how soon after radiation?
hi all,
i'm looking for some feedback. i had a bilat mast. in feb with tissue expanders. just finished radiation 2 weeks ago, and went to see my PS yesterday. he said my skin looks good and to come see him again in october, and that probably he could do my exchange-for-implants surgery before this year is through. i had always heard/thought that we need to wait at least 6 months after completing radiation, for the skin to finish changing and healing? i asked him this and he said my skin looks good, so we'll see. i had 33 radiation treatments.....28 and then 5 boosts. my skin was really fried, blistery and awful but it's healing up quickly. anyway, i wonder what everyone else has heard about this timeline? thank you ladies!
christine
Comments
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I had a bi-lat, chemo and 33 radiation sessions (28 regular w/bolus and 5 boost). I was told to wait at least 6 months or longer for the healing process, but I was also told not to do implants because the radiated tissue won't be as soft and flexible and over time it will much more noticable with an implant. I talked to a few surgeons and they all seemed to agree that because of the radiation I should stick with DIEP.
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Hi Christine,
I am about at the same point too, I finished rads in June and actually had "forgotten" the time frame on my reconstruction! Ha! My Mom had been pestering me that her friend (who was a RECEPTIONIST at a doc's---NOT an onc either---years ago) kept saying to her "I don't know why she hasn't had that done already---so and so had hers done during the surgery---blah, blah, blah"! OMG I am getting pissed just typing that. People can be SO annoying. They have NO idea how different each person's case is. So, anywhoo I have an appointment w/my PS Sept 10 to go over my options and a time frame. I am going to Johns Hopkins and they do not reccomend implants if you've had rads for the reasons Jenn mentioned, as well as the high failure rate because of the skin condition. I will probably do DIEP too, although of course there are issues there, some being the long surgery time, as well as an at least 3 day hospital stay, plus there is always a posibility of rejection. I'll know more after the 10th and will be sure to fill you in. I'd like to hear how you are doing too!
Take care,
Sharon
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Hi Christine,
I am about at the same point too, I finished rads in June (bilateral mx, chemo, rads) and actually had "forgotten" the time frame on my reconstruction! Ha! My Mom had been pestering me that her friend (who was a RECEPTIONIST at a doc's---NOT an onc either---years ago) kept saying to her "I don't know why she hasn't gotten that done already---so and so had hers done during the surgery---blah, blah, blah"! OMG I am getting pissed just typing that. People can be SO annoying. They have NO idea how different each person's case is. So, anywhoo I have an appointment w/my PS Sept 10 to go over my options and a time frame. I am going to Johns Hopkins and they do not reccomend implants if you've had rads for the reasons Jenn mentioned, as well as the high failure rate because of the skin condition and the fact they are not considered "permanent" meaning implants need to be replaced eventually (more surgery later). I will probably do DIEP too, although of course there are issues there, the long surgery time, as well as an at least 3 day hospital stay, plus there is always a posibility of rejection. I'll know more after the 10th and will be sure to fill you in. I'd like to hear how you are doing too!
Take care,
Sharon
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I had bilat with TE, chemo, rads and ooph.....PS likes to wait at least 6 months post rads to do exchange.....had my exchange almost 7 months post rads.....my skin has done well.....but implant fell 6 weeks after exchange and had a revision 4 months after the exchange....implant fell again, though not much, but since I didn't like the implants I wanted them out and a year later had both swapped out for smaller ones....2 years later all is well.....a freind just had a DIEP following bilat...it was a 2nd primary and she had rads the 1st time....it was a rough go for her with PS having to go back in twice, next day and 2 days after DIEP....I was afraid of a long surgery so never looked into it....my surgeon does not do them and I was not a candidate for lat flap.....in clothes, I look pretty much like I did before BC, but of course, naked they are not the same!!! and no feeling.....all the best to you...
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I would wait at least six months. The skin may look fine after rads, but it still heals more slowly that it used to. I think it's best to be safe. Congrats on finishing rads!
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Sharon - I just wanted to say I know how you feel about the people who "think" it's their business to know when and why we're doing our surgeries. I'm pretty open about everything, but have come across quite a few people that don't understand my waiting. In all honesty, I'm waiting because DIEP is a long surgery and I'd like to be in better physical shape for the surgery, I'm tired of doctors and I wanted to spend this summer with family not sick and get my daughter off to college without distractions. I rescheduled my appt with the PS to December because I just didn't want to deal with it right now.
Christine - I wanted to add to my earlier post that while the dr's feel that I should have DIEP, it's the decision they feel is best for me. I reread what I wrote and felt that I sounded like DIEP is the only option for people with bi-lat and radiation. I am no expert, I meant to just give the information I had based on my own experiences (so far).
