasts squished together all the time.  For the next few days, it is sports bras for me, but that is fine.  I have plenty.

    I hope everyone enjoys their 3 day break!!!

  • ddlatt
    ddlatt Member Posts: 448
    edited May 2009

    kt57 - when i was a patient at kaiser in san francisco, we had to pay for our parking at the doc's office and even at the hospital!! there was a ticket machine in the lobby where you had to stand in line and then pay for your parking. can you imagine treating patients like that?  and the parking was in a huge garage, not at all convenient. when i moved to reno and then was diagnosed with cancer, i think my biggest shock of all was the FREE parking everywhere in reno, and the special parking for cancer patients at the hospital. i've lived here almost a year and still can't get over the free parking. amazing.

  • Cruise4life
    Cruise4life Member Posts: 394
    edited May 2009

    Aloha girl...I am still wearing my underwires....they are the only thing that can hold me up...LOL

  • Anonymous
    Anonymous Member Posts: 1,376
    edited May 2009

    Alohagirl - I am also wearing mine.  I typically wear a 38-B, and they told me at the radiation facility that I'm on the small side (?), and that the underwires shouldn't be an issue.  I've had treatment #9 out of 26 yesterday and I have no chafing or anything, just some mild-to-moderate swelling near the lymph node and extreme side of my breast area.  I did stop wearing any bras that might have been really tight, just to make sure I'm comfortable, but so far, so good.

  • Bold
    Bold Member Posts: 692
    edited May 2009

    Hope that everyone is having a wonderful weekend!!!  I start on Tuesday with final sims and maybe even rads. I am all marked up for the weekend you could see it in a tee shirt!Yell I am going to go swimming this weekend I will just be careful and not stay in long enough to fade there markings.

    I am so glad to hear that no one is experiencing bad SE. It is very encouraging.

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