April & May 2015 Surgery Sisters
Comments
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JackBirdie, No one can be strong all the time. That's why we have this place. So we can offer strength when we have it and so we can receive it when we need it. Downdog said it exactly right. Our journeys are all very different, but we are together in the fight.
Sometimes I feel like I don't belong here since so far my journey has been pretty simple and straight forward. Then I read a post like yours and I realize that I do belong here because I can give love and support when someone else needs it. Today it's your turn to receive. Accept our love and support and when you are out of the pit, I know you'll be right there it handing out like before.
We're not just surgery sisters, we're breast friends.
Suzy
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SummerAngel, keep an eye on your temperature and I hope your fever breaks soon. Best wishes for your return to work next week. I hope the transition is easy for you and you don't find it too tiring.
Ladies, I'm abandoning the CYP2D6 and am thinking of looking into ER receptiveness a little more.
Sisters, I have tried to encourage you all to push yourselves a bit and exercise to your tolerance and ability levels. It will help you recover faster and energize you. Just as everyone's BC is different, our recoveries are all different. I am now in my 7th week of recovery and have made a full recovery in almost all areas. I went into this with a super high level of fitness, no other health conditions and overall very healthy eating. After reading Kris Carr's Crazy Sexy Cancer, I started making daily cancer smoothies for several weeks with broccoli, kale, wheat grass, berries etc, but the fact was, they didn't taste all that great, so I don't make them as often. My diet was pretty clean before; nonetheless, I've improved it a bit and only buy organic produce and dairy and grass fed meat now to avoid hormones, pesticides and antibiotics. I like good food and I am still going to eat it. I am in the camp that cancer is a crapshoot, just like Jackbirdie's MO said. I'm not tossing out all my makeup and skincare. I will wear fragrance when I feel like it. We all have to decide the extent to which we want to eliminate things from our lives that may trigger cancer. All humans have the potential for cancer inside them and whether it's stress, inflammation, environmental toxins, whatever, their immune system can't overcome it and kill the beast. Shit happens. Cancer robs some of us more than others. I have decided that I am not going to live my life thinking of BC and a possible recurrence. I am going to live as full a life as possible, learn and try new things and continue to challenge myself. The 401 is a 16 lane highway, with 4 lane dividers, that runs across the top of Toronto. Drivers are aggressive, with a few psycho drivers thrown in. I have not calculated the statistical odds, but I wouldn't be surprised to find that my chances of a bad accident/death are greater driving on this highway than those of a recurrence. Yet, every time I get on that highway, I don't even think about the chances of an accident happening. I refuse to live my life in fear. You never know what the future holds in store, but need to make the most of what you have now, each day.
As for my recovery, I am naturally such a high energy person that resting for two weeks was trying, but I knew was necessary for healing. I used my arms minimally for the first two weeks. I first noticed the impact on my pecs trying to grate parmesan cheese the first week. I couldn't do it. I couldn't open jars. I couldn't use a whisk, because the feeling in my pecs creeped me out. When I told my PS at my 4 wk follow up about not liking the feeling of dynamic pec contractions and that I found them cringe-worthy, she said I just had to work through it. So that's what I did.
