February 2012 MX
Comments
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Carolyn, yes it is incredible how different surgeons sem to have different opinions om compression wear, types of bras, etc. I have read on some of the reconstruction sites that some PSs didn't want their patients in anything but sport bras for months; others wanted underwire bras for support of the new breast; others say ABSolutely NO underwire. Some have their DIEP and TRAM patients in the compression girdles 24/7while others don't push it at all. So much of our treatment seems subjective it can maddening...how are we supposed to know what is best when the doctors can't agree?
For now, I am in the torture girdle my PS sent home with me. It is very thick and tight..the kind off fabric you think,of from girdles from the 1950-1960s. It's a longline garment too..covers my torso all the way up to just under my breast, with heavy tummy panel to push hard on the abdominal incision and it continues all the way down my thighs. My husband finds it hysterical.. He teases me and tells me its incredibly sexy bc it has an inch of lace on the legs! Like I said..it is extremely uncomfortable..but I do feel it pressing on that abdomen and that is what is supposed to do..help those tissues knit together.
This is what the fat necrosis along the abdominal incision felt like...hard lumps and I mean really hard just below the surface of the skin beneath the suture line. And like you, I am cut from past one hip bone to the other. The fat necrosos felt like hard ropes all across the abdomen. I can see that I will have the little dog ears people mention..little extra flaps of skin at ends of the abdominal suture..PS says he will remove the during Stage 2. I wear the Torture Girdle as much as I can..stand ..at least 15-18 hours a day. But when I absolutely can't stand it and need a break I switch to Spanx that I got at Lane Bryant. The Spanx are what used to be called a panty girdle" but the material is softer and doesn't dig into me so badly. It does not give as firm of tummy support as the compression girdle from hospital but I will wear the Spanx for an hour or two just to give myself a mental and physical break. For bras I found two good sports bras. They were expensive..$68 apiece but worth it. I got one at a specialty bra store and ordered the other one online. I can see being in those for a long time until the swelling in the new breasts goes down. The sports bras seem to provide good support without digging in or hurting the incisions o the new breast.
Someone else mentioned ongoing nausea. I still have mild nausea too.. I think it is from the pain meds. I was trying to wean off Percocet bc of the nausea and constipation, but since I had yet another surgery 2 days ago it's just not possible yet. I am lucky in that I can take the pills for nausea (promethezine?)but even with that I get "the queasiness" and have tried some other home remedies. Tru drinking ginger ale or ginger tea.. Stick to bland foods. Popsicles help me too for some reason.
Hope everyone is making good progress! Hang in there and lets keep sharing tips. I know I have gotten more helpful tips here than from my doctors, that is for sure!
PelicangirlSpeechpro -
Bern 25 - That really blows.....try not to worry about that pain, but do talk to your MO about it. I have had pain in my rib right under my right breast for several weeks. I too am going to mention it to my oncologist when I see her next month.....I will pretty much say I want a bone scan now that I have 2 positive nodes.......Its so disappointing!
Gina - IMO, get the nodes checked, believe me. I've had two MRIs, one PET scan, and one CT scan since my diagnosis in September and they've told me all along my nodes looked good. What that meant was that my nodes were not swollen, or enlarged, which would indicate there was involvement. You may NOT have lymphedema if you get the nodes taken out?? I just had 20 nodes taken.....I think that is a good number......I feel secure in the knowledge that 20 nodes taken out and checked......but its not too many that I am overly concerned about lymphedema. I just want to live.....that's all I can think about right now......
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Am I the only February girl who has had axillary node dissection two weeks after MX to remove more lymph nodes? If not, just wondering how you are feeling? I was doing great after the MX but this has really set me back on my ROM.
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Well 3-2-12 wasn't the best day on our thread. Lots of annoyances, worries, pain etc.
Wildrumara and Bern25, hey you guys are on the other side with the rest of us. So glad to see you're back! The two of you have the bone pain and Qs to unite you as well as your mutual surgery dates. Wildrumara, 6 hours on the table means lots of anesthesia and pain meds. in your system. You might want to cut yourself some slack and read earlier pages where your Feb. sisters shared those SE.
My leak from where the aquarium tubing from where my drain was removed is under control. I am to just do what I did. Change the gauze pad and band-aid,clean, anti-biotic ointment and tightly replace the band-aid and tape so there is pressure. No plans to aspirate me. I so appreciated that post BTW. Thank you. If I get a fever, redness, or swelling, I'm to contact the PS. Glad I went. Relieved. Won't stew over the weekend. I might marinate.
