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Yulia View Drop Down
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    Posted: Jan 03 2010 at 11:00am
Hi there! I am Yulia, 27 years old. I was diagnosed with triple negative breast cancer in July yhis year when I was 26 years old. No family history of breast cancer, sport everyday, ate healthy....
 
I already went through 4 Chemoes already and am waiting for my operation in the 20th of January.
I'm from Moscow, Russia and I'm sooo glad I found this website because we don't have anything similar.
 
I'm doing pretty well now and will get more Chemoes after the operation but I still don't understand where did this cancer come from...Confused
 
 
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Post Options Post Options   Thanks (0) Thanks(0)   Quote tasoulla Quote  Post ReplyReply Direct Link To This Post Posted: Jan 03 2010 at 11:08am
Hi Yulia!
 I want you to know that here all the members are helpful and very supportive....
I feel very confident here and all my queries concerning triple negative, therapies, etc are answered and everybody here makes you feel nice!
How did you discovered the tumor and what is the status of your report? Are there any lymph nodes affected?

Wish you all the best,
Tasoulla


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Yulia View Drop Down
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Hi Tasoulla!
 
Thank you for answering.
 
Medically speaking, the cancer I am fighting with is T2N0M0. So, it is stage 2, lymph nodes do not seem to be affected but they will examine them after the operation anyway.
I discovered it accidentally one morning in July 2009 and it turned out to be triple negative bc.
 
I just wonder if there are many of those who were diagnosed at the same age and without any family history of breast cancer... And I really wonder where it came from...
 
Thank you for your support!!!
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tasoulla View Drop Down
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Post Options Post Options   Thanks (0) Thanks(0)   Quote tasoulla Quote  Post ReplyReply Direct Link To This Post Posted: Jan 03 2010 at 11:44am
My mum is triple negative, diagnosed in September at her yearly mammograph, at age 53 with no family history.It was a big shock for us and we didn't accept it yet!
From what i read, researching and talking with people, it affects and women at your age.
I can understand what you are feeling but you have to fight and big strong and believe you will be a winner!
What chemo are you having and what is the size of your tumor?

Tasoulla
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Post Options Post Options   Thanks (0) Thanks(0)   Quote unklez Quote  Post ReplyReply Direct Link To This Post Posted: Jan 03 2010 at 11:46am
Dear Yulia,

Welcome to the TNBC Foundation. There are several women here who were diagnosed young and without any family history. Please feel free to ask us any and all questions.

Curious  to know what chemo are you getting.


Wife Dx: Jul/09. Age: 37. Size: 3cm. BRCA: -ve. Lumpectomy: Aug/09. Micromet 1/9 node. Chemo Start: Sep/09. E5103. DD ACB-> DD Abraxane (Taxol reaction). Zometa (S0307). Canadian Fraction Rads.
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Yulia View Drop Down
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Post Options Post Options   Thanks (0) Thanks(0)   Quote Yulia Quote  Post ReplyReply Direct Link To This Post Posted: Jan 03 2010 at 11:56am
Thank you for welcoming!
 
I'm on CAF Chemo scheme, went through 4 rounds prior to the operation. I am not sure if we will continue with the same scheme after the operation, I will find it out later this month.
 
I read some articles about the CAF scheme and it seems to be very effective. Tongue I hope it is.
 
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Yulia View Drop Down
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Post Options Post Options   Thanks (0) Thanks(0)   Quote Yulia Quote  Post ReplyReply Direct Link To This Post Posted: Jan 03 2010 at 12:00pm
Tasoulla, you have to be strong too! To me it seems that my famile took these news worse than I did. And it really seems to me that cancer does not know the age! Anyone can get it.
 
I forgot to say that the size of the tumor was 2,5x3cm prior to the Chemo. I will get my mammogramm in 1.5 weeks ad will know how much did the Chemo reduce it.
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Post Options Post Options   Thanks (0) Thanks(0)   Quote unklez Quote  Post ReplyReply Direct Link To This Post Posted: Jan 03 2010 at 12:11pm
Thanks Yulia. To easily let everyone know your tumor size, chemo etc add these details to your signature.

Wife Dx: Jul/09. Age: 37. Size: 3cm. BRCA: -ve. Lumpectomy: Aug/09. Micromet 1/9 node. Chemo Start: Sep/09. E5103. DD ACB-> DD Abraxane (Taxol reaction). Zometa (S0307). Canadian Fraction Rads.
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123Donna View Drop Down
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Post Options Post Options   Thanks (0) Thanks(0)   Quote 123Donna Quote  Post ReplyReply Direct Link To This Post Posted: Jan 03 2010 at 12:13pm
Welcome Yulia,

I'm glad you found this site.  Yes, there seems to be many of us here that don't have any family history or any of the high risks for bc.  Yet we ended up with tnbc anyway.  Please let us know how your mammogram goes and wishing you good results.

