Rug pulled out from under me!
This is my first time on this board. I am 40 years old and have spent years going through infertility treatments. I had just had a miscarriage in July and had been pretty devastated. After a long road both mentally and physically we had finally made the decision to move on to donor eggs and had scheduled for January. Since I was over 40 I had to have an updated mammogram. I was completely shocked when it came back abnormal and I had to go back. I was diagnosed last week with intermediate DCIS 1.5cm in my right breast. I had my MRI on Monday and I am waiting for my test results. To say I am shocked and depressed in an understatement! I am devastated that I have to put the baby on hold indefinitely. I know I cannot take Tamoxifen if I want to get pregnant. I am trying to put my head around the best treatment options and how to get through this. My Mother also had dcis and had her breasts removed. She died at 52 unrelated to bc. I have always considered myself a very strong sane women. That seems to have gone out the window! My husbands best friend had just died a month before this and my husband is still reeling and seems to be emotionally unavailable.
Sorry to vent! I just need guidance.
Comments
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RRN - you have come to the right place to vent!!
First of all, tamoxifen may not be recommended for you, second of all, if it is, you get to decide whether/when to start/stop it. check this out: http://www.breastcancer.org/tips/fert_preg_adopt/fertility/tamoxifen.jsp, there are discussion threads on this topic, use the search function while you are in the discussion board section on this website or even do a general google: tamoxifen pregnancy
You are going through the worst time now, diagnosed with breast cancer, but not having all the facts yet, and not having a plan of treatment. You will have options. Hopefully this will just be a bump in the road/a slight detour on your way to fulfilling your dreams.
Julie E
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I just received my MRI results and he said it was good and under 2cm. He recommended lumpectomy with 6 weeks radiation with or without Tamoxifen. He said he would support my decision if I wanted to have a mastectomy. I don't know what to do!? The Dr. suggested genetic testing if it would change my decision.
Thanks for the support!
Thank you for the link! -
rrn - That's good news. Did you have a biopsy as well. This will tell you if it is grade 1, 2 or 3 and will also tell you if you are ER/PR positive or negative. This might help you make the decision. I had genetic testing in September and still don't have the results back so I didn't have that information in time to help with my decision. I had a lumpectomy followed by a mastectomy. If my cancer was grade 1 and I didn't have multiple tumours in two quads of my breast, I would have been very comfotable having a lumpectomy. Although, in truth I was hesitant about having radiation over my left breast but I think if my margins would have been clear, I still would have gone with a lumpectomy.
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ARRRGHH!!! I just typed out a really long post with my story and some suggestions, and my Internet crashed... I'm late for an appointment but will try to recreate it when I get back... the short version is, I can totally relate to what you're feeling now (my husband and I have been TTC for years and have had four miscarriages), but there is HOPE! Much more later! Hang in there!!
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ARRRGHH!!! I just typed out a really long post with my story and some suggestions, and my Internet crashed... I'm late for an appointment but will try to recreate it when I get back... the short version is, I can totally relate to what you're feeling now (my husband and I have been TTC for years and have had four miscarriages), but there is HOPE! Much more later! Hang in there!!
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Hi again... sorry about the misfire earlier! What I was saying was... I'm close to your age. My husband and I have been trying to have a baby for several years. We've had four miscarriages, the last one in 2008. This last one sent me into the most overwhelming depression and despair... I truly didn't know if I would survive.
This summer, I was finally starting to see light at the end of the tunnel and pulling myself out of my depression, and was even looking forward to trying a new fertility treatment.
Then the bomb hit. I was told by three different doctors that I had cancer and that it was most likely invasive.
I knew from friends having gone through invasive cancer that this meant chemo + radiation + Tamoxifen (five years' worth of induced menopause)... and therefore no hope of ever even trying again to have a baby.
Thankfully, my third doctor's biopsy showed that my cancer was NOT invasive, that it was DCIS... so ironically, I was thrilled beyond belief to be diagnosed with "only" DCIS. This meant no doctor was going to force me to do fertility-destroying chemo. Targeted radiation, I can handle since that doesn't affect fertility. It's just a 6-week detour on the road to Mommydom -- a far cry from having to wait 5-6 years -- and that I can handle.
As for Tamoxifen, of course that's a personal choice, but I strongly urge you DON'T DO IT!! My DCIS is fueled by estrogen (ER+) so I know my doctor will try to put me on it, and with your fertility history I suspect you will turn out to be ER+ too, but there are better, safer ways to bring your hormones back into balance without a drug that complete shuts off all estrogen (not to mention the side effects, increased risk of uterine cancer, etc.).
Have you checked out the alternative/complementary board here yet? There are some great threads about balancing hormones naturally. BTW, "conventional medicine" failed me for two full years while my husband and I were TTC. What worked for me was NOT a drug... it was using natural (diet/lifestyle) means to bring my hormones into balance. I know from that experience that natural means are so much better than throwing chemical drugs at the problem.
