Got Cancer? AGAIN????
Comments
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Hi Ladies,
First diagnosed: 1996 - DCIS, lumpectomy and radiation
Second diagnosis: 2007 - DCIS, lumpectomy but margins not clear; June 8, 2007 - left breast mastectomy -
Hi Diane, that really is crummy you've had c come back and had to go thru a left mastectomy.
We've fought it off before so we'll just do it again.
It certainly is a shock to hear it's back.
Best wishes -
Hi, I'm not sure if I have a reoccurance or not. The last pet scan should a suspicious 'something' right around my mastectomy site that I had Dec 06. The radiologist recommended another pet scan in three months which will be Oct 07, so now I'm just waiting. My oncologist says 'it's probably something from the surgery' but she also mentioned my liver ( in the same breath) which I didn't understand. I'm just a little anxiously waiting for the next scan. Thanks for all the information on this site. It helps to know so many people do so well.
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I had a suspicious something too- and my BS waited a year.
I paid the price for it by having a much larger new cancer and four positive nodes with extra-nodal extension and have been in chemo since April.
Please don't wait.
Get it checked out sooner rather than later.
Good luck to you,
g
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Tessie, I had my 6 month CT scan in July which came back clean (NED) but 10 days later found a very small lump just above my mastectomy scar. The surgeon did an ultrasound and thought it was a lymph node but said it had to come out to know for sure.
We did the surgery the very next day and fortunately it turned out to be scar tissue and a remnant of an old suture that my body reacted to with an inflammatory process. Obviously that was great news to me!
My point being that I agree with Nosurrender. I feel it is better to get these things checked out so that you either get good news and can stop worrying, or else you find out what has to be done and can start taking treatment steps before things get too far along.
Hope things work out well for you. Let us know.
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Well ....
I DO have cancer again for the 3rd time, but not Breast... this is NEW cancer I am told, I have stage 1 Lung Cancer.. BIG shock... I thought it was stage IV Breast, But I guess its better to have the Lung Cancer, instead of stage IV breast. I am scheduled for Lung surgery in 2 weeks..... I dont know anything about LUng Cancer, I never smoked..Dr thinks its from 2nd hand smoke from my parents, My Mom died from lung cancer in 1993, she always smoked around me. closed car. in the house. She had an ashtray in every room. She smoked about 3-4 packs a day.....I will always keep you ladies in my prayers and in my thoughts, DONT GIVE UP
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Golden Eyes - check out this article. I realize you have done a lot of research and wondered if you know more information about this procedure. I also have several lung nodules where the largest was biopsied as benign granuloma however, I'm being watched by a pulmonary specialist who mentioned removal if changes seen during my next CT in Oct. I came across this article last year prior to my lung biopsy and saved it. Best wishes! Joann
http://www.news.harvard.edu/gazette/2001/03.15/07-surgery.html
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first dx i was 39 stage 1 no node involvment triple negative tumor
had lumpectomy and radiation
10 YEARS LATER ! thought i was in the clear after 5
redx same breast this time stage 3b * (and thats with yearly mammos and sonos! ) mammo did not pick it up both times due to dense breasts- should have been doing MRI
had adjunct chemo and dbl mast and reconstruction- NED for 1 yr
never dreamed of having bc nevermind having it twice it was quite a shock since i had perfect mammo and sono the year before - i believe it was there at that point but becos of dense breast tissue would only have been picked up by mri
well now dont have to worry about dense breast tissue since i have NO breast tissue but very happy with my reconstruction and i loved all my drs at memorial sloan kettering in nyc
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1990, cervical cancer, hysterectomy, no follow up treatment. I was dumb about cancer. Didn't get a copy of the pathologists report, have no idea of a classification or if there even was one at that point.
2005, breast cancer, 3c, er+ pr+ HER2-, 18 of 18 nodes positive, left mast, node disection, chemo, rads.
Now I'm watching a bruise on my right forearm with a small lump. I go to the GP on the 19th and will ask him what he thinks. (An aunt, father's sister, had breast cancer then a few years later had to have her arm amputated for cancer.) Frightening! Makes me wonder if it's best to know of these things or not.
