Member Since: August 28, 2008
Last Login: November 19, 2008
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| Diagnosis: | Dx 9/19/2008, IDC, 2cm, Stage IIa, ER+/PR+, HER2- |
| Diagnosed: | September 19, 2008 |
| Type: | Invasive or Infiltrating Ductal Carcinoma |
| Recurrent? | No recurrence |
| Metastatic? | No |
| Stage: | Stage IIa |
| Lymph Nodes Removed: | |
| Positive Lymph Nodes: | |
| Tumor Size: | 2cm-2.9cm |
| Tumor Grade: | |
| Hormone Receptor Status: | Tumor has both estrogen and progesterone receptors |
| HER2/neu Status: | Tumor does not have an excess of HER2/neu receptors or genes |
Posted in:
Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Nov 18, 2008 08:28 pm
Third Chemo QuestionsThis Post was deleted by Lonewolf. |
Posted in:
Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Nov 9, 2008 05:36 pm
Perhaps a stupid question but.....This Post was deleted by Lonewolf. |
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Tests, Treatments & Side Effects + Just Diagnosed, Created: Nov 2, 2008 01:47 am
Down Syndrome woman diagnosed w/BCI dont quite understand how this has been determined "inoperable". Dx 9/19/2008, IDC, 2cm, Stage IIa, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Just Diagnosed, Created: Oct 31, 2008 11:34 pm
I broke down todaySure seems that way doesnt it? Tell them you are a "hard stick" and insist on a butterfly IV needle for this stuff. FYI - It took me about a month to get to the point where my chemo port was tolerable. Dx 9/19/2008, IDC, 2cm, Stage IIa, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Oct 17, 2008 06:06 pm
Spiked WBC After NeulastaThis Post was deleted by Lonewolf. |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + IDC (Invasive Ductal Carcinoma), Created: Oct 17, 2008 05:58 pm
starting chemoFor the first week after my first chemo I was pretty germ phobic and then started going out a bit more. As for having people over no one who is sick is allowed in my house and I am not above wearing a mask when I sit in the waiting room for medical appointments. In my case the first chemo lowered my white cell count and the shot of neulasta given afterwards raised it to three times what I was before starting chemo. So you might want to see how much your counts go down first before you start being more active socially. Also tis the season for flu out there so better safe than sorry. Dx 9/19/2008, IDC, 2cm, Stage IIa, ER+/PR+ |
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Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Oct 16, 2008 09:31 pm
Spiked WBC After NeulastaThis Post was deleted by Lonewolf. |
Posted in:
Tests, Treatments & Side Effects + Just Diagnosed, Created: Oct 14, 2008 03:43 am
please helpI keep having recurring dreams about treatments not working or not being eligable for treatments (I have had one of 4 chemo treatments so far), etc. Dx 9/19/2008, IDC, 2cm, Stage IIa, ER+/PR+ |
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Not Diagnosed but Concerned + High Risk Women, Created: Oct 13, 2008 07:25 pm
PET ScansThis Post was deleted by Lonewolf. |
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Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Oct 13, 2008 05:11 pm
PET scansFrom what I understand the Pet scan will "light up" any rapidly dividing cells. It not only showed my breast cancer and its spread to my lympth nodes but also adenomas and polyps I had and both of those are supposedly non cancerous. Dx 9/19/2008, IDC, 2cm, Stage IIa, ER+/PR+ |
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Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Oct 11, 2008 07:12 pm
Neulasta Bone Pain QuestionOh wow, all that pain and your counts still went down? My God there ought to be a law...is that typical? Did you end up hospitalized?
Dx 9/19/2008, IDC, 2cm, Stage IIa, ER+/PR+ |
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Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Oct 11, 2008 03:41 pm
Neulasta Bone Pain QuestionHad shot on Thursday and today I have intense pain in the tailbone area and the leg muscles feel very weak. How long does this typically last? How have others coped with this?
Dx 9/19/2008, IDC, 2cm, Stage IIa, ER+/PR+ |
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Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Oct 11, 2008 03:16 pm
ER+. Her2Neu+ and Fish+I dont know about bombarded but I am getting four rounds of both the A/C and the Taxotere at the same time instead of the customary 4 weeks each and I have not yet been scheduled for surgery.