Interestingly, you'll find that most of the diet/lifestyle change recommendations for improving fertility are the VERY same recommendations for fighting cancer! Things like drinking 2-3 cups of green tea every day... sleeping every night in total darkness (not even a nightlight or clock radio light showing)... getting 15-30 minutes of sunshine exposure every day (when possible)... doing some kind of exercise every day... it's amazing how several small changes can make you more fertile, AND fight cancer, ANNNND help with depression, weight management, ADD, and who knows what else!
At this point, as terrified as I was when I was newly diagnosed, as you are, I actually see this diagnosis as a blessing. I was going down a self-destructive road (after the last miscarriage, I sort of gave up and started eating junk food, drinking way too much caffeine, etc.). This was a wake-up call to get back on track with the very lifestyle changes I HAD to make if I ever want to become a mother. So, for that, I am grateful.
This is a completely different post from the one I wrote initially, but I can't remember what all I had typed earlier, so I may add more as I think of things! In short, though, you are going to be OKAY!! I feel so certain both of us have Motherhood ahead of us! What an amazing story we will have to tell later... how we faced infertility and CANCER, and came through it with flying colors!! Please feel free to PM me if you have ANY questions at all... in the meantime, keep your chin up... DCIS is really the "best case scenario" kind of cancer for us future Moms.
Oh, I had mentioned a book that gave me a lot of encouragement. It's called You Can Get Pregnant Over 40, Naturally by Sandy Robertson. She and her husband started TTC when she was in her late 30's. She was only able to conceive with IVF, and it ended in miscarriage (6 miscarriages total). Then, she decided to cast off modern medicine and use natural means (diet/lifestyle) to conceive naturally. She did... and had her beautiful, healthy daughter at age 44! See why I think there's hope for us young'uns?
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Thank you Julia! I sent you a pm. Thanks everyone for your help.
When the surgeon called I asked about the grade and if I was ER/PR negative/positive? He said that you could not tell until I did a lumpectomy. I had a stereotatic core biopsy two weeks ago that I am still hurting from. I have scheduled my lumpectomy for next Thursday. I am completely confused! My family thinks I should have a mastectomy, husband thinks lumpectomy. It is my body and I have not idea what I want. The only thing I know for sure is I will not take tamoxifin.
Any suggestions are appreciated!
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Hi, rrn ~ Of course you're confused. A bc diagnosis usually comes out of the blue, and it also sounds like everything is happening extremely fast, especially if you are dealing with pure DCIS, which is a non-invasive bc. Are you seeing a breast surgeon or a general surgeon? One reason I'm asking is that I don't understand why he can't tell you your ER/PR status from the biopsy. If he had a copy in front of him, it should give him that information, which is usually something a breast surgeon is anxious to confirm with you because it may influence your decision. And the results from your MRI will be one more piece to the puzzle re. whether you choose a lumpectomy or a mastectomy.
If you haven't already, you might want to go to the Symptoms & Diagnosis section of this website (at very top bar) and read the Diagnosis of DCIS page. At this point, and barring any factors we may not know yet, I would tend to agree with your husband. A 1.5 cm area of DCIS is quite small and if there isn't any more of it, lumpectomy should be an excellent option.
Have you considered getting a second opinion? Not all surgeons will give you the same advice, and the more people you talk to, the more it will help you shape your decision as to what is right for you.
Here's hoping that the discovery of DCIS will be a hidden blessing and allow you to get your body back into balance so that you will have a much easier time getting pregnant very soon. Deanna
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I was just able to get a copy of my pathology report after stereotactic biopsy.
My path result says DCIS Right breast cores 12 o clock 2 cm from nipple. Intermediate grade with focal necrosis and calcifications involving multiple core biopsies in all tissue blocks at least 1.3cm in greatest dimension.
Under microscopic description:
Multiple sections are examined in multiple levels and reveal core needle bipsies of breast tissue featuring at least partial involvement by dcis of cores of all four blocks. The tumor shows a solid pattern w foci of central necrosis and calcification. The grade is intermediate. Some stromal fibroplasia and chronic inflammation is seen, however no definite invasive tumor is identified in these sections. The greatest expanse of tumor is 1.3cm, however this may not reflect the true size of the tumor as it is present in multiple tissue blocks and multiple core biopsies.
What does all this mean?
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Hi rrn, Im so sorry this happened to you. I was 40 at diagnosis and also struggled with infertility and miscarriages. Dont worry too much about you path report they will know more when you get the lumpectomy. Intermediate grade is the middle grade but again they get a better picture when they take the whole thing out. Necrosis is what happens when the cells outgrow their blood supply (cell death)also shows up as calcifications on mammo. I got a prescription for xanax when I was diagnosed -it helped me get through the panic stage and all the dr visits and such(I had a bit of a panic attack at oncologist office) . I no longer need it now but it was a big help. Good news, the wire guided lumpectomy is not as painful as the steriotactic biopsy.
