Do you call DCIS "breast cancer"?
Comments
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Dixiemine - no worries on the name.
A beach house sounds awesome. Funny story - my hubby knew all along that Disneyworld was my destination of choice and was cool with it. I even told him we were staying at Polynesian and paying the big bucks.
Then we do our taxes and were bummed to owe more than we thought. He says to me "maybe we should scale back on DW." You know that look we can give our husbands...you know... "THE LOOK!" He sees it and then said "No. Of course not. We won't do that." Good boy! You just redeemed yourself! So funny.
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There is a tab at the top for Private Messages. Click that and you'll see where to send PM (short for private message). I'm no expert on the shorthand but I know these:
mx - mastectomy
unimx - unilateral mastectomy
bmx - bilateral mastectomy
rads - radiation
ps - plastic surgeon
onc - oncologist
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Thanks - I'll start my dictionary!!
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Go to this thread: http://community.breastcancer.org/forum/131/topic/773727
This is a very helpful list of abbreviations that is provided by the Moderators. If this link does not take you there, go to the Forum Index, Welcome to Breastcancer.org, New to this site? and you'll see the list there.
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I told everyone that I had breast cancer that was caught as early as could be.
I think the way I explained it to my 7 and 10 year old children had the most meaning for me. In the fall of 2010, when I was diagnosed with ADH, I told the kids that cancer is cells that grow like crazy and therefore are dangerous to the normal cells around them. I told them that I had ADH which were cells that were not yet dangerous, but could become dangerous, so we were removing them.
Then, when I was diagnosed with DCIS this fall, I told the kids that I had dangerous cells this time, but they hadn't yet been able to cause damage. The doctors were removing the entire breast to be sure there were no cells left that were dangerous.
I explained that IDC is when the dangerous cells have started causing damage, but that wasn't happening in my case.
I think, in essence, that is all accurate. At the time, it helped me come to terms with what was actually happening. I felt much reassured, as did my children.
I personally feel very lucky. They caught my cancer at the first moment and I had all sorts of options and choices available to me. I, too, was nearly vegan and worked out extensively and quit smoking years before and rarely drank...etc... A couple of times, I thought, why'd I bother?? But mostly, I was grateful that I was in such good shape and it allowed me a quick recovery from surgery. I wonder if it also caused my cancer to grow much more slowly. I will never know, but I am not going to second guess myself by knocking myself down. I am glad I am in good shape and I believe that it HAS helped me in relation to cancer. I didn't get cancer in spite of my lifestyle, I am surviving cancer in style because of my lifestyle!!
I feel for all of you who are so newly diagnosed. Those first months are really a roller coaster. It is getting better now, but I still feel newly diagnosed, 5 months later. Wishing you all the best...hang in there...it gets better.
Claire
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Deleted as a repeated post.
Turn your face to the sun and the shadows fall behind you. ~Maori Proverb
Diagnosis: 9/15/2011, DCIS, Stage 0, Grade 1, 0/1 nodes, ER+/PR+ -
CLC - I love this statement you made..."I am surviving cancer in style because of my lifestyle!!"
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VG -- There is no such thing as too many or silly questions here. Ask away :-) I have found the body has a remarkable ability to make tears because I've shed buckets of them. The first couple of weeks I began to wonder if I had also developed a personality disorder because I could go from normal to angry to weeping all within 5 minutes. It's A LOT to process, feel what you feel and know that we are here to support you. We know what you are going through and it's nice to have somewhere to turn for answers. This forum is wonderful and there are so many knowledgeable ladies here....I love it!!!!
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That is quite a list of short forms . . . oh my! Much to learn . . .
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Unfortunately, you'll be a pro in no time :-) I swear I have never in my life spent so much time thinking about and talking about my boobs....haha.
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VeganGal - a couple of other terms that I find kinda funny...
Foob(s) - fake boob(s)
Fipple(s) - face nipple(s)
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A list of abbreviations can be found on the forum index. If you go to the forum index at the top, then go to the "New to this site" forum, there is a thread with a list of abbreviations...
Here is the url
http://community.breastcancer.org/forum/131/topic/773727?page=1#idx_1
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You chicks are awesome!!! Thanks for making me laugh for the first time in almost two weeks . . . and . . . yes. . . I don't think I said the word "boob" outloud so much in my entire 43 years of life as I have in the last 10 days . . . so funny . . . and I've never looked at so many sets of boobs online either!! Boob, boob, boob, boob . . . . I may write a boob song . . . or a Bye, Bye, Boob song . . . I was even considering throwing a Farewell Boobie Party before my surgery . . .
