December 2011 Rad

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  • seacretgardn
    seacretgardn Member Posts: 269
    edited January 2012

    Michelle and Ann, thank you for your replies.



    Michelle I too am angry about the TEs. I definitely felt "talked into", and unfortunately was alone during my visits. The bs was also under the impression prior to surgery based on my MRI that I would most likely not need chemo/rad. I was under the impression that I would NOT get the expanders if node involvement was found.



    My poor family listens to me complain more about these darn peace robbers than anything. They make my arms numb and my pec muscles spasms constantly. I knew I would hate them.



    I have refused fills and agree with you, I can feel the fluid moving around and cant understand how

    they would not interfere with rads.



    I will def push for removal prior to rads.



    Thank you so much and Ann good luck with your rads and future reconstruction and Michelle you too!

  • kennylynne
    kennylynne Member Posts: 152
    edited January 2012

    Congrats to the ladies that finished!!!! Love the poem!

  • Ralsper
    Ralsper Member Posts: 352
    edited January 2012

    Michelle- Thank you!

    Windlass - I am with you 100%

    Ann Alive - Even though I will begin my rads on January I also joined this threat because I was in a threat with a lot of these women during chemo and I missed their wisdom, courage and good heart. My RO answered the same as yours: What's to aim at for the boost? I do not have enough info, but I know that if I insist I can get the boost, but... do I want it?

    Secretfardn - I had the same chemo treatment (4 AC followed by 12 Taxol).  I highly recommend you to read the threat June2011 AC & T Groupies Unite! and please do not hesitate to send me a PM if you have any questions. While on chemo I didn't read anything about radiation and I think that was a mistake. I had my first appointment with my RO 3 weeks before I finished chemo (11/29/2011). AnnAlive is completely right about the TE and radiation. When I met with my PS 8 months ago, he explained to me with details the procedure and he decided to perform a "special" surgery in case I would need to have radiation.  They place the TE underneath the muscle and add a piece of "skin cadaver" to support and protect the TE from the radiation. The fills are not painful, but the TE is uncomfortable. They filled most of my TE during chemo and PS finished filling completely 1 months ago (for all the reasons AnnAlive explained). Well, one week ago my RO suggested that the liquid of my TE should be removed (not the TE just the saline), so my skin doesn't get too damage (basically just cosmetic reasons). Well, if the TE does not interfere with the main purpose of the radiation and my RO wants it removed for cosmetic reasons, he should discussed it with my PS as I asked him to do it 2 months ago!!! Anyway, he finally called and my PS prefers not to remove the saline and I trusted his opinion completely. I keep you post it!

  • Anonymous
    Anonymous Member Posts: 1,376
    edited January 2012

    Wheee! I got #25 done today, so the lymph node rdiation is done!! Now three more treatments to the chest wall, then five boosts, then I am outta there! (Blister-free and mostly pain-free, so far.)

    Shelley: You've inspired me. I plan to write a poem to the radiation techs I have been so surly to. I did apologize today and tell them my quiet demeanor was not their fault and that I am grateful for their help.

    Pebee: Wow - Congratulations. How are you feeling about being done? Has it even sunk in yet? 

    LuvRVing: I am also at DFCI (getting TDM1 every three weeks, but rads elsewhere).

  • AnnAlive
    AnnAlive Member Posts: 450
    edited January 2012

    Ralston - Good grief (re: your story to Seacretgardn)! So PS fills and then RO wants to unfill? They should get their plan together. Undecided  I have read of part of someone's fill being removed if the TE is full enough to block the ideal angles for radiation. I asked at simulation if mine was OK (not that full at 420cc on the non-rad side) and the tech said no problem. I do have the cadaver skin "slings" PS called them -- but mine are from calf skin, not human. He didn't say they were there to protect from radiation, but to help close a gap from not enough muscle to cover the bottom of the pocket as the TE is filled. It is there to support the TE and subsequent implant, or they could extrude. When he went in to replace/remove it, he said the sling had grown well into the muscle on that side. I haven't heard anyone say that emptying the TE will cause the skin to get less damage cosmetically--interesting. Doesn't this make you feel like we are all in the experimental stage of this procedure!

    Actually, the question "What's to aim at for the boost?" (after mastectomy and excision of the original scar) is my question to my RO. I hope to find out Friday at my dry run whether he still wants to do boosts, if I don't see only a tech that day. I hope I see RO to hear the whole plan. I also do not know whether I do or don't want the boost, so in this case will defer to RO's expertise.

