February 2010 Mastectomy
Time for a February 2010 mastectomy club to get started. Let me know if you need added to the list!
Jan. 21 Shannon12 Bilateral mx
Jan. 29 ReginaR Unilateral mx, node dissection, TE
Jan. 29 lim822 Bilateral mx, SNB, node dissection
Feb. 1 lovemygarden Bilateral mx, sentinal node biopsy
Feb. 2 groundhog Bilateral mx, sentinal node biopsy
Feb. 2 nieves Unilateral mx, axillary node dissection
Feb. 2 hbowser Unilateral mx
Feb. 3 funsizejen Bilateral mx, sentinal node biopsy, TE
Feb. 3 charua Prophylactic Bilateral, sentinal node bx, recons.
Feb. 3 Olivia218 Unilateral mx, immediate DIEP
Feb. 4 Faith316 Unilateral mx, axillary node dissection again
Feb. 5 Paintressa Unilateral mx, sentinal node biopsy
Feb. 5 PiscesMoon Unilateral mx, sentinal node biopsy
Feb. 8 cornellalum Bilateral mx, sentinal node biopsy, no reconst.
Feb. 8 toni67 Unilateral mx, node dissection, reduction
Feb. 8 Chalex Unilateral mx, node dissection
Feb. 9 lilacsandoldlace Bilateral mx
Feb. 9 mommalu Bilateral mx, sentinal node biopsy
Feb. 10 bodhi Bilateral mx and DIEP
Feb. 10 LTK Bilateral mx, sentinal node biopsy, implant
Feb. 10 dangergirl Bilateral mx and TE
Feb. 10 hunter11 Unilateral mx, SNB/node dissec., alloderm/TE
Feb. 10 CNSTP Bilateral mx, no reconstruction
Feb. 12 banana4me Unilateral mx, TE, delayed TRAM later
Feb. 12 MiachelJ2009 Bilateral, sentinal node biopsy, LAT flap
Feb. 12 Kayne Bilateral mx, immediate TE
Feb. 12 Cooltrainer Bilateral mx, immediate TE
Feb. 12 toughtitties Bilateral mx, TE
Feb. 16 Lillies4Laurie Bilateral mx, delayed reconstruction
Feb. 18 DeeCee Unilateral mx, immediate reconstruction
Feb. 18 MNLinda Bilateral mx
Feb. 22 LauraM Bilateral mx, immediate TRAM
Feb. 22 rockermom Bilateral mx, no reconstruction
Feb. 22 Jen112263 Bilateral mx
Feb. 23 Leeinvegas Bilateral mx
Feb. 23 caltex_catlady Bilateral mx, sentinal node biopsy
Feb. 23 TaminMo Bilateral mx, sentinal node biopsy, TE
Feb. 24 CyndiS Unilateral mx, immediate TE reconstruction
Feb. 24 thibaultm Bilateral mx
Feb. 24 black-cat Unilateral mx with DIEP
Feb. 24 guardienangel Bilateral mx with TE
Feb. 24 star-light Bilateral mx, SNB, TE
Feb. 25 sejnboys Bilateral mx with DIEP
Feb. 25 dickisonmomma Bilateral nipple sparing, TE
Feb. 25 dbdaze Unilateral mx
Feb. 25 slh_tn Unilateral mx, delayed reconstruction
Feb. 26 lostindecisions Unilateral mx, sentinal node biopsy
Feb. 26 hereandnow Unilateral mx, node dissection, TE
Feb. 27 TokyoSing Unilateral mx, SNB
Mar. 4 cakeisgreat Bilateral mx with DIEP
Comments
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February 8 - bilateral mastectomy with sentinel node biopsy, no reconstruction.
I am ready to be finished with this whole fiasco.
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I am new to this forum. I got my diagnosis in early Dec and have had to wait to get my insurance changed (Jan1) so that I could have my bilat DIEP in Seattle on Feb. 10.
I am so trying to be patient and accepting but I am scared and ready to have the surgery and get on with healing. I know I am supposed to be exercising before surgery. I have been spendng all my focussed energy on making arrangements, studying about the disease and the docs that I feel wasted by the end of the day.
I am grateful that this was caught early and that I may be spared chemo and radiation but until they do the surgery there is no way to really know.But I have had bouts of mourning for the loss of life as I have known it. Grateful and very sad.
All best wishes to you and to those of us on this journey.
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Faith316 - thanks for starting this list, please add my name.
Feb. 2 groundhog bi-lateral mx w/sentinel node bx, no recon
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I guess your Feb. 2 date is appropriate for a groundhog! I'll add you.
