Member Since: September 6, 2003
Last Login: November 17, 2008
Birthday: December 31, 1971
Location: clayton, nc United States
Occupation: supermom
Homepage URL: www.myspace.com/kancion
| Diagnosis: | Dx 8/25/2003, IDC, 2cm, Stage IV, Grade 2, 12/20 nodes, ER+/PR+, HER2- |
| Diagnosed: | August 25, 2003 |
| Type: | Invasive or Infiltrating Ductal Carcinoma |
| Recurrent? | |
| Metastatic? | |
| Stage: | Stage IV |
| Lymph Nodes Removed: | 20 |
| Positive Lymph Nodes: | 12 |
| Tumor Size: | 2cm-2.9cm |
| Tumor Grade: | Grade 2 or medium 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:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Nov 17, 2008 02:53 pm
pet/ct tomorrowI had indifferent news. there are two tumors showing in the liver, that didn't image the last couple of times, but I have a fatty liver so that could have been hiding them. ((But, a year ago there were innumberable tumors -- so I see this as 'whatever' news. Onc wasn't too concerned, so we're going to wait until scans in Jan to see if they grow.)) The bones are stable, but a little more 'bright' on the bone scan in the pelvis and left femur. Staying on the same chemo for now. So, all in all cancerland is fine -- if I could just get rid of the 'normal person' sicks that I've been having. Bladder infections, ear infections, colds, etc..... Hopefully it will be all better soon. Looking forward to going home to see my family in WV for Thanksgiving and 2 weeks at Christmas... I think I'm just in a funk and having a hard time getting on myspace or here to post much..... Thank you guys for the concern..... Dx 8/25/2003, IDC, 2cm, Stage IV, Grade 2, 12/20 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Oct 21, 2008 07:14 am
Numbing Spray for Port Banned by Joint Commissionmy hospital uses an 'ethyl chloride' spray which is manufactured by a company called Gebauer. They just used it yesterday, so it must still be ok to use. Dx 8/25/2003, IDC, 2cm, Stage IV, Grade 2, 12/20 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Oct 16, 2008 08:54 pm
pet/ct tomorrowwill get results on monday. worried as usual, just asking for prayers.... Dx 8/25/2003, IDC, 2cm, Stage IV, Grade 2, 12/20 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Oct 15, 2008 09:27 am
Waiting stinks...oh vicki -- they're not joking about the severe part.... Its very hard to keep it moving with this junk.... stay on top of it, stool softeners every day (I take mountains of stuff to keep it working...) Dx 8/25/2003, IDC, 2cm, Stage IV, Grade 2, 12/20 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Oct 15, 2008 09:20 am
oh no! I am in such trouble....seriously guys, I think we've gotten it handled. I appreciate all the offers for help, I really do. I have money on the way and some offers of help that are just perfect. I was really scared and overwhelmed yesterday, we always seem to be in money crisis mode because I can't work (yes, I get SSDI, but my claim started when I was 31 -- I didn't have too many work credits, so my check is about 40% of what my income was...) We just struggle to keep the lights on and vehicles on the road and our roof over our head -- this was just yet another shock to the budget and I snapped. Deep breaths, everything will be just fine..... I'm not crying, people have it much worse than we do - but it really stresses me out sometimes... Dx 8/25/2003, IDC, 2cm, Stage IV, Grade 2, 12/20 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Oct 14, 2008 11:28 pm
oh no! I am in such trouble....susan -- i just want to hear them say it and make sure that it means that they can be re-refrigerated. Its the whole little 'e-coli' thing on it and the onc saying that they're no good. I just want a verbal... If it is that easy then I'll be a dancing fool and gladly returning some cashola. ((And I'll feel like a heel for crying and being stressed most of the day)). I still can't really settle down and i'm pretty ativaned and xanaxed up.... Dx 8/25/2003, IDC, 2cm, Stage IV, Grade 2, 12/20 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Oct 14, 2008 04:50 pm
