Radiation post reconstruction - anyone doing it??
Comments
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Thanks muska for the info. We are over inflating my TE so that there might be extra skin to use of some is too damaged from rads. Not excited to have it in me for so long but I am slowly getting used to the rock
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I will have a UMX with immediate DIEP reconstruction this Friday. I will start radiation sometime in July.
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So sorry not buying it and now apprehensive, I start my rads today, I had a mastectomy 2 years ago with saline implants at the same time. I'm so nervous about the possibilities, also the second time for radiation so more room for problems. You are not alone, it stinks that the treatments are so hard to endure. Best of luck, Stephanie
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Hi aff, I did not know you are having rads post reconstruction, we have one more thing in common. Strength for all of us this week. Stephanie
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Radiation after reconstruction surgery is not the usual path. My PS is confident that following DIEP reconstruction the flap will hold up well to radiation. He said that with a strong blood supply he believes the only issue will be minor shrinking. My new breast is actually a bit larger than my natural breast to accommodate any shrinking. Here's praying that our rads road is uneventful
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I had rads about 8 weeks after a UMX with DIEP. The breast & skin held up really well as it was also built a little larger to allow for rads shrinking. It did get a bit lifted and tight, but my PS was able to fix it in an outpatient revision procedure. In fact, I think he pretty much took the DIEP apart and put it back together in a 45 minute procedure. He also did some minor fat grafting as a touch up. I declined a lift to the good breast because I am small so the difference was negligible.I was fortunate in the whole reconstruction process. Because my tumor was high on the chest wall at the 12:00 position, My BS spared the skin and areola and the PS build the DIEP from that location, there is a small scar but I can wear anything. I came out with a stage 1 nipple.
From speaking with the RO, it seems that rads after reconstruction is actually pretty common around here (NY) although from reading these boards I realize that is not the case in most places. No one suggested I delay it.
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Rmanmom - That is great news about the breast holding up well. Thank you so much for your response. I start rads tomorrow and have been a bit anxious about it. Not like I was before surgery, but a bit. I had skin sparing but not nipple sparing so I'm still trying to decide between nipple reconstruction or 3D tattoos. I have a while before I have to worry about that.
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Good luck you will do fine! Just keep up with the creams (aloe or whatever your RO recommends). I was nervous too because especially after the rough DIEP surgery and recovery I certainly didn't want my new breast destroyed by radiation, but that did not happen at all. -
just had my year exam post reconstruction then Rads - PS says looks very good - soft - no shrinkage - no dimpling - but did warn, as Muska did, that sometimes things don't happen right away - it's been 2 months since Rads & i am hoping things stay the same.
I know it is difficult (i know it was for me) but the main focus is to rid ourselves of the cancer for good!
for me it's on to the last question - to nipple or not nipple?
the outcome was not the fairy tale they fed me - the left side will never look like the right - when i yawn or sneeze it contracts like a muscle - it sits high & round while the right side is more triangular & sags a bit - not totally sure that if someone had showed me a picture of this outcome i would have endured all it took to get here . But here i am - still alive & kickin - slightly different on the outside but still the same old me on the inside.
Best of luck to all of you - listen to all the advice & comments but remember than everyone's story is a little different
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I'm almost halfway through rads, 12 of 28, and so far so good. I'm slightly pink but no skin reaction, no tightness yet and no itching, and no shrinking yet. I know it very early but I'll take each good day I have. Saw my PS on Wed and he was very happy with the way my skin is holding up. I won't see him again for 2 months. I won't have any revisions for at least 6 months post rads so I have lots of time to decide on nipple or not.
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sounds like your doing good!! hang in there! i saw my PS and he said it looks good - so far still no reprecussions from the Rads
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Ladies, I had follow-up appointment with my PS yesterday. It has been three months since I completed rads. I am happy to report that everything looks very good. The left side that was not radiated looks excellent, the right side - radiated - looks very good. No adjustment needed. Both are symmetrical and the same size, everything looks perfect in swimsuit and when dressed.
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wonderful news!! did you have any Lymphnoid involvement? I had 15 removed & i now think that's what is causing my tightness under the arm & new breast - i do have an area of scar tissue i can feel & i'm wondering if that can be removed.... i have an appt on the 21st with a different PS - just to look things over & tell me what he thinks i should do going forward - pretty sure i will do the nipple recon & my right side (i had a reduction) needs a tuck under my arm. Otherwise i am pretty happy with the girls
in a bra & suit no one can tell - tho my new "breast" does sit a little higher & firmer - i am hoping the nipple addition will make it more triangular & maybe sag it a bit Ha!! never thought i'd wish for that!
anyway - glad you are happy with the end result!!
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Hi notbuying, yes I did have lymph nodes involvement and was radiated in the armpit. Good luck with your consults!
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but no tightness?? makes me a little crazy sometimes....how are you doing on the Arimidex?
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No tightness. I have been doing stretching exercises through chemo and radiation and increased exercise load since radiation ended. Do a 30 minute session with personal trainer once a week (muscle conditioning with low weights), 1-2 zoomba classes a week, a lot of walking, try doing a yoga class on Sundays - very good for stretching. My PS also recommended delicately "moving" the implant on the radiated side every morning (moving is not the right word I guess...) and I have been doing this since radiation ended. She told me to continue b/c shrinking and hardening might continue.
Speaking of Arimidex, I do have some stiffness in the joints that I never had before that is greatly helped by exercise and some increased vaginal dryness but no major side effects so far. No hot flashes, mood changes or sleep problems. Sleep is actually much better than while I was undergoing chemo. OTC lubricant is enough to take care of the dryness. Also, I was pre-menopausal at diagnosis and was put into menopause by chemo so I am not sure what it would be like even without Arimidex.
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