Donna
DX IDC TNBC 6/09 age 49, Stage 1,Grade 3, 1.5cm,0/5Nodes,KI-67 48%,BRCA-,6/09bi-mx, recon, T/C X4(9/09)
11/10 Recur IM node, Gem,Carb,Iniparib 12/10,MRI NED 2/11,IMRT Radsx40,CT NED11/13,MRI NED3/15

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Yulia View Drop Down
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Thank you all so much for your support!
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Post Options Post Options   Thanks (0) Thanks(0)   Quote trip2 Quote  Post ReplyReply Direct Link To This Post Posted: Jan 03 2010 at 3:47pm
Hi Yulia and a warm welcome to you.
 
 
Do you have any family history on your father's side?
 
There is what they call sporadic breast cancer.  It just appears and they don't know why.
 
TNBC tends to come to the younger woman although we have women on here in every age group who have been diagnosed.  I believe at one time we had a 25 yr old.  It's a shame someone as young as you has to go thru this, do you have good family support?
 
You have our support, come here often and let us know how you are doing. 
 
Heart
Stage 2 2003
Stage 1 2007
BRCA 1+
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Post Options Post Options   Thanks (0) Thanks(0)   Quote girlpower731 Quote  Post ReplyReply Direct Link To This Post Posted: Jan 03 2010 at 4:42pm
Hi Yulia,
 
Welcome to the site.  I'm interested to haer whether any cancer showed up on a mammo at your young age.  When I went for the mammogram and ultrasound, nothing showed up on the mammo, partly due to my age and partly due to the fact that I have dense breast tissue.  I didn't use the digital imaging machine either.
 
This site offers imazing support and it really helps during treatment.  We share a special type of bond since we are all going through similar experiences.
 
I may have missed it in the reading, but did you say what type of surgery that you will be having?  I had a lumpectomy back in August and I will either being having more surgery to clear the margins or a masectomy, I will know more in the coming weeks.
 
I recommend you going to the tips and resources section of the site.  I found invaluable information there and I keep going back to read new things.  There is a good section on chemo tips (I know you said you've been through chemoo  to reduce the size of the tumor, but you may find something useful if you need to continue chemo after the surgery. 
 
The best advice I can give is have a great attitude.  Don't let the cancer get
 the best of you.  Whatever is thrown at you, you can handle it, with the help of your loved ones, your doctors and all the men and women on this site. 
 
Keep us informed of your progress as we are all rooting for you for a speedy, healthy recovery.
 
Girlpower
dx: age 31. Stage 2a, BRCA1/2 -, Lumpectomy 8/09, AC/Taxol dense dose 9/09-1/10
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SagePatientAdvocates View Drop Down
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Post Options Post Options   Thanks (0) Thanks(0)   Quote SagePatientAdvocates Quote  Post ReplyReply Direct Link To This Post Posted: Jan 03 2010 at 5:47pm
Dear Yulia,

well I am half Russian. My grandmother came from Odessa (when it was part of Russia, I believe) in 1902...

The following study, I believe, is important-

BMC Cancer. 2009 Mar 19;9:86.

The prevalence of BRCA1 mutations among young women with triple-negative breast cancer.

Young SR, Pilarski RT, Donenberg T, Shapiro C, Hammond LS, Miller J, Brooks KA, Cohen S, Tenenholz B, Desai D, Zandvakili I, Royer R, Li S, Narod SA.

Women's College Research Institute, Department of Public Health, The University of Toronto, Toronto, Canada. sryoung37@aol.com

BACKGROUND: Molecular screening for BRCA1 and BRCA2 mutations is now an established component of risk evaluation and management of familial breast cancer. Features of hereditary breast cancer include an early age-of-onset and over-representation of the 'triple-negative' phenotype (negative for estrogen-receptor, progesterone-receptor and HER2). The decision to offer genetic testing to a breast cancer patient is usually based on her family history, but in the absence of a family history of cancer, some women may qualify for testing based on the age-of-onset and/or the pathologic features of the breast cancer. METHODS: We studied 54 women who were diagnosed with high-grade, triple-negative invasive breast cancer at or before age 40. These women were selected for study because they had little or no family history of breast or ovarian cancer and they did not qualify for genetic testing using conventional family history criteria. BRCA1 screening was performed using a combination of fluorescent multiplexed-PCR analysis, BRCA1 exon-13 6 kb duplication screening, the protein truncation test (PTT) and fluorescent multiplexed denaturing gradient gel electrophoresis (DGGE). All coding exons of BRCA1 were screened. The two large exons of BRCA2 were also screened using PTT. All mutations were confirmed with direct sequencing. RESULTS: Five deleterious BRCA1 mutations and one deleterious BRCA2 mutation were identified in the 54 patients with early-onset, triple-negative breast cancer (11%). CONCLUSION: Women with early-onset triple-negative breast cancer are candidates for genetic testing for BRCA1, even in the absence of a family history of breast or ovarian cancer.

