How did you find out?
Hi Ladies... if you're comfortable sharing, I'd appreciate learning about how you discovered your recurrence and/or metastasis. I'm 2 years out from my initial diagnosis (stage 3, her2+), and I admit I'm still a hypochondriac. I'm wondering what I really should be looking out for. Thanks. I pray you all are feeling well.
Diane
Comments
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I found accidentally looking for a infection pocket post reconstruction. Turned out it was a superficial infection, but they found 50 small mets all over my lungs! Surprise! I had waited a year to do reconstruction and had completed all and was on vacation and noticed one implant was red. Two years out now from all of that...not Ned but almost are gone and staying gone
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I couldn't breathe and forgotten all about the BC I had 10 years before. At first they said it was COPD but when nothing they tried worked, I had a CT which showed a pleural effusion in my lungs. They just told me it was there, not what it might mean and had me admitted to the hospital to drain it. Eventually the labs came back, but I was relieved because now that they knew the real problem, they were able to fix it. Which was lovely after having breathing problems for five months.
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I found my local recurrence by finding the lump. They were "certain " it was scar tissue, but I politely requested a biopsy. Thankfully, they agreed.
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I was like KBeee, I found a lump almost under my lx scar but to the side a little. My MO acted quickly and local recurrence was confirmed. Salvage MX with immediate diep followed.
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I found a lump in the same breast in nearly the exact same location as my primary from 2008. Breast self-exams have saved me each time! I can't overstate how important it is for bc survivors to continue monitoring their breasts for any changes. They won't always show up as lumps, but you should check anyway.
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In my case my back muscles started to spasm. Two months later I sneezed and fell. Needed crutches. Eventually they did an x-ray. Lo and behold my back was broken. Mets had eaten L5. Major surprise to everyone.
The first treatment got me to NED. I wouldn't be doing any better if they'd found it earlier. Maybe I could have avoided the week in the hospital but I doubt it. By the time my muscles started to spasm it I would have needed surgery.
Diane, I realize it's hard, but you need to not worry about this. Someone quoted at Stage IV lady who said that when mets were found you never wished you worried more. Live your life. Worry less. If mets appear, they appear. There's not much you can do about it. Live well.
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I wonder if it appears before symptoms or does the scan pet or ct or MRI catch it I have had some twinges and aches near hips and left arm and I am scared its mets although I haven't had surgery yet. Doc says its in my head
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Occasional twinges and aches are not typically concerning. They are things many of us had, but ignored prior to cancer. Now they get our attention. Ongoing pain should be reported
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I'm still waiting to find out. Should find out something on Monday. But I have been going through the back pain and muscle spasms since I fell in late July. I went to the chiropractor and then the orthopedic Dr. Although I talked some to my oncologist about it, mets never came up and I was really just informing her of what else was going on with me. I didn't realize ongoing pain was an indicator. But as pajim referred to; I don't think it would have mattered if I had gone straight to my oncologist. If I have mets; then I have mets. While it is very hard to not worry, I try to remember that I've read so many posts on these forums and the overwhelming message is I'm not alone and live. Whether that living is just today and for many day/years to come; still live!
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Diane, for what it's worth, here's my story...
Around October 2014 (almost 6 years out from my original Stage II dx), I developed a severe lower backache that I chalked off to the change of seasons and going from wearing flip flops every day to boots, as well as carrying a lot of heavy stuff. I'd also lost about 10 lbs., which I assumed was due to stress. We had had a serious flood in our home in August that necessitated moving first into a hotel and then a rental home and putting everything we own in storage (no small task) for 5 months while our home underwent extensive repair and renovation. In the midst of all that, while we were still living in a rental home and overseeing reconstruction of our home, my DH decided to follow thru with knee replacement surgery scheduled prior to our flood, which meant more lifting and additional stress. So it was easy to explain away my earliest symptoms of an aching back, overall exhaustion, and just not feeling well. Then, in December, after a week in Las Vegas and expecting to come home to a finished house that wasn't, I got literally the sickest I've ever been in my life. I thought I'd picked up an exotic bug in LV, but when I wasn't getting any better after about 10 days and two trips to Urgent Care, I decided to see my onc, who initially reassured me that I was not dealing with a recurrence but had a very nasty viral infection. But the labs he did came back showing a CA27-29 of 155 (my normal range was always 10 - 12), as well as sky high Alk Phos levels. A CT Scan was ordered, and it divulged extensive bone mets.
The best advice I can share with you is the advice I got from UCLA shortly after I finished up my early stage tx -- which was, if you have an ache or pain that doesn't go away in 3 weeks' time, get it checked out -- if only for your peace of mind. In my situation, both prior to my re-dx and since then, everything that's ever bothered me that wasn't mets -- no matter how achy or painful -- seemed to go away in that 3 weeks time. It was only when my backache and other symptoms didn't improve and actually worsened over several weeks that it turned out to be an mbc recurrence. And I personally feel that stress was a huge factor. I think my body reached a point where I just couldn't deal with the stress and stay healthy.
Another thought that might be worth sharing with you... Even though I have had a recurrence, I clearly remember at one point when I was like you -- worried about every ache and pain -- and it occurred to me how foolish it would be if I constantly worried about a recurrence and it never happened, I would have wasted all those years worrying for nothing. And if it did, I still would have wasted all that time worrying. So it's fine to be vigilant, but don't let worry ruin your life now. (((Hugs))) Deanna
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I have just completed standard chemotherapy two months ago. I had surgery last month. After my surgery, I started feeling some kind of imbalance/dizziness/lightheadedness whenever I move or shake my head. I had brain MRI and they didn't find anything. A day after my Herceptin infusion (which I must complete for a year), I experienced abdominal pain and went to the ER. They did CT scan and found thickening which they thought must be investigated. Thus, I am seeing a gastroenterologist next week. I know I may look like a hypochondriac but cancer recurs/metastasizes. I have accepted the fact that, even though my pathology report says cancer is not there anymore, it will be a lifelong affair with the disease.
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