continued Tissue expander pain!!
Comments
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I was started on Lorazeoam and it really helps with th tightness.
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Hey 40somthingMom,
Not that I deserved BC any less (or more) than the next gal, but if I have to go through this, I damn well plan to make the most of it. I was not naturally endowed, so this wildly alluring cleavage has been a gas. Once I forget all the discomfort, I'm going to be very happy with the new me. Silver lining, Baby.
That being said, I don't have a daughter.
You have to live with the new girls. Be happy.
Carol(AZ)
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DITTO!!! When you get handed lemons...make lemonaid baby. Make a positive out of the negative you were dealt (you did not choose to have BC!)
I went from a barely A to a small C (just had exchange surgery last Fri) and l love the clevage and they way my clothes fit! When one asks if you are going larger 1) mind your own business or 2) why not?
As for your daughter, focus on the healthy, cancer-free aspect, not the size.
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Hi all,
I'm new, but I'm having second thoughts about implants. I only have one more expansion left to do before surgery,but I have read only negative things about implants. I WAS thinking about Saline implants, but now I am not sure it implants are right for me. I do not have enough "fat" for the TRAM. Has anyone else felt like this before?
Any advice or encourement would be very helpful.
Thanks
trish
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Hi Trish,
I have second thoughts sometimes too -- my exchange surgery is Oct. 9 and I'm getting silicone. I don't have enough extra tissue for flap recon either. I know there are drawbacks to implants, but there are drawbacks to all types of recon, so I figure if I could have the choice, it would probably just be a harder one! My suggestion would be to find some women on these boards who have already had their exchange surgery and see what they think. Maybe also talk to your PS about the specific concerns you have. My PS is really good about taking as much time as I need to to ask questions, and in a couple instances it turned out that what I read was "old" info, and things had changed. In the end though, it's about doing what's right for YOU, and you need to be comfortable with your decisions. Sometimes that "gut" feeling is the biggest factor, though, so you shouldn't ignore that either!
Sheila
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sbmolee & Carol-- THANKS VERY MUCH FOR THE REPLY, I just needed to hear that and I am over bothering my husband with my emotional roller-coaster ride- I wish you both the best with your journies
trish- I have heard good things about implants & that saline is as safe as silicone, I'm going with silicone they are suppose to be softer - I did not have enough "fat" either, I was very interested in the DIEP but again no fat-- good luck with your decision, just another, in this (seems to be)never ending disease we call BC
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pufpig - There are pros and cons as well as risks and benefits with all options after mast. If you are anxious, best do research and discuss with your doctor to determine what you feel most comfortable with and what the best option for you is. It is not uncommon to get anxious or "cold feet" but even implants can be reversed if you are unhappy or uncomfortable with them.
Best of luck! Hugs.
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I'm now about 5 months out from my exchange. I have silicone implants, 425cc, and am a large B/small C cup. When I saw my PS last week, he asked me if I was happy with the size, and was shocked to hear me say I wish they were smaller. (Most women seem to want bigger.) My problem with the size is the heaviness of them. I have a constant pulling sensation at the sides of my breasts, and it is worse on the side that suffered a nerve injury post-op. (I'm still on Neurontin for that, but it's way better.)
I've postponed getting nipples done, thinking I don't want another surgery. And I don't want to be stuck with ugly nipples (hi-beams on, or else shrinking away.) I most likely will get the 3D tatoos, but I don't want to do that till I'm 100% sure I'm keeping the boobs. I'm 95% sure I will, but there's that niggling part that's just not thrilled and too uncomfortable right now...
On the other hand, they look good in clothes. And that's really why I did reconstruction. I just don't care for the weight of them, how they restrict some of my chest exercising, and how freaking cold they feel.
If I had it to do all over, I would have traveled for DIEP or SGAP. The other muscle-based surgeries weren't acceptable to me.
It's such a hard decision to make. We fly on emotion and blind faith, despite all the research we do and opinions we get. My basic advice is, if you're not 100% sure you want reconstruction, just wait. You can get it later if you change your mind.
Anne
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Thanks for the replies, sistergirls!!