Good luck- PM me if you need any info.
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Hi RRN:
I agree with Deanna that your tumor sounds small and lumpectomy plus radiation (if indicated) should be enough. Your breast surgeon is a great resource. My surgeon was not specifically a breast surgeon, but he had done enough breast surgeries over the years for me to feel comfortable with his experience. As for the ER status, it took a few days after the initial path report for them to make that determination and it did not come with my original path report (it noted "pending"). So yours may still be on the way - check with the surgeon for an update.Good luck!
Janet
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I decided to have the genetic testing done to make a more informed choice. The waiting on the results is going to kill me!
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http://www.hopkinsbreastcenter.org/artemis/200912/11.html
an upbeat article on fertility treatment and breast cancer !
and you may want to subscribe to this newsletter for more general info
Julie E -
Julie/Jelson, great article... thank you for sharing that!
I do have to say, the way the term "fertility preservation" is used (not just in that article, but in the medical industry generally) is a bit misleading... in my mind, "fertility preservation" means that one's fertility is not irreversibly destroyed when undergoing cancer treatment. The medical industry, though, uses the term "fertility preservation" to mean egg retrieval/freezing or IVF/embryo freezing, specifically... which is great, and certainly the best option for many cancer patients, but it would be reassuring if more care were given to truly preserving fertility (and there are many available, such as ovarian suppression and ovarian transposition, but they haven't been researched as well as the more standard and less reliable methods of cryopreservation). That's just a minor beef I have which doesn't apply to rrn or me... since it's really chemo and Tamoxifen that harm fertility, not surgery or radiation.
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Thank you for the article. Unfortunately the Dr's say my eggs are already bad. We were having to move to donor eggs.
I am a little confused. The one thing I had definitely decided not to do was take Tamoxifen. My surgeon told me it was only about a 5% difference if I took or not. I took my cousin to her oncologist appt today. She started asking about me. He said he definitely recommended Tamoxifen, since it decreased recurrence by 30%. That is a huge difference.
Still waiting on my genetic testing. Should have tomorrow. If I test positive I am not sure if I want to go through with the lumpectomy. DECISIONS! DECISIONS!
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rrn... the author of the book I mentioned above, Sandy Robertson, was also written off as having bad eggs... from what I've researched, I'm convinced that most fertility specialists don't understand that even women with "bad eggs" can have their biological clocks turned back, with certain nutritional/lifestyle changes... but, I know that's totally not where you're at right now, just wanted to throw that out there as food for thought for AFTER you get over this DCIS hurdle and are ready to think about having a baby!
As for Tamoxifen, remember that "success rate" statistics can and ARE manipulated. After researching it, I personally have chosen NOT to do Tamoxifen for many reasons, even if it decreased recurrence by 50% (which is the figure my surgeon gave me!). I know all these decisions are so hard, but if you make sure you research them well instead of just blindly believe everything your doctor tells you, you'll be sure to make the right decision for YOU. Good luck!!
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rrn it sounds like you have just had an encounter with the huge difference between absolute and relative benefit statistics. It may well be that the 5% and the 30% are the same thing.
For instance, if without a drug 15 of every 100 women will get cancer, and with the drug only 10 of every 100 women will get cancer, that is a reduction of 33% (5 fewer women is 33% of the 15 who were getting it) but it is also a reduction of 5% ( since now 10% rather than 15% of women will get cancer).
In that case, 33% is the relative risk reduction, and 5% the absolute risk reduction. It is the absolute risk that I choose to focus on. In my case Tamoxfen had a relative risk reduction of 33% but an absolute risk reduction of only 6%. I chose not to take it.
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My BRCA 1 and 2 tests both came back negative. YEAH! I am so relieved!
I had my lumpectomy Thursday and should have the path reports on Monday. Feeling alot better mentally.
Thanks for all your advice and helping me cope the last few weeks.
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Hi I was on fertility treatment and was also diagnosed with breast cancer 13 years ago aged 32....I had a lumpectomy, chemotherapy, and radiotherapy .
I was absolutely devastated when I was diagnosed.. but it put everything into perspective for me I had a fantastic husband and loving family and decided that after treatment for the cancer I would stop all attempts to have a child and just enjoy my life with my husband.
A year after all the treatment stopped I began to feel poorly again and was terrified my cancer had returned... it turned out I was a couple of months pregnant naturally, I gave birth to a beautiful daughter 6 months later. She has just turned 10 years old.
I know that at the moment you are taking everything in and I can still remember that awful feeling of hopelessness. Once my treatment started I started to feel more positive about things and I know you will too.
Thinking of you and know that you will be okay and most of all keep smiling xxxxx
Manchester/England
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