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mbordo Joined: Mar 2007 Posts: 280 |
Aug 30, 2007 10:47 am
mbordo wrote:
Laurie- I'm sending you a PM
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mbordo Joined: Mar 2007 Posts: 280 |
Aug 30, 2007 11:33 am
mbordo wrote:
Oh yeah - if you think you need help with the anxiety thing, please ask your doc!! I needed a little Valium so I could sleep/deal/relax in the days before my surgeries. Very normal request - please ask your surgeon! No need to suffer - this is something major to deal with on a mental level - so stress/anxiety are to be expected! Take care! Mary |
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lvtwoqlt Joined: May 2007 Posts: 2431 |
Aug 30, 2007 12:26 pm
lvtwoqlt wrote:
I am 47 and I was dx with DCIS this spring and had a bilat mast with recon/expanders June 1. The expanders are not too bad if they go slow with the fills, my PS went with 60cc at a time. I have been on a roller coaster ride of emotions over the last 2 years with DX of ADH in each breast. We all have fears about the return of this dreaded beast known as Cancer. I was fearful after getting the diagnosis of DCIS. I was fearful wondering if I made the right surgery decision prior to the final scheduling with the breast surgeon and plastic surgeon. I was fearful going into surgery, not knowing what the final outcome would be but also knowing that this was the best decision for me. I don't know if the fear will completly go away. I just take it one day/step at a time. I am fully expanded and waiting for everything to relax prior to the exchange surgery. Best of luck to you. As Mary said, don't be afraid to ask for meds to help the anxiety/stress. Sheila |
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3girls4me Joined: Jul 2007 Posts: 123 |
Aug 31, 2007 04:22 pm
3girls4me wrote:
Hi Laurie, Welcome to the group! I understand first hand all the things you mentioned in your post. And we are not alone! I have DCIS stage 0, low-grade, non-comedo. I was diagnosed in June, and after much thought and other tests and re-excisions that didn't get it all, I am opting for a bilateral with reconstruction. Having my surgery September 12. You've got to go with your own gut feeling, and no one (unfortunately!) can make that decision for you. The hardest part for me was during that time of not knowing what I was going to do. Once I made the decision, I felt LOADS better. I think you will too. You'll just "know" what to do. Now I have not gone thru the surgery part yet, so I really can't help there, because I don't know yet! But there are so many great ladies on this board who have, and I have gained so much strength from them! I trust everything will be just fine. Don't let the anxiety part of being having to help you out get you down. The people around you WANT to help, just like you would help them if it was the other way around. I struggle with this as well, and feel guilty. I'm always the one in charge of everything and helping everyone. But I've also got a husband and 3 kids who need to be fed, so the offers to bring dinner are welcomed! You'll do the right thing! Leslie |
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LaurieK22 Joined: Aug 2007 Posts: 5 |
Sep 3, 2007 12:10 pm
LaurieK22 wrote:
Thank you Leslie for your kind and supportive words. I will be thinking of you on Sept. 12. Please let me know how you are doing when you can. I have 3 children as well, plus a supportive husband. I hope your recovery process is as easy as it can be. You have got a great attitude and I hope to achieve that once I schedule my surgery. I am comfortable in my decision for surgery, but the time between now and my surgery date will not be easy. Laurie |
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jade Joined: Sep 2007 Posts: 564 |
Sep 11, 2007 10:00 am
jade wrote:
hi everyone I to am leaning on bilat mast. My dcis is cribiform,intermediate grade and comedonecrosis associated w/ microcalc. I am truley greatful to hear everyones storys. I am begining to digest what I have to do and get controle over my life.....today at least:<}. I am going to stop trying to be strong and let some of these tears out. I havent cried with my mom yet. She is going through soooo much taking care of my dad who is going through chemo. I am trying to be strong and not....who knows....sorry I am carrying on. I need to go out and buy a journal and just write my little heart out. thank you all So much for sharing your stories |
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Jenny812 Joined: Apr 2007 Posts: 216 |
Sep 13, 2007 07:57 pm
Jenny812 wrote:
Lauire, It is a radical decision and I made the same. Maybe, if you haven't already, check out the reconstruciton thread. There's different types of reconstruction with pros and cons on each - but there will be one right for you. I had a DIEP 3 months ago. It was a long haul but I'm whole again! Good luck. Jenny J. |
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Julie216 Joined: Aug 2007 Posts: 24 |
Sep 15, 2007 12:48 pm
Julie216 wrote:
Laurie, I was diagnosed with DCIS in left breast (grade 3) in early June. After spending my summer consumed with researching and getting other opinions, I decided to have a bilateral mastectomy with implants. My surgery was September 5th and so far, I have no regrets. It was a very difficult decision to make, but after much soulsearching, my gut told me this was the right thing for me to do. Follow your gut, Laurie. Also, my implants were placed at the same time as the mastectomy (no tissue expanders). My ps thought that I was a good candidate for this procedure given my size (c cup) and the fact that my breast surgeon was able to be conservative with the amount of skin she took during the mastectomy. I am a little uncomfortable, but not in pain. My breasts are shaped a little odd, for now, but with massage and time, my ps assures me that they will look great and I have the utmost confidence in her. Good luck, Laurie. I wish you all the best with making this difficult decision. Best regards, Julie |
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jade Joined: Sep 2007 Posts: 564 |
Sep 15, 2007 02:07 pm
jade wrote:
julie what kind of implants did you get? I too am getting a bilat and I have not seen my ps yet but my surgeon told me I would need expanders. I am a C cup too. who knows? Dx 9/4/2007, DCIS, Stage 0, Grade 2, ER+/PR+ |
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Julie216 Joined: Aug 2007 Posts: 24 |
Sep 15, 2007 03:28 pm
Julie216 wrote:
Jade, I have Allergen silicone implants. My ps used Alloderm to help support the implant. She did say that I may end up a little smaller, but not much (she mentioned this before the surgery). Ps said that she is just starting to do this procedure (while I am not her first, I am one of the first dozen or so that she has performed immediate permanent implant placement). I trust her and have confidence in her judgement -- she believed that this was a good route for me to go. Most of her patients have the expanders. Good luck! Let me know what your ps says about this procedure. Take care, Julie |
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jade Joined: Sep 2007 Posts: 564 |
Sep 15, 2007 04:26 pm
jade wrote:
julie thank you, I will let you know. I wouldnt mind skipping the whole expander thing if I could. I cant wait till this is all done and I can exhale alittle. Dx 9/4/2007, DCIS, Stage 0, Grade 2, ER+/PR+ |
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Julie216 Joined: Aug 2007 Posts: 24 |
Sep 15, 2007 09:20 pm
Julie216 wrote:
Jade, I know what you mean. For me, getting past the surgery was a huge step. Good luck. I will keep you in my thoughts and prayers. When are you meeting with your ps? Julie |
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Wren Joined: Sep 2007 Posts: 207 |
Sep 16, 2007 02:58 am
Wren wrote:
I am also considering this double mastectomy with reconstruction. I see the plastic surgeon next week. My DCIS is also grade 3 and I just don't want to mess with this ever again--nor do I really want radiation. Thank you for sharing your journey here. I don't feel as alone now. I also, didn't know anyone personally who has been through this decision (DCIS and how to treat it) before. |
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JODI Joined: Sep 2007 Posts: 19 |
Sep 16, 2007 09:23 am
JODI wrote:
Julie hi all couldnt get in under jade....so i used Jodi. I am going to the ps on this Friday and my oncologist on the 26th. I know how you feel wren about NOT EVER wanting to deal with this again!!!!! I dont either. I have been hitting ALOT of reconstruction sites (doesnt that sound odd) and preparing myself. I cant wait till I can ex hale again ....you know. I am 36 years old and I feel like I am 10yrs old when I go to the dr. Thank goodness I have my husband with me so he can translate. |
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Julie216 Joined: Aug 2007 Posts: 24 |
Sep 16, 2007 02:56 pm
Julie216 wrote:
Jodi, Good luck with your upcoming doctor's appointments. Keep us posted on your decision. You are fortunate to have a supportive husband (this helps A LOT). I do not think it sounds silly to have spent a great deal of time researching on the internet. I too spent hours and hours researching, trying to find something that would help me make my decision. You will be in my thoughts and prayers. Julie |
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JODI Joined: Sep 2007 Posts: 19 |
Sep 16, 2007 06:56 pm
JODI wrote:
thank you guys I cant begin to tell you how much hearing from you all helps. I will keep you all posted. This is a wild ride. I am going to visit my friends before my surgery....they are having a "say good bye to my boobs, hello new ones" party. I always had the pretty breast among my friends...at least the only real ones.:<} |
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avasmom Joined: Sep 2007 Posts: 26 |
Sep 17, 2007 02:09 pm
avasmom wrote:
Laurie- I'm not sure if you made your final decision yet. I just wanted to give you my input. I don't know if you have read another thread of mine or not, but I had a large amount of dcis, 2 lumpectomies, rads and now tamoxifen. I was 37 at dx last year. Had we known that I had that much dcis to remove prior to the second lumpectomy, I would have opted for a double mast. In retrospect, I wish I had a double mast because I need recon and a radiated breast does not do well with reconstruction. I also have a suspicious area in my other breast (though only mildly suspicious) that I am going in for a 2nd mri on in october. With a lumpectomy, you always have to worry about a reoccurance....and the opposite side is the most at risk. There are pros and cons to both options. I want you to know that radiation is not all that bad and it certainly is easier than a mastectomy. I have a family member who had a double mast and although it's totally doable, it's a major surgery. She is fine and doing great, but I don't think anyone would tell you it's easy. Radiation sounds more scary than it is. I did have some burning issues, but I still don't look back at it as a horrible thing. It's more time consuming than anything....going every day. I think you need to look at the size of your dcis first and go from there. Also, if you would ever consider having reconstruction, radiation is not the best option in my opinion. Ultimately, a reoccurance is what we all want to avoid...talk to your surgeon/onc about your fears and concerns. |
