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Old 12-03-2007, 11:18 PM   #1
harrie
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Location: Hilo, Hawaii
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Farign,
It is not impossible, but improbable that you carry the breast cancer gene with the family history your wrote about.
I do have a strong family history of breast cancer and a history of it myself. I was NOT going to be tested because I thought I was being monitered close enough and I assumed that was sufficient enough for me. I have 2 sisters and they were interested in knowing if they had the gene and they have never had br ca. It made the most sense for me to be tested first because I had DCIS twice, so for their sake, I had myself tested. The reason for this is because if I am tested +, then for their testing, all they had to do was look for the defective part of my results and for my sisters it meant their testing would become much less extensive and more narrowed down, looking for the defect that I had (if that makes sense to you). (I will be glad to reword this for a better explanation if anyone is interested)
After genetic counselling, I discovered that if I am tested positive, my survellience would be different, it would consist of annual MRI's and annual mammograms.
So I was tested and it turned out to be positive for BRCA2. My sisters then were tested (50/50 chance they also carried the gene) and they were both tested neg. My daughter (50/50 chance also) tested negative.
My genetic testing ran about $3,000, although my insurance picked it all up, and my sisters and daughters test ran around $300.
I hope this information benefited you.
Remember, just because you test positive is not a guarantee you will get br ca and it also holds true that if you are not a carrier of the BRCA gene it is not an assurance that you will not get breast cancer.
Maryanne
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*** MARYANNE *** aka HARRIECANARIE

1993: right side DCIS, lumpectomy, rads
1999: left side DCIS, lumpectomy, rads, tamoxifen

2006:
BRCA 2 positive
Stage I, invasive DCIS (6mm x 5mm)
Grade: intermediate
sentinal node biopsy: neg
HER2/neu amplified 4.7
ER+/PR+
TOPO II neg
Oncotype dx 20
Bilat mastectomy with DIEP flap reconstruction
oophorectomy

2007:
6 cycles TCH (taxotere, carboplatin, herceptin)
finished 1 yr herceptin 05/07
Arimidex, stopped after almost 1 yr
Femara
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Old 12-04-2007, 07:30 AM   #2
janet/FL
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Maryanne
That was a very clear explanation for me though I won't need it for my particular case as I don't have children and neither do my siblings. Thanks
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Janet
Endometrial Cancer 2002
Mammogram 11/2004
Lumpectomy 12/2004
Stage 1, 9mm DCIS, grade 2, Her2+++, ER/PR negative
Refused A/C as recommened by two oncs.
35 treatments of radiation that ended March 4, 2005
Changed oncologists and began
Taxotere/Herceptin August 2005. Finished Herceptin July 2006
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Old 12-04-2007, 07:45 AM   #3
tousled1
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Location: Acworth, GA
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Fargin,

Have you been tested for the BRCA 1 and 2 genes yourself? It would be futile to have your daughter tested if you were not tested or if you were negative. Most HER2 cancers do not tend to be hereditary. I have a very strong family history of both breast and oarian cancer on both sides of my family and I esed negative.
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Kate
Stage IIIC Diagnosed Oct 25, 2005 (age 58)
ER/PR-, HER2+++, grade 3, Ploidy/DNA index: Aneuploid/1.61, S-phase: 24.2%
Neoadjunct chemo: 4 A/C; 4 Taxatore
Bilateral mastectomy June 8, 2006
14 of 26 nodes positive
Herceptin June 22, 2006 - April 20, 2007
Radiation (X35) July 24-September 11, 2006
BRCA1/BRCA2 negative
Stage IV lung mets July 13, 2007 - TCH
Single brain met - August 6, 2007 -CyberKnife
Oct 2007 - clear brain MRI and lung mets shrinking.
March 2008 lung met progression, brain still clear - begin Tykerb/Xeloda/Ixempra
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