October Rads. 2009

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  • PauldingMom
    PauldingMom Member Posts: 927
    edited September 2009

    Of course you can join!! Silly Woman! Embarassed We are all about sharing. 

    I was also told Aloe. Picked up some on Saturday.

    I've never had a CT scan. How does that go? I also have questions about long term effects. Anyone have any insight on that? Since going through chemo. and now rads. will I ever be able to donate blood? or organs? or does having breast cancer just cancel all that out?

    Looking forward to my speech in October, but scared too. Any suggestions on what to tell a bunch of very young women about B.C. would be helpful.

    Thanks, Lisa 

  • Kimmer51
    Kimmer51 Member Posts: 26
    edited September 2009

    Hi!  I am so happy that I found this site.  I've learned so much..

    I have had 3rd treatment of 12 Taxols.  I'm seeing my oncologist tomorrow to see how I'm doing and to talk about when to start radiation.  At my last appt with him he seemed to think I could start radiation WHILE doing the Taxol.  However, when my oncology nurse tried to schedule my appt with the radiation doc, the scheduler said she likes to wait until Taxol is over with.

    I can't find any information on this site about this.  I did talk to my best friend who is a nurse at Mayo Clinic about it.  She said that she had heard they were starting to do this.

    It is something I really want to do so that I can be finished with all my treatments by the end of the year (I hate to start all over with my deductible). 

  • jaelsne
    jaelsne Member Posts: 82
    edited September 2009

    Hi Lisa,

      I was on the bone marrow donor list, but I called to let them know about my cancer and they dropped me from the list.  I'm 99 percent sure that would be true of blood donors, and most likely organ donors.  I sure wouldn't want blood from a cancer patient, would you?  We'll have to find other ways to help those in need...  (actually, I've been knitting baby blankets for Children's hospital's neonatal unit in my now copious spare time....)

    Jo Anne 

  • Eph3_12
    Eph3_12 Member Posts: 4,781
    edited September 2009

    HI all,

    Appt with Rad Onc tomorrow to find out particulars-Paulding-thanks for your info from your visit.

    talk soon

    Joni2

  • strngwmn39
    strngwmn39 Member Posts: 77
    edited September 2009

    PauldingMom, 

    Sorry, once you have cancer, you can no longer donate blood or organs, since they have the potential of developing cancer (and therefore giving cancer to another person).

    A CT scan is no big deal - you may have an IV so they can inject a tracer dye at the end for the last few pictures, and you are in a machine that is a donut like scanner that whirrs around and takes pictures. The deal is this, they don't order the scan unless they know the information from it will positively impact your treatment (in other words, if they wouldn't do anything different with additional information, then subjecting you to the scan isn't appropriate).

     Michelle 

  • liztaylor1
    liztaylor1 Member Posts: 95
    edited September 2009

    Hello, Ladies,

    Nice to meet you - I've moved from board to board as this journey progresses.  Dx'd with DCIS on 8/24; lumpectomy 9/18; path report comes in tomorrow.  If clear margins, on to Rad Tx.  Met with the radiation oncologist last week.   I'm supposed to have a total of 35 treatments but we are going on vacation right before Thanksgiving - so, I need to start rads next week (10/1) with simulation this Friday.

    My poor breast is all bruised from the lumpectomy.  I've been using Arnica gel to help speed up the healing so I can move forward.

    This whole thing started only a month ago.  My husband and I are still in shock, I think.   Our support has been tremendous - but it's still happening to us.

    I'm so glad to have you with me and to be with you in the 7 weeks or so.  I read all of your posts (read through most of the September rads group posts already).  SO HELPFUL!!!

     Liz

  • liztaylor1
    liztaylor1 Member Posts: 95
    edited September 2009

    Hello,

    Surgeon called last night with path report.  I have 5mm of clear margins (tumor was 2.5 cm or 1 inch).  YAY!!