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thank you for this feedback! it has me really thinking, maybe i should get a second opinion on this one. i had heard there is a significant chance of issues with implants following rads, but i was never advised that i should go in a different direction, and after everything, i have just wanted the simplest surgery. i thought about DIEP too and even went to houston for a consultation with a surgeon there who specializes in that only (i'm in california). she said she would do the DIEP flap WITH an implant. at this point i don't care that much about the cosmetic outcome....i'm actually fine with my stupid tissue expanders.....i just don't want complications. i am worried about more loss of sensation too.....my boobs and axilla and part of my underarm, completely numb....so i was avoiding flaps since i think(?) there would be more loss of sensation? like across my belly? anyway i appreciate the responses! it's so wonderful to be able to reach out and get a different perspective or to hear about a different experience, especially when people live in other parts of the country...i think the advise we get changes slightly, regionally.thank you friends! christine
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I am going to see my PS today (BMX with expanders on Tuesday). I found out after I met with him the first time that radiation was highly likely for me… but my BS always knew this and felt that I was not a candidate for TRAM (I don't even have enough fat on my stomach to make one breast A cup let alone 2.) I'm not sure if I could do DIEP. I don't want to take muscle from my back because I already have some neck/back issues. I personally feel I need that muscle to keep pain at bay.
So in my case it seems like its implants or external prosthesis. I'll see what my PS says today. Granted there are surgeons that can take tissue from my butt or thighs (I do have fat there) but I don't want to go that invasive. That can fail too. I feel failing from implants isn't going to be as much as a disappointment than doing a more invasive procedure.
I'll let you know what he says. He does fat grafting and I have read that helps with radiated breasts (reduced capsular contraction) but that would be in conjunction with lat flap with implant.
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UPDATE:
Plastic surgeon seem fairly confident we can do implants… of course no garuntee and no radiation would be better. He feels that since I'm not trying to go large (currently an A or smalland the use of fat grafting that there is a good chance he can make this work. He stated that there are arguments on both sides, one to wait on the reconstruction and one to start with the implants as mastectomy. He feels it's best to start right away. (Ironically I read that on Dr. Susan Love's site too:
scroll down to Radiation After Recontruction http://www.dslrf.org/breastcancer/content.asp?L2=3&L3=2&SID=167
He says radiation isn't quite like it used to be. They really pinpoint the area now.
My husband went with me this time. He feels this doctor is very smart and knows what he's doing… but quirky. He thinks my BS is quirky too.
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thank you for the update! i'm pretty small too so maybe i have that advantage going for me. i have never heard of fat grafting.....sorta like a DIEP but fat from somewhere else? it makes sense to add some healthy tissue to the radiated area. so you are thinking you'll go straight to implants, or start with tissue expanders? i def need a second opinion i think. GOOD LUCK with your surgery! mine was pretty easy....one night hosp stay, then home and took it really easy for a good 10-12 days, but i could get up and move around right off the bat. take pain meds and let people do stuff for you. i'll be thinking of you and sending good vibes your way.
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Expanders first. I will be there 2 nights. With expanders there is a little more pain involved and longer surgery. I think they want to be sure I have my pain managed properly. I was told its about an 8 hour operation to do both that BMX and the expanders.
Glad I'm not going to be awake for any of this. I don't really like blood and guts
Fat grafting isn't like DIEP. It's more like they lyposuction it from one place and inject into the other. A lot less invasive. They have to put in extra because the body does absorb a lot of it. At least that is what I read online
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fat grafting.....interesting.....wonder if they would take it from my stomach? i could use a little less in that area! will look into it. hopefully your surgery won't take too long. mine was a little under 4 hours and i also had tissue expanders put in place at the same time, plus an axillary dissection on one side and sentinal node on the other. they only kept me one night, about 18 hours altogether. they had me on an IV of morphine at first, and it worked but made me a little nauseous, so they switched it to dilaudid.......love dilaudid, worked like a charm. then home with vicodin and percocet. here's something that may be helpful, i am especially sensitive to feeling sick to my stomach after general anesthesia, so i made a LOT of noise about it beforehand to the anesthesiologist.....talked to him on the phone the night before. anyway he gave me extra anti-nausea meds and i woke up and didn't feel pukey. groggy for sure but not sick, which was good. oh another thing, i had an oncu-pump (SP?) in place for 6 days....like a little plastic ball full of local anesthetic, with tiny tubes, one going into each breast. i wore it in a fannypack type thing around my waist. anyway it REALLY helped with pain once i got home. i have two friends who had bilats without it and they had a much harder time moving around after surgery. so you might ask about that. the med just seeps in over a period of time...i had to go have the little ball refilled after a few days, and then on day 5 or 6 after the surgery they took it all out. GOOD LUCK!!! soon the cancer will be OUT!
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OMG me too. BMX level I axillary on left side, sentinel on right. Maybe my doctors are older and move slower
I was told only 2 myPods (my name for drains). I'm actually going out right now to fill my prescriptions:
Colace for constipation, Sofran for nausea, Valium for anxiety, Norco for pain, Cleocin antibiotic and percocoet for really bad pain. I haven't had that many drugs in, well ever! and certainly not at one time. Maybe have all those drugs in me will get my body ready for Chemo.
I'm not going to fill the Colace because I use Milk of Magnesia. If that doesn't work I'll fill it. I have a feeling I won't need the Valium and possibly the Sofran either as long as I don't take the drugs on an empty stomach.
They are planning on keeping me 2 nights granted they first night will be practically over since surgery starts at 2:45 + 8 hours= after 11pm some time. It is possible a 3rd but we are all not planning on it. I have a doctor's appointment that 3rd day with the PS.
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