December 2016 Surgeries
Comments
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Welcome, Armecia! I've added you to the list. Will you have immediate reconstruction?
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To each her own but noreconstruction for me.
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JCN16: Thank you. I hope and trust I'll receive as much clarity as you've received! Sounds like you have a solid plan in place and are mentally moving forward. It certainly brings some relief once you've made a decision. Praying I get that Thursday!! Will be praying for and thinking of you and your medical team Friday. :-)
Armecia: Did you strike gold with her or what? :-) I've never even heard of such expertise and that has been one of my main concerns, developing lymphedema. How fantastic that you have access to someone who specializes in lymph node mapping. Sounds like the 2.5 hr drive from your home will be well worth it!! Will be thinking of you this Friday, too! -
Armecia, I've updated your info! I'm glad you've joined us!
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HI all,
Bilateral w/no reconstruction, this Friday, Dec 2nd. Scared witless!
(My first post but I've been reading the boards for almost six months now.)
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I'm having Bilateral surgery Dec 13th...scared also!
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Seems strange to say, "welcome" but hello, nonetheless, NorthBrooklyn and Truper! Someone here (can't remember who or what thread) said they were scared until they read where someone mentioned that we're not getting a limb or organ removed, it's primarily dealing w/the incision after surgery. That provided some comfort...at least momentarily. :-) I know we'll get through it!!
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Absolutely. I kept trying to remind myself that during chemo.
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NB: You've already had chemo? Then I trust the worst is behind you. I won't know if I'll need it until after surgery. More waiting and wondering. I'm just thankful for narcotics ;-)
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Yeah, I did neoadjuvant. Which didn't work as well as hoped, unfortunately.
Last chemo was Oct. 24th. I'd felt some heaviness in the bad breast this past week but this morning I noticed that it's starting to look wonky again. I feel like I did the chemo for nothing.
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NB: Did they already do scans following chemo? I'm guessing that's the only way to know for sure if it was successful. Sorry, I'm so new to all of this myself and I don't know what I'm talking about half of the time. I'm just full of questions and no answers or good guidance. :-(
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Welcome, NorthBrooklyn and truper! Glad to have you with us, but not glad you have to be here!
I've added both of you to the list!
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RedemptiveSufferer, that helped me a lot, too (no muscle or organs). I'm focusing on that so I won't be so worried about the recovery.
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truper, are you having reconstruction, too?
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Hi Ladies! We are closing in on December and I wish you all luck. Looks like as of right now I am last on the list...I will be crossing fingers for everyone that heads in before me. I am in tons of pain, and my left breast is basically all-encompassed on the medial side. My mobility decreases each day, and I basically had an emotional breakdown in yoga today. I am exhausted and sore and frustrated, and the more I try to project positivity, it seems the more exhausted I get...put on that smiling face as they say. I have been on HRT from my hysterectomy in 2012, and had to stop that already as I am ER+, so I am in full blown menopause right now - not sleeping, hot flashing, and down right cranky. I had a followup with my surgeon today to go over a few things. This is what we covered....I wonder if anyone has any of their own experiences to share, and hope you all are having good experiences with your respective surgeons and their teams:
1. She suspects the increased pain I am having could possibly be from the development of a hematoma, but they are unsure. If it is not a hematoma, it is most likely inflammation of the surrounding tissue as my tumor area is so large. Regardless, it will all be removed so they are not going to investigate or test or remove it this close to surgery.
2.I need genetic testing. I don't have an official family history of the disease, but because I have a family history of lymphoma, and I have developed BC, there is concern that there is a link, and there are genes that do this. None of my treatments for my lymphoma to this point would cause anyone to think I should have developed BC as a secondary to lymphoma (I didn't have radiation, etc), so I am considered to be a highly probably candidate for a genetic link of some sort. I don't need to find this out before surgery.
3. I will be having node mapping the night before surgery to see if any are involved. However, because I had 7-9 nodes removed in two different surgeries for my lymphoma, there is high concern that the dye won't map properly to trace the BC. If the dye doesn't map, they do not want to simply remove the rest of my nodes as a precautionary (basically going blind not knowing if there is cancer in them or not) and I will be monitored for development of further BC in the chest area after my surgery (wtf).
4. We discussed in-depth my preference for placement of my incisions. I am kinda sassy and won't be donning turtlenecks for the rest of my life so I want less scarring on the front of my chest, and she will be working to place them to the side and under my arms as much as she can. I have zero inclination for reconstruction - ever- so she will be taking as much tissue and skin as possible to make me as flat and seamless as possible. (so weird to say that).
5.Because my incisions will be more under my arms than in front, my recovery will be longer and my temporary mobility will be more compromised. I will be assigned to a physical therapist.
Hope you all are hanging in there.
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Welcome, thekeensheep! I've added you to the list, but I don't think you're last (if your surgery is 12/12). Let me know if I got it wrong!
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I love that this group is so diverse - some with reconstruction (immediate and not), others going flat, some UMX, others BMX, others lumpectomies, some both (me!). And I love that we'll be here to support each other. But I hate that we have to be here at all.
thekeensheep, did they give you anything for the pain? It seems like an awful long time for you to have to deal with that kind of pain.
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What have all of you done to prepare for surgery? The only thing I've done (or my husband has done for me because I hate to shop), is buy three flannel, buttoned shirts.
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I have my list of things to get, dry shampoo I need to wash my hair kinda vain about that lol. But maybe after surgery I wont care what I look like. I do have button up shirts, need new button jammies for home, socks with the gripper bottoms a gift from a friend. I do have smooth tea for the constipation I have seen ladies mention.
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I also wanted to post some things that I have done that have been SUPER helpful!! Maybe helpful ideas for you all.