    I'm officially moving over to this board now.  Reading all of the September posts, too, since there are so many gems of wisdom.  Simulation is this Friday (9/25) with rads starting next Wednesday.

    Liz

  • shadow38
    shadow38 Member Posts: 76
    edited September 2009

    First of all, CONGRATULATIONS on your clean margins and no chemo, Liz.  I'm really happy for you.  My margins weren't clean.  I had my re-excision on 9/3 after Chemo.  This time, I was free and clear of cancer.  YAY!!  Laughing

    I went for my initial set up today and it went well.  My tech was an absolute sweetheart and answered so many of my questions!! 

    First, they made the mold that will fit around my body to keep me in position during my treatments, then she did some markings with a permanent marker and took pictures, and finally, I had the CT Scan.  Piece of cake.  The whole thing took a half hour or so. 

    I go for my simulation Wednesday (9/30) and start Rads the next day (10/1).  I'm going at 10:30 every morning.  That seemed like a good time.  I'll be finished on November 12th. 

    I'm nervous.  It's the fear of the unknown.  I was told that after having gone thru Chemo, Rads would seem like a walk in the park.  I hope that's the case.  I couldn't stand it if it was anything like Chemo.  I felt like crap by the end of that and I'm just starting to feel better now.  Also hoping my skin holds up.

    I bought Dove body wash today and a big tube of Eucerin Calming Ointment.  I think I'm going to pickup some of the pure Aloe you girls have mentioned as well.  Can't hurt!!

    My very best to everyone as we continue this journey together!! 

  • liztaylor1
    liztaylor1 Member Posts: 95
    edited September 2009

    Dear Shadow,

    Pleased to meet you!!   We are on this radiation journey together.  Whatever a simulation is, I am having that tomorrow morning.  Surgeon took out the stitch today.  She was so good - operated around my nipple (saving the nipple).  When it heals, you won't even able to see where she operated on me.

    The two things that worry me the most about radiation are: the skin burns (?) and the fatigue.  I've loved reading these boards to prepare myself for the next step.

    As an aside, I'm 60 yo - had "suspicious" cevical cells at my yearly exam in late July plus HPV+.  Culposcopy showed the same thing - precancerous cells.  So, I'm now thinking that I'll get through this rad thing this fall - enjoy the holidays - and then discuss a hysterectomy for the winter time. 

    It's back to playing golf in the spring!!  By then, I will be CANCER FREE!!

    Isn't there a t-shirt that says: Liz 1

                                               Cancer 0

    Liz

  • vnelson
    vnelson Member Posts: 15
    edited September 2009

    Hi,  I just finished my chemo yesterday and will be starting radiation within the next few weeks. I have had first consult visit and will be going in for my marking soon. My question is regarding the porta cath - did you have one and if so when do you plan to have it removed? Mine is scheduled to be removed October 8 and some folks are telling me that is too soon.

    Dx: 3/18/09 IDC; 2.5cm; grade 3; stage 1-2; ER/PR+

  • PAP
    PAP Member Posts: 142
    edited September 2009

    VNELSON....My onc wanted to wait till radiation was finished before having port removed.  I wasn't happy about that since it really bothers me and is very sensitive, so he agreed I could have it taken out.  My veins are good so lab work shouldn't be a problem.  Had the port removed yesterday....hallelujah.  I'm still not sure why they want to wait unless it is just in case you need more chemo.  I had no lymph node involvement, so it's not likely for more.  Anyway, had it removed with just a local and it's still really tender around it and I suspect will be for several days, but soooooo glad it is gone, gone, gone!  Patti

  • sakura73
    sakura73 Member Posts: 467
    edited September 2009

    Hello all,

     I had my first radiation treatment yesterday and would love to join this group since i'll be going all through October.

    I did AC x 4 and Taxol x 12, finishing on Sept 8 (I am in the March Warrior Princesses chemo group)  and had the port out  on September 16. My onco was happy for me to have it out that quickly as my blood counts had always been fine. 

