Looks like battle #2 begins...
Comments
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I have been diagnosed with a return of cancer close to the same area treated last year. Has anyone experienced this. I had a lumpectomy in Dec 2010 chemo ACx4 dose dense followed by 12 weeks of taxol. Followed by 7 weeks of radiation. I meet with dr tomorrow for multi dis meeting again. I had lots of staging tests done last week. I am trying to stay positive and strong but am very nervous to hear what they have to say.
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I am sure there are others who have experienced this. I had a new cancer show up in the opposite breast after 8 years. For some reason I think it is harder the second time.
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Hi Kerglid24 -
I was diagnosed with a return of triple neg cancer close to the same area last fall just six weeks after my one year "all's good" follow up appointment. I had the same initial tx you did in the early part of 2010. I was told I have lymphatic invasion now (not good news). I had a mastectomy in October and just finished up 4 1/2 months of chemo. I'll start radiation on Monday. I'm 48 and was in pretty good health when i was diagnosed. (I hike daily with my dog most mornings in Colorado, not overweight, healthy eater).
From what I've read and heard (I saw the head of breast cancer research at the University of Colorado in Denver), this cancer IS responsive to exercise and nutrition. I'd tell you not to be scared but the truth is, this is scary stuff. My advice? Don't overthink right now. Focus on the next baby step. Don't think beyond that. Focus on what makes you happy in the next hour, the next day. That's it. Be kind to yourself and trust that you are strong. Make yourself your number one priority. Ask yourself what you promised yourself you'd do after the first diagnosis but didn't. And make healing your ONLY (only, only only!!) priority. Everything else can wait. family...friends....work...everything.
Its scary but every case is different. Obviously, they've caught this early. That's good news. And don't forget...one baby step at a time.
Wishing you healing and peace,
B
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I am awaiting news on the results of my biopsy on my other breast. Would have been four years cancer free and was starting to relax a bit. In some ways, this time around I'm more calm because I know what to expect. In other ways, I'm more scared because I know what to expect. Some days I just want to say farewell to the girls and let 'em go feed the fishes. Other days I think my sagging boobs are the most beautiful things in the world. Conflicts galore! Had my biopsy Friday and hope for results today but will most likely be tomorrow by which time I'll be a complete wreck. One thing I know, I got through this before and can do it again. My DH assures me he can do it again, as well. Will be 68 the end of July and I've got more living to do, hopefully.
One question. Once TN, always TN for new cancers?
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Nope, not necessarily. It does seem common that TNs recur with TN, and ER+ with ER+, perhaps because our bodies are predisposed to harbouring and stimulating the growth of those particular tumours, but there's no hard and fast rule about that, no. You will find some TNs on these boards whose subsequent tumours tested ER+... even some metastases that show different pathology from original tumour... Sorry you're dealing with this all over again, but it sounds like you're in the fighting spirit!
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Got the biopsy results of cancer in left breast and it's TN again, too. Readying to start the battle. Now if only I could sleep. Maybe now that it's confirmed, I will. So far, I'm comforting family and friends. Am tired and going to bed.
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kane: Thinking of you, and wishing you well. Hope you'll keep us posted on your treatment, going forward. We're here for you.
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I am Stage IV, TN and If I was able to be NED,for three months... there is always hope for you all that are stages I-III. Staying positive is one of my survival mode ; staying buizzie with my Home Daycare; and just trying to keep everything normal
I try my best to keep everything the way it was before I was dx; my dailey routine, my sleeping habits ( is my biggest challange); But the way I eat is the one thing I have changed. Trying my best to keep the sugars down; since I had gotten Thrush twice now and of course my cancer came bk after three months. Remember I am stage four; so I have to expect it to come bk; but that does NOT mean I give up on the possabillty of going into remission again.I will never give up and you should NOT eather. Stay positive girls and LIVE YOU LIFE TO THE FULLEST
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My mum is in the same boat. She had a lumpectomy in July 08, 4 mos chemo and 5 weeks rad, for a small TN tumour with no lymph node involvement. Mammograms and various body scans every 6 mos and then in Jan '12 they found a wee tumour on her breast. Mastecomy, all lymph nodes removed were positive, and confirmed bone, liver and lung mets. She starts chemo next week and rads to her leg where the tumour is in the bone.
