ILC - The Odd One Out?
Comments
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I was pretty tired in the year leading up to finding my lump. I was also getting every cold that was going round. Both were unusual for me. I had a new job that was pretty stressful and thought the tiredness was from that,and it could have been, but I normally handle those sorts of stresses really well. I was always the sort of person who thrived when there was a job to be done, juggling 40 balls in the air and deadlines that couldn't be moved.
I was getting one cold after another, and that certainly wasn't normal for me, I usually shrug off most colds that seem to be going round. Funnily enough, since dx I've probably had two colds lol.
I would panic every time I had a scare after chemo had finished. The year after chemo and herceptin I had three scares and that was very stressful. First one was when I had a persistent pain in my lower back that my chiro couldn't help with. Was sent for a bone scan and that turned out to be arthritis. Second scare was when I found a lump in my "good" breast. That turned out to be a fatty cyst. Third scare was when I had a routine fecal test that everyone in Australia gets a kit for when they turn either 50 or 55 (mine was at 55) and there was blood found. That turned out to be benign polyps.
Now that I'm having unexplained pain in my abdomen, I'm not so scared. It is what it is, it will in all probability turn out to be something other than cancer, and if it does turn out to be sinister, then I'll have to deal with it then. I refuse to be worried over everything that goes on in my body now. Life is too short to spend time worrying about what something "might" be.
I'm not saying it's not in the back of mind that ILC is sneaky and has a tendency to turn up in places different to IDC, but I'm not going to stress over it. I would like to find an answer though - persistent pain isn't good.
I now have a less stressful job, have turned my passion with photography into a business which is doing well and life is slower and better. If it hadn't been for bc I would still be working in a stressful job without the time to follow my dreams.
Trish
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I did not experience any fatigue prior to my dx (just after I turned 50) that was out of the ordinary. I am a group ex instructor (teach 4 classes a week & workout every day), work full-time as an attorney, and have 2 youngish kids, both in grade school. I had no prior medical concerns and was not taking any medication. I would catch the occasional sickness from my kids, but most of the time I was able to avoid whatever they picked up at school. I don't recall any loss of energy or having a feeling that I needed to slow down prior to dx. I have been extremely fortunate to be able to keep up my classes (but I had to take 6 weeks off for the BMX and again for the exchange surgery).
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I was extremely healthy prior to dx. I am a school teacher, and I am exposed to every sickness the kids come in with. I haven't had a cold In 3 years. I did have a lot of stress the 5 years before DX. My husband lost his job, and started a landscape company, which due to the economy, hasn't been a great money maker. My younger daughter had depression, and in order to pay for my girls college, I was working every night and Saturdays. I was always tired, but I do remember one night feeling sheer exhaustion, like I do now with chemo. I remember thinking that was odd, but attributed it to my hectic schedule. I definitely think stress was a large contributing factor.
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I definitely attribute extreme stress and depression as contributing to my cancer. I had a horrible accident and was unable to do the work I love.
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Jumping right in -- I would love a data base of our characteristics. It seems so few doctors are savvy about ILC and, in turn, we aren't educated enough about it until we have it. I had such blind faith in my family practitioner and my annual mammogram.
So, here are my stats:
age at dx: 48
height/weight: 5' 6 1/2", 140 lbs.
smoke: never, but grew up in a house filled with second-hand smoke
BCPs: yes, age 17 until week of bmx (except when trying to get pregnant, being pregnant or nursing)
periods: first at age 12, nothing since surgery; normal
alcohol: moderate/heavy until dx (I LOVED wine at night with same exceptions as with BCPs)
exercise: walk 3-5 miles daily for past 14 years; spotty exercise before that
children: 3, first one when I was 29
breast feeding: yes, 1 year each kid
DES: nope
stress before dx: lots of nonsensical anxiety for past ten years, major real stress last two
family history: no
BRCA: no
breasts: small, dense, cyst removed 25 years ago in good breast
blood pressure: freaky low
cholesterol: good
diet: childhood filled with processed food and transfats, none in adulthood but could eat a few more veggies each day
Maybe it was the wine and birth control pills that got me, but it's probably just that I'm alive and
havehad boobs. -
Dear all,
I was not tired before my dx, and was about as fit as could be, not overweight, etc. but was still ovulating at age 53 with no sign of perimenopause/first period age 11/2 surgeries for multiple fibroids.