    I elected not to have tattoos so have six large crosses on me covered by clear stickers! First treatment yesterday was a complete anti-climax - I was only on the table for 15 minutes and most of that was them getting me into position. I am  using Vitamin E cream but am also going to get a calendula cream after reading about it elsewhere on the Radiation board.

    My naturopath has told me to cut down on carbs and especially sugars - apparently a low carb diet 'cools' your body which helps counteract the effect of radiation. Anyone else been told this?

  • LittleRed
    LittleRed Member Posts: 223
    edited September 2009

    Dear vnelson: I have been advised to leave my port in until my next mamo in March.  I did have node involvement, so my onc wanted to leave it in for 5-6 months post chemo.  I'm not happy about waiting, but I'll just have to get used to it...

  • vnelson
    vnelson Member Posts: 15
    edited September 2009

    Thanks so much! All of this info really helps me and I believe I am going to go ahead and have it removed on the 8th. Mine has been aggravating the crap out of me also Patti. It became inflammed on one occasion and scared me goofy! I just want it out. Mine is pretty deep and will have to go to OP surgery to have it removed. Good luck to all you guys and we'll just keep hanging on for the next adventure.    Virginia

  • kimby
    kimby Member Posts: 32
    edited September 2009

    Hi Ladies,

    I start rads on 12 Oct can't wait to get onto the next step. My final chemo tx is tomorrow. Praying that all goes well. I've been reading all your posts. V. helpful. I hope as we go through this next step of our journey that we can all be of help and support to one another.   

  • Eph3_12
    Eph3_12 Member Posts: 4,781
    edited September 2009

    So, had the "pillow" molded today, as well as the CT & the tattoos.  1st rad scheduled for 9-29-09.  I have an appt with onc on 10-1 & I'm going to insist that the port-be-gone!  Have hated it the whole time (thankful to have had it on chemo days tho', hated it the rest of the time).  Thanksgiving will mean alot more to me this year than in years past is all I have to say.

    Joni2

  • strngwmn39
    strngwmn39 Member Posts: 77
    edited September 2009

    Hello Everyone, 

    I had my sims appointment last week and my first radiation appointment is scheduled for 9-30-09. I'm wondering how many people on this list are having radiation after mastectomy (like I am) versus radiation after lumpectomy? I believe the side effects from treatment will be a bit different for us, as I learned my treatment field will be a bit larger.

    I had the tattoos - and I found them to be very tiny, and the pain was less than a bee sting. I have four of them. The difficulty I am having is that I cannot get my arms all the way above my head so the position I am in is very awkward and painful. Physical therapy is difficult and I am hoping I can get over this hurdle quickly.

    Michelle, age 40 

  • LittleRed
    LittleRed Member Posts: 223
    edited September 2009

    Dear strngwmn39:

    I had my mx in late April, so I've had a while to gain back my strength and flexibility.  My surgeon said to do my exercises, and when I thought I couldn't go any further, to go another inch.  It was painful at first but I am greatly improved at this point.  I still have pain when I extend fully over my head, but even that has reduced. 

    I finished chemo 3 weeks ago and start radiation on Monday 9/28.  I think you are correct, the field of treatment will be larger that it might be for lumpectomy, but I don't know if that will mean different SEs or not.  You might want to ask your onc about taking something for the discomfort prior to your treatments - Tylenol or whatever.  The treatment sessions are not that long, but you could ask about pre-medicating to see if that makes you more comfortable. 

    Best of luck - take care of yourself.

  • jaelsne
    jaelsne Member Posts: 82
    edited September 2009

    Michelle,

      I'm having radiation after having a mastectomy in March followed by about six months of chemo.  Originally they hadn't recommended rads, but since I wound up with positive lymph nodes they siad I should go ahead with it.  I go for my tattoos on Tuesday.  I was told that my rads would be a lesser dose and higher up than someone say, with a lumpectomy followed by rads.  I think my rad onc is going to focus on the area around my upper chest and neck...  so any little traveler devil cells would get wiped out before they hit my brain...