I am the fittest recon patient my PS has ever had. She told me I would bounce back quickly and advised that exercise would help me heal faster, so she supported as much exercise as I wanted, subject to her restrictions for that particular period of time in the recovery process. No arms above 90°. No vigorous exercise for the first two weeks. I walked the halls the night of surgery and did leg lunges. When my PS & BS made rounds together the next day I was doing yoga leg exercises in the air and lower ab work. They just laughed. The first day home I slept. Every day after I walked. I did stretching and modified yoga within the limits of my restrictions and my abilities and tolerance at that time. I did stairs. At week 3 my PS gave the ok for lower body, so I started cycling and did leg machine workouts. At week 4, all my restrictions were lifted with the exception of not lying on my stomach until week 12 and no waterskiing this summer. I started running (needed to wait to week 4 to wear a sports bra), swimming, tennis, returned to my hot yoga studio, pushups, weights, kayaking, soccer, you name it. For most, I was able to perform at my pre-sx levels. At week 4 isometric pec exercises (e.g. plank and holding it for several minutes) were no problem; however dynamic pec exercises were a different story. My challenge was in becoming accustomed to the kinesthetic changes in having my pecs reattached at a higher point. I couldn't do a pushup the first time I tried - I had to start on my knees. I couldn't do a real pushup until week 5. Today I can only do 25; pre-sx I could do 150 without stopping. I am up to 5 with pushup stands (allow you to go deeper with added height). I used to be the pushup queen; I'm not sure I will be able to reach the same levels. Time will tell. I am motivated and will give it my best shot, but am ok if I can't. Swim strokes were all good at 5 weeks, with the exception of butterfly. My arms don't fully lift after the initiation of the stroke. I think in another 2 weeks I will nail fly. I also can't use an ab wheel with a full extension yet, but I'm working on it. The limitation is at the lower edge of the Alloderm slings where they were sutured to my upper abs. One of my favourite ab exercises is stir the pot on a stability ball. I couldn't do it until week 5. When I do it, my implants move like people doing the wave at a sports stadium. Something I didn't like in my pre-sx research was seeing extensive dynamic pec distortion on youtube videos and PS websites. I found it freaky. My right side is my dominant side and has virtually none, which both surprises and pleases me. My left breast has a little bit, so I will strengthen that side with light weights to eliminate the need for compensation and hopefully get rid of the distortion. I will also talk to my PT about it when I see her in a couple of weeks.
Pain-wise, I have lucked out. Did my physical condition play a role? I would imagine it helped, but really don't know. I know my condition helped my flaps heal. My PS had been worried that I might get necrosis because they were so thin. I had no nipple or skin necrosis and my nipples looked healthy from day 1. After the first week, I consider that I have had no pain: no iron bra whatsoever (which I attribute to my 6 weeks of pre-op dedicated pec development), no twinges, no nerve zaps. My PS said nerve regeneration sometimes feels like a burn, but I haven't experienced that so far. I did experience discomfort with stretching as I regained ROM and also pushing past the creep out factor of dynamic pec contractions.
I am very happy with my results. Two weeks prior to sx, I went to see my PS again, to fully clarify my expectations. I didn't want any surprises or disappointment. I look just like she said I would. I haven't had, nor will I experience any 'drop and fluff', according to my PS. Not sure if this is due to precise pocket work, size (weight) of implants (since mine are smaller than most of yours), or a combo of these factors, since I didn't ask her why. She told me that it takes up to a year for nerves to regenerate and that she has only had 2 patients who regained nipple sensation. I derived a lot of sexual pleasure from my breasts and nipples, so I tasked my DH with discovering new erogenous zones. I do not resent or feel bitter about losing sensation. I made my decision of NSBMX knowing full well that I would lose sensation. My expectation is that I will have none and if I develop any over the course of the next year it will be a bonus. I can't change the past. I have got rid of all my bras, as I go braless all the time now, except for sports bras for high impact activities. Now that it's summer I will be wearing a lot of yoga tops and tennis outfits. They are all stretchy, so no issues with fit. I donated some clothing that was too fitted in the bust and is now too small, so had to go shopping!
I wish you strength to get through your respective tx, whatever they may be. Be gentle with yourselves when you are fragile and don't demand too much of yourselves when tx has made it impossible. I wish you lives full of peace, beauty, love and light. Be the best that you can be. Challenge yourself. Take up a new hobby, learn another language or perhaps a craft, read some good books, volunteer somewhere - anything that interests you. Try and squeeze some exercise into your day. Namaste.
New dress #1 I bought for myself. It's dark navy. The camera strap is black, which I didn't realize had fallen in front.
I bought this dress for DH, because he's an ass man at heart.
Here's what my implants look like at 7 weeks. My camera is heavy, so the side holding it is lifted a tad. They really are perfect mirror images. The dark circle at my neck is the shadow from the lens.
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You look fabulous!!!! Thank you for sharing these pictures. You're definitely an inspiration.