I am so deflated when I read upon receiving our final path reports that some of the Feb. club gets smacked with more worries and DECISIONS to make. Heavy sigh.
Gina9195, here's what I don't understand in your case. I presumed that the norm if one was having an MX, would be to do a sentinel node biopsy- when they have you on the table unconscious and are removing your breast- period. Regardless of if you have DCIS or invasive. If they are so concerned about DCIS that a MX is warranted, then why wouldn't you be at least given the option of having a SNB during the MX? That's when they did mine (I was IDC and DCIS). I did not have the option of node biopsy SNB- nada pre-MX. I didn't know until I awoke the preliminary node results that were done during the MX. I too had elective implants prior and it's true the eventual implants were an easy surgery for me. The TE is crummy and I already have the "parking garage" for it ready with minimal need for skin to be stretched. PS filled me almost to my pre-surgery size 270 ccs during MX because I had had the implant.
Susanes, you got the diagonal international "no" scar, too??? I am not alone! I teased DH that I might put red tape over it and add a red circle so he knows which one to avoid.
mma59 I got my "fluffy" at the cancer store at the hospital. But here's the deal. All it is is a poly-filled nylon oval that looks like a roll. It looks like the nylon shoulder pads we used to have in the eighties (no velcro to irritate) only lightly stuffed. Check your local fabaric store if you get desperate. I always place one ply of thin gauze over my MX site with a tiny piece of tape at the corners to hold it in place. Lots of air gets to it. I just don't want anything to accidentally irritate my scar because I can't feel a darn thing on foob!
I'll share what I know and have done regarding lymphedema as so many of us had node surprises (either in number takenand/or results).
1. I ordered a stainless steel medical bracelet from the American Cancer Society www.tlccatalog.org that says "no needles, No BP on Rt. arm". It reminds ME to watch it. I read all about lymphedema on this very site at the top of the opening page. I even did the test provided by this site from the San Antonio (?) conference where the South American presenters had a calculator exercise to estimate one's risk. To cut to the chase on that: one must convert ht. and weight to metric measures etc. so have your googled converter ready unless you are on the metric system. For me (with no Rads nor chemo), the BMI (body mass index) seemed to be the predictive variable. I had no idea what my BMI was. The same site allowed me to calculate it. It didn't even ask me how many nodes were taken! It asked all this other stuff.I have a 7% risk for what it's worth. Very low. Time will tell. I could screw it up.
Next benefit with the bracelet. I carry around a very heavy purse and my MX is on my right side (naturally, I'm right handed). Seeing that bracelet is training me after decades of habit to carry the purse on the other shoulder. If you're BMX I think the breastcancer.org says you can have needles in legs and there are novel ways of taking BP that never occured to me (and never wanted to know). Check it out. I also because of having read about it prior to my MX, I elevated my arm on it's own pillow every single night when I slept until the drains were out to avoid lymphedema. So, if I get it. It wasn't because I didn't do my part.
DebbieOs and FYI for Janice too some people like fruit for constipation- for me I eat a whole raw carrot, preferrably with skin on and eat at least one a day. Due to a past history of constipation (under active thyroid for decades) it has spared me all the previous side effects of constipation (if you know what I mean). I don't take laxatives except post anesthesia/surgeries. The raw whole upeeled carrot (not the little dainty sticks already sliced up) work terrific for me. They turned out to be an unexpected weight control tip. I never get in my car for errands, appts., shopping, or a drive somewhere without two of them in my car. Less calories than fruit, greater ruffage, cheaper, year round availabilty and it buys me more time to choose a healthier meal on the road, or just tides me over until I get home. I keep a Costco sized bag in the garage refrigerator unwashed ('cuz I'm tired after a Costco run and don't want to wash 5 lbs of carrots). I grab them as I jump in the car. I squirt them with my water bottle that is in my car and wipe em off with a kleenex. This way I don't have to make a big deal and plan ahead. With my luck, it'll probably be listed as a carcinogen and I'll be denied that,too.
KatieP1388, so good to see the delight in your posts regarding how pleased the nipples came through the surgery. I'm so excited for you! Very encouraging. Question: Out of curiosity, how was chemo decided for you prior to BMX for a tumor size of 1 cm? (If I didn't get that infr botched up).
Cajmi, you cracked me up about the scar. I am amazed how you gals withstand ABDs, trams, Dieps, BMXs etc.I'm held together with glue, tape, and I'm spouting leaks.