    Windlass - so encouraging to hear how well you've done! Blister-free and mostly pain-free is a good thing!

  • Anonymous
    Anonymous Member Posts: 1,376
    edited January 2012

    Ann: I suspect we IIIC's are pretty much automatic candidates for the boost, unless there is a bad skin reaction to the primary radiation treatment.

  • YaYa5
    YaYa5 Member Posts: 667
    edited January 2012
    michelle, i had #24 full breast today and then they marked me up for the boosts under my arm which start friday.  i wanted to tell you that one of the rads therapists showed me a brand new pen that he had put my name on!  they marked me up a lot today, so i was really happy that i had a new pen, but i never would have thought about it without your posts.  the therapist who got the new pen is also the one who gives me his arm when he gets me in the waiting room.  i think i have a LOT to be grateful for!
  • LuvRVing
    LuvRVing Member Posts: 4,516
    edited January 2012

    To be clear, my TE needed to be removed because the RO said it was covering my heart.  In order to use several angles to hit my chest wall and skin yet avoid my heart and lungs (11 different zaps), the TE had to go.   I made a comment to Dr. Harris about MDA requiring patients to have their TEs drained before radiation and he said they also would have wanted it removed.  So there was something unique about my anatomy probably complicated by the fact that I had already received Mammosite radiation in that area. 

    #29 is done, I'll finish tomorrow so long as the weather is not too nasty (storm predicted). Otherwise, I will skip #30.   The area of my mammary nodes is improving and the rest of the skin has held up just fine.

  • Ralsper
    Ralsper Member Posts: 352
    edited January 2012

    AnnAlive - I also hope to see my RO to hear the whole plan. I haven't heard from them, so I am calling tomorrow. Believe me, I will not hesitate to change RO if I don't feel comfortable (I learn that from Michelle... Oooh, I remember perfectly what she went through) If my TE is blocking the ideal angles for radiation, I will not have any problem removing it, but my RO was just concerned about my skin getting more damage with the TE. I remember perfectly 5 minutes before my UMX, my PS told me again that he was going to place the TE taking into consideration that I may need radiation in the future and made sure that I understood that it would've been a totally different surgery if radiation was not in the picture. I want to believe that they know what they are doing, but it is hard...

  • bgail84
    bgail84 Member Posts: 94
    edited January 2012
    LuvRVing, am so excited for you today!!! Laughing
  • LuvRVing
    LuvRVing Member Posts: 4,516
    edited January 2012

    Thanks, Gail!  It's snowing and nasty here this morning.  It needs to switch over to rain this morning, as the forecast indicates.  I've been looking forward to this day since early April!!!

  • twistedsteel
    twistedsteel Member Posts: 156
    edited January 2012

    Best of luck, Michelle. I am so happy that you are so very very very close to the finish line! Safe driving.

  • LuvRVing
    LuvRVing Member Posts: 4,516
    edited January 2012

    Still snowing and now a little sleet, too.  It's supposed to warm up to the 40's but it's going to have to hurry up!  We are supposed to go to dinner with our best friends tonight, to celebrate THE END!  The latest forecast says it will switch over around 2, which will work. 

  • YaYa5
    YaYa5 Member Posts: 667
    edited January 2012
    michelle, i hope the weather gets better in time for you to finish.  good luck and (hopefully) congratulations!!!
  • michelleo13
    michelleo13 Member Posts: 342
    edited January 2012

    Good luck today Michelle!!!

    Tx #20 for me today. Only 10 more to go. So far so good!

  • Southamptonmom
    Southamptonmom Member Posts: 491
    edited January 2012

    #12 for me. I have blisters already! I can't wait for the kids to get home so I can shower and get some of the itchiness off of me!
    Michelle, be safe and congrats! We should cheer with a glass of something tonight!

    Congrats Shelley and Pebee!!!

  • Ralsper
    Ralsper Member Posts: 352
    edited January 2012

    Rose - I am sorry about your blisters. Isn't too soon for blisters? What are you using to protect your skin?

    Michelle - Please try not to stress about the weather and be safe! Today you have so many reasons to celebrate!!! I am with Rose. We should celebrate with a glass of something tonight Smile

  • LuvRVing
    LuvRVing Member Posts: 4,516
    edited January 2012

    I went and I am done!!! On my way to dinner and drinks...more later.