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I had DCIS in 1998, age 56, mastectomy with A(bad) saline implant reconstruction after three lumpectomies did not result in clear margins, no other treatment. Then in 2004 I had a second primary IDC in the other breast, 1.4 cm, node-negative, Pr+, at age 62. I had lumpectomy, radiation, turned down chemo with consent of my oncologist, and am on year 4 of Arimidex. I had the usual aches and pains, carpal tunnel, dry skin everywhere, thinning hair, short-term memory loss... but nothing I can't live with and so far am doing fine. I take Fosamax and extra Vitamin D and calcium, and my bone scans are normal. I still have checkups with all my different specialists every 4 or 6 months, so there's someone poking at my breasts every few months, and a mammogram twice a year. I'm always waiting for the other shoe to drop, but so far so good. I wish everyone well -- haven't posted for years, but I still read, usually in the middle of the night when I wake up and the Demons are lurking.
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Hi Girls
I'm a newbie from the UK. Don't know whether I should be adding to this thread, but here goes.
1981 Lumpectomy (age 34) Left-hand side - no other treatment
1983 Lumpectomy same side - no other treatment
1985 Radical mastectomy and lymph node removal - no other treatment
1990 Reconstruction - done twice as surgeon got it 'wrong' the first time!
1995 Silicone implant removed - leaking
2007 (Christmas) Lumpectomy and node removal right-hand side. Just finished 20 sessions of radiotherapy, taking Tamoxifen for 2 years then switching to Arimidix for the duration!
Fighting with Attitude! -
1999 age 41...lcis in left breast
2000 age 42.... benign lump.. started tamoxifin (left breast)
2001 age 43.....idc....very small.. lumpectomy/w rads...doc takes me off tam. said maybe it caused my cancer, as a small cancer should not have broken through
2007.... age 49... dcis and small microinvasion...(left breast).. bilateral mast... no other meds
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Hi All,
I had my first b/c in 2006
April 2006 lumpectomy no clear margins
June 2006 r mastectomy 4 dense dose A/C
Found lump in Dec. of 07
Jan dx recurrance.
I will have surgery to remove the cancer and axillary lymph discetion next week or so.
I finally found the oncologist of my dreams (this is my 3rd opinion) she is out of Chicago area, and is doing two clinical trials on triple neg metastic breast cancer, so I'm lucky enough to finally have someone who specializes in my type of the disease Yeah!! I will have 4 or six rounds of carboplaxin tanetere and avastin. Anyone have any input on the drugs, side effects, and so on...
Thanks
Leesa
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Yes, it is back again! So, here goes the saga.
Nov 1998 we had just spent a year planning our daughter's wedding. They married Sat., Jan 3 and Monday I had a lumpectomy, followed with chemo, and rad, and Tamox. Spring 2006 my annual mamo showed something suspicous on the right breast. All I could feel was the scar tissue. Sure enough, it came back in the very same spot. I said, fine. Take them both off. June 2006 one surgeon took them off and the ps came in to begin the recon. I was going to have the tissue expanders. I was excited when I could eventually go in for the injections. After 2 weeks, of expanding, the right breast burst at the seam and liquid ran everywhere! Naturally it was a Sat. We called my ps. He said to meet him at his office. Well he was afraid the previous rads would have done too much damage to the tissue to hold the expander. The following Tue he took the right expander out. After a fashion he said Plan B would be to put in the implant plus my own tissue on the rt. After 5 hours of surgery it was done. It was recommended that I do chemo - I did one session and thought I would have to get better to die! No vomitting, but abdominal cramps were beyond description!! Two weeks of them! After that I said no more! I believe it was the nasty beast Taxol. I finished all recon surgery July 2007. I am not 100% pleased but considering what the ps had to work with on the rt side, it's better than nothing! Several months ago I noticed a itchy rash along my bra line. My reg dr said "oh it's dermitis" and gave me a cream. After 2 weeks it was still the same I did as she suggested and resorted to a dermatologist. We are baaaack!!!!! By this time there were bumps all across both breasts and was starting to move to the back on the rt side. My onc said no surgery. He said rads and Arimidex. I have finished the rads, have the ct scan of the chest this Friday. My chest looked like a road map! I had 4 areas for rads every day for 20 days! I am exhausted! My onc said the only way he would recommend chemo is if it moves to another area. In the past 10 years it has (thankfully??) stayed in the one area. I have been SO depressed! Have cried my eyes out! The year of recon surgery sent me into a horrible depression. They say the anesthetic is what does it. I ended up at a Psych's office - still on 300 mg of Effexor/day. And still on Ambien at night so I can sleep. I wonder if I will ever get rid of the Ambien. It has been very difficult...I had no idea there were so many others who had bc return like mine. Thank you all so much for being here, I am ready to cry again this time for thankfullness!