      Jo Anne 

  • debnyc
    debnyc Member Posts: 111
    edited September 2009

    Hi Everyone,

    I have my first appointment with the radiation oncologist on Wednesday. Can you please tell me what to expect? Also, I met with a medical oncologist yesterday. He gave me my first prescription for tamoxifen. He said that I could start taking it immediately, or wait till after radiation. Is there any benefit for waiting until after radiation or should I start now?

    Deb

  • liztaylor1
    liztaylor1 Member Posts: 95
    edited September 2009

    Hi, Deb,

    During my initial meeting with the radiation oncologist he did a brief physical exam (this was two days before my lumpectomy).  We talked for about an hour - thanks to these boards, I had pretty specific questions.  He explained radiation therapy, number of treatments, etc. We talked, mostly, about side effects (skin changes and fatigue). 

    I had my surgery on 9/18.  Today was the "simulation".  Normally, he likes to start rads a month after surgery.  We are going on vacation right before Thanksgiving, so this whole process needed to start earlier.

    The simulation took about 40 minutes.  I met with the doctor for 15" or so - to finish asking questions and to sign the consent.  Then, it was on to a room for "molding". For this, I just laid on a table with my arm over my head (this was the only hard part...) for 20" or so.  During this time, the table went in and out of a CAT scan machine.  They put wires or something on my chest to help with "markings" (these came off after the process was over).   Then, they put 4 large X's in different places (these are made with a permanent marking pen - that may "wear off" on your clothes over time) and, I think, that's where the "tattoos" were put.  These tattoos are so tiny - they were like 4 tiny bug bites. 

    I have a very low pain threshold and found this whole thing to be just fine.

    Hope this answers a little bit of your questions?

    My official rads start next Wednesday (9/30).  Looking forward to getting a move on this process.

    Best,

    Liz

  • liztaylor1
    liztaylor1 Member Posts: 95
    edited September 2009

    Hi, Deb,

    During my initial meeting with the radiation oncologist he did a brief physical exam (this was two days before my lumpectomy).  We talked for about an hour - thanks to these boards, I had pretty specific questions.  He explained radiation therapy, number of treatments, etc. We talked, mostly, about side effects (skin changes and fatigue). 

    I had my surgery on 9/18.  Today was the "simulation".  Normally, he likes to start rads a month after surgery.  We are going on vacation right before Thanksgiving, so this whole process needed to start earlier.

    The simulation took about 40 minutes.  I met with the doctor for 15" or so - to finish asking questions and to sign the consent.  Then, it was on to a room for "molding". For this, I just laid on a table with my arm over my head (this was the only hard part...) for 20" or so.  During this time, the table went in and out of a CAT scan machine.  They put wires or something on my chest to help with "markings" (these came off after the process was over).   Then, they put 4 large X's in different places (these are made with a permanent marking pen - that may "wear off" on your clothes over time) and, I think, that's where the "tattoos" were put.  These tattoos are so tiny - they were like 4 tiny bug bites. 

    I have a very low pain threshold and found this whole thing to be just fine.

    Hope this answers a little bit of your questions?

    My official rads start next Wednesday (9/30).  Looking forward to getting a move on this process.

    Best,

    Liz

  • elimar86861
    elimar86861 Member Posts: 7,416
    edited September 2009

    Coming from Aug. Rads, via Sept Rads and I expect to finish on 10/9.  I've just finished 23/33 treatments; the last 7 will be boosts.  It seems like a lot of you have done chemo, but I didn't have that.  Anyway, as I go into the "homestretch" I'll post on this thread too.

    People just starting Tx will find a lot of interesting info. on those Rads threads from the months past.  My opinion of Rads is that it is freakishly unatural, but I was/am too scared NOT to do it and leave a nasty bit of cancer behind. 