1. I created a closed group for family and friends on FB so that I can keep them up to date and put more specific progress and treatment info out there to those that are really invested, and its not all over FB.
2. I created an Amazon wishlist with many of the recovery things on the shopping list included above, plus gift cards. You can adjust the priority of each item, and how much of them you want. I put everything from the Brobe, to foam wedges for sleeping, to compression sleeves and bras, to vitamins, plus many other things on there and within a couple days it had all been purchased. I receive boxes each day (my mailman really has to wonder what I am up to!), and as gifts come in I send a thank you note on FB or write a card and stick it in the mail, and then enter the info into an excel spreadsheet so I can keep track of who sent what, mark off that I sent them a thank you, and keep track of their addresses. Here is a link to my wishlist - you can see what I put on there - sort by purchased/unpurchased. http://a.co/g5SsR9M
3. A couple of weeks ago I bought tons (literally like 4 cases) of wide mouth ball pint jars and plastic lids for them, and asked for help cooking on FB with my dietary restrictions. I put many of the jars on my back patio, and people came and picked up empty jars and then dropped them off full of food. I have an extra freezer full of food now and don't have to worry for quite a while. I also asked for fresh canned goods (I have tons of friends that have farms or gardens), and offered to barter - all declined the need for a barter. I just keep track of who's jars are who's as I use them so I can return them when this is all over. (I also keep track of this on a spreadsheet - there is no way I will remember everyone who helped when this is all over, and any bit of help matters - big or small!)
4. I am finding the desire to ensure I still feel feminine as I move through this -especially with no reconstruction, so I have been working hard to find little things that will help with that so I don't feel so gross with drains and what not. These are a gem! - http://brilliantcontours.com/ and the lady that makes them is awesome - great customer service and you can put them on your amazon wishlist, they carry them! I put two pretty ones on my wishlist and two different friends got them for me. I already have received them and they are soft and comfy and will be great after the first couple days or so after surgery.
5. Here is a great surgical bra site: http://www.gentlet.com/
6. Here is the Brobe: http://a.co/1G38HSj
Happy prepping ladies!
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Hi MyJourneys - you have me listed twice. My surgery is Dec 14th.
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TKS: I second MJs input. That's a long time to be in pain that could hopefully be eliminated w/some pain meds. Were any suggested? Or are they wanting you to avoid them prior to surgery?
MJs: Great question. I've purchased very little. I've purchased 1 flannel, buttoned shirt, a few zip-up jackets that could be worn as tops w/a cami underneath, a front-fastening bra, a couple pairs of sweat pants, and my husband bought me a cape (don't think Wonder Woman, lol) so I won't need to slip my arms into coat sleeves if I go out. I don't have anything for drains and come to think of it, I don't know if I bought the cami I was eyeing online. Hmmm. Gotta check that. -
TheKeenSheep, you are all over this!!! You have amazing suggestions! Thanks for passing along!
GoinCrazy8, you've done your homework, too. Like the dry shampoo idea. I have some that I use occasionally w/my daughter who doesn't always wash her hair to my liking ;-) Didn't even think it might be handy for me coming up! Glad you shared. -
No pain meds for me. Ugh. I am also on call in case there is an opening before my date - so I have been staying off everything. I most likely will reject a new date if offered one at this point as I have scheduled my mom and son to come in around my dec 14 date. They said tylenol only for me, and that is nasty stuff, so I am just stretching as much as possible, and oddly also being rather aware of the pain so that I can really and truly appreciate it when it is gone! lol.
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thekeensheep, I've corrected the list - you are last now... but not least!
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Great ideas and links, KeenSheep! I don't have any front-clap bras. Do you think I need that with just a MX on one side?
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I ended up ordering the Brobe and the shower things (drain holders) tonight. I think those, and the flannel button shirts will get me through for now. My husband and children will cook, etc., for me, so I'm not as worried about that.
I'll probably need some front-closure bras, too. Going to take a look at the ones KeenSheep linked to next.
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Oh, glad to find this forum. My surgery is Dec 21st. I have done nothing really to prepare as of now...arghh...but I am reading up now. I have posted on another forum so just pasting below.
I am very confused regarding my upcoming surgery. My cancer is very aggressive and I am mostly concerned about that at the moment so reconstructions is so far away from my mind.
They suggested to have an immediate expander placed during the removal of my breast. I have large breast and my tumor size is 6,5 x 4 cm and has grown that size during 2 years It has not noticeably shrunk during the neoadjuvant treatment so they are planing to remove the entire breast. I will start radiation beginning January, every day for 2 months as well as hormonal treatment, which kind I am not sure as of yet. I have a friend of a friend whom is a professor of breast cancer, she strongly advice me against placing the expander and using silicon at this point and instead just focus on getting rid of the cancer. She also said chances of complications of the implant might make the breast very hard and not comfortable at all. I will have the opportunity to speak with her on the phone tonight to ask more questions. I am more interested in reducing the size of my healthy breast, keeping the nipple to just make it more bearable for the years I have to wait for reconstruction, they said approx. 2 years since my treatment herceptin ends next September.
Any thoughts here would be very appreciated. I understand it would be great to immediately get a breast even if hard but I am more worried about the cancer spreading and complications with the silicon. From what I understand now a flap is softer and more comfortable in the long run.
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Just remembered I intended to order Pink Pockets for the drains and didn't do it. Has anyone bought those and do they work? My surgery is Friday, so I probably wouldn't use them until I get home.
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Kattis, I wish I had more knowledge about radiation and chemotherapy and could answer your questions. I've read that a lot of plastic surgeons won't do anything until after radiation and chemotherapy. Have you had a chance to talk with your friend's friend yet?
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