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Suzyq- thank you for your kind words.
Downdog- you are truly a beacon. Amazing person, so strong and so giving. Meanwhile being a super hottie! Love the dresses. You indeed do look fantastic! But your insides are just as beautiful.
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SuzyQ42 and Jackbirdie, thank you so much! If I can inspire or help any sister I will be happy. Hugs to both of you.
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Downdog, you're inspirational, a beautiful mind, body and soul. Thank you for all you do. You and the rest of the BC sister survivors got me through the scariest part of my BC journey, BMX with reconstruction. When I left my home to go to the hospital for my surgery, I felt you all with me, I knew I was being carried with prayers and love. The night of my surgery it took me an hour to post to this board, I kept nodding off, but I wanted to reconnect with all of you, that's how strong this bond has become. I thank, bless and continue to pray for all of us, for healing, for peace, and for the courage to face the future.
With all my love 💝💝💝💝💝
Audrey
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downdog - you are smoking hot!! I hope my rack will get there soon!!
There is no bond stronger than that of a BC sister. You are all truly amazing. I am so blessed to have met all you here to share all the highs and lows with. May we all find peace and acceptance of the new normal.
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Thank you, Audrey and mjh1! Audrey, I hope I can inspire you to incorporate fitness/exercise into your life and stay committed. You are such a beautiful person. mjh1, so true. The sisterhood is one of compassionate camaraderie. I am rooting for you big time that your August revision sx delivers on giving you the results you want.
Sisters, ask yourselves what makes you come alive. And then go do that. Be your most passionate self and live a fulfilling life.
Have a great day, everyone!
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Downdog, I'm a runner. And avid Weight Watcher. BC won't stop me.
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Excellent, Audrey...and very impressive! That's the attitude. Don't let BC take away your power and stop you from doing what you want.
Sisters, if you have access to a pool, even gentle movements standing and walking in water can be very therapeutic, if are weakened from treatment. The resistance can help build your strength.
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hi BC sisters - been a few days so just catching up!
Downdog - you are amazing & an inspiration - thank you for your post & sharing your gorgeous pics! I love how you say to find ways to challenge ourselves! I have never been wild about exercise and then in 2010 I had a very serious neck injury & was almost paralyzed! I came thru it thankfully after major neck surgery & months of rehab! With all that the only exercise I can do is walk & after reading your post I plan to hold myself to push myself to walk everyday!
So I will get my 1st fill this coming Tuesday - 200cc's in at time of surgery so curious how much PS will put in. Any tips out there on fills? Do they hurt?
My appointment with MO was originally set for 7/27 has now been moved up to this coming Wednesday since 2 nodes were positive? Anxious for this appointment to start discussing Chemo & if radiation is also a definite!! I know Tamoxifen is definite as my BC was 95% pos both ER & PR! Has anyone had radiation with implants ?? I will also search other threads... I think they will want to do some radiation since the cancer in one node showed outside the node! Have read horror stories of radiation & TE's / implants!
On a brighter note celebrated my Birthday yesterday (46) & funny how birthdays take on a new meaning after diagnosis! While I have always enjoyed birthdays now I want to shout them from the rooftops🎂👍
As always thanks to all for sharing
Mary
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Happy birthday, Mary!
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Downdog and Audrey, you guys look amazing and I am so inspired by you! I thought I had to wait until 6 weeks post-op to start exercising (I don't remember where I got that number) but after reading your posts, I started to exercise today (almost 4 weeks post-op). I feel great and my breasts didn't hurt to exercise! I did the elliptical for about 20 minutes and a lot of gentle stretching today. I used to run before but I don't think I should run for a while because I'm afraid of my implants bouncing up and down too much, even with a tight sports bra on. I'm healing nicely and I'd hate to mess with that. How long do you think I should wait before running?
Another big change: I've decided to go back to work tomorrow, just a few hours a day. My job is a desk job so not physically demanding at all. It feels great to gradually reclaim some normalcy in my life!