  • Anita333
    Anita333 Member Posts: 45
    edited January 2012

    Full breast radiation #25 done!!!!!!!! Cool

     Starting 5 boosters tomorrow. 

  • YaYa5
    YaYa5 Member Posts: 667
    edited January 2012

    anita, you and i are in exactly the same place with radiation.  i know you're as excited about having that part over as i am!  congrats!

    by the way, i've found something that is really helpful for burned areas.  has anyone heard of it?  it's called mepilex and it's a bandage-like cover to place over your burned areas.  it helps because my clothes don't rub against my breast.  i've really been happy with them.  here's a website:

    http://www.healthproductsforyou.com/p-957-molnlycke-mepilex-soft-silicone-absorbent-foam-safetac-dressing.html

  • Anita333
    Anita333 Member Posts: 45
    edited January 2012

    Congratulations YaYa5!  

    oh yes I am happy. I even did a happy dance in front of the technicians today. Smile

    They said that my skin did extremely well. It is in some parts a bit pink but not everywhere. They said that they would be really surprised if my skin would cause any serious issues.

    All I am using is some aloe vera gel in the evening (usually every second night).

     

  • kennylynne
    kennylynne Member Posts: 152
    edited January 2012

    Congrats Michelle!!!! Enjoy your supper.Smile

    #20 for me today 5 more to go!!!! Skin is starting to break down and have a nice looking rash which just started today.

  • kennylynne
    kennylynne Member Posts: 152
    edited January 2012

    Congrats to you too Anita!!!!!

  • Ralsper
    Ralsper Member Posts: 352
    edited January 2012

    Congrats to all the ladies that finished rads! Thank you for posting your experiences, because it has helped me to know what to expect.

    Well, I think I had bitch so much that the head of the department called me today. She apologized about the confusion my RO created suggesting to unfill my TE. She told me that since I had a sparing skin mastectomy, they will radiate my chest wall and probably my skin will break (she said we have to hope for the best, but prepare for the worst) because it  has been already pulled, streched, cut, etc., but she will meet with me every week to make sure everything goes according to the plan and take care of my skin. I feel much better. I am been treated at the Seattle Cancer Care Alliance, so definetely this is what I was expecting from them.

  • bgail84
    bgail84 Member Posts: 94
    edited January 2012

    So excited!! I will finish rads tomorrow. On the other side, I have a younger friend who was told today she has BC. This disease hits so many of us! Makes me so angry.

  • LuvRVing
    LuvRVing Member Posts: 4,516
    edited January 2012

    Congratulations to everyone getting it done!

    As Papa Smurf said, "not much longer now, my little smurfs!"

    We went to dinner with friends, I had a couple glasses of Prosecco, and I don't have to go back to Dana Farber until June.  What on earth will I do with myself???

  • Ralsper
    Ralsper Member Posts: 352
    edited January 2012

    Michelle - I love you!!! You are such a funny, brave and positive Lady. Well, believe it or not, I got depressed after chemo, because I had all this extra time in my hands without visiting doctors or having treatments that I had the same thoughts as you. I think I understand better now the purpose of so many therapies to help you understand your "new life". Best wishes.

  • YaYa5
    YaYa5 Member Posts: 667
    edited January 2012
    michelle, i'm so extremely happy for you.  you don't have to go back until june???  WOW!  i'll bet you're ready to get in that RV and head out.  i hope you get to do it very soon.  CONGRATS!!!
  • Anonymous
    Anonymous Member Posts: 1,376
    edited January 2012

    Congrats to Michelle and all the other great ladies on here who have finished rads or are about to finish.

    Ralston: I am gld they are finally listening to you and addressing your concerns. Good luck!

  • Vicks1960
    Vicks1960 Member Posts: 473
    edited January 2012

    Michelle, and all you other ladies finishing Rads!!!!!  CONGRATULATIONS!!!! Sealed

    I finished mine November 18, (internal brachytherapy) My breast is almost back to normal, other than still looking toasted on the lower side  (where tumor was)

    It is WONDERFUL to have this behind us.  I  have diagnosis April 17, see MO the 18th and the RO on the 19th.    Have been on Letrozole (generic Femara) since Nov 21.  Only SE is more hot flashes than I had going thru menopause, and some sleeping problems during the night, but those are small prices to pay to keep the devil away!!!!>

    Here's to a healthier year for everyone here.

    Vickie

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