Dx 9/19/2008, IDC, 2cm, Stage IIa, ER+/PR+ |
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Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Oct 11, 2008 01:54 pm
today is my birthday and my chemo-versaryHappy Birthday and thanks for the words of hope. I had my first chemo on Oct 1st. Then surgery and then its anyone's guess. Dx 9/19/2008, IDC, 2cm, Stage IIa, ER+/PR+ |
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Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Oct 8, 2008 08:16 pm
Who Do I Believe?Okay my social worker got a copy of my report (thank goodness someone did) and it is IDC and NOT IBC so the surgeon happily is wrong!!!!!! Just a note....I was told that the oncologist is the real cancer specialist and should typically know more about what cancer is and what treatment will be most effective than a surgeon would.
Dx 9/19/2008, IDC, 2cm, Stage IIa, ER+/PR+ |
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Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Oct 7, 2008 05:27 pm
Who Do I Believe?I suppose I better double check another topic of disagreement....My sister (who I live with) and I typically both get flu shots every year. There seems to be some disagreement over her getting one as she could infect me and a LOT of disagreement over if I should. Onco wasnt sure, surgeon didnt know, Onco nurse said I should cause its a killed virus.....yikes. So did anyone get flu shots while taking chemo or have people they lived with get one?
Dx 9/19/2008, IDC, 2cm, Stage IIa, ER+/PR+ |
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Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Oct 7, 2008 03:03 pm
Who Do I Believe?I'm going for labs and a meeting with a nurse practitioner at the Oncology Clinic this thursday so I will demand a copy of that and the pet scan results then. I prefer the lumpectomy as I was supposed to finish my social work degree starting this semester and since he told me I would only be "busy" for 3 or 4 months I told them I would start in late January instead. I've never been through this before so I am not sure of the normal time frame but I know my 4th (and supposedly last) round of chemo is going to be around Dec 5th. So what happens after the last round of chemo for someone who got chemo first? Another PET scan I would presume? How long do they wait after chemo to do surgery? I thought the whole purpose of getting the chemo first was to prevent me from having to have radical surgery. I will post here in this forum the results so hopefully someone can tell me who, if anyone to believe. Dx 9/19/2008, IDC, 2cm, Stage IIa, ER+/PR+ |
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Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Oct 7, 2008 02:41 pm
Who Do I Believe?My surgeon did a biopsy, ordered a pet scan and then sent me to an Oncologist who I was told would explain everything. The Oncologist told me I have Invasive Ductal Carcinoma that its 2.7cm and that I was staged at 2a. He also told me that he had someone just like me who he cured with a combo of taxotere and red devil (4 rounds) and then a lumpectomy. He told me I would be "busy" for 3 to 4 months and that my problem was fixable. When I saw my surgeon yesterday so he could check the site of my chemo port installation he seemed to feel it was IBC and would require a radical mast plus rads... Now there is quite a difference between the two in every respect but I was trying to read upside down when I was in with the Oncol and believe the biopsy report did say Invasive Ductal Carcinoma. These two had better be on the same page by surgery time because I am not about to let someone cut me up and later find out I wouldnt have needed that invasive an approach. As it is I have already been hospitalized a week in the past for a condition that I didnt really have and which could have been treated at home. Dx 9/19/2008, IDC, 2cm, Stage IIa, ER+/PR+ |
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Not Diagnosed but Concerned + Not Diagnosed but Worried, Created: Oct 5, 2008 02:15 am
I just "feel" I need to do moreNo you arent over reacting. You need to do whatever you need in order to find out what's causing your problem and do it as quickly as possible. Dx 9/19/2008, IDC, 2cm, Stage IIa, ER+/PR+ |
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Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Oct 4, 2008 04:20 pm
Odd Things HappeningI am officially at day four after my first chemo treatment and am experiencing some weird things and I wonder if anyone else has gone through. 1. Overall I feel like someone recovering from the stomach flu......okay but not ready to return to work yet. 2. A weird smell....like something rotten in the fridge...in my nostrils and all over the house. I'm sweating too so I dont know if the smell is coming from me or what. 3. Odd pains in the affected breast......each lasting for a few seconds and in no particular order.....like being stabbed, then like being stabbed with a hot poker and then finally almost numbness. 4. Feet feel like I've been walking barefoot through desert sand but dont look any different. I put 4 coats of nail strengthener on toe and fingernails so hopefully the taxotere (or red devil) wont make them fall off. 5. Restlessness and frustration yet feel weak as a kitten. 6. Odd body pains especially in spine where I was diagnosed with arthritis. Other than those listed above and wanting to rip this chemo port out I'm doing pretty good. Dx 9/19/2008, IDC, 2cm, Stage IIa, ER+/PR+ |
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