Jan 2008--Ain't it Great?
Comments
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Carol....I'll be the first to agree with you about the diamonds. My neighbor used to give his wife some kind of diamond when she finished a round of chemo...I say before is better incentive. lol
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Carol....I'll be the first to agree with you about the diamonds. My neighbor used to give his wife some kind of diamond when she finished a round of chemo...I say before is better incentive. lol
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D1
Xeloda is a pill form of chemo. I have to take 9-500mg pills a day for 14 days, then off for 7 days. Then repeat.
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Nine pills in one day, Lori? Holy moly! Although I'll admit, I'd love to get my chemo in pill form. I'm scared sh*tless of needles and am getting mine via IV. Should be a real treat. At least the nurses have ordered my blood counts to be done via fingerstick whenever possible to avoid as many needles as I can. No one wants to see me make a fool of myself when they bring the needle around more often than I have to.
Anyway, sounds pretty intense. Is this the same tx you had last time?
D1
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Hello January Jewels!!
Thanks so much to Determined1 for starting this thread, and to everyone else for sharing their stories.
I had a bilateral mastectomy November 1 with positive nodes, so chemo is part of my treatment. Had a meeting with my onc today and in the second week of January she will start me on 6 rounds of FEC, 3 weeks apart (via IV).
I am Stage IIIa, T2 (4 cm) N2 (6 positive nodes out of 22) M0 Grade 1 with excellent margins (from 2.5 cm - 10 cm), ER+/PR+ HER2-.
The cancer centre is so busy here, I'll have blood tests done the day before chemo, so each round of chemo will require two trips to the hospital.
I go for my MUGA scan on the 24th, my chemo class on the 28th and then it's get down and fight this thing. I don't know what my experience will be like, but it is an honor to have such a wonderful group to go through this with.
Thank you all, so very very much.
twinkly
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Hi fellow Jewels! Had my MUGA scan yesterday-- a piece of cake. I almost fell asleep during it-- such a difference from the MRI where I freaked out. I think I'll get at least 2 more MUGAs during treatment. The chemo talk was uneventful. I thought I'd be seeing my onc as I had tons of questions, but I saw a nurse and she didn't know the answers to most of my questions. I intend on calling my onc when he's back in the office next week. One thing I did learn is that the Decadron I do the day before, of, and after chemo in combination with an antiemetic I'll get the day of chemo should be very helpful with N/V. Yay! I think the antiemetic I'll get is called Aloxi-- I've heard others talk about it favorably. I also have an RX for Zofran to have at home just in case. I am more freaked out now about the constipation it all causes. And I had some bad dreams last night about hair loss. The mind is a terrible thing! I got tons of literature about what to eat, etc. So as I read it, I'll share the info if it's good. Did you all know about doing mouthrinses 6-8 times daily with baking soda? It's supposed to lessen mouth sores. I'm supposed to do it daily during my 4 rounds (so for 12 weeks). I'll try anything that helps. I also signed up for a Look Good, Feel Better class and am pretty excited about what they can teach me to look less yucky during chemo. Got my "cranial prosthesis" RX, too and will start shopping after Christmas. So much info at once. Oh, and I got a good book--- "the chemo cookbook"-- at our cancer center's library. I'll share that, too as I browse through it or try stuff. i can get anyone the true title and author if you want to look it up, but it came highly recommended to me and so far a quick glance looks promising. Gotta go. I'll check in later.
P.S. Welcome Lori to our group. So sorry to hear of your recurrence. We have a great group here that will be supportive for you. What is your HER2 status?
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Hello January Jewels!!!
got the haircut last night. Brought some hair home for my hubby(he wanted to save it) I lost about 7" of hair..everyone loves my hair..sexy and sassy they said
Waiting to hear from the hospital to see what time surgery is tomorrow and trying to figure out what i need to bring for spending the night...toothbrush/brush/slippers..anything else you can recommend? I will try to get on the boards tonight if i feel the need to talk. (vent) LOL. I will try to get on line sometime Saturday and let you know how i am, if i can't type i will make my hubby be my secretary and i can dictate to him...It is so weird, i feel like i going to miss all of you only for a few days...HUGS to the Jewels....
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Vettegal - just did my AND last Thursday, hoping to get drain out today!!!! Waiting for results today too. I found my IPod was my best thing I could take to the hospital, although it may have been a little rude to zone out my dh, it helped me relax as much as possible prior to surgery, as well as after when I was doozing in and out. Here's to your speedy recovery and a no positive nodes found ! Carol
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(((vettegal)))
We are all with you tomorrow. I had a bilat with no reconstruction and only stayed in the hospital overnight. Wasn't really in a lot of pain, just uncomfortable from the drains. I can't remember what surgery you said you were having, but if you need us this evening (or anytime for that matter) we will be here to listen to you vent.