Linda,
Arizona
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Hi All,
I will add my story:
DX June 06 with mixed IDC/ILC 1.5 mass er/pr +, 0 nodes stage 1 grade 1. Did lumpectomy, rads and tamoxifen. I am Braca neg.
DX Jan 08 with.6mm ILC same area of first tumor, er/pr +,stage 1 grade 1. The recurrence was found on MRI was not visible with mammo or Ulra sound.
April 29th bit lat w/immediate recon and oopherectomy so that I can start AIs. Chemo began 6/11.
I hope this is the end of my story with ILC!!!!! Here is to moving on to new Foobs and a healthy future!
Valerie
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Hi Ladies!
I was dx with 1st go round in Aug 05 her/er ++ stage 3. I did TAC for 12 weeks and radiation for 6 weeks. Chose not to take tamoxifen. I was dx with recurrence on Apr 25. I started chemo on May 1...phase III study of Avastin/taxol...3 weeks on, 1 week off indefinately. I have multifocal mets to right lung, both hips, both femurs, groin, sacrum, and spine...lovely huh? I was 34 when I was dx the 1st time and 37 now. I haven't had the best attitude, esp since I had to lose my hair AGAIN, but if last time is any indication, I will start fighting just as soon as I get over being FURIOUS. This site is great and I think it is helping, esp seeing that other people have had to do all this bull over again, so maybe I can too. You are all in my prayers...take care.
Ali
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Hang in there azsunshop. You have been through hell it sounds like, but thank goodness the CA hasn't changed or spread. You are in my prayers and thoughts
Ali
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Hello Ladies,
I was first diagnosed in August of 2001. I had an area of (right breast) microcalsifications that was watched every 6 months X 4 years with mammograms. In 2001, a second area appeared an my mammogram and the doctor ordered biopsy. My biopsy was on a wed and late Fri afternoon my doc called me to say the lab could not tell if it was cancer yet or not. So it was sent to larger lab in New York. New York had the same conclusion, did not say it was B9 or cancer.
After talking to my doctor, the radiologist and my surgeon, I decided to have a mastectomy with reconstruction. Ionly had the one surgery and since it was so early I did not have to have rads or chemo, I only missed two weeks of work and everything went so smoothly. I woke up from surgery and a nice little round implant.
Piece of cake. Wish they could all be that way.
This go around, I had my yaerly mammogram on March 19,and before I left the room the rdiologist sent me over for US,Ten minutes to 5 the US doctor came in and said it does not look good and he was calling my doctor to order a biopsy. My doctor called my surgeon the next morning to set up an appointment for the following week to discuss the biopsy. I walked in to the exam room adn my surgeon was standing there looking at my mammogram films and before I could sit down e said: "it doesn't look good, I don't like it". My dh and I just looked at each other and I said OK now what?. Surgeon said he wanted to do a biopsy and I asked when and he said right now. After to biopsy he said he would know the results in 48 hours, he called me the next afternoon and said I have cancer. He asked if I wanted to have the surgery and reconstruction at the same time as before and I said sure. The only problem with that is my ps does not do total reconstruction any more and gave up his priviledges at the three local hospitals b/c he opened his own surgery center. The only PS in that county takes medicare or $5,000. up front.