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Yeah, surgery date suggested the screen name. Not very creative I guess but, oh well...at least this way it's easy to remember when to send positive vibes and prayers for me (and my surgeon! - steady hands, not too much coffee but neither too little!!). {{hugs}}
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Hi February Ladies,
This is Regina. If any of you need an apron for drain bulbs after surgery PM me and I will get you one made and out ASAP! I would love to help you if I can.
((HUGS))
Regina
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Thanks Regina, that's so cool of you to do....
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Joining the February club! Bilateral mx with SNB and TE on Feb. 3rd.
I'm scared.
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funsizejen - welcome to the club, no one wants to join but glad you're here to go through this with. I'm a day ahead of you Tues 2/2 & also scared. But it's what I have to do so I'm doing it. Like you bmx w/bi-lat SNB but no recon. I'll be under 4 hours as it is and that's long enough! Good luck and I will be thinking of you Weds 2/3.
Faith316, cornellalum and bodhi - how are you tonight?
{{hugs}} to all
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Hi everybody!
Just noticed that so far, I am the only one not doing bilateral mx. All of my oncologists are telling me not to take the healthy breast because it isn't likely to spread to the other breast. If something shows up there it would more likely be a new primary. At one point, I thought I was gonna do bilateral, but decided I really want to keep the healthy breast. Don't want to lose all sensation. I, too, plan to do reconstruction but just not immediately. As aggressive as inflammatory breast cancer is, my doctors want me to wait a bit. They haven't given me a timetable, but I'm thinking maybe next fall I will have DIEP.
I also seem to be the only one who wasn't recently diagnosed. (Cornellalum, just wondering when you were diagnosed, if you want to share.) This is my second dx. Originally IDC, now IBC which started while I was still on chemo and radiation for the IDC. You can see what all I have been through in this nearly two year journey in my signature line below.
Wondering if any of you have been through chemo or radiation or if surgery is your first step.
Faith
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Faith, surgery is my first step. I'll know more about next steps after node bx and maybe oncotype.
Added: my family history was the deciding factor w/bi-lat. Of course, that will be different for you.
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Bodhi - I am sort of in the same boat. I am currently scheduled for a unilateral mastectomy on Jan. 27, but if I wait until February I have new insurance that has dramatically better coverage. I am in the process of trying to move everything out... I was losing it when I first found out all the problems I was about to face (with insurance) but am thinking now it was a blessing in disguise. As long as I can tolerate the wait. So, I may be joining the February ladies! I've been in the January forum all month. This is such an odd journey...
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Ladies, I went down this path last March. Faith, this was my 2nd diagnosis as well, having had lumpectomy and RADS with the first go-round (2006). Excellent Oncotype score (which measures risk of distant recurrance, not local). I opted for BMx this time. My BS wanted to do the affected breast and leave the other one. My intuition told me otherwise, too much fibercystic, too many scares. I changed BS's. I had the BMx plus SGAP reconstruction at the same time. It was a wise choice - the healthy breast was not diseased but had some atypical cells and they found LCIS in the Dx breast along with the IDC they already knew about. LCIS was a marker of increased risk, so they would have recommended the BMx had they known. So, what is your intuition telling you? What has your past history been? Calcifications? Any atypia? Only you can know what will make you feel more at ease. A recurrance was a lot more scary to me than the thought of mastectomy. The recovery from that was quite easy. The reconstruction recovery was tough but doable. Exercise and getting yourself in as great of shape as possible is key. PM me if you'd like additional info on my experience and research on flap surgery.
Check out the flap reconstructions on the NOLA site, breastcenter.com. Some reconstructions look better than the originals. So if having breasts are important, think about that. I'm glad I went this route and happy with the results. I understand you are scared and upset - I sure was! But as someone who is on the other side, who thanked my breasts and then said goodby, I am now much more calm and I know without a doubt that I made the right choice and minimized my risks.
I won't kid you - losing sensation was the pits. But a funny thing happened and now my arm and neck skin are sensitive - woo-hoo!! Of course, it's NOT the same, but it is nice!
Good luck, ladies., I will be praying for you.
Please listen to the docs and exercise - take 20 minutes daily and jump rope, hoola hoop, jumping jacks, whatever you can do - this is important! Practice deep breathing and get oxygenated! Ask you docs if you can take multivitamins plus additional C - it will help in the healing process. You will heal faster so preparation is critical. Take care!
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CyndiS -- Let us know if your surgery gets moved to Feb. and we'll add you. If not, good luck in January. Hope everything goes well for you! Let us know how things turn out!