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JODI Joined: Sep 2007 Posts: 19 |
Sep 18, 2007 06:40 am
JODI wrote:
thank you for your story. I feel like I made the right decision (bilat mast), but I do tend to secound guess myself out of pure fright!!!!! I am going to my ps this friday and will see my oncologist the following weds. Ive read SO MUCH info that I dream about it. I want to avoid further operations in my future. My microcalcification grew in one year and formed cancer. My dr. did tell me that even if the cancer doesnt come back (after lump and rads} my calsicication prbably will and I will WORRY.....I know I feel like a broken recored. Just trying to grip my reality:<} thank you sooooo much for being apart of my mind restoration:<} Jodi |
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JODI Joined: Sep 2007 Posts: 19 |
Sep 18, 2007 06:40 am
JODI wrote:
thank you for your story. I feel like I made the right decision (bilat mast), but I do tend to secound guess myself out of pure fright!!!!! I am going to my ps this friday and will see my oncologist the following weds. Ive read SO MUCH info that I dream about it. I want to avoid further operations in my future. My microcalcification grew in one year and formed cancer. My dr. did tell me that even if the cancer doesnt come back (after lump and rads} my calsicication prbably will and I will WORRY.....I know I feel like a broken recored. Just trying to grip my reality:<} thank you sooooo much for being apart of my mind restoration:<} Jodi |
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Debinaz Joined: Apr 2008 Posts: 8 |
May 8, 2008 03:10 pm
Debinaz wrote:
Hi, I too had implants in at time of mast. have you had any issues with dying tissue or infection?? I have had some tissue dye and am now back on strong antibiotics for another week or so. I have noticed some drainage from the bandage in the last day. Debbie |
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Marian Joined: Jan 2008 Posts: 216 |
May 8, 2008 03:41 pm
Marian wrote:
Wow Laurie reading your story well I could have written just those words! Everything and I too made the difficult decision to have a bi-lateral. But before I made that decision the anxiety was so intense I started to loose my hair, what was left turned grey I don't think I sleeped through the night for 2 months, my emotions were all over the place. It is a difficult decision and I remember thinking what if I don't make it through this surgery, here I am trying to save my life and I have to go under general anethetics and I may have cut it short by doing that! It is an incredible frightening thing. But ultimately the anxiety of the possibility of the cancer returning after a lump. was too much for my mind to comprehend and so I made the decision. I also wanted to avoid radiation if possible and I was lucky enough to do just that. My initial response was good actually I was going to wait and watch, but when I started to see all the surgeons and doc's to get opinions I was scared into it. I can say more than a year later and 6 months after final silicone implant I don't believe I made a mistake with the bi-lateral only with the selection of my first ps. So if you do decide to have a bi-lateral interview lots of ps (I interviewed 4 all together and that wasn't enough).. I'm sorry about your needing to be here and I wish you all the best in your decision making - I'll be thinking about you! Best Marian |
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ijl Joined: Apr 2007 Posts: 668 |
May 12, 2008 09:50 pm
ijl wrote:
Here is my short summary. DCIS in left breast led to a lumpectomy . The margins were not clear. Then I had a unilateral mastectomy and DIEP reconstruction. I did have a genetic test done to make sure I was not BRAC1 or BRAC2 postitive. I briefly considered a bilateral one, but my gut told me to go with the unilateral. One thing I would like to suggest is that if you did not reserach DIEP reconstruction to do so. I am very happy with my results, it feels very natural. It bounces just like the original one and matches it almost perfectly. I haven't done my nipple yet. DIEP require a lot of upfront investment (i.e. at least 3 weeks before you can stand up and walk straigth) plus a very experiences surgeon. But it is worth considering. |
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DAPHNESPLAC
Joined: Apr 2008 Posts: 42 |
May 12, 2008 10:31 pm
DAPHNESPLACE wrote:
ijl, did your insurance cover the genetic testing & are you saying you do not carry the gene? My mother & at least 2 second cousins had breast cancer & I would like to consider genetic testing |
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