Long story short, I ended up going to a Women's Center at the advice of the office manager in my surgeon's office. I say the newmsurgeon the next day, the PS the followigmMonday, had my surgery on April 19, 08, IDC, 2 cm, StageIIb, Grade2, 2/11 nodes, HER-Neu- The path report showed an unclean margin and my second surgery was May 16. No cake here this time. Anyhow I am schedued to A/C once bi-weeklyfor 4 months and Taxol weekly for 12 weeks. Now as soon as the drain from my surgery is out I can begin the chemo journey.
Anyhow HUGS to everyone and we will beat this monster.
Sandy
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Sandy,
Wow, what a ride. I don't think it's every a piece of cake, really, but I'm sorry you're not having as easy a time of it right now.
In a way, for me anyway, second time around seems easier emotionally (in that I know much more) but harder physcially (more ectensive surgery, and ofter heavier treatments.)
But, yes, we hang in there and do what we need to do. That's what counts.
anne
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Yes I was on this site in 2005 had a lumpectomey chemo and rads and now its shown its ugley head in the same breast, having chem (taxol) at moment. On the third session and its been a killer, extensive joint pain and sickness so I am feeling very down at the moment.
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Age 29 IDC, mastectomy and CMF.
Age 48 this year DCIS with micromets to the sentinal node, mastectomy and dose dense Taxol anmd Adriamycin. What a Trip that has been!!!!
Ovaries coming out in August. Two is enough for me!
LA
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Two years ago I told the recon surgeon "I was going to be one of the lucky ones that didn't get IT again" when asked if I wanted to have both breasts removed. I figured with a 70% chance of it NOT coming back, why remove a healthy breast. It was not to be.
My first journey with cancer started with thyroid cancer when I was 22 and a newlywed. I had total body scans for 10 years and felt blessed when nothing ever showed up.
In Feb. 2006 the mammogram showed a large lump filled w/cancer. Needle biopsy confirmed it. What was really weird was that it was a lump I had had my whole life. As I had gone thru menopause, lumps disappeared. This one had not gone yet. Dr. said it was very unusual for a lump to fill with DCIS. Initial area started at 4cm. After the lumpectomy (actual partial mastectomy by the time she was done) area ended up st 9cm. Even then, 3 margins were not clean. Surgeon said I probably would not be happy after wider excision and then rads so I went with mast & immediate recon using SIEA, done by Dr. Allen in Charleston, SC. Recovery for me was very quick. Course, this was my 18th & 19th surgeries since 1971.
I'm a pro. Ha, ha. Had BRAC testing and was negative.
2007 mamogram was clear. 2008 was not. DCIS is now in the left breast. I am now waiting to hear from the Plastic Surgeon who now does the perforator flap surgeries here in MI to see if I will be able to have recon surgery using tissue from my thigh. She trained with Dr. Allen and he has developed this new method. I should know Friday.
Can't use implants because of RA. Because of the RA, I really didn't want to go the route of lumpectomy and rads, especially since it is my left side.
I'm sure I don't have to tell anyone how devastated I felt when they said cancer again. It doesn't matter that it is "only DCIS" - I'm still losing my other breast and having another surgery. This will be 22 and 23.
It seems that one minute I'm OK and then the next I'm in tears. No sense to it, just pure emotion. I'ts not fair, but then as I tell my son, life's not fair; you just do the best you can every day.
I am so thankful for this site, I wish I would have found it 2 years ago. Only someone who has gone thru or is going thru bc knows what it is like. The sisters writing on these boards do. God bless you all.
Sunkist in MI
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Hi Second Timers,
It has been a while since I checked in here.
I was just reading up on some of your stories - wow. What everyone has been through is amazing.
I want to say hi to everyone and to the most recent posters,
Sunkist, good luck with everything. I didn't know you couldn't get implants with RA. I just had my exchange surgery and I am pretty happy with it. "Only dcis"- we know it is just as devastating. Stick around this board, lots of places to get input on every stage you are going through.
Super, my first chemo was CMF too. Then I upgraded to the Adria, Abraxane and finally Xeloda for the second time. I had IDC the first time and ILC the second as well. My ovaries are history too, probably in the fall.
Anne, that is exactly how I felt. Easier emotionally- but physically, not so much! How are you feeling now?