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I'm glad to have some fellow travelers on this journey. My story started in June 2009 with microcalicifications on my regular screening mammogram. A needle biopsy turned up classic LCIS and DCIS, and a lumpectomy in November also turned up pleomorphic LCIS without clear margins. My surgeon initially wanted to do a re-excision to try to get clear margins, but due to the aggressive nature of pleomorphic LCIS and my family history, a bilateral mastectomy was definitely the way to go. No chemo or rads yet, and hopefully none will be needed. We'll see, right?
CharlestonGirl - exercise?? Sounds like work!
One of the most frustrating parts of this whole thing for me have been that we, as patients, are expected to make these huge decisions about exactly which treatment route to take. While my BS (and my second and third opinions) gave me the options, ultimately it was up to me to make the final decision. That certainly made for some sleepless nights, and endless pondering. But I will admit this: once I made up my mind (about two weeks ago), I was done with the thinking about it. I am very sure that this is the right way to go. Now I just need to wait until the date. I wish it was sooner......
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Cornellalum - my story is similar -- routine mammo in Oct. identified microcalcs, stereotactic bx in Nov. found DCIS and possible IDC, surgical bx in Dec. confirmed IDC. Had first onc appt 12/22 so that's my official diagnosis date. Onc was great, squeezed me in before the holiday and still spent a lot of time talking, explaining path report, even drew pix!
I needed time to think things through so called surgeon right after C-Mas to say let's do the bmx. He explained that, due to his vacation in mid-Jan. and not wanting to leave me in the lurch in case of post-op issues, we either needed to do it next week or in a month. AAGH - a week? No way, too soon, I was able to wait the month and boy has it gone fast! Yes, I want the cancer gone but oh how I will miss my breasts!
The wisdom and support here is amazing, I do not know how I could do this without y'all!! {{hugs}}
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Feb 12 - Unilateral mastectomy left side with recon (expanders). Will have TRAM flap recon later. The PS wouldn't do it immediately because I just quit smoking a couple of weeks ago. But at least I quit!!
I was originally going to have a lumpectomy on Jan 27th, but since I decided to change to mx, the date had to be pushed back. I'm a little nervous about putting it off longer, but I'm also relieved that it's now three weeks away again instead of three days...
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banana4me - hi and welcome - just some encouragement, I quit smoking last year and you can do it too! {{hugs}}
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Welcome banana4me! Interesting username. Good for you for quitting smoking! That is wonderful!
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Thanks for the support. I quit smoking after learning about the increased risk of complications with reconstruction. It's sad that it took a BC diagnosis to get me to quit.
BTW, the username came from my banana fetish. Banana every morning, first thing. Otherwise I'm grouchy the rest of the day.
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Yup, same here, I was down to one a day, but it took the ca dx to snuff the habit for good. (Sorry that was a groaner.)
It's interesting in hindsight that I craved bananas and really increased my consumption when I quit smoking. FYI, from google: Bananas can also help people trying to give up smoking. The B6, B12 they contain, as well as the potassium and magnesium found in them, help the body recover from the effects of nicotine withdrawal.
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Well, I guess a banana addiction is better than a nicotine addiction. I've been eating one every day for longer than I've been smoking - let's hope I can keep it down to just one...
On another, more serious note. Had bloody discharge today from the diseased breast. First time that's happened. I've had a weird, blackish discharge before, but never bloody. Is this cause to contact my Dr. or is it "normal" for a breast with IDC?
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Pam - if it were me, I'd call the doc's office. S/he needs the info and you need the peace of mind!
There's a discharge thread in the Not Diagnosed but Worried forum, author is inspireme, may be some help there? Good luck!
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Bodhi,
Misery will have company on Feb.10th. I'm in New York City, having a unilateral mastectomy (for widespread D.C.I.S.) and sentinal node biopsy. It's a skin-sparing (although not nipple-sparing) surgery with immediate reconstruction. The plastic surgeon will put in an implant. Hopefully, the newly constructed breast will match the healthy sandbag on the other side! (Going on 40; two breastfed kids. Gravity's been at work on my chest.)
I'm brand-new to this website. And, 2.5 weeks away from surgery, I've just been "building myself up" mentally to face this challenge. It's a mental game, and I'm determined to be a tough competitor against fear. You know in the Olympics, when you get a glimpse of an athlete warming up, listening to music, doing some moves, psyching themselves up before their sport? That's how I've decided to prepare myself. In fact, goofy as it sounds, I've been feeling the urge to punch the air with both my fists--boxer-style-- just to assert my strength. I will NOT let this mastectomy and my fear get me down. In your face, mastectomy!