oh no! I am in such trouble....I kept the shots, if they can stay at room temp for a time.... ((I'm going to call Amgen where they're made and find out)) My dad sent me some money to buy some and my church is willing to chip in some and I can buy a couple. My onc had no luck with the insurance company. However, I am going to call my homeowner's policy and check into that one. What a great idea. I am just really stressed out and upset about it. I can't believe I lost that many shots. I know that no one left it open intentionally. However I have prevented it by happening again. Target has a mini-fridge that holds only a 6pack of soda, plugs into the car and wall. I'm picking it up tomorrow and plugging it in on my nightstand. I'm good for this next cycle and have a little time. My PCP said that I can come over and get my counts checked every day if I want, they do it in-house and he's literally a mile away from my home. I'm working on a game plan here and you guys had some great suggestions - thanks a million (or at least several thousand, huh?) Dx 8/25/2003, IDC, 2cm, Stage IV, Grade 2, 12/20 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Oct 14, 2008 11:56 am
Waiting stinks...actually jeanne46, I get mine in a push and I have a port. They just flush with a small bag of fluid afterwards... Dx 8/25/2003, IDC, 2cm, Stage IV, Grade 2, 12/20 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Oct 14, 2008 11:53 am
oh no! I am in such trouble....Someone at the house left the refrigerator open last night and my neupogen shots were in the door. They were not the least bit cold. The onc said that I could use one now, but that the others were bad now. My counts drop way too much to not use them. I called my insurance company and they won't pay for more until next month - I still need 12 to get through this cycle. They said that I could purchase them at the insurance discounted price, but that is still $2700 and we don't have it. I know I could ask my family for help - but I am so tired of doing that - it sucks. My doc can get me 2 as samples, but I've called Amgen and the compassionate whatever program will take too long to get started, and financially we don't really qualify since the insurance usually covers them - this is our fault in their eyes. I'm just sick with this and wanted to commiserate. I am so tired of being broke and having bad things happen that I'm overwhelmed with it. Makes living so long with this not so appealing sometimes.... Dx 8/25/2003, IDC, 2cm, Stage IV, Grade 2, 12/20 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Oct 13, 2008 05:27 pm
Waiting stinks...oh yeah, the navelbine is a 'push' drug, so they get it in through a syringe and it just takes about 5 minutes.... Dx 8/25/2003, IDC, 2cm, Stage IV, Grade 2, 12/20 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Oct 13, 2008 05:26 pm
Waiting stinks...its navelbine (or as I call it 'navy bean') its not too bad and I get it weekly. mine is paired with avastin. its not too major weekly, but its not lots of fun. i don't have anything really weird other than stomach pain the day of treatment and the day after, and it makes your counts drop. still have my hair with the weekly plan. i also have neuropathy now and don't know if that is the navelbine or the avastin... oh yeah, how could I forget the constipation? it should be easier than the xeloda though. from what i've heard, its tougher to handle -- but I haven't taken it. good thing is that its held me stable for a year (so far) and has shrunk the liver mets enough that they don't see them on the PET/CT anymore.... Dx 8/25/2003, IDC, 2cm, Stage IV, Grade 2, 12/20 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Oct 13, 2008 08:13 am
Do you ever take a break from this?also weekly chemo for a year now, monthly before that for a couple of years. I have taken a week off before to travel (and am taking 2 weeks at Christmas - onc doesn't know that one yet....) I'm also afraid to take too much of a break, and it has never been mentioned... Dx 8/25/2003, IDC, 2cm, Stage IV, Grade 2, 12/20 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Oct 13, 2008 08:05 am
The Truth - The scans are NOT goodI've had it happen as well. Mine told me that she didn't want me too overwhelmed all at once... Nice, but misleading. I also can pull up my scans and bloodwork and stuff online, which I think is FABULOUS! Wish they would post them sooner (a week delay), but I guess I can't have everything.... I'm sorry and it sure does stink. I know that I felt totally betrayed by my onc and seriously began searching for another (however, I had chosen her for a reason, so I stayed.) I did tell her that I wear my big girl panties for appointments and wanted nothing less than all the facts from that point forward. Hope you can come up with a solution that works for you.... Dx 8/25/2003, IDC, 2cm, Stage IV, Grade 2, 12/20 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Oct 13, 2008 07:58 am