However, I "knew" that there was something wrong with me...for a year before I had an inkling that something was up...not sure what. I just felt a vague threat near me, as though something was just "not right". Like when the sun shines, but you are under an unbrella with a shadow?
Anyone have that sixth sense before their dx?
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Claire, it is weird, but true. I had the same feeling of dread; like I knew something really bad was going to happen. I attributed it to depression, and I was going to make an appointment with my PCP, but I found my lump and made the appointment with my gyno instead. My sister gave me a surprise 50th birthday party on Fire Island, and I was in a fog the whole time, couldn't enjoy it because I knew something was up. Really freaky.
I was not even close to menopause either. I went off bcp in January, 2013 and was showing no signs of slowing down. Chemo has halted my periods, and my doctor says I will probably be in permanent menopause after, but I am not so sure. I started at 10, and my ovaries seem content to keep on going. Because I am BRCA negative the docs don't want to remove my ovaries. They say menopause will do the same thing, but I don't want ILC creeping in there, and I want them gone. I need to figure out a way so the insurance would cover it.
I don't know if any of you have seen this; a study that suggests a correlation between root canals and breast cancer. I don't know how to post a link, but I'm sure you all can find it in google. Anyway, this study in England looked at the number of women who had had root canals and then developed BC. I had a root canal 12 years ago, and over the past three years had all sorts of periodontal surgery on my gums. The study suggested that bacteria gets into the root canal and the body is fighting that bacteria and not cancer cells. I don't know if I buy it 100%, but it was interesting theory.
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Interesting...I've had two root canals, gum graft surgery, orthodontia as an adult and have horribly receding gums.
I didn't have a feeling this was happening, but I think I've had a feeling for years that there would be some sort of crisis in my adult life. I thought DD's struggle with depression was that crisis but, in the end, I think the way I handled that caused so much stress and that stress is one thing that made it easier for my cells to go wacky. It's funny...even though I definitely have anxiety about what my future holds for my kids and DH, I think I'm more at peace now than I've been in a long time. I guess I feel like the crises have happened and it's a relief.
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its interesting to read all of everyones info.
I was 46 at dx I was told I had cancer for probly 7 or more years so i was in my 30's when it started. iT went un- noticed somehow even though I had been mammogrammed every year for 10 years I also had a few ultrasounds on breast also did not show up. at time of dx I had 9.2 cm tumor in breast 1 cm and 2 cm tumors in nodes and 17 cancerous nodes. I was tired but also my business was very busy so I am not sure which wore me down.
my cancer all of a sudden became aggressive I had a lump that you could actually see on my breast and it grew fast. and still did not show on mammo or u.s.
I did notice in the about 6 month range before dx that I craved sweets at odd times of the day and not just period time. it was a strong craving for sweets. my hair started to feel like straw when wet which is odd because I had never colored or highlighted ot permed my hair and use no hair products. I have virgin hair.
I did take birth control pills for about 10 years.
got period at 11 years old.
got pregnant at 28
no family history of any cancer.
i was a healthy weight drank green tea ate blueberries stayed active
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Well, ladies, I need to back away from this thread. I just discovered the pathology report from my mx. No notation of ILC, just not sure why my notes say I am. Not sure what I am except triple negative. Will check this out next MO visit. Wishing all you dear friends the very best. Jan
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Hi All - I've been lurking on this topic for a bit and decided to add my info.
Dx at 41, ILC, 4cm, no nodes, grade 1, ER+/PR+, HER -
I'm tall and on the thin side and always have been. Super dense breasts.
Bilateral mastectomy - one prophylactic
Family history - yes (mom, premeno BC, not sure what type - she died when I was 20)
Menarche: 15 (I was a serious athlete),
As someone else said, crazy low blood pressure
No birth control pills ever (mostly because I was keenly aware of my high risk status)
Active/fit, though not a super athlete like I was as a kid.
A good job, not super stressful.
Light/moderate drinker (glass of wine with dinner most days since I was in my late 20s). I've stopped, though I'm not sure it's entirely reasonable.
Two successful pregnancies - first at 30, second at 33. Breastfed both for at least a year each. No miscarriages or trouble getting pregnant.
DES daughter? Possibly. I was born in early 1972, and all the literature says it was banned in 1971. I might not have been directly exposed to it in utero, though my mom had significant issues staying pregnant and had had several miscarriages prior to me (her only successful pregnancy), so I'm pretty sure she would have fit the profile of someone who'd have gotten DES for those prior pregnancies in the late 60s, 1970.