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Anne, can I ask how much your expanders were filled? Is the size of the expanders a good indication of the size you are after exchange? I know that the PS will adjust the pocket some at the exchange surgery, and the implants tend to sit lower than the expanders, plus they're softer, and I'm wondering if the implants look or feel smaller than the expanders do. I'm filled to 400cc, and I'm getting 400cc implants, so it's going to be an "even" exchange, but if the implants feel as heavy and big as the expanders do, I think I'd rather go smaller too. I heard about how cold they are too. A friend described it as having a couple ice packs on her chest when she's outside in winter. Too bad you can't take them out and microwave them like those hot/cold packs!
Thanks!
Sheila
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I too had chemo before bilateral mastectomies.my Chemo was cytoxan and taxotere.By the 6th time i had had all i could take.I am 3 wks post mastecomy surgery,and yes,the expanders"ache",i wont lie,but my main complaint is not being able to sleep on my stomach!I also take tamoxifan and the heat flashes at night keep me awake.By now you can imagine,it is hard to find the strength for any more battling,but i have to.Its always scary,every part of it,and then i say when one part is done-ITS DONE..I cross off all the days on my calenders that had visits or procedures,and every day i let myself cry a little-but next year at this time,i will be DOne..there is a light at the end of this tunnel,and its not a train,it our life richer fuller and worth going to war for!!!!!!!!!!!!!!!!!!!!!!!!!!!Ill pray for you every day.
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I was told today, that due to rads, I will need to be fully expanded before rads. They think this will need to be done within 6-8 weeks because delaying rads is too dangerous. So ladies.. if this ends up being MY case.. how much pain is this little B+ cup going to be in?
Laura
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Estepp - it will be uncomfortable if not also painful. How many cc's are they taking you from and to? Did they give an estimate? Muscle relaxants help as well as ice packs. Sleeping was the worst to try and get comfortable - ended up with back pain and knots.
Good
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Sheila,
I was filled to 500cc before going with the 425s for the exchange. It's so hard to know--even with the implant website that gives you all the dimensions. So hard to visualize what it really translates to, or what it feels like behind the muscle.
I know so many women who have no problem with their foobs--don't even know they're there. I wonder if there's a correlation between what we feel and how much we engage the pec muscles? Or is it a function of our nervous systems, or chest dimensions...
Oh, well. It is what it is, right now.
Anne
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Hi Estepp,
My PS waited 3 wks before starting the fills, then did 60cc/wk. It took about 10 wk to become a full C (as far as I can tell). Some women can take more than 60 cc(and some less) comfortably. Your health takes precedence. Later, after you've beaten BC, you may be able to enlarge.
Pain med taken before and after fills, and finally a muscle relaxant helped fill faster.
Health and happiness to you.
Carol(AZ)
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Hi All,
My expander pain is OVER! I had my exchange yesterday. I was filled to 600CC on the right side (ca side) and 550 on the left. I hurt bad all through my fills. I have not seen my boobs yet but I was told I would be a little smaller than the expanders. They want a little wiggle room so they don't fit so high and tight on the chest.
I had initial fill of 50cc each. The second fill in 10 days was another 50cc each. Then I moved up to 100cc with each fill. At the end, I had to wait longer because the pain was getting unbearable. At 550cc on the left I had to stop.....it hurt to bad. I had my expanders put in on 6/10/08 and I think I had 5 or 6 fills. It still matched the right side because more tissue was taken from the right side. I hated the way my expanders bulged under my arm...was hard to shave. And they were so damn hard! When I hugged my dh, he always commented. That is now gone...I can just feel a little through the gauze and tape but it feels so soft.
Anne, I totally understand about the size. I don't want to be too big either. I got my nipples done at the same time. I just now have to wait for the healing to get my tattoo's. I do aerobics and always had to hold my old boobs during some the jumping part (I work at home). After the mast, I loved exercising and running. I also thought about no recon but I hated the prosthesis and all the acoutrements with them (special bras, cami's bathing suits, etc.).
After my fills, I took Lortab 7.5 mg and did all through the expansion process. Toward the end, the pain got so bad that he moved me up to Tylox for the first 4 days after the expansion. The meds let me keep my active life going. I had a bunch of gardening to do (transplanting, digging, new beds, etc) which I could not due to chemo fatigue.