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Happy birthday Mary! Fills are ok. I was filled 400cc at surgery then three 100cc fills and one 50cc fill in the PS office. And now I'm done. The PS will use a small hand held device to find the port in the TE, like a stud finder. He will insert a needle and attach a very large syringe to the needle and push the fluid in. I was numb on my right breast so never felt the needle. I did feel the needle on the left side though but it's only a second and it's over. Getting an IV is 100 times worse for comparison. For me I would get two syringes per breast equalling 100cc each. I would just talk to the nurse and PS throughout the whole process, about 10 minutes. They must talk about me and call me the yapper but it's how I dealt with it. I wil let others speak to radiation.
MsryAgatha, I went back to work last Wednesday. Prepare to be tired at night. It's awesome to get the normalcy of life back though. I don't have a dr apt until 8/4, surgery preop. It's nice to have a little vacation from medical procedures, surgeries, poking and prodding.
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Mary, happy birthday and hope you had a great day! I am so proud of you for making a commitment to walk more. If you are able, try and walk through chemo to help reduce SEs. If you can't, don't beat yourself up. Some days will be better than other days. That is an amazing recovery from near paralysis. If you get moments of doubt while going through tx, recall the strength you had to get through everything you went through and know that you absolutely have the inner strength to get through your bc tx. I hope you like and trust your MO and have a good appointment on Wed.
MaryAgatha, check with your PS to get the OK for running. They all have different instructions and your PS can see how well you're healing. I had to wait until 4 weeks to wear a sports bra and that was only if it didn't bother my incisions. You need to feel comfortable running, so make sure you like your running/sports bra. Personally, I don't like sports bras that compress and squish into a uni-boob. I think you get better support with ones that separate the breasts and I find underwire better. Underwire felt fine on my incisions. My favourite high impact sports bra is Athleta's Glory bra. I have other brands, but I like them the best. Try different brands and styles on and run on the spot in the change room. If you will be doing other high impact activities, do a couple of squat jumps. The impact of hitting the ground is a great way to see if you get bounce with the bra. Good luck back at work tomorrow.
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Happy Birthday Mary! 🎂🎂🎂
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Happy birthday, Mary! We're very close to the same age, I turned 46 in April. I've been having fills done every week since my surgery, the first one 5 days post-op. I started with 100 ccs at surgery time and have had 3 fills of 50 ccs each. No problem, but there is some tightness for the first day or two after. I can feel the needle and I do bleed each time, but there's very little pain associated with the fills.
I'm still running a fever, never higher than 100.9. My oncologist's office called a second time to say that Tamoxifen is NOT causing my fever. Nice that they have no idea. Sigh. I think it's an unrelated virus, actually. I don't feel too terrible, just tired and sometimes dizzy, and both of my daughters are feeling the same way.
Starting back to work today, 20 hours this week. I work from home full-time so I'm not concerned about the strain.
It's good to read stories about everyone's exercise after surgery. I'm excited to start back up again. I've only been doing my physical therapist's recommended stretches so far, along with some light housework and walking. I'm not sure how much to do while I still have a fever, though. I have an appointment with my PT later this week, hopefully she'll be able to shed some light on what's safe for me to do. My biggest fear is developing lymphedema so I'm careful with my arms.
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Happy Belated Birthday Mary!!!
Audrey, you look FANTASTIC too! You and Downdog are really inspiring me.
JackieBird, I hope you're feeling better! I was away for a business conference this weekend, but I was thinking of you and sending you healing vibes.
Happy Monday to us all!
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thanks all for the Birthday wishes 😎
QQ - trying to prepare questions for MO... My path report showed 1 Sentinel Node positive with focal extranodal extension and then 1 axillary node positive with No extraodal extension.. Anyone have similar findings - advice on it?
Also when i asked BS how many nodes were taken she said she has no way to tell that - I was only advised 2 were tested & they were positive! I want to push to know if all other nodes were clear.. Any thoughts? Path report does not show a # of total nodes. Did any of you have to push for add'l info on path report??