No significant health issues prior to this, though shortly before diagnosis I'd had some arthritis issues flare up (which are now gone post surgery)
From menarche to my early 20s, my periods were irregular, then became regular in my early 20s, but they were long-cycle (32-35 days), became a little shorter in my early 30s (fairly typical 28-30 days) and then really shortened up in the last three to four years (24-25 days). I'm convinced the short perimenopausal periods are a sign of too much estrogen
I had my first mammo at 35, and then several afterwards. Last mammo in summer 2012 showed nothing. Ob/Gyn felt lump ( thickening) in my annual check up in the fall and sent me for mammo. Again, they saw nothing on mammo, but US showed something to the techs. BS did ultrasound and said hmmm. He then offered to schedule me an MRI or do a biopsy right there in the office. I said biopsy, and here we are.
Surgery was pretty easy (no recon), and I'm waiting for my oncotype score (and am on tamoxifen in the interim. MO is pretty sure I won't need chem.) Then probably radiation as the margins were close.
Tamox has been mild so far, just warm waves.
Anyone else with large-ish tumor but neg nodes? did you do chemo?
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Claireinaz, I definitely had the 6th sense of doom & gloom. When I called to set up the mammo, which was my yearly exam, I had very strong premonition that I would have bc. All he women in my family were dx in there 60s, and I am 58, so this was not a huge shock. Having it spread to 6 nodes and growing outside the nodes was/is a bitch. I had had a exam by my PCP shortly before. She did not feel anything.
It seems like I am one of the older ones on this thread. Only 1 root canal. I think I took bc for 18 years..
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no root canals here (only ever had 3 fillings)
Definately Very low BP since a teenager eg when pregnant dropped to about 80/40 !! But always hovered around 95/60.
Momine have you got any theories yet ?
I am thinking 49, stress and EtOH -
I am also thinking a survey of stage IVs to see % of ILC vs IDC ( and TN) and also the % from stages I , II and III that go on to actually develop stage IV assuming chemo, rads and hormonals have been done as needed ( my gut says about 10%, 20% and 30% respectively)
There seem to be soooooo many variables once you throw in +- nodes +- ECE, margins etc etc - hollanders example is extremely sobering !!
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Hi ladies--
I'm continuing to read everyone's comments with great interest. I've had two root canals, but as I recall, the area of breast tissue thickening that turned out to be bc was already there when I had them. No DES exposure. My bilateral mx showed clean margins , with nothing "suspicious" or questionable remaining. All the docs who reviewed the path report were very pleased with the results, and felt like I was well on the road to recovery. I was divorced six years before dx, and while it was a stressful 2-3 years before that, it was a good and smart decision for me. I actually get along really well with my ex and his 2nd wife, which is a little weird, but life is too short to hold on to those old issues. Plus it makes life better for my kids! My current job is somewhat stressful, but I'm glad to have it, and my health insurance is paid for. No depression, fatigue or sense of something being wrong before my dx-- my life was great!
It is so hard to try to pinpoint an issue or event that could have been the trigger that kicked my bc into action. I've learned to let all of that go (well, most of the time), since there's nothing that can be done about it. All of my docs have said that they can't tell me why or when it started. Or why it came back. I don't need to dwell on what I could have done differently since there's a very good chance that there's nothing I could have done to change the end result. What I do know is that I had 6 years following my initial dx (and tx was over) when I thought I was cured, and I lived my life without the black cloud of "what if" following me every day. It was great. And I recommend that all of you try to do the same, as much as you can. Don't worry about "what if it comes back" until it actually does. Don't waste your precious time and energy on something that you can't really control. Eat well, be active, get rest, do regular follow ups and check ups, be happy and enjoy life. Everyone has struggles, difficulties and bad things happen in their lives-- it's just part of being human. But don't worry and second-guess that anything negative will cause your cancer to come back!! Think of all of people who have bad things happen, or who don't take of their health, diet, drink too much, smoke, etc. who never get breast cancer. I think it's such a crap shoot, and if you get it, you just do your best to deal with it any way you can.
I wish I could say "just do this", or "avoid doing that", and you'll never have to worry about breast cancer again. But until more research is done to find the cause, and the magic bullet cure is discovered, all we have is treatment that is more reactive than proactive. I am so grateful for everything that's out there now, so that we can treat this as a chronic disease, bit I do wish we knew more about ILC-specific treatments.