.............

At your age, in my opinion you should speak to an expert in genetics, even though you don't have a family history of breast cancer. As Pam mentioned above, sometimes the men in the family can carry for several generations the BRCA mutation even though they have never had breast cancer. I, for example, do not have cancer (that I know of) and yet, I am BRCA1+ and passed the mutation on to my daughter. I don't know if there are any in Moscow or if BRCA testing is available but for sure, it is available in the UK. I know a Dr. Rosalind Eeles at Royal Marsden Hospital in London. Here is her contact information. Maybe she can refer you to someone closer to you.

Dr. Eeles details-

Dr. Ros Eeles  MA; PhD; FRCP; FRCR
Reader in Clinical Cancer Genetics
Team Leader, Translational Cancer Genetics Team
The Institute of Cancer Research

Honorary Consultant in Cancer Genetics & Clinical Oncology
Royal Marsden  NHS Foundation Trust
Downs  Road
Sutton
Surrey
SM2 5PT
UK

Tel 44-208 661 3642 (Academic)
Fax 44-208 770 1489
e mail   Rosalind.Eeles@icr.ac.uk
www.icr.ac.uk

NHS Clinical Contact Details
Cancer Genetics
Tel 44-208 661 3375
Fax 44-208 770 1489

Urology
Tel 44-207 808 2788
Fax 44-207 811 8017

Private patients
(Cancer Genetics and Urology)
Tel 44-207 808 2788
Fax 44-207 811 8017

The Institute of Cancer Research: Royal Cancer Hospital, a charitable Company Limited by Guarantee, Registered in England under Company No. 534147 with its Registered Office at 123 Old Brompton Road, London SW7 3RP.
............

if you wish please feel free to send me a PM and I will send you my email address. Happy to try to help.

you shall be in my prayers. I hope everything goes well for you..

good luck,

Steve







Edited by steve - Jan 03 2010 at 5:53pm
I am a BRCA1+ grandson, son and father of women affected by breast/oc-my daughter inherited mutation from me, and at 36, was dx 2004 TNBC I am a volunteer patient advocate with SAGE Patient Advocates
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Yulia:  Sorry to hear your diagnosis, but please stay strong.  My daughter, Ashley, was diagnosed with TNBC at 22.  She will be having her 6th chemo this coming Thursday.  Two more after that, then radiation.  She had a mastectomy of the left breast prior to chemo, and will have another mastectomy and reconstruction after chemo and radiation is over.  She's a member on this site and would be glad to talk about it if you want to talk with her - her member name is adaniel.  Let us know how everything goes.
Bonnie
Bonnie - Daughter Ashley dx TN 8/09 @ 22; St3, BRCA1/2-; AC&Ixempra done 2/10; mets to lung 3/10; G/C 3/10; PARP 6/10; sternum mets 9/10; NK012 failed; mets to liver, spine, kidney; Avastin/Xeloda
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Post Options Post Options   Thanks (0) Thanks(0)   Quote scared Quote  Post ReplyReply Direct Link To This Post Posted: Jan 04 2010 at 12:10am
Hello Yulia,

I am sorry about your cancer diagnosis, it is almost unheard of for somebody your age to have it.  On my wife's side she had some family history of cancer, and she had a genetic test done that came back negative so she somehow just got it too.

So, will your treatments be in Russia?  It has taken us over a year in dealing with cancer and we are still going through the muck.  It seems to wear your spirit down at times, so when I feel like that I come here for support.

I hope you have good support from your family and friends, or even your pets.  I know without our friends and family we could not have made it, and Jeff our cat would purrr next to my wife's breast that had cancer and it would be like he was trying to heal her, it did help to calm my wife down.

Wishing you the best with only positive outcomes!

Dave
Wife diagnosed 7/08 stage 2B 4.78cm with 3 nodes. 15 weeks of Adriamycin and Cytoxin, Mastectomy, 12 weeks of Taxol, and 6.5 weeks of radiation.
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Yulia View Drop Down
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Post Options Post Options   Thanks (0) Thanks(0)   Quote Yulia Quote  Post ReplyReply Direct Link To This Post Posted: Jan 04 2010 at 8:17am
Thank you all so much for your support!!!
 
Dear Pam,
 
thank you for the link, will read it now. My grandgrandfather had lug cancer. He did not receive any Chemo at all, he was just operated and lived 20 years after the operation. He died from heart attack and not from the cancer. This is the only cancer case I know...
I've got a really good family and friends support. I did not even imagie there are so many wonderful people surrounding me!!!!
 
Girlpower731,
 
thank you for your support! Yes, I agree, this website is something awesome!!!
 