Nel, our dear founder, I hope you are having a good weekend. I want to post on this board later to you about looking at the scar.
Deborah2012
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Deborah,
I saw my PS today and they too noticed a GIANT hematoma on the incision site....they said that they were surprised as it should've swelled my chest, but didn't, and I should've had lots more pain than I had. They are squeezed it for about a 1/2 hour (oh, the joy...) and they're having me put triple antibiotic over it and are seeing me this upcoming Monday.
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Deborah- my reason for chemo first is quite complicated but to keep it short i had a lumpectomy, clear margins.. Then wasnin the debate chemo or no chemo .. Got many opinions. Chemo was decided to be safe since im 23 yrsnold. Started ivf egg freezing pre chemo just incase i got stuck in menopause.
Turns out my shitty local hospital missed that my cancer was multifocal (cluster of separate tumors) which is different thant multicentric ( seperate tumors in many areas over the breast)
So they missed three dcis that then became invasive during the fertility preservation and grew to a larger size. The largest being the same as my first and the other two less then half of that. Thisnall happened in a wek. So then i needed mx, but with the idea one boob could produce 4 seperate cancers in a short time and i have a long life ahead of me i opted for bmx.
My first lumpectomy was in august but it was already october and they were worried about me systemically all tho 3 snb was all clear. Basically i was loosing the boobs reguardless and they wanted to protect my whole body first because it was grade 3. So i bgain chemo the nexxt week! I know rypically they only o this for bigger tumprs or node involvment but my case hasbeen completely out of the box amd they just wanted to be extra safe -
Pelicangirl....yes, I was one of those with TONS of nausea...spent last night in the urgent care again...gads. They gave me zophran, phenergen, raglan (sp?) and atavan! What a cocktail! However, this morning I feel great once again..Phew. I'm back to eating applesauce and gingerale for a while however. I think my problem was that I was trying to cure the constipation first with raisin bran, etc, without really realizing how that was going to upset my stomach.. So, I'm focusing on the stomach first...once that's under control again...then the constipation....
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Good morning DebbieOs (I'm on west coast).
So tell me a liittle bit more about this hematoma.
1. Did you have seroma exiting your body after a drain was removed? As in the little hole was streaming seroma if direct finger pressure wasn't applied to It? Mine stopped after a 2' gause pad and a band-aid.
2. Whaddya mean they applied pressure for 1/2 hour? Are you kidding- as in someone in the medical field at their hourly rate and patient overload, actually applied direct compression for a half hour by hand to your foob (you do have a foob?) without a machine?
3. Could you see black & blue, green or yellow discoloration under the incision site yourself?
4. Did you notice the giant hematoma yourself or just felt the pain?
5. Did your cheast/lungs feel like when someone has pneumonia (heavy) but can breathe perfectly normal?
My guy didn't say anything about any hematoma.
Thanks.
Deborah2012
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3rd fill yesterday!!. For some reason it didn't bother me as much as the first two...yes, I felt tight and "full" but not as much discomfort. We went shopping and even took the scenic route home.
Last night while trying to sleep and this morning....YIKES!!....pressure!! A sports bra, a muscle relaxer and a 1/2 hour later...I was right as rain again. I don't know why my brain didn't come up with that solution at 2:00 am....duh!
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Deborah2012, thanks for the information on lymphedema. I'm going to chek it out. I'm also going to see a PT that specializes in that. Since the axillary node dissection, my ROM isn't that great. Thanks again for keeping track of everyone!
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Hey ladies - Thanks for the words of encouragement. I have to share with you. Had a home health nurse come in today......when she looked at my new foobs she gasped and said "These are the nicest set of reconstructed breasts I've ever seen"......Her comment actually put me in a pretty good mood!! I think I deserve some good news........anyway, had to share with you. Glad I did the direct to implant....kuddos to my plastic surgeon!!!
Pain seems to be under better control today.......took a shower which actually wiped me out, but now that is over, I'm glad I did. My husband is such a trooper....he got soaking wet trying to help me and I'm yelling at him when all he was trying to do was help! Trying to figure out what to do these three drains, besides hiding them in the inside pockets of a sweatshirt....any ideas???
I will definitely keep you posted on my final pathology report. Should talk to surgeon's office on Monday.
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Deborah2012: I agree, I'm not sure why they didn't take the nodes during the biopsy. Their reasoning was that DCIS was non-invasive, and didn't warrant it. Of course, now they've admitted that you just have to weigh the options and likelihood, and sometimes the wrong decision is made at the time.
