A bunch of premature, crybaby, self-absorbed hysterical women
- I posted in the category of unusual radiology results I didn't get a single solitary answer. Now I know why Sandy Walters called breast cance.org a bunch a gang banging crybaby women before she passed away suddenly last year from stage for breast cancer complications
I've come to the conclusion that this wesite is all about htsterical newbies wanting to get free advice and jumping the gun before they should get really get their shorts in a knot. You newbies need to chill.Un you have a radiology report like my then you could cry a river
Chill you get a report like this.:
I had an MRI done five days ago and yesterday I got the report. Not good. Actually it's a crazy report telling me that I need 4 biopsies!! Apparently, have an enlarged axilla lymph node in a breast that never ever had cancer and still does not, according to this new report. In the other breast I have now a suspected local recurrence including a node in the IMN chain. Has anyone else here ever been told they need to get their IMNchain biopsied? Has anyone here ever been treated for a disease that lymph node in the IMN chain? There's just not a lot out there about having a diseased lymph node in the breast itself
This is what I been able to find for a summary of what this diagnosis is:
For over a century, there has been considerable interest in the management of regional lymph node metastasis in patients with primary breast cancer. Since the advent of sentinel lymph node biopsies, there has been renewed interest in the management of patients with metastasis to the internal mammary nodes. The appropriate management of these patients has not yet been established. Some investigators propose that biopsy of the internal mammary sentinel node may provide additional prognostic information which might be used to guide the administration of systemic adjuvant therapy. Additionally, it has been suggested that patients with metastasis to the internal mammary sentinel node may benefit from radiotherapy to the internal mammary nodal chain. Clinical trials are needed to resolve these issues. Internal mammary sentinel node biopsy in patients with primary breast cancer should be considered investigational, and conducted only in the context.
As I was saying, you newbies really have nothing to be so panic stricken about. This group is not all free advice from those of been there, but rather from those just looking to vent prematurely.
Comments
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I had a sentinel node biopsy when I had my mastectomy. The MRI and pathology found no cancer in the node just the 2 tumors ILC and IDC. No radiation suggested. My oncodx was 34 but I did not do recommended chemo just 4 years AI drugs. Both tumors were 95% ER amd 0% PR which was probably significant in determining my oncodx number.
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Actually, you posted in the thread about less common types of BC, not unusual radiology results - 18 hours ago, on a weekend, when this site is typically slower - asking if anyone else had had result a similar to yours. No one responded - in 18 hours - so now we're all a bunch of “gangbanging crybaby women" (whatever that's supposed to mean)?
Seriously - no one's forcing you to post here if it's truly that awful. I've found nothing but support through my first...second...and third diagnoses. Sounds like maybe this group isn't providing the instanteous support and answers you need. good luck.
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A breast cancer scare or an actual dx are scary and fraught with a multitude of emotions and reactions. We all deal with them differently. I am stage IV but I understand that even the worry about bc and waiting for tests, biopsies and doctors appointments can have a huge emotional impact on many. Let's just support folks wherever they are and hope, in the end, that they really do have nothing to panic about. Crybaby, self absorbed, hysterical women? I disagree as we all react differently when confronted with the possibility of bc. And what on earth does gangbanging mean in relation to worrying about possible bc? The name calling is not necessary at all.
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I had to google and find a medical site to even see what IMN was. Maybe that's why your responses have been few. Most people on this site are new to cancer and don't know what to think or not to think. Sorry for your frustration and rage but we all feel that way at one point or another once cancer is our new norm
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