Sandy you have had some time of it. I started my second course of chemo in April in 2007 and finished in December. I have hair again! What a difference a year makes between last summer and this summer. Next summer will be much better for you too.
Grandmaberyl, I hope you can talk with your onc and find a way to help you with the pain. I did Abraxane not Taxol. I still had joint pain but it was managable. Maybe you can switch?
Ali, how are you feeling? How is the chemo combo treating you? I hope well.
Valerie, I never heard of ILC being Tripleneg. I always thought that was saved for IDC. I was tripleneg the first time with IDC and er+ the second time with ILC. I hope you are doing ok.
Azsunshop/Linda, how are you? I have heard that about anesthesia too. I hope things are going ok.
Anyone checking in here who has been diagnosed for a second time, last summer I was totally bald, in chemo that wouldn't end until December and it seems like a long, long road to haul.
This summer, I just had my exchange surgery last week, I have about 3 or so inches of hair and am hoping that two times is the charm and I don't have to get on the cancer bus again.
hang in there everybody!
g
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currently going through second bout 1st in 2004 had AC and Radiation now 2nd mastectomy and about to commence chemo Taxotere and cyclophosphamide. Would dearly love to find someone who has been there, currently there and experience with this chemo regime
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Thanks 'nosurrender'. The reason I mentioned about not having the implants with RA is because of my cousin. She has lupas and RA and had the implants. She had a terrible time because her body sensed invasion and encapsulated them. Both had to be removed and she ended up with horrible scars and both breasts a real mess. My RA dr. said he would not recommend implants either.
Thank you for your kind words. Heard from the PS Friday and sounds good the the recon using tissue from my thigh. I will be scheduling a CAT scan tomorrow to make the vessels a viable for the microsurgery to the breast then if they look good, get a date set. I think at that point, my emotions may settle down. If the thigh won't work, I'll have to go back to Dr. Allen since the PS here doesn't want to do the GAP on me due to my sciatic nerve problems. She's relatively new with these procedures and would feel more comfortable with Dr. Allen's experience w/the GAP and my situation. I'm praying the thigh will work, mostly since she is in-network and participates w/my insurance. We are still paying for the recon on the first breast that Dr. Allen did. Sure would not like to have to add to that home equity loan.
Take care.
Sunkist in MI
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Well done No Surrender I admire your tenacity and determination. Must admit to finding it harder to accept this time round. Developed massive infection and have been having dressings done every second day for the past two months just to get the op site healed. Supposed to start chemo next week.....If the wound is healed. Lets hope two times is the final time. Best of luck.
P
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Age 34- married w/ 3 daughters (ages 3, 14, & 15 YIKES!)
DX- July 06- days after 33 birthday
Stage 0 DCIS intermediate grade 30% ER positive.
2 lumpectomies (to clear margins) 33 rads 5 year tamoxifen.
D&C July 07 excessive bleeding due to tamoxifen use- No uterine cancer just hormonal imbalance
Recurrence Nov 07
Stage 1 DCIS high grade w/ 6mm of invasion 70% ER positive (so much for tamoxifen) Quit tamxofen due to excessive bleeding and it not working anyway! Anemic from tamoxifen use.
Dec 10 2007- Bilateral Mastectomy w/ tram flap on left side and tissue expander on right. Blood transfusion. Sentinel node clean- BRCA tests negative. No chemo recommended. -
Hi Staci,
Did they doctors recommend mastectomy or did you ask for it?
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Inet has been down a home until this past weekend. Sorry not to have written. I had my first chemo tx on 06/19. From all I have read onthese threads, my side effectswere minimal and short lived. Hope it's a repeat when I take this weeks tx on thursday.
I converesed with GoGators on another thread and she and I are going to the same cancer center and during my first tx she was there for bloodwork and we actually got to met. She's is awesome. wish all of you could met her.
Well gotta go for now
Hugs and Prayers
Sandy
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2003..... right breast, lumpectomy, chemo, rads and tamoxifen
lets fast forward to present 5 years later
2008..advanced breast cancer to pelvis in bones, right lung and right breast again near scar line...Lupron injection, Femara pill and Zoledronic Acid iv
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