Hope it's ok to pray for you too.
Deb
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Vettegal: Good luck with tomorrow's surgery. Take a shoelace or some kind of lanyard to put around your neck and pin your drain(s) to it so they don't get pulled. It's also nice to have slippers b/c the floors are so cold at the hospital
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Yes Deb, you can pray for me. I am on so many prayer list right now. i feel so touched by them. Still waiting to hear from the hospital.
KathyL thanks for the tip on the lanyard I have many of them.
I am have the ANB my SNB showed 2 micromets .2mm each and I am going back for more nodes. I pray for positive nodes tonight!
Hey golfer, how bad was the drain really?
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Hey Jewels,
I love that gals from the 2007 group have popped by to say hello and offer their words of encouragment. Thank you....without those who have gone before helping us through this...we'd be muddling along without direction. Just think, in a year from now, we will be doing the same for another group of women.
To those who are having tests, treatments, or surgeries...I'm sending out postitive energy into the universe for you...
To those, like me, waiting to begin chemo, enjoy the holidays....don't think about it or let it worry you as worry only takes away precious time that can be better used doing something way more fun...like drinking a good glass of red wine or a cranberritini with appetizers guaranteed to be 'bad' for you, and the love and laughter of friends and family.
My sisters and friends are all convinced I haven't experienced much pain with my bilateral mastectomy with immediate expander placement-15 days ago- because I sent it out to the universe to have each of them take on what they could for me...all of them have been saying their breasts hurt for me. Now, those are good friends and loving sisters! :-)
Just got back from the oncologist-start chemo after the 1st of the year- TAC (Taxodere, Adriamycin, and Cyclophosphamide). I'm all for the magic number three-Strike One, Strike Two, Strike Three...and you're out a there!!!!! Every three weeks is also working for me.
I wrote a poem out of the blue yesterday. It wanted to be written, and who am I to deny it that?
Cancer slinked in quietly dressed in black… unnoticed,
acting all nonchalant so as not to draw attention to itself.
Never suspecting its eventual discovery, it made itself at home.
Caught like a thief in the spotlight of modern medicine, it was
extricated from my breasts and sentenced to death.
Reclaiming what has been stolen from me is impossible;
nevertheless, I am content, for I have emerged the victor.
I have survived to tell the tale.
What more could one ask for during this holiday season? 100% Alive Today!!!!!!
Merry Christmas Jewels,
Your SIS(Sister In Survival)
Kimberly
P.S. Deb, now that I think of it, yes, I do work for the government. Technically teachers do work for the government since our pay comes from the state coffers, after each District has shaken out their budget, and I know how in love with acronyms they are...it's contagious. -
Hello there I would love to join in with you. I found my lump October Had Biop. 1 day after my 43 rd B-Day Dx on 11/26 I will get my port 12/27 and begin Chemo 1/2 I am not sure what Chemo meds I will be on yet. I am joining a clinical trail Nooadjuvant Therapy so it will depend on my group A,B or C
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Vettegal - so the drain removal wasn't bad at all. She cut the stitich, told me to take a deep breath and I had to ask if it was out!
Unfornunately my path report was not as great. I have 2 more nodes out of a total 34 removed positive. I can't believe they took two levels according to the path report and they got 34. I'm actually pretty thin, especially my arms and I guess I assumed they would not get that many.
Today I did not see a doc, just the nurse who gave me a copy of the path report. I will not go over those results with a doc until next week after Xmas. Thus I guess I need to update my profile...here's to better luck for you, Carol
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First of all, good luck tomorrow, Vettegal. I'm with Carol--take the iPod. Music is my first line of defense. I may date myself, but a personal favorite during this has been Pink Floyd's Comfortably Numb. Takes my head to another space and time. Plus the guitar riff at the end makes my heart swell. Don't forget the charger! I'll send my best vibes your way.
Carol, my heart sank when I read that you have 2 more positive nodes. You said they took two levels--did that clean out your pit, or is there another level lurking? I can't believe they gave you a copy of your report without a doc's translation. I couldn't get ANYTHING out of my nurses--the doc had to order all communication with me. So annoying. I hope when you talk to your doc that you're going to be able to stay on schedule. I did loads of waiting, myself, and it was not fun. I wish a good outcome for you.
Kimberly SIS JJ--I think you missed your calling. There must be a place where poetry like this is published. Your work deserves to be there. When is your chemo start date?