My mammo did show the cancer although they had to verify the diagnosis with ultrasound, biopsy and core-biopsy later. I know that the structure of breast at 27 differs from that you will have at 40 or 50 but the mammo still showed the tumor.
As per the operation I still do not kow. As I already wrote my oncologist decided to start the Chemo before the operation to reduce the size of the tumor. I will know details of the opeartion later this month. Honestly speaking, if I was the one to decide I would have mastectomy of the both breasts and get implants later.Smile
 
Dear Steve,
 
thank you for the article. We do have a lot of medical centers where you can be tested for BRCA. I was thinking about it lately and will speak with my oncologist. Anyway, I think I will be tested for it.
Thank you for praying for me!
 
Dear Bonni,
 
I hope Ashley will get a speedy recovery!!! What king of Chemo if she getting?
I will get 8 Chemoes as well. 4 before the operation, 4 afterwards + radiation.
 
Dear Dave,
 
yes, I am going through the treatment in Moscow. Cancer patients who are citizens of Russia are getting the Chemo for free here although we spend a lot to help maintain the liver, heart etc.
You are totally right about the pets! We have got two newfoundlands!!!
I hope your wife is doing fine now andthe cancer will never get back to her!
Diagnosed with TNBC at age 26. Stage 2a,Grade 3, size 2.5x3 cm. 10 - 12/2009 4 CAF Chemo rounds. Radical resection 19/01. Started paclitaxel.
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Post Options Post Options   Thanks (0) Thanks(0)   Quote Bonnie Quote  Post ReplyReply Direct Link To This Post Posted: Jan 04 2010 at 8:24am
Yulia:  Ashley is participating in a clinical trial called TITAN which is 4 AC treatments followed by 4 Ixempra treatments.  She's doing really well.
Bonnie
Bonnie - Daughter Ashley dx TN 8/09 @ 22; St3, BRCA1/2-; AC&Ixempra done 2/10; mets to lung 3/10; G/C 3/10; PARP 6/10; sternum mets 9/10; NK012 failed; mets to liver, spine, kidney; Avastin/Xeloda
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Dear Yulia,

If you go to PubMed and enter Narod SA in the inquiry box you will find 370 papers by Dr. Narod's growth..many of them on BRCA and some on TNBC. He is one of the world's leading experts on BRCA. I would suggest printing the study out that is available free of charge(just click on the yellow box on the right hand side) and bring it to your oncologist. Your family hx certainly does not indicate a typical BRCA family but your very early age, in my mind, warrants a test. Better safe than sorry, in my view.

the link for PubMed (our country's primary medical library, over 19 million citations) is

http://www.ncbi.nlm.nih.gov/pubmed/

good luck to you,

Steve




I am a BRCA1+ grandson, son and father of women affected by breast/oc-my daughter inherited mutation from me, and at 36, was dx 2004 TNBC I am a volunteer patient advocate with SAGE Patient Advocates
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Yulia View Drop Down
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Hello everyone!
 
I had radical resection on the 19th of  January and is scheduled to 3 courses of paclitaxel at the moment. I had the new Chemo 1,5 weeks ago and it wasn't bad at all. Previous Chemo (CAF) didn't work quite well, so now I'm hoping this new Chemo will kill all the cancer cells. Anyway I'm trying to visit other oncologists these days to get alternative opinion on the Chemo scheme. I read they usually recommend 4 courses of taxanes when it's stage 2a.
 
My nodes were not involved although they say that the lymph goes to parasternal lymph nodes when the tumor is in inner quadrant of the breast. Anyone heard of that?
I would like to get a CT of mediastinal but my doctor say I do not need one. Probably I'm just nervous and scared? Cry  I just want to do the maximum now in order to live longer after the treatment!!!
 
I also tested for BRCA mutation couple of days ago and am waiting for the results on the 11th of March.
Diagnosed with TNBC at age 26. Stage 2a,Grade 3, size 2.5x3 cm. 10 - 12/2009 4 CAF Chemo rounds. Radical resection 19/01. Started paclitaxel.
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Post Options Post Options   Thanks (0) Thanks(0)   Quote Carol (Tenn) Quote  Post ReplyReply Direct Link To This Post Posted: Feb 18 2010 at 8:35am
Dear Yulia,
Welcome to our home. I am so sorry that you are going through this at such a young age.
I am an exception to the rule, at 68. I was 66 at diagnosis. I had no history of cancer of any kind and yet, here I am. Cancer is no respecter of persons. It can and does strike anyone, anywhere.
One thing is for sure, you have come to right place for encouragement, information and support.
Please join us on the Spiritual Support thread if that is your desire.
Love and Prayers,
Carol
 
St 2 Gr 3, A/C/T, DD
Radiation x35
Rec chest wall 07/09
Radiation x28
NED 10/24/11
NED 10/5/12
NED 03/15/13
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