Also thanks for the advice on fills - looking forward to getting started but also a little concerned they may want to do radiation and the impact of that on my reconstruction
Happy Monday All
Mary
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Suzy-Thanks! feeling a bit better..... Just in time for last chemo on Thursday! I know it will take a while to bounce back and I am in terrible physical condition- but I'm hoping the knowledge that I'm now done with the worst (I hope!) of the treatment, I will be inspired to do more to help myself make a BIG COMEBACK!
Hear that Downdog?
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SummerAngel, take it easy while you still have the fever.
mdoc524, I am a bit puzzled by your situation. Sentinel nodes are most often Level 1 axillary nodes. There are 3 levels of axillary nodes. ALND takes levels I and II and they are removed as a chunk of the axillary fat pat. In an ANLD, the surgeon will not know how many nodes were removed, because they are embedded in the fat pad, but they will be counted and reported by the pathologist. Did you sign a consent form for only a SNB? I think your surgeon may have removed 2 nodes for your sentinel node procedure, which is not unusual. One and a spare. If you have a radioactive tracer, and particularly if your tumour is in the upper outer quadrant, the whole area is lit up and the fat shows hot as well. This can make it difficult to discern if there is only one node, so the surgeon often take a couple of the hottest nodes, which are usually close together. Same thing for blue dye. Sometimes two are equally as blue. My best guess is that you had a SNB, two nodes were removed and you have the info about those two on your path report. The path report typically describes the entire specimen in the labelled container. Is there any language on the path report that states the contents of the container, i.e, two nodes, perhaps a bit of fat and then expands on what specifically was found in the nodes?
If you only had a SNB, I am finding it hard to believe that your BS did not record the number of nodes in her surgical notes. What did she do, remove a big pad of fat with embedded nodes? That's not a SNB procedure. Phone the office and ask her to check her surgical notes and confirm what she did and how many nodes she removed. Did she do a SNB? Only a SNB? How many nodes? See what info you get. If your path report doesn't state how many nodes were in the lymph node specimen container, then you should follow up there too. They can't remove body parts from you and not have a record of it - they need to be in compliance with whatever practices are prescribed by your state's college of physicians and surgeons. It's crazy that you have to chase this info down; you are entitled to know. BTW, did you have any pre-sx imaging that indicated suspicious nodes? Good luck with finding out more info.
Jackbirdie, I am going to hold you to that!!
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Hi downdog - thanks so much for the info and your thoughts .. initially prior to surgery my BS advised she will take 1st Sentinel Node - check it or them if more than 1 and if she sees anything abnormal she will take all nodes underarm -which is what she shared after surgery. The path report though only indicates 2 nodes and no where on it does it say how many nodes were actually included .. here are some screen shots from the report - just cut and pasted anywhere it mentioned node********
Left breast, mastectomy: Invasive ductal carcinoma (measuring 3.4 cm, see note). Nipple/areola are uninvolved with tumor. Surgical res ection margins are negative for tumor. See s noptic report. C. Left axillary lymph node #1,excision: Metastatic carcinoma present in one lymph node (1/1) without extranodal extension. D. Left axillary sentinel lymph node #1, excision:Metastatic carcinoma pres ent in one lymph node (1/1) with focal extranodal extension.
Microcalcifications :Present in nonneoplastic tissue Lymph Nodes Sentinel and Non-Sentinel Nodes Total Number of Lymph Nodes Examined (sentinel and nons entinel): 2 Micro /MacroMetastases : Present Number of Lymph Nodes With Macrometastases > 2 mm): 2 Number of Lymph Nodes With Micrometastases (> 0.2 mm to 2 mm and / or > 200 cells ): 0 Size of Largest Metastatic Deposit: 5 mm Extranodal Extension: Present Sentinel Nodes : Sentinel lymph node biopsy performed Number of Sentinel Lymph Nodes Examined: 1
Specified in the Latest Version of the ASCO / CAP Guidelines : Yes Fixative: Formalin Stage (pTNM) Primary Tumor (pT): pT2: Tumor > 20 mm but <= 50mm in greatest dimension Regional Lymph Nodes (pN): pN1a: Metastases in 1 to 3 axillary lymph nodes , at least 1 metastasis is greater than 2.0 mm
C. TOUCH PREP IMPRESSION: LEFT AXILLARY LYMPH NODE #1: No malignant cells seen on touch preparation. Findings called to Dr. (GS). D. TOUCH PREP IMPRESSION: LEFT AXILLARY SENTINEL LYMPH NODE #2: Positive for metastatic carcinoma. Findings called to Dr.