Wildrumara: I agree with you too. Although it will stink to have another surgery, I need to know that the cancer has left my body.
My gf came to visit today and was surprised to see a bump already. Because of my pre-augmentation, my TE is a fairly decent size as someone else mentioned it was also for them. -
I had my post op visit with my BS yesterday. I received an "amended" pathology report....WTH.
Intermediate grade ductal carcinoma in-situ, cribiform and solid patterns with necrosis, 2.5 cm in greatest extent; two foci of microinvasion present (each less than 1mm); deep margin negative for malignancy; fibrosystic changes; benign nipple.
Also, she thought she got a lymph node but it isn't showing up in the sample. She said if it was her she wouldn't go back and get a node, there was such a teeny-tiny chance there would be anything there and the risk far outweighed the possibility. She said I could make an appointment with a MO if I wanted to but they would tell me the same thing. Ugh!
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Gina9195 -- Looks like we are in the same boat. My BS said since mine was a microinvasion (less than 1mm) that she wouldn't go back in for SNB if it were her. I'm just sitting here wondering if doing nothing is the right thing to do.
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Hi Dixiemine30,
"That sucks! I want to understand more about your crap"
I don't recall the details of your orignal final path. report. If I umderstand your post, you have a microinvasion that no one knew about until the BMX. So, iIf one has a "microinvasion" does that put you (and Gina9195 also) into the IDC and DCIS category (Stage 1)? Or do you stay DCIS? How are microinvasions treated is what I'm curious about. I'm getting that lymph information in some cases is sought post the BMX/MX and in other cases (oronc. preference) they are not.
Also, prior to your BMX, did you have DCIS is one or both breasts? Were the microinvasions limited to the suspect breast or both (if you had a prophylactic BMX)?
Wow. If I was a DCIS woman following this thread, I would ask BEFORE- if I have the option of a SNB while I'm undergoing a MX or BMX.
Thanks for the fill information and tips for soreness.
Deborah2012
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Wildrumara,
You could juggle them. Ha, ha.
Deborah2012
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Katie1388,that is really poopy that the hosp just found out it was multi focal. However,they might have been waiting on the final path report and just not yet have known. My surgeons had all warned me that things could change up to the final path report and then we would wait and send the finals to the oncol cuz he could not do anything for me without the final surg path. Been taking Arimidex for a few days now he gave me and its suppose to make you gain weight but I have dropped almost 10 lb since Wed whoohoo,get rid of all the pre surg flab I was so anxious I was eating day and night to sooth my nerves. The Ari does give me drenches at night,hot flash and anxiety out of nowhere but so far not noticed any joint pain yet.
Wildrumar-did you do bmx with immediate implants? I have heard of those but never saw too much about women who had it done that way. I imagine it would be better than the TE which are the 2 alien babies on my chest,I already gave birth to the one in my stomack aka the Q pain pump LOL
Carrots for constipation? have to try that,I love the organic baby carrots but I guess you mean the regular long carrots cuz I think the baby org are pre peeled. They look like they are. I ate some prunes but nothing happened and took Ex Lax and Colace,every time I take the Tramadol or tyco#3,the plumbing acts up. Never had that problem b4 bc. I guess my life is now divided into BBC(before breast cancer) and ABC (after breast cancer)
Fiance moving out today,it will be nice to no longer have mud tracked in and leaves. I am chafing at the bit cuz the PS says no sweeping and no vacumning til 6 wks is up and no lifting over 10 lb. (altho I am sure the door to my hosp room must have took a great force to get it open so I could do my little walks past the dr and nurses so they would think I was better and let me out of purgatory aka the hospital)
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"two foci of micorinvasion present (each less than 1mm)".....this is the only thing that changed from my first post-surgery pathology report to this amended one that was sent 5 days post-op. BS said anything under 1mm didn't require treatment since it had just started. It was on my left (DCIS) breast. My right breast didn't have anything before or after surgery.....I just didn't want to have to go through all of this again.
Per BS....I remain DCIS and my BMX remains a curative procedure.