Why do I sleep 20 hours a day?I know that its probably a lot of things making you sleep so much, certainly the WBR doesn't help much. When my liver mets were bad before I started treatment for them I was sleeping like 18 hours a day. I still sleep wayyy too much, seems like I can't get enough of it (unfortunately it doesn't happen often enough at night). Sleep is a time for your body to try to mend, but it sure feels like you're getting nothing accomplished, huh? I'm sorry honey. I know its miserable..... Dx 8/25/2003, IDC, 2cm, Stage IV, Grade 2, 12/20 nodes, ER+/PR+, HER2- |
Posted in:
Tests, Treatments & Side Effects + Lymphedema After Surgery, Created: Oct 11, 2008 04:31 pm
i can't believe i'm so slow....no, the weightloss is entirely the navelbine/avastin -- but I had plenty to spare, so I'll take it.... I found a sleeve that I got once upon a time that I never could wear because it was too small -- it fits pretty good. (It was mediven and I liked the fit of the jobst ones) If I could just find a gauntlet it would be great (I know I have them somewhere....) Plus, the jovipak still provides enough compression. It is already not tender to the touch anymore, so I think I may be able to skip the therapist this go-round. I'll give it another week and see how it goes.... I could swim, but it would have to be the indoor pool and then I'd be all cold - I'm just not a pool person in the fall/winter. I'm already babying the arm and lotioning it up and doing the exercises again -- but it sure was nice to have it gone for a while..... Dx 8/25/2003, IDC, 2cm, Stage IV, Grade 2, 12/20 nodes, ER+/PR+, HER2- |
Posted in:
Tests, Treatments & Side Effects + Lymphedema After Surgery, Created: Oct 7, 2008 07:43 am
i can't believe i'm so slow....My affected hand has been HURTING lately. I have neuropathy in several fingers from the navelbine and I was just kind of passing it off as that. While I was cleaning in my room I came across my Jovi-pak and wrapping stuff and it kind of dawned on me. Stupid LE is back, that is why my hand and forearm are so sore to the touch... I haven't even worn a sleeve or anything since early spring when I started swimming every day. Now, I haven't been to the pool in a month and TADA -- its back! I have no idea where any of my sleeves are or if they fit anymore (I've lost like 60 pounds since I was last fitted) The jovipak is compressing, because the pain in my hand is really minimal after just 3 nights. I am just STUNNED that after all the LE stuff I've gone through that it really slipped my mind THAT much when the symptoms came back....... Guess I need to make an appt for some MLD and get remeasured.... Dx 8/25/2003, IDC, 2cm, Stage IV, Grade 2, 12/20 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Oct 2, 2008 11:16 pm
MRI tomorrow to rule out brain metswill definitely add you to my prayers, tamantha. Dx 8/25/2003, IDC, 2cm, Stage IV, Grade 2, 12/20 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Oct 2, 2008 11:14 pm
mets/elbow?speak of the devil....... Geeta, you're so funny! I was going to call you and tell you to check out this post...... stack -- hope that its something else, also..... I'm so bad with details that I was sure I'd screwed something up, but I was SURE it was your belbow geets.... Dx 8/25/2003, IDC, 2cm, Stage IV, Grade 2, 12/20 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Sep 30, 2008 03:26 pm
mets/elbow?actually geeta75 had it present as bone mets in her elbow.... weird spot, but it sure went there on her.... Dx 8/25/2003, IDC, 2cm, Stage IV, Grade 2, 12/20 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Sep 30, 2008 02:55 pm
Are you treated at a National Cancer Institute?I'm at Duke. While I LOVE my onc (we've had our ups and downs, but she's been my doc for 5 yrs now) I get frustrated with the "being a number" that happens with scheduling and such. I know all of the chemo nurses, the valet parkers, the people at the check-in desks, the nuclear medicine peeps, and they call me by name, even if I'm just walking by them in the hall. But, if I have to make a phone call about a problem (not medical) or call scheduling to change an appointment -- I think it would be easier to do brain surgery on myself.... Granted, it means that I spend hours and hours there for chemo, and a whole day there if I have scans or see the onc, but I made the choice initially to go there because of its rankings and can't see changing to something more convenient (especially being stage IV now....) I have gone with friends to different cancer centers and there is one local one that is like a spa and I really liked the atmosphere, but couldn't imagine being treated by the onc there... I think I'm too resistant to change to make the jump to somewhere else...... Dx 8/25/2003, IDC, 2cm, Stage IV, Grade 2, 12/20 nodes, ER+/PR+, HER2- |
© 2008 Breastcancer.org. All rights reserved.