The stats I mentioned earlier were from another thread on this site- can't remember which one. I've read that "early stage" includes stages 0-3, and also seen that it includes 0-3a. Not sure who determined that, and I don't think there's any tracking of the break down of each stage and % that develops mets. Just one more problem with the current way this disease is handled...But there are women who have had every stage of bc (even 0) who have ended up with mets. It just doesn't make sense, but it's just the way this awful disease works. Don't mean to scare or discourage any of you-- we just need answers that don't exist (yet).
Big ((((HUGS)))) to all of you!
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Smlvr--it took me over a year, but I finally found an OBGYN who agreed that the ovaries should come out. Oncologist was never for it. Once the OBGYN decided to do the surgery, I had no problems with the insurance company. I am so glad that I had them out because two months later, I saw a new oncologist who said that probably the cause of my breast cancer was use of synthetic progesterones as birth control so to the extent that my ovaries could have been making progesterone still, I was glad to have them out. The doctors only look at one type of estrogen hormone, estradiol, in the blood and then declare you to be in menopause.
Maybe it was easy to get through my insurance company...they don't even seem to realize that my breasts are gone. Sent me a notice today that my mammogram is two years over due, and that small cancers can be picked up on the mammogram with early detection leading to better outcomes. I wanted to throw up.
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Nocompromises, no, none. I am struck by how many of us were in the latter half of our 40s when DXed, and it is tempting to think that hormonal changes might be some sort of trigger.
A lot of people mention stress, and I also had loads of it in the years prior to DX. However, and this is my own completely ungrounded little theory, I think it is fine to be busy. What I think is damaging when being busy, especially when we are busy taking care of everyone else, is that we set our basic needs aside. By that I mean the need for healthy food at proper meal times and some exercise. I have become quite insistent on keeping to my meal times, eating what I want and need to eat and making time for exercise.
As for the root canals, I read what I could find on that at some point, and my take is that it is complete bunk. Also, I have never had any. I have one, small filling that was done when I was 12.
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Our stats are so similar:
dx at 49
menarche @ 13
Very low Blood pressure - 70/40 (hypotension)
very dense breasts - large
Birth control pills when I was a teen and in my 20s.
Excellent Health, no medical conditions prior to dx.
Athletic, in great shape, worked out daily
Healthy diet - low carb.
heavy drinker, but not in the 10 years prior to dx
bouts of depression, anxiety.
Very high energy, single working mom,
Son born at age 31.
high-tech, very, very stressful job entire 6 years leading up to dx.
Perimenopausal for 3 years prior to dx.
No family history - adopted.
had mammos and ultrasounds of breasts every 6 months - fluid and cysts. Told everything was benign.
Had a sixth sense something wasn't right, everything in my life was a huge stress and on verge of nervous breakdown. In the back of my mind I intuited that the story would turn out to be cancer. I just never imagined it would be so advanced. My tumor was 12.5 cm. Yes, misdiagnosed by lots of specialists and docs who I believed. My psychic side ruled in the end. (I hate that my psychic abilities always are strongest with the negative, dark side).
If you ask me what I think is the major factor in cancer dx, it's stress. The Israeli's believe this in addition to a non-alqualine diet, and I agree. I have eliminated all stress from my life. I meditate, pray, and have slowed way down. I don't let things bother me and I think this has a huge factor in my remission. NO STRESS.
My son is away in college now and I'm an empty nester. It's a great life. I don't think or worry about recurrence other than to remind myself that I have to live as though I have a short time left and get my bucket list out of the way. It's fun. The question now is "how are we're living" and not "how are we dying".
Hugs,
Kat
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Hollander, thank you for all your posts and your very wise words. You have a wonderful attitude and outlook, and it's very inspiring to me. ((Big hugs)) back to you, too!
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gemini4. I could agree more.
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gemini4. I couldnt agree more.
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Amazing how alike we all are. No root canals; really good teeth so far (knock wood). But dense breasts--with no warning that dense breasts should be examined more closely and in different ways than a regular mammogram. I think that's what did it for me--lack of knowledge so I could be proactive earlier than I was.
I asked my gyno NP why she exclaimed over my dense breast tissue during an exam years ago...and she never said anything out of the ordinary that made me think I was at higher risk of not finding BC involvement. Had she shared that, I might have paid more attention even when my regular mammos were clear.