Hang in there ladies, it is so worth it....just to get out of the pain. I just have some pain where the incision is. I feel great!
Debbie
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Thanks for your input ladies... did anyone have to have more fills after rads... if they could not get all fills done between surgery and rads? If it was just to painful to go that fast?
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Hello Estepp,
I had both expanders and all of my fills after the radiation. I finished radiation in April, 08, then had the other breast removed in June 08, first fill was Sept. 5 08, second was last week, and exchange yesterday. The radiated side is copromised so it did not stretch like my good side, but it stretched enough that I have little breast mounds. My PS said, I would not be able to be very big, and I'm totally okay with that. The radiated side is definitelymore painful. I hope that answered your questions.
Take care - Lilyj
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Congratulations, Debbie!!! Whoo-hoo!!!!
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Lilyj,
Do you think that if all your fills would have been done before rads, your radiated side would not have been compromised?
TY
Laura
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Hi Ladies,
I've been gone from the boards for a while but want to add my 2 cents about the silicone implant... I had the mast in July 2997 and the implant put in in Dec 2007. I HATE IT! For me, it's almost as bad as the expander (just a bit softer). I still have muscle spasms and am working on getting it removed in December. I just have never adjusted to it and I'm just tired of dealing with it. It looks beautiful though...it just doesn't feel quite right. I talked to the ps almost 6 months ago about it and he said it was "To soon to remove it and I needed to adjust to it". I'm going for another checkup in November and hopefully will get a date to get it removed.
Hey Anne W...long time no see! Glad to see a name I recognized from last year! It looks like things are going well with you. I never got the nips or tattoos for the same reasons you stated above. I just didn't want to be "on" all the time. Better to have just one nipple to shield from the cold instead of 2!
Yall have a good night.
Margaret
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Good to see you again, Margaret! I'm sorry things haven't gone well for you with the implant. I do understand. No point in keeping it if you're not happy. I'll give it a little more time to see how it goes for me.
I hope work is going well for you.
Don't be a stranger!
Anne
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Hi Laura,
I'm not sure how it all would have worked to have the expanders put in before the radiation. I think my skin would have been so stretched and then burned on top of it. The radiation was more important at the time than any reconstruction, so there wasn't much of a choice. I did burn quite a bit and that will always make my skin thin looking. I don't think there is a better or easy way... they both are difficult!
Hang in there.
thanks,
lilyj
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Margaret, I feel so bad for you that you're not happy with your implant. That has to be hard, after everything you have to go through to get that far. I was going to ask some of the post-exchange women if they're still having muscle spasms. Now that the pain from stretching is pretty much gone for me (I'm fully expanded to 400cc), the muscle spasms are the worst thing. Massage helps a lot, but I can't exactly do that if I get a muscle spasm at work! I can see where that could be a deal-breaker for me too.
Good luck with getting your appt for the removal -- I hope your PS is good about it.
Sheila
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Hi ladies,
Just wanted to share some hope with you. Day 2 after my exchange and in NO pain at all except a little sore at the incision site. My back hurts from sleeping on it. I tried sleeping on my side but the stitches hurt too bad.
I am sorry Margaret that you are having a tough time. My PS gave me valium for the muscles spasm. I did not really have any but it helped me to sleep and sometimes helped my back ache. I had a really tough time with the expanders. I stayed on pain meds the whole time....sometimes 6 a day! But now I am off of them. Thanks to all the women who shared their experience and strength and hope. I hope I can do the same for those of you still suffering with the awful expanders.
BTW, I asked if I could have my expanders. Thought they would make a great centerpiece for a dart board. No....new regs say they cannot give those to patients. A long time ago, you used to be able to get your gall stones, kidney stones, appendix...etc. Darn, I really wanted to see those things and punch them a couple of times.