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Layla- it didnt have anything to do with the pathology report. I had a lumpectomy clea margins, the multifocal was seen on my original mri and mammo images from the first hospitAl. The first hospital was lazy or fucked up. I was just answering as to why i had chemo before bmx, when i was only stage1. Thankfully none of this matters bcuz chemo did its job and my bmx path report completely clear no cancer anywhere
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I have been upgraded from DCIS to Stage 1, IDC 6mm. BS said had my first biopsy been just a fraction deeper they would have detected it. I really won't know until Tues. if the onc will suggest removing some nodes. I too did not have any nodes show up in the tissue removed from the MX. I do say to anyone diagnosed with DCIS to request a centinal node biopsy at time of MX. I wish I had. I feel so much better right now, except for the pressure of the TE, and now to take some nodes will be so invasive under my arm. I'm sure it will set me back with my recovery.
PS, I'm going to buy raw carrots today! -
Layla - The procedure that was performed on me is called oncoplastic surgery. There are only a few dozen doctors in the country who perform this. Yes, I went straight from a double mastectomy to implants. No tissue expanders. There is quite a bit of information regarding this procedure on this forum. Its called a skin-sparing direct to implant reconstruction using Alloderm. I live in Pittsburgh and my doctor was actually trained in NYC when he lived there 10 years ago. It really is wonderful. Not everyone is a candidate though.
Now that two positive nodes were found and radiation may be in my future, these implants might not do as well with radiation as say tissue expanders, but I will worry about that at the time. May have to have some tweaking done.....So bummed because they really do look good, even all swollen and bruised (LOL
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Grrr, my seroma is filling up again. I'll have to go in Monday for another drain. I'm so tired of my husband needing to drive me to really short appointments. I can't figure out what to do about the seat belt when I drive. How have others cushioned their mx?
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a bed pillow works well!!
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Wren44 -- I use a heavy winter scarf folded to the size it need.....not as bulky as a pillow and still does the trick.
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Nel,
I am squeamish. I can see blood, but I have never been able to look at gory stuff, surgical photos etc. For example, when the news says "warning some scenes may be graphic or distrubing"- I don't look.
Prior to my MX, I wanted to see what a post MX breast site would look like (the healed scars). I had seen the MX diagrams (cartoon renderings) in the brochures from the BS handout pamphlets. I was afraid that in my search for viewing an actual healed MX I would stumble on some live you tube in progress MX surgery or something like it. Here's my personal journey of being able to look at my own scar. However, for me my fear was avoiding something gory, repulsive in appearance, or graphic.
1. I was able to eventually find a photo on line (could have had someone else locate one for me, too) that showed a BMX (I'm a MX) that obviously had a TE. I was at first a bit shocked. I quickly looked away. Didn't want to look at it again-two giant white horizontal scars across the entire breast/s- no nipples.
2. In the hospita,l I had DH look when PS came to seeme post op. I didn't look at it. I didn't even look down. DH didn't flinch and his genuine reaction was that it looked good. It also had the steri-strip piece of tape over the incision.
4. When I gopt home after I slept some, I could see that I had a good-sized bump for a breast (TE), knew the actual incision had some modesty with steri-strip covering it, recalled DH's reaction, and decided to look down first. Remember my fear was all about the "gory" not the I"m disfigured. Not bad at all. Some discoloration but not a big deal.
5. Next day, stood in front of mirror and looked at my torso with the steri-strip taped foob. It was not gory. I did feel sorry for my poor body. I thought, awwww you have really been through a battle-zone. It was really weird. It was like it was a separate animus from me. I also had the node removal scar with black threads too by my underarm. My poor body. It's ok. I feel good and I'll take care of us. I gave myself a few days to get accustomed to my foob with the modesty steri-strip. I got used to seeing myself in the mirror and how it looked on my torso. I would alcohol wipe it and care for it. It made my existing breast look saggy. Hmmm, this may turn out to actually wind up being an eventual improvement.
6. Next step. I closely examined the incision with the steri-strip on. I could see a black line and a little bit more about the size and width of the scar. It was big, reddish.
7. At my PS first visit, he went to remove the steri-strip. I nervously admitted I hadn't peeked. He said I could look away. DH was there and again- no reaction of revulsion. I looked down. I had an earthworm and I could see black line stuff. I was ok. So my first naked viewing was in the presence of PS and DH. I don't think I walked over to the mirror in the room and looked at it on my torso. I asked that the steri-stsrip be re-applied.
8. After a couple of days, I gently removed the steri-strip, wiped it with alochol. and it no longer was an issue.
9. It heals super fast! I no longer have the earthworm. It is almost flat, pink not red, no black line stuff etc. no discoloration. Now, I am happy to see it. It is the model of where my other saggy boob is headed- upwards!