I've always hated exercising, but today--despite the cold and drizzle--I took my first brisk walk outdoors just to help bolster my confidence going into Feb.10th. A good competitor needs to be in good shape, right? It was fantastic. I highly recommend this. I felt powerful, using the muscles in my legs and braving the cold. I've decided I'm going to make this a regular thing for the next 2 weeks, regardless of the weather, and compile my own mix of inspiring songs to accompany more these walks. Actually, lousy weather adds to the challenge, in a good way. If I can handle cold wind in my face, raindrops, etc., it reminds me that I am TOUGH for whatever challenges lie ahead.
I'm writing on and on... oops. The reason I signed on to the website tonight, for the first time, was to ask about recovery. Does anyone know--for a unilateral mx and sentinal node biopsy, how long can I expect to feel sore? My parents are coming into town to help with my two young kids, and I don't know for how long I should ask them to stay. We need to plan for their accommodations.
Soldier on, February ladies!! Glad to know that I have company.
LTK
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Sounds like your spirit is strong! Wonderful and welcome to our group. Since none of us have yet had mastectomies, you might want to ask your questions about recovery in a separate new thread. I doubt that many people who are not having Feb. 2010 surgeries will read this thread. I'll add you to our group list above.
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I am have a PBM on Feb 3rd with recon (not sure which method - either TE or one-step).
I had Hodgkins lymphoma in 1996 and was treated with chemo and chest radiation. The radiation raised my risk for breast cancer so I began mammograms at 25. I have had at least 10 areas biopsied and all have been benign. Unfortunately my most recent biopsy in September 2009 found ALH. Considering my history and risk, I decided to do PBM. I am 32 and have 2 kids (4 and 2 years old).
I am VERY nervous that the biopsies will show cancer. My BS doesn't think that will happen and was even planning on skipping the SNB. I convinced her to do the SNB but she isn't doing a stain in the OR. She will only send off the tissue to be analyzed.
In September, I had a breast MRI, ultrasound and mammogram so I am hoping nothing has popped up in the past 4 1/2 months. The thought keeps me up at night though!!
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Welcome LTK and Charua! We will all get through this together!
Charua, we'll be going through the same procedure on the same day. I have ALH in one side and IDC in the other. My breasts are out to get me!
My pre-op with the plastic surgeon is tomorrow.
Jennifer
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Hi ladies, hola from Spain!
I had Hodgkins lymphoma in 1991-92 and last month I was diagnosed a cancer tumor with only 12 mm diameter, but as I received a huge amount of radiation to cure Hodgkins desease, radiotherapy is not a chance now. 3 days ago, my doctors told me that they had been studying my case and had decided that what they will do is mastectomy of the affected breast
and also to extract all the lymphatic nodes from that side
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Next february the first I´ll enter the hospital and the operation will take place on Feb the 2nd . I'm awfully scared, I just can't swallow this bad news so easily and I dont trust in my own body, that seems to betray me again.
I see some of you are good warriors and I need to put myself together and keep going one way or another.
I send you big hugs and best wishes.
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Welcome charua and nieves! Sounds like you girls have a similar circumstance with both previously having had Hodgkin's lymphoma. We will ALL get through this together. Glad you found us!
Jen -- good luck with your appointment today!
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LTK: I am a visitor from the Jan. thread. I had a BMX w/SNB on one side on Jan. 8th. I had family staying with my children for the time I was in the hospital and the first 2 days I was home. My kids are a bit older than yours, I think (16,14,11). My husband and I were fine on our own after that. I had a couple of friends take me to the grocery store, and my kids helped with laundry--with much detailed direction from me. I haven't lived in New York for many years, but can you still shop and pay, then have it delivered to you?
I am still a bit sore, especially at the end of the day, and I'm not sleeping quite as long as I would like at night. But, I do feel much better than I expected to at this point (2.5 weeks). Each of us recovers differently, so it's hard to predict. My oldest friend came from NY to stay with me last week while my husband was on a business trip. I was happy to have her help, but the greatest benefit was psychological. I was pretty worn down emotionally from the whole ordeal. I guess what I'm trying to say is that it's a guessing game when trying to plan for your parents. Just don't forget that some of the healing you need to do is emotional, so don't forget to factor that in.
The January thread is a good place to read about the varied experiences of some different women as we've gone through this. Best wishes to you for a successful surgery and recovery.
Maura
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