I have no idea what to expect. I need my mother around. She's only 60.
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Anyone still on this thread? I have same situation. 3.5 years out, now with a local recurrence. Will have bmx, dread the thought of AC and T again. If any of you still read this thread, please let me know how you're doing. I'm just trying to rally for round 2.
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Hi crs, most likely most that posted here have forgotten about this thread unless they happen upon it like I did. I was diagnosed in 2002 and 2011, opposite breast. Are you getting AC again? Most doctors won't give the A part again, but mine did. I am doing ok now (said with fingers crossed). It is rough to go through again, but doable, so hang in there!
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first dx 7/12. stage III grade 3 TN with lymph involvement. DD 4AC, 1 Taxol, 3 taxotere (bad reaction to taxol). bmx 12/12, skin sparing with recon TE's. 6 wks rads ending 3/22/13. at last RO app, everything looked good. that very night (5/9/13) I found a peasized lump on the same breast. Yes, only 10 hrs from seeing the dr. biopsy pos TN, PET scan shows no systemic disease, but in 1 wk 2 more lumps showed up . will be meeting with 2 different onco's to compare treatment options. Has anyone else had skin sparing recon with TE's and experienced such a fast recurrance? BS says i need to do chemo 1st (again) before i can even think of removing TE and breast skin. I'm not even 1 year from original dx, so all this is new to me.... very scared.
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Bump.... 2nd opinion suggested xeloda. started taking it yesterday. From what I've been reading, Xeloda is used primarily for mets. Has anyone had it prescribed for local recurrance for stage III TN? I'm thinking it's because my tumor came up only 6 wks post rads, literally grew to peasize in 10 hrs. Hoping it stops it in its tracks. Prayers to 2 close friends who just got dx also. Seems very odd that we are all being dx around the same time, all about the same age. I really believe either environment or food and packaging are the reason.
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Hello ladies. I was dx last May with IDC, TN,Stage 2, grade 3. Had a lumpectomy followed by 4 cycles of AC, then, 4 ctcles of Taxotere. Started radiation in Jan. of this year, finished March 8th. About 3 weeks ago, i was gaerdening, did alot of diggin. Noticed lymphedema to the right breast, same breast i was treated for. Went to my onc. last week because the breast was red, swollen, heavy. He sent me to a surgeon who deals with lymphedema. Saw that surgeon this Thursday, he thinks i have inflammatory Breast Cancer. I am getting an ultrasound of the breast next Tuesday with an MRI ordered if something shows uo on US> I did research on this, poor prognosis. Getting ready to tell my kids and i dread it
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fishinurse, I'm so sorry to hear about this issue, but please don't jump to conclusions about IBC. My initial symptoms had me convinced I also had IBC. Went to bed on a friday night with no lumps or symptoms, woke up next morning with my right breast 2x bigger than left. Gyno thought macstitis (Ididn't), but sent me to BS anyway. dx stage III IDC with lymph involvement. My skin had the classic orange peel look, discolored and warm. Scans showed a mass. Apparently, IBC grows in "sheets" on/in the skin, not as lumps. My tumor started to invade the skin and lymph system, hence the swelling, but not classified as IBC. I know what you're experiencing and it is scary, but try not to pull the cart ahead of the horse. Wait to hear what your bs says, take it one day at a time. TN dx can present in many ways. my recurrance has to be in the skin since i had bmx, and 2nd time it showed up as lumps, no swelling or pitting. It's still not classified as IBC even though its in the skin.
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Thanks so much for the reply. As time goes by,I reminded myself, no matter what it is, I will deal with it as it comes. Knowledge is power, once i know what it is, i can move forward with a plan. Like you said, One day at a time!
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Had a mastectomy oct 1213 but its back am booked for craniotomy on Thursday am so afraid it seems so much bigger than breast cancer the good news is that the tumour is superficial but will be away from home for about a month It feels like forever and I haven't left yet. I am not giving up but it is definitely scareier the 2nd time around I am taking one day at a time this op has to be done I do not have a choice .
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