KathyL, I was glad to hear the MUGA was uneventful. I'm taking Decadron, too (isn't that one the steroid one? Can't remember.), but that's the only drug on your list we have in common. It sounds like you're ready to go, though. Good for you.
Welcome, Twinkly. You must be in Canada or Europe, taking FEC. We're happy to have you in our group.
Some bad news here. My oldest daughter, home from college for break, went to the high school to p/u her sister for me today. On her way, a kid on a scooter shot off the sidewalk into traffic and hit my daughter's car. He started on the bumper and flew off his bike into her windshield--shattering it with his helmet. Luckily, he was not hurt (thank God for the helmet), but my daughter is totally traumatized. The kid is kinda sketchy--told the cops he was 16 so he'd be the legal age to drive the scooter, but turns out he's 14. Then gave a bogus address to the police. Our insurance company is warning me that there is probably no insurance on their end, so our uninsured motorist plan will pay for the damages and even tho they say our premium won't increase since it wasn't her fault (fortunately, at least a half dozen people gave statements saying just that), I'm skepical. And pissed. Now I have to get the car repaired, get ready for Christmas, go to NYC, and start chemo all in the next week. Why do I have to be tested so? Argh.
At least my dh ordered my last meal. I want ribs from the Rendezvous restaurant in Memphis. So we're having them delivered. How extravagant!!!
Okay, I'll get off my rant. Thanks for the read.
D1
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D1 - as easy as it is for me to say, try your darndest to have a great time in NYC. I'm not the first to say that cars can be repaired and as long as no one is seriously injured, you have other things to put your energy towards. Hoping your daughter can erase this ugly memory as well. We as well have two daughters (my step daughters) home from college, it was pretty funny as they noticed no gifts under the tree, I said "that is a correct statement", and laughed. We're planning on alot of gift certs. this year.
I personally celebrated having my drain removed with a couple small glasses of vino tonight and a steak dinner. We've been lucky to have friends bring food all week long, but I hate to say it, I can't do another casserole at this point. I'll deal with the reality of more nodes involved tomorrow!!! Carol
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Carol and D1... man does that all suck. I feel for you both. Remember though, it has to get better after something like this... and truly you are only handed what you can handle. I hope you both can enjoy your holidays. And Carol, remember-- better to know about the xtra nodes and DO SOMETHING than not know they were lurking there... knowledge is power I say.
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Hi Everyone,
I go back to my oncologist Dec 28th and thats the day I guess I sign off on my life too. I will find out what kind of chemo and for how long and if I need a port or not. I have had 2 lumpectomies and SNB, and they are telling me they finally got it all out of my breast, I have my clear margins. And I also had a biospy above my nipple, no cancer found. So in Jan I'm chemo bound! The reason why I was told i'm having chemo is because of the size of my tumor, it was 2.3 cm. So I'm ready to join everyone, hoping and praying its the best year for all of us. Everyone have a Merry Christmas!
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I do agree with KathyL, Carol, better to figure out the node thing now and get it taken care of.
I had a moment today. I decided to treat myself before we head off to NYC in the morning and had a mani/pedi (I'll get the car to the shop later--I come first!). The girl was so sweet. She's Vietnamese and doesn't speak much English (and I speak no Vietnamese), so I was content to lean back and close my eyes like I used to see my mom do (that always annoyed me cuz she looked so stupid!). Suddenly I hear the girl tell me how pretty my hair looked. Oh schnap! Almost lost it. All that kept looping through my head was f me, f me, in 3 weeks' time it'll be gone! I seem to be going one step forward, then 3 steps back with my mental prep on this. Guess I'll get there by Thursday!
If I don't wander back in tonight (my kid has a basketball game), then I'll see you all after NYC.
Have a great weekend.
D1
Vettegal--thinking of you.
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D1 - enjoy your weekend and time with your family, we'll all be here when you return home!!! Carol
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Good morning Jewels,
D1-Thank you for your compliment regarding my poem...I don't know if there is a thread for that or not.
Carol-WhooHoo on the drain removal. Wasn't it a relief. I got mine out yesterday. The node thing-3 of 34 is not a bad number at all considering the percentage of positive to negative, 9% neg to 91% pos...in my profession you've earned yourself an A. ;-) I have 4 of 10, but even with 40% to 60%, I'm sure between the chemo and radiation that will take care of any lingering cells. You'll be fine, sweetie, I'm sure of it. I'm wondering why they took so many nodes. Did your surgeon do the blue dye sentinal node test while you were in surgery? I knew I had a tumor-in situ in my nodes, so I knew some would be removed, but the test apparently showed her that only 10 needed to be tested. I suppose if more had come up positive, I'd have had to go back in for more lymph removal-thank goodness I passed by the skin of my teeth with a 60%. :-)
Welcome WVgirl and SheShe48. OK, so Miss Acronym, here, has more to learn. What is ANB and SNB? JJ?