Debbie
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Hi Ladies,
Anne, I was wondering how your implants restrict some of your chest exercising? I find that my chest does get tight with lifting and driving for a long distance. I can always feel my implants. I have the gummie bears which are tear drop shaped (in Canada) My exchange was done on June 6/08, so not that long ago. I am afraid to really get back to my light weights yet. I will give it a bit more time before I try. My muscles anywhere on my body can get really tight with exercising and I do need to do stretching regularly.
Margaret, Sorry to hear that you are not happy with your implant, after all that you went through during the expansion. I hope that things work out for you.
Debbie, That is too funny that you wanted your expander for the centerpiece for a dart board!!!!! They could be used for many interesting things. I wonder how the Dr. can get them out of the little incision, they seem soo hard to flatten out and get them out. Glad you have RELIEF.
Kes
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Finding this website has been SUCH a blessing to me! I had B mastectomy with tissue expanders two weeks ago. I am very sore, but getting better each day. Needing motrin and flexeril. It feels like to rocks on my chest. I will go in for my first injection next Monday. I pray all goes well. It's comforting to know that I'm not alone. I feel a certain sense of comradeship with all of you, in that we are going through this together.
God bless you all!
Sue
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Sue
Glad you found the site too! It is such a great place for support and information. An incredible group of people! You are definately not alone in this - so many here have been through so many trials and remain strong. They are a real inspiration.
My fills were really nothing, except for the last which was 100cc and I wish I had said I wanted to keep it at 50. The 100 was a bit much for me - very tight and I had muscle pain. But the first two at 50cc were not bad at all. To me the drains were the biggest drag! Good luck with your continued recovery - sounds like you are doing well!
Amy
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Good Morning Ladies,
Thanks for all the kind words.
Sue, this site saved my life going through recon. There were so many days I felt like crap but there was always something humorous to get me through the day here.
Debbie, I wished I could've kept that "beotch" implant too! I'd have liked to see just how much it would expand to until it popped! I was at 720cc's when they did the swap and it felt like it would come apart in my chest. I still have a prescription for flexeril but can't take it and teach (I haven't learned how to sleep and lecture yet!). I may take one on the weekend if the muscle spasms get bad. Overall though I'll take the spasms over breast cancer anyday!
Sheila, I warned my students I may be touching my breast during class and I assured them it wasn't just for fun! They're kinda used to it now. College student's are much easier to explain things to than the little ones for sure!
Anne, the college's great and so are my students. I gave my BSE talk in my sexual behavior class and some wanted to see and feel the implant, etc (just the ladies!) but the conversation was great! I've got 7 guys in the class (and 21 women) and the guys listened just as intently and asked as many questions. This is my first time back to teaching a full week in a yr. and it is an adjustment (not being able to nap when I want sucks!). They guys did get a little uncomfortable when I switched from breast cancer to testicular cancer. They didn't like the idea of the digital rectal exam (WIMPS!).
The nurse practitioner at the ps office is great and totally understands where I'm coming from. She told me 6 months ago it sounded like the implant was on a nerve (of course I said "It's on my LAST nerve!") and that removal would be the way to go. PS not wanting to destry his beautiful work (they do look spectacular!) wanted me to wait so I'll wait until the end of the semester to get them out. If he won't do it I'll get a scalpel and some butterfly bandages and do it in my kitchen!!! Or the alternative, find another PS to do it!
I'm going to get a basil cell carcinoma removed from under my eye today (yea for me...more stitches!). My body's looking more of something you'd find in a Rand-McNally road atlas everyday! Yall have a good day.
Margaret
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Debbie,
Thanks for sharing, I am so happy that you had your exchange surgery and that all went well. I wish you a very speedy recovery.
Only 67 more days until my exchange surgery (not that I am counting). I do have to say I was in agony all the time and could not see it getting better but this last week I think I finally streched outward and the expanders are not digging in under my arms and not squeezing my lungs. Now it only hurts when I cough or sneeze. I am still uncomfortable and suspect that I will be until my exchange surgery but it definately has gotten better.
I am looking to get some size and feel no pain no gain but my PS feels that I have expanded enough. Do I listen to him or do I keep pushing it? Any advice? I have about 400CC's in now and want 400 CC silicone implants. Does that work? I am tired and confused, I just don't want any regrets.
Thanks ladies.
I
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