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Claire, I had dense breasts also. There was never any indication from any medical professional who I saw that this could lead to other things and should be monitored. I was told that dense breast tissue was common among younger women. Being in my 40's, I thought cool-- at least part of me still looks like a twenty-something! My aunt mentioned that one of my cousins (10 yrs. younger) also had dense breasts. Like me, she was slim, had good health habits, etc., so I figured maybe women in our family just had dense breasts. Well, she was diagnosed with IDC the same week I found out I had mets. Not a good week for our family.... But hers had a "cause"-- lots of radiation due to 2 bouts of Hodgkins. Her doc told her that if she ever had any cancer show up after Hodgkins treatments, it would be breast cancer. And it showed up 10 years later. Luckily they caught it early. That was OT, sorry.... but it sounds like dense breasts and other "activity" like micro calcifications, etc. may be warning signs worth monitoring closely with MRI's, not mammograms or US, since ILC very often only shows up on an MRI. It will probably be an uphill battle with insurance companies to have that become standard practice for dense breasts. We can only hope that enough docs and knowledgeable patients will start to push for this to become the norm.
Thanks for all of your kind words. I wish there was some way that my experience could somehow prevent anyone else from having to go down this road!! But it's an easier road with all of the support from the sisters here at BCO. Here's to the good life, however long it may be!!! (((Hugs)))
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Dear all
new here and first public post, if there are some mistakes with my English, please ignore it because its my second language and still working on it....lol
here is mine:
no family history, at twelve had first period, had my only daughter at 28yrs, breast feeding about two months, pretty healthy all the time, and very active person. one thing I noticed that like some of the sisters here, I barely catch cold, no matter what, some times even all my co workers were sick one by one, I am always the only one never got it. before I was so proud of it, now I think that is something wrong with my immune system. they are not fighting properly.
dense and small breasts, the thing pi$$ed me off, I barely have breasts and i have breast cancer!
Iots of stress in the past 15 years, from marriage and job.
Had problem with my periods for years since after had my daughter. always heavy bleeding, and painful that have to take meds. Had IUD inserted last year for half year then took it out on Sept. had mammogram each year since 2008, missed 2012, then found in 2013 march, even in Jan. 2013 my mammogram showed nothing changed, but I found a lump in my breast and went to my gyn who referred to BS and did biopsy, turned out BC..... I found that my temper was really bad and was really easy to be irritated before my DX...
best wishes to all
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What a great, bright group of women. I enjoy reading posts and think the tenor of the group is to support each other, find out if there are commonalities, and just listen. I like that. Don't have it anywhere else.
I try not to look backwards, thinking this is where I'm at now- what's the best way to move forward. But if I wanted to I could be upset with the medical establishment that never warned me to be more vigilant due to obvious risk factors. I was told to tell every OB or gyn I ever saw (really the only drs I saw yearly, (up til BC, freakishly healthy - never had the flu, hardly had colds, etc.) that I was a DES daughter (my Mom took it for most of her pregnancy with me.) I did this from the age of 14 onwards and was carefully watched for vaginal cancer. Not one dr ever told me that DES was a risk for BC, which it seriously is. I might have even read about it (though there wasn't internet then
but didn't think much of it since we had no fam hx, and no dr ever said anything. I thought if it was important enough, surely a dr would have mentioned it. I, too, was told that I had very dense breasts and always had to have an US in addition to a mammogram. Never thought much of this either...some people just have dense breasts, right? Never thought to ask as mammograms were always clear, mine just took a bit longer. Wow did I not pay attention. BC was just not on my radar screen. A family full of heart disease, but no cancer except distant cousins. Now I do hope that drs are warning patients w DES histories to be timely with their mammograms. Not sure if they are.Also, I sometimes wonder if BC more often strikes a certain personality type. One that takes on too much and harbors stress like air. I was always a person who never said no, and multi-tasked until I was exhausted. Even when I didn't have terrible things going on (thank God) I juggled four kids, a stressful career, a husband's stressful career, extended family stress, and all of the other craziness that we impose on ourselves. I slowed down post BC and have to work at not allowing it to all creep back into my life again, because it is my tendency, to overload. I'd been successful for a while, and was happier. I still have occasional harsh deadlines and I see that this is simply not for me; I feel physically worse and of course worry that it will usher in new BC! Worry about worrying!
Good weekend to all.
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Ladies, this thread is going somewhere so very interesting. Dense breasts, stress, and overall health. So I will add my 2 cents worth on these topics if you don't mind.