Left breast 12 o'clock long, 3 o'clock short, left axillary contents Type of Specimen: Modified radical mastectomy Received: Fresh Specimen dimensions : Breast: 22.0 x 20.0 x 6.0 cm Axillary tail: Present measuring 8.0 x 5.5 x 2.0 cm Skin/Scar: 14.0 x 5.0 cm. **********So it looks like the ALND was completed because the specimen included the Axillary Tail but nothing about the total # of lymph nodes and it is confusing where at first it states in the beginning that there is carcinoma present in Left Axillary node but then where it says Touch impressions - Left axillary lymph node - No malignant cells ... ?? seems contradicting
My plan was to ask about all of this with MO because that appt is tomorrow and if I do not get the answers I want I will then call BS .. thanks for looking at it and sending me the questions you would ask .. just want to make right decision on treatment - I am confident Chemo and Tamoxifen are in my game plan but not sure about radiation if it is really needed .. everything I read is that if less than 3 nodes radiation may not be needed ...
thanks and I am sure there maybe other threads or articles - I have downloaded the path report from this site and browsed the articles and everything is telling me that I should have been given more info
Mary
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My first week back at work is going really well so far! I have a great job and very supportive co-workers. What a blessing!
My breasts look great with clothes on (maybe even better than the original because they're a bit bigger and perkier now) but without clothes on, my breasts still look kind of mangled and very very fake. Only my DH and I will ever see my naked breasts so why should I care? I'm not sure why it matters but it does bother me whenever I look in the mirror. I hate the thought of another surgery but unless I see some dramatic changes in the next month or so, I think I will ask for a revision.... maybe...
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mdoc Belated birthday wishes! Downdog and Audrey you both look amazing! You are both inspiring! Downdog I am taking your inspiration and trying new exercises. My reconstruction has me somewhat limited because if the incisions in my thighs. I did 4 minutes on the recumbent bike and I had a tight band feeling all day after- I didn't get discouraged just had to laugh and make light of my inabilities. Audrey I too don't have any appointments until Aug 5 to the BS which will be my first post op with him he let the PS do all the post op appts. And then the PS on Aug 6 for a pre-op apt for stage 2. It feels good but I must say sometimes I am worried to go that long without being checked.
Downdog I read your post about nipple sensation- I didn't ask my PS about it but I was wondering...your PS has had 2 people regain some sensation? Out of how many? Since most women do not have NSBMX I would think the number isn't as high as we may think? I guess we can only hope to be one of the few.
Summerangel its great to get back to work but its true you will be very tired! The days I work I try to take a power nap in the middle of the day just to make it through. And that is very much not like me normally. But I am trying to get used to my new normal for now...
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Mary, OK, now it makes more sense. Your BS did a SNB removing 1 node. This was examined by the pathologist during your surgery. The results are under the 'Touch Prep', where the sentinel node was positive and the results called to your BS. Often this intra-operative testing is done by frozen section and it is about 90% accurate (false negative, not false positive error). The formalin fixed slides are done later, take more time and are more accurate. Your BS likely proceeded with the mastectomy while waiting for the results, the pathologist called the OR and then she proceeded with the ALND, because of the positive sentinel node. This is standard procedure. I did not think it was typical to do an intra-operative test of the ALND and you have the axillary node results listed under the Touch Prep info, so I am not sure why this was done. Normally, your axillary fat pad would be dissected with the lymph nodes embedded in it and your BS wouldn't know how many nodes were removed. This whole specimen would be examined by the pathologist and the total number of nodes in the sample should be noted. Say for example that your BS only removed 4 nodes with the ALND, plus the sentinel node. This would only be a total of 5 nodes and would not be considered a full ALND. Your MO would not have confidence in accurately staging the cancer with this number of nodes in the ALND (usually 10+). Your MO is going to want to know the total number of nodes removed for accurate staging. You need to know for your own info, so you can determine what is the appropriate treatment and have confidence that your tx plan is appropriate. Your risk of lymphedema increases with the number of nodes removed. You need to know to manage your risk and if you consult with a lymphedema specialist or PT, that person is going to ask how many nodes were removed in total. The axillary tail (also called the Tail of Spence) is breast tissue. It is a prolongation of the upper outer quadrant extending into the axilla. Axillary node(s) can sometimes be attached to it when it is removed as part of a mastectomy - this is more likely to happen in large breasts. Your pathology report would indicate this, if this happened (yours doesn't).