    Some of you might be worried about side effects?  I was.  Surprisingly, my skin is still good, just 3-4 shades darker.  I get tired, but not all day, every day.  I recently developed some reflux, supposedly not due to Rads., but I disagree.  You can all come to your own conclusion on that. When you think of how many women have went through this before us, you know we can make it too, right? 

  • Dolores81035
    Dolores81035 Member Posts: 82
    edited September 2009

     Hello Ladies,

    I started with AccuBoost Breast Cancer Radiotherapy procedure on Sept 22.

     I start radiation on Sept 30. Anyone else start with AccuBoost Cancer Radiotherapy Procedure?

  • LittleRed
    LittleRed Member Posts: 223
    edited September 2009

    Ladies:

    I'm starting radiation Monday and heading back to work part-time on Wednesday.  My plan is to start 3 days a week (8:30-2:00), have rads at 3:30, then head home to my son. I have a min. of an hour commute to and from work.   Hopefully, I can work my way up to a full schedule.

    Has anybody already started rads and work?  How's it going?  I feel stronger now that I'm done with chemo, but I'm concerned about my stamina with the rads.

    Thanks -

  • Eph3_12
    Eph3_12 Member Posts: 4,781
    edited September 2009

     Dolores, I don't know what that Star Wars sounding procedure is, so I guess I'm not having it.

    Little Red, I've been told that for some gals who have had chemo & are going into rads that you actually start to feel better as it proceeds because you are recovering from the chemo, so you feel better each day & the radiation doesn't zap as much as the chemo.  Of course, everyone is different, but I'm hoping that's true in my case!  I've been working all through chemo with just a day off here & there, but it's definitely been a struggle.

    Joni2 

  • Sunris
    Sunris Member Posts: 120
    edited September 2009

    Hello fellow Oct. Rads women...

    I will be joining you all for the Oct. experience. My first appt is Oct. 6 for simulation.  Sure hoping I will be able to get my arm lifted as far up/back? as they want it.  I am 5 weeks post lumpectomy and have good range of motion in my own opinion, but it's still sore for sure. 

     I see that there are more Triple Neg. women out here other than myself also starting Rads in Oct.  Ladies, let's hope these rads kill the crap outta them lingering little cells as we are already at higher risk of recurrence.  

  • dsgirl
    dsgirl Member Posts: 276
    edited September 2009

    Hello again

    I had my first 5 rad treatments this week, and going back for # 6 on monday, so I will be a little ahead of some of you, I have been reading both here and Sept. Rads group.

    So far so good, I have been using the aloe vera as instructed, and have no "sunburn yet, I do have a swelling around the nipple, it's looking just like the bad reaction I had to the blue tracer dye, it did not show up until today, I will be sure to ask doc about this tomorrow as aloe vera does not relieve the pain associated with the swelling. I wear cotton inside my bra, and that seems to help, without a bra any movement does create some pain. The treatment is very short for me, I am in and out in 8 to 10 minutes. I can feel I tense up when the actual radiation is going on, can't help myself, it's no more than 12 seconds on one side, then it buzzed over to the other side and zaps me again for 15 or so seconds, I try to breathe normal, but so far have failed there. The techs are kind, say I am doing ok, and breathing is allowed, heehee.

    dsgirl

  • LittleRed
    LittleRed Member Posts: 223
    edited September 2009

    dsgirl:

    Thanks for the post - I start tomorrow.  Just a little nervous...I know what you mean about the breathing! (LOL)

    It's encouraging to hear you did OK week 1 - Good luck this week.

  • Laurie09
    Laurie09 Member Posts: 313
    edited September 2009

    Hi all

    I'm starting radiation on Wednesday this week. 

    I had neoadjuvant chemotherapy first - finished Mid July.  I had a mastectomy end of August. 

    I'm looking forward to getting this next phase out of the way.  I'm planning on working full time - hoping radiaiton doesn't take too much out of me. 

    Good luck to everyone!

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