waiting for reoccurance
Comments
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Thanks Shelly, I guess i just assumed because it was triple neg and I missed out on treatment that it might be more often. I am good with this.
I just noticed the thread was for stage 3. My apologies....getting old.
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I'm like so many of you. I'm about a year out from treatment and my last scans. It's time to go back in and see my Dr. this month and it's stirring up a lot of emotions for me...thus here I am on BCO again. I felt strong while I was on Herceptin, but now that I'm done, some days I just feel like I'm holding my breath waiting. My breast surgeon believes in scans so I guess I'll know in a couple of weeks. Breathe...breathe....breathe.....
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i went to oncologist for six month check up today, asked what my risk was and quite shocked by the reply - 50 to 60% chance local recurrence or getting cancer in remaining breast........but for cancer elsewhere risk is same as rest of population he says...........i am concerned as ca15.3 goes up at every blood test.... Still within normal but higher than it was three weeks pre surgery two years ago!
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I'm Stage IIIc and was told my chance of distant recurrence or metastases is 50-60% during the first five years. i'm not sure what my local recurrence chance is and probably don't even care to know because this is other is so much more serious and daunting.
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I was not told that I was at high risk for reoccurance. Instead, because I'm doing neoadjuvant, my onc tells me that my reoccurance risk all hinges on how well I've responded to my chemo cocktail. Bad response, high risk, great response, low risk, average response, it's a crapshoot. It makes me so nervous for finishing chemo and surgery because I feel like whether I will live or die all hinges on what is found during surgery.
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Aryas...I so relate to where you are. Please, know the waves of hopelessness you are feeling does lessen in time. The waves hit less and less and don't take you as deep into the darkness. You speak of children and I will say that was a powerful force for me to fight my way out of the darkness over and over again!! If by proactive you mean choosing foods, exercise and such....keep proactive!! I promise it will become a new way of life and one I feel you will find rewarding. Yes, I live proactive in hopes to stay NED, but it also has giving me such better health over all. I went from a size 14 to size 4 ( I am 5'8)....and feel wonderful even with my daily Als!! My children also have learned from all I have learned and adapted healthier life styles!!
The fear is exhausting and over time you will let go of it more and more as it is such an overwhelming burden. Yes, I still very much can have the fear and hopelessness hit, but I am more stable and less in shock to handle it better...you will too!! Keep coming here as this is where we all know what you are feeling!!
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I think the main things that make me high risk according to my onc is family history (2nd degree relatives), and grades 1-3 in my tumor. She also claims this was only growing for 6-12 months, but am not sure I believe that. They seem to say that about Stage 2 people too -- at least in one case I've heard.
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My onc claims I have a 70-80% chance of remaining cancer free for the next 10 years. It is all a complete crap shoot.
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thats 20 to 30% chance of recurrence Momine, i dont know if I am kdding myself but women who have never had breast cancer have a 20% chance if getting it dont they?
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not the thread i am suppose to be on but I just wanted to say hang in there and have fun. Live fully. I do have mbc. Recurrence 2 1/2 years ago 8 years diagnosis. At this time I am still living a GREAT life. Enjoying more than I thought possible.
My doc keeps telling me not to change anything I am doing cause I feel so good still. I do not believe he knows proseco is part of my feeling good treatment..lol don't like red wine but do love my proseco .
And I do walk and excessive a lot. I feel when you engage in any aerobic activity you really feel alive.. That helps me a lot...and of course...the proseco !!!
Wishing health and happiness and no fears for all...take care
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Lily, I am really not sure. What the onc says is also what cancermath.org says for my case. Where my risk is a lot different than the average woman's is that if mine comes back, it will be stage 4, and I am not sure the risk is that high in the general population anyway. That may be the risk of getting a DX, but we are not talking DX here, we are talking death basically.
Your numbers and mine would be different because we have had different treatment. However, if the crap comes back the end result is the same either way, and stats mean little on an individual level. I always keep in mind that my mom's chance of 5-yr survival was 30%, when she was DXed with ovarian cancer ... 7 years ago. She is fine, great in fact. I was there the other day, and she was on her way to ballet class, on her bike. The woman is 74.
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i firmly believe stats do not take in to account lifestyle or diet changes and i dont see stage 4 as death as I know a few people with this who lived or continue to live for ten years plus post stage 4 diagnosis. So I am not attaching myself to statistics, just to being healthy and happy as possible, ruthlessly so where friends (some now ex friends) are concerned
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Lily, I hear you and same here.
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Susan3 - why hijack a thread in Stage III, when you are Stage?
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Kicks, that is not a "hijacking." I am glad some of the former stage 1-3 ladies still hang with us.
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open communication is a good thing. I love that Ebru name is stagefree & always welcomes us to her threads.
Susan, I am a red wine drinker, but have had proseco & it is light & yummy.
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The written word is open for SO many intererations. Especially over the internet. We can NOT see the person, their tone or body language. Can only go on the first words written - "not the thread I'm supposed to be on'. I will agree that there was positive posted BUT that was did not start the post. To ME - The positive should have been first on this thread - then once written something along the lines "I've been there, you can too".
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Thanks hopefour for you kind compassionate response. Apparently, I was having a reaction to my post op meds that put me in a deep funk when I wrote in such despair.
I have no idea of my odds of recurrence and it is frustrating because I have always been the kind of person who reads the end of the book first. It frustrates me that my doctors have no interest in speculating.
My ONC will not do the blood tests or what she deems unnecessary scans. It just gets to me sometimes. Maybe this is a lesson for me. In patience. I have had enough lessons.
And nobody irl gets it. Why I didn't want to eat cake when treatment was over. I like cake but I didn't feel like celebrating.
Anyway, today is better. Not great, but better.
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Totally get it, AryaS.
By the time I'd finished all my treatments last September, I was so tired, and people couldn't understand why I was not, like, "WHOOP! WHOOP!! I JUST KICKED CANCER'S SORRY !@#$!!" It took time to get my energy and enthusiasm back up.
And then this February, I had a scare, a lump on my scar line. And for a month I was scared and depressed until I got the results. My doc phoned to let me know, and I was like "OK, thanks for letting me know" And she said, "So its GOOD news, right?!", as if she thought I hadn't understood, but it was merely that, when you've been so down and anxious, its difficult to just stop, and be back to normal!
It took a couple of days to come to terms with a benign diagnosis, and then I got news that my mum had a stroke. She passed away April 23, and I am just getting back on track again now.
I feel happy and healthy, just now, and see a PS for reconstruction decisions this week. At present I am not stressing about recurrence .... not to mean I don't fear it though ....
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