How did you get hooked into the medical trial SheShe?
Got my treatment option- my cocktail-to be referred to from now on as my chemo-tini- is a combination of Taxotere, Adriamycin, and Cyclophosphamide (TAC). I'll start soon after the new year, but won't know until next week exactly what day-the oncologists office needs to get approval from my insurance company. Radiation will follow that daily for 4 to 6 weeks.
Take care my sweet sisters.
Your SIS(Sister In Survival)
Kimberly -
Kim:
I have a similar chemo-tini: I'm doing taxotere and cyclophosphamide (cytoxan), and herceptin. We can share info along the way. I start Jan. 16. Are you getting a port?
I think SNB is sentinel node biopsy... at least that's how I refer to it. Don't know what ANB is though.
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Kimberly, I think the doc was surprised himself as to how many nodes were found. They did not do the dye test, my incision is about 2 inches long. While reading The Breast Book, Dr. Love talks about everybody having different amounts of nodes. I guess the pathologist also makes a difference in those numbers with how thorough they dissect the specimen. The surgeon (who called last night at 9:00pm) told me that its easier to find the nodes when your thin, they don't have to look through the fatty tissue so much. Yeah, for skinny armpits!!!
I meet with the onc next Thursday to discuss my cocktail, and I have a second opinion scheduled for the following Monday with the Seattle Cancer Care Center. I figure it won't hurt to hear two opinions.
Until then, hope you enjoy your holiday, Carol
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ANB, I'm assuming that the reference is to Axillary Node Biopsy (or Dissection).
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Kathy, I had my port placed during my bilat w/expander surgery.
Carol, glad to hear your doctor is on the ball! I hear that people have different numbers of nodes as well...isn't the human body an interesting thing? I have an identical twin and we joke around a lot about splitting things...we may have split the number of nodes we have...we know we split a bladder as we both have the bladder of a peanut (not literally, just that we never pass up a good opportunity to pee). :-)
Thanks for the clarification on ANB, so SNB must be sentinal node biopsy. Still don't know what JJ means....it's not a cancer related acronym as I've seen it used in regular email.
Your SIS,
Kimberly -
hi jewels, back from my surgery..
came home yesterday really sore. Got percocets for pain. i wanted to tell everyone HELLO..my hubby is taking care of my drain. I going to take off the bandage this morning to see how big the cut is and finally see the drain.I have missed so much on the boards, hope everyone is well...i will try to talk later...
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Hey Sweetie, so glad you posted. Glad to hear all went well. Rest and let your loved ones take care of you...recovering from surgery takes energy. Let us know the results as soon as you know...here's to negative nodes!!!!
Your SIS(Sister In Survival)
Kimberly -
Welcome back vettegal! Hope the percocets keep you comfortable. One big step done-- next will be getting that darn drain out. But remember, for now it's your friend. At least you're home; I found it much more comfortable being home:)
Does JJ stand for "just joking"???
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I guess I'm in the club too.
First chemo is 12/27. Dose dense (AC 4x2 weeks). Then probably Taxol, maybe Taxotere. Won't know about anything else til final biopsy results come in (er/pr, her2/neu).
Had chemo training last week.
Scared of the nausea. That was the only bad thing about getting the port put in -- they gave me Fentanyl and it made me feel very very sick when I woke up. Next time no pain med. Give me a rag to bite on. No narcotics.
I'm doing chemo before surgery, so they can't nail the stage: they figure 2b/3a, since they can't tell how many nodes are involved. They may never know, as the chemo may clear up some of them. The primary tumor is 3.1 cm and IDC. The axillary node is 2.4 cm. It may be a matted aggregate of nodes.
I wanted a second opinion but can't get any appointments until mid-late January. By then I'll probably be through AC. What would be the point? Plus no one wants to consult without having full pathology results. I don't want to delay treatment that long.
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Welcome to the Jewels LJ13. Bummer about having to do chemo first before even knowing much about what you're dealing with. It is so interesting how everyone's treatment plan is so different. I had three tumors-the first detected by annual mammo, the second and third by PET scan and confirmed by MRI.
Two in the breast and one in the axillary node.
I hope all goes well for you on the 27th. Keep us posted. My chemotini doesn't occur until after the first of the year. I should know the for sure date by next week.
Kathy-I don't know if JJ means just joking...maybe D1 will let me know when she returns from NYC...
Hope you're having a great time D1...I love NY. Even though I've only been one time, it left a lasting impression.
Your SIS(Sister In Survival)
Kimberly
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