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VG - I am 43 too. Too young for the real or fake cancer!
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Merritmalloy . . . sounds like we have a lot in common . . . it is a pleasure to "meet you" . . . .
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Well, girls...I am an old lady compared to you...I come in at the ripe old age of 44...:)
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CLC - maybe you should head on over to the DCIS/AARP board. ;-)
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Several ladies have had farewell parties for their "girls". One even had an awesome boob cake...haha. If I can find that link I'll PM (private message) it to you. It was great!!
I know!! My husband and I have both been looking at boobs for weeks....sometimes we both crack up at ourselves. I am almost positive that before January 3 had I come home and found him looking at boobs on the internet there would have been a huge fight. Now I just ask him if he's boob shopping...LOL.
VG -- you are going to be fine. Is it fun? No!...but it is doable!!! I am also 43...one more thing in common.
Love & Hugs ~Karen
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CLC . . . I really need to embrace some of the comments you made about doing better through this because of my lifestyle . . . not inspite of it . . . thank you for that!!
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Merritmalloy -- real or fake breast cancer?....totally cracks me up. I will be 43 in July :-)
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Karen . . . so great - so funny . . . I can't believe that we are all the same age . . . all with DCIS . . . all the same experiences . . . I didn't know what it would be like to come on this board, but I am grinning ear to ear right now because of all of you . . .
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Hello girls, I had to chime in w/ a thanks for making me laugh and making me feel relieved that there are others out there like me who have been completely blindsided over the past few months. I was diagnosed in Nov 2011 w/ DCIS. I wanted a BMX from the beginning , knowing that I would worry myself sick for the rest of my life worried that it would come back. I've had many people that are super supportive. I do feel very lucky that my cancer was found so early. Biggest complaint... I've had a few people that have had breast augmentation comparing their recovery to mine.... REALLY??? So I'm forced to either smile and nod (knowing that they just dont have a clue) or ...kindly remind them that these are very different surgeries since I had cancer..
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Welcome to the "gang" . . . I am leaning towards the same decision . . . I am a worry wart . . . and don't want to live like that . . . did you have immedicate reconstruction? I want this but I understand that some surgeons push back? Did you have nipple tattoos . . . I've checking these out online and they look very cool . . .
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I am so grateful for all the feedback regarding this question.
I started out actually feeling somewhat guilty when explaining DCIS to my family at least (go figure, I'm Canadian) and then had an about-face after going through surgery. My sister had a more aggressive form of breast cancer, so that might have had something to do with it. Plus my surgeon did say "you don't have cancer" which really confused me. I realize that surgeons see in black and white at the cellular level at least.
I think I am in the "anger" stage also. I had some surgery complications this past weekend, which didn't help matters because it might mean more surgery even though I have clear margins.
And the fact that I haven't been able to return to work as soon as I would have liked doesn't help either. So, it does add up.
I'm very grateful to everyone who has chimed in on this. It has given me much food for thought, and it really helps to "talk" to people who are going through the same thing.
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Here is the thing about being lucky, someone is always going to be luckier and someone is always going to be more unlucky. It is a very vicious and ugly game to play. My brother in law was saying how he thought he had a bad year until he compared himself to what I went through....I told him how I felt we had a bad year until I compared myself to my other SIL who lost her 4 year old daughter to cancer. That sister in law recently posted about how badly she felt feeling sorry for herself when a woman she knows who lost a child to cancer was recently diagnosed with stage 4 cancer herself. There is always going to be someone worse off then we are, and there are always going to be someone in a better situation.
We all have to deal with the situation we have. Whether your doctor feels it is cancer or not, it still needs to be treated, whether it is mastectomy or lumpectomy, whether you take tamoxifen or not, radiation or not. If doctors truly did not feel it was dangerous, then they would all just "watch and wait". I've read and seen to many post by women who started with DCIS, who did the BMX or the uni-MX, who take the tamoxifen or not, then years or months later, see it return. Sometimes as something worse. It is dangerous and it needs to be treated.
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Well said Emaline.
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Yes Emaline, you hit the nail on the head.
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Love this thread! Thanks for making me laugh and cry at the same time....
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Hear Hear Emaline . . . Agree Wholeheartedly!!!
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