I hope that the answer to dense breasts is improving the current imaging....not sending more of us for MRIS. But until we have better imaging, we ILCers need to advocate for diagnostic mammo/ultrasound with alternating MRI. MRI's are a double edged sword and not without their own risks. Tomography offers great hope. In the future, I am hopeful that there will be other reliable, safe screening methods so that all women of all ages will qualify for breast cancer screening and it will reliably find our ILC tumors before they get so big and nasty.
I have read with interest the connection we draw between cancer and stress. I am definitely one of those people who over-function and definitely had periods of time in my life when I was very stressed, unhealthfully so. I even have pictures to prove it. Ha! The silver lining for me in this heinous disease is that I have stopped overfunctioning for underfunctioning people. Life is really good now on that front. Who knew?
And as far as overall health...I too am one of those people with perfect attendance....during school, work, etc. nothing could take me down. I wonder if the high performing personality is what gives us the illusion of good health, meaning that we have a cold, the flu, etc....we just ignore it and climb the ladder. Just a thought.
Anyway, I really enjoy this thread. It is so interesting to hear your stories. I wish there weren't so many of us!
Love, MsP
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Music67, no worries, your English is fine. My I ask what your first language is?
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Hi all!
I think this thread is awesome! Thank you MmeJ for starting it! I've been lurking since the beginning and thought I should chime in.
I have a strong maternal family history of cancer but not breast cancer. I was diagnosed at age 44. I have two children, 14 and 8, both breast fed for 6 months each. My first period came just shy of my 12th birthday. Periods were never regular. Was on BCPs off and on 10-15 years. I had the Mirena IUD for 5 1/2 years up to date of diagnosis. Had it removed ASAP! I have very dense, small breasts. I have had two root canals prior to diagnosis. One of which caused an abscess because the dentist DID NOT finish the root canal! I had that tooth pulled. Found out that abscess is what had been causing my sinus infections for years. My BC tumor was on the same side as my root canals. I do not necessarily believe this caused my BC. I also loved my glass or two of wine in the evenings prior to diagnosis. Scared to drink now. I lived in the Central Valley of California for ten years, in the LA area for three years, and then in Cairo, Egypt, for 8 years up until the revolution in January 2011. I feel the environment may have contributed to the BC. Cairo is highly polluted and the tap water is heavily chlorinated, LA is highly polluted, and the Central Valley is full of pesticides from farming. Can't think of anything else to add right now.
Hollander, you've touched my heart. Thank you for sharing your story.
Hugs to all!
~ Amy
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This is truly a great thread. Thank you all for sharing.
I also had a short temper and quick to anger in the 3-4 years before my dx. I didn't even recognize myself. After dx I immediately attributed my bizarre behavior to the Cancer.
I too never missed a day of work and put in 70 hours a week on average. I also couldn't believe how I never got colds. I was taking lots of supplements and telling my co-workers and friends they should try them since I hadn't gotten a cold for 3 years. I used to say "I don't ever get the little c". How ironic as I had the Big C the entire time.
We have legislation in California that passed last year changing diagnostic tests for women with Dense Breasts. The protocols now include MRI and Biopsies since 40% of women they say have dense breasts. This legislation passed just after my dx. You all might like to get a copy of it "Simitian Bill" and send it to your state senators and congressional reps.How many of you gals have MO's who track your tumor markers?
Hugs,
Kat
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Katarina, my onc does tumor markers, but she never volunteers the result of my blood work at each visit nor has she ever had a discussion about how she uses them for surveillance. It really bothers me that I have to ask for and drop by to pick up a hard copy of my blood tests the day after my test/visit. My onc never talks about nutrition or exercise or mental well being....all things that I think are important and that I would like to hear my doctor "rah, rahing" I had to ask her why she chose Femara for me. I hate having to ask important crap like that. I have now learned to tell her how many questions I have at the beginning of the visit...so that she doesn't make me chase her out of the examination room. And I limit it to 5 or less. I am retiring soon and will be moving to another city....otherwise I would have already broken up with this onc. Thankfully, my tumor markers have been and are in normal range, so there have been no issues to date. I definitely know what kind of onc I want in my new city and it isn't this type. (Sigh) Sorry for the extra info you didn't need or want.
MsP
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Kat, thanks for a good reminder about that legislation. My mastectomy bra/foob fitter had mentioned it, but I never looked into it since I didn't need to at that point. Timing is everything, eh? Of course, I was diagnosed this past summer! I am so glad, though, for others who get to have better diagnostic tools available to them.
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- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team