Nel, I guess what I'm sharing is that you might want to think about specifically what is the frightening part of looking? That you have "hurt" or wounded your once intact body, that it is the simple gory aspects of it that are disgusting/scary, that you worry that you may damaged goods or unattractive, or some other reasons? Once you get that sorted out, you may think about meaningful steps you could do that would address the fear before you decide how to gradually plan to "undress" your surgery site and accept your body in it's wannabe underconstruction stage.
Deborah2012
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Hi Deborah2012 and ladies insterested in the aspiration of a seroma
In brief, all that happened was that I had swelling on the outside of my right rib (where I had the mastectomy) and a nurse inserted a needle and sucked it out.
I was still numb from the mastectomy so it didn't hurt, although it did make me a little queasy.
By the way, very sorry but forgot to say that I did not have a reconstruction after the mastectomy because I may have to have rads.
Perhaps that why I healed so well and so easily!!!
Next year, after chemo and immunotherapy and possiblly rads (second opinion thinks it may not be necessary) I do hope to have a recontstruction and am prepared after reading all your posts. Thank you!
I loved your joke Deborah2012 re marriage guideance. Sad to say but sounds just like a friend's husband...Glad he's not mine!
AlicetheCat
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Hi All,
Home after a great weekend work event (Fri night thru Sun mid day) I manage a small non-profit and once a year we have w eekend away for about 10-15 teen girls and a parent,lots of pampering, fun,food and info that applies to their disability. Everyone is excited for next year annd hopefully by then I have hair again. I am tired, but when I was dx, wasn't sure I would feel well enough to participate , so very glad I was able to and what a great distraction. Compared to what some of you folks are going thru,I only had a mx with no reconstruction,so tho I have some discomfort around the surgery site and under my arm,an feeling generally well.
Deborah2012,
I am not sure what I am frighteend of. I have always had small breasts, never defined myself by how I look, just sort of freaking out. Steri strips etc have been gone for week or so. Now it is jsut taking the first look.I know the anticipation is making it worse. I am going to reread your thoughts and see if I can do it bit by bit.
Wishing all a gentle week,
Nel
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Let me throw these out there and see what happens.
Does any one else feel a knot at the outside edge of the breast? This is not about the incision. Fwiw, I had a skin-sparing bmx. This is on the side that did not have any node surgery.
The side of the SNB has at the outside edge of the breast seemed to be a bit swollen. It's been building for over a week though. Initially I'd feel something uncomfortable and couldn't figure out precisely where it was, felt like the inner arm but nothing would react when I'd feel around. Within the past day or two I've had no problem determining where the problem is. Just now when changing ito jammies, I looked at it again. The skin fold is getting some pink not quite red areas under it.
It just so happens that I'll be up at the VA for various appts Monday and Tuesday so I'll call the Breast Clinic when they open and see what they want. At least no fever so that's a good thing.
Thanks, Sally
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I had a weird experience today, sort of similar to what you are describing. I also had a skin sparing bmx and above the snb site, I had a big bulging lump, hard as a rock. I think it was a muscle spasm, but should I have a big muscle bulge here? It is the area of breast tissue (fat?) next to the armpit. It softened up after I laid down, but it is still swollen in this area.
I have been feeling pretty good these past two days so maybe this is from overdoing it a bit. That is, if you consider sitting up chatting with a friend for a few hours and then eating dinner, at the table, overdoing it.
Has anyone else had an experience like this? -
Finally touching base. My surgery was Wednesday, 02/29. I came home on Thursday, 03/01.
I feel great. Needed very little pain meds while in the hospital, and have only had 1 Vicodin since coming home (this is my 4th day at home). I've been able to sleep in my own bed since my first night home. The drains are annoying, but bearable. I was very happy to wake up and find that I only had 2 drains, not 4.
The SNB Quick Look, while I was in surgery, showed no cancerous cells. They removed 2 nodes. I'll get the final path report later this week at my follow-up appointment.
I was surprised that there's almost no pain from the incisions. The pain is muscle pain, and it's definitely tolerable. I know that I'll have nerve regeneration pain before too long, but the pain immediately following surgery is what I was kind of nervous about. What a relief that it turned out to be minimal!
I've had a couple of times where I felt pretty sad, a sense of loss. But that didn't last long. Overall, I'm so relieved that I made the decision to do BMX. I haven't regretted the decision for one second. Everything has gone more smoothly and easily than I anticipated.
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- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team