Talk to your MO tomorrow about this. He/she may even have already contacted the pathologist to obtain the total number of nodes removed. I can't see how the MO will proceed with recommending your tx plan in the absence of this info. If rads end up being part of your tx, then your RO will want to know as well, since the axilla isn't usually radiated if a full ALND has taken place. Let us know how your appoint goes tomorrow. Good luck.
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Mary, just to further clarify, the reason why I say I don't believe they can confidently stage the cancer without knowing the total number of nodes removed is that they need to know that the sample size of removed nodes is sufficiently large enough to have confidence that the two positive nodes are the extent of the nodal involvement.
MaryAgatha, great news about your job. I am sorry that you are unhappy with your implants. You ask why should you care and the fact that you don't like them is all the reason to care. I think if you still unhappy with them after a few months, you should consider a revision. I never requested access to the picture forum, but if you haven't done so already, you may wish to. You will be able to see what kind of results women get with different implants and FG and what is possible for body types similar to yours. I do think if a woman wants recon to deliver natural looking and feeling breasts that perforator flaps are the best option, if she is a candidate and willing to undergo the surgery. Get the breasts you want.
lovevt, that's a great attitude not getting discouraged and being able to laugh at yourself. It's all about resilience. I didn't ask out of how many, but I know from research that it's a very small percentage who regain sensation. I don't see my PS again until Aug, so will try to remember to ask.
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downdog - thanks for the clarification - I did get that which is what has been making me question it - I know that if it really is only 2 nodes still Stage 2 but the more nodes the more risk it has spread further so I want to be sure & just disappointed it was not on the report!
Got my 1st fill - 60 cc's on top of the 200 PS put in at surgery! Did not hurt going in but hurts now - right side worse than left but glad the fills have started!
MaryAgatha & lovevt - Congrats on getting back to work - must be nice to get back in the groove! I have 2 more weeks & then 2 weeks vacation time I saved up all year so looking forward to getting away!
Very anxious about MO appt tomorrow - really hope to get my add'l questions answered or I may have to consider another option ..
Hope everyone is healing well - have a good night
Mary
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downdog - replied to your clarification & then I saw your post before that with just such a wealth of info - Thank You so much .. I have typed out a full list of questions for MO appt tomorrow so hopefully she will have answers!!
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Good luck at your MO apt tomorrow Mary.
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Hi Ladies, tried posting this on the general surgery thread but no one replied. Thought I'd try on my "group" thread. Hope someone has some insights they can share. So had a PBMX with TEs on May 21, incl removal of 5 sentinel nodes. Had my first fill of 60 cc a week ago (ouch!!). A few days before my fill, I began experiencing pain on the top of my ribcage--- just on one side. It runs the gamut from piercing to aching to burning. Asked my PS and he said likely it was from the tissue being pulled off the ribs during MX--- making it sound like my "shock absorbers " were removed, if that makes sense. Some days it's bad enough that I need a pain pill (or two).
Anyone experience this? Does it resolve on its own? Does the tissue that used to act as a shock absorber grow back? Might my being short (5'2") and short waisted contribute (ie, my bra band sits on the top of my ribcage)?
Thanks in advance and positive healing thoughts to all
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- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 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