Calling all Stage II Sisters!!!
Comments
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Hi Raffomimi! Like voraciousreader said, this isn't a place any of us wanted to be, but thank God it's here!
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Just popping in, haven't been on this thread before. I am stage IIa. Still trying to figure all this stuff out.
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Hello all new to this thread, I'm stage 2, no surgery yet, on last half of chemo on Taxol weekly had 3/12 so far.
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Hard to believe a little over a year ago I was dx with Stage II B/C at the age of 50. Almost 3 weeks after dx had lumpectomy. With a low score from the oncotype DX I did not have to have chemo, only 6 weeks of radiation, and 2 years of tamoxofin before switching to a differnt one.
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Hello everyone I am just sooo....happy to find this thread. I now have a home here. I have posted on several threads but have always just felt as it I was just visiting. I would love to join you girls. I was dx on 11/11/11 with stage 11a, My Oncotype was 2 so I didn't do Chemo. Still worry if that was the right decision. Thinking maybe I should have thrown the kitchen sink at it. I hope those people who do the onco test know what they are doing. I had a nipple/skin sparring BMX on Dec 9th with TEs and the exchange was done on Feb 16th. Everything went well and I am healing. I don't like the looks of my new foobs though, they are uneven and have indentions in them especialy the side that had BC. I want to complain but then I think they may not be pretty but hey there is no BC in them right. I am on Tamox and have had several of the SE's, Hot flashes, joint and bone pain...ect... again not realy complaining because its keeping the stray ba@#$rd's away right. So gald to meet you all and hope eveyone is doing well tonight
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Welcome naan and Janie.
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Thanks Christina for the welcome. Hope everyone is having a really good day
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Hi Ladies,
I am stage IIa and just had my one year checkup. All labs normal!! I am so relieved and I am beginning to think it was all just a bad dream..Anyway, I am also a year out of chemo and I feel just great. There is light at the end of the tunnel, and most times I don't even think of the dark days. I am back to sleeping soundly, altho I have mega hot flashes. Life is precious and I am enjoying every minute.
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What is your secret to sleeping soundly? I haven't had a good nights sleep in months. Night sweats make sure of that. Glad things are going good for you. Enjoy life!
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Paula congrats on your good 1 year results!!!
I am stage II as well. I am at the "1 year since my hair fell out" mark.
Which was extremly tramatic for me! Good news is that it is growing back...just not FAST enough for my liking!
I am very lucky when it comes to sleeping...I never had a problem sleeping. If anything, I had the opposite, I would need to sleep 10 to 12 hours every night. I do have the hot flashes, but they are manageble.
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Hey stage II ladies. I am going in for an MRI to look deeper into what is causing this breast infection. I passed my one year since diagnosis. Now approaching my surgery day anniversary on March 15. Wow. Hair still short, but alive and kicking .
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Congrat!!!! Paula, Cyborg and FLwarrior on the one year mark. I am looking forward to my 1st year cancerversery.....
Cyborg good luck with your MRI. Let us know how it goes and I hope you figure out whats going on so you can get rid of the infection once and for all
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Hi Girlies,
Just checking back in to see how everyone is. Greetings to all. Best wishes to you Cyborg with your MRI.
Blessings
Maria
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Hello Raffomini gald you checked in. Are you doing ok?
Cyborg have you had your MRI yet? I hope the infection is getted betdter
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Hi ladies, Hope all is well with you all!
Cyborg, Hope your infection is getting better! Best wishes on the MRI.
Naan, How are you doing with the chemo? I hope you are tolerating it well.
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{{{{{{{Cyborg}}}}}}.
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Helooooo FLwarrior glad you are doing ok. I bet the weather in Fl. is starting to heat up
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Hello all I am stage IIA recently diagnosed, had lumpectomy and ALND and start chemo Monday. 6 rounds every 3 weeks then RADS, then hormone therapy. It is so good to read of so many a year or two out who are doing so well living life...thank you for sticking around to share.
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Hi Stacie,
I just passed my 3 year cancerversity -- I had a similiar diagnosis -- 6 sessions of TAC (Taxtor-Adriamycin and Cytoxan) followed by seven weeks of radiation. I've been on Femara since November 2009 -- getting close to the half way point on the hormone treatment.
I've been relatively lucky with side effects and have graduated to yearly visits. It does get better.
One thing I found helpful during chemo was to do something fun and totally unrelated to the cancer the weekend before the next treatment -- when I had the most energy, like a movie. Before the last one I took a improv class with Second CIty it was a hoot.
Pretty much the basics are drinking lots of water, get enough protein ( the Boost and Ensure drinks with extra protein are good when appetitie is weak). I also found that eating Greek yogurt helped to prevent getting thrush during chemo.
It's kind of like an obstacle course, but you've got lots of cheerleaders who've run the gauntlet before. Listen to your body and know we're all rooting for you.
All the best,
Meg
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Hi Janie, Thanks. The weather here has been absolutly beautiful!!! It gets warm in the afternoon, but not too hot...yet. I like it and have been enjoying it.
Cyborg, how are you doing? Healing thought to you.
Stacie, Welcome, but So sorry you have to join us. What chemo regimen are you having? I had 6 rounds total. The first 3 were FEC and the last 3 were taxotere. I agree with Megadotz, it is good to plan something FUN to do the week or weekend prior to each treatment. You will be feeling better and your blood counts will be back in the safe range.
Megadotz, Congrats to you on 3 years!!!
Hi to everyone and hope you are all doing well.
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Every 3 weeks x6 plus 4-6 weeks of RADS. NOT sure which chemo. I find out Thurs. Waited to ask so i could worry about specific SEs later LOL
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Well I just wanted to stop in and check on everyone. I hope everyone is just busy with there lives and the beautiful spring weather.
Stacie I am so sorry you had to find us. I am hoping you get through the chemo with little SEs. I think you will find lots of helpful information here and on other threads
Megadotz. Congrats on your 3 years!!!!!!
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Glad to meet you all. IIA here. I've had my lumpectomy. With an oncotype score of 9 my MO isn't recommending chemo. But I need to do rads (30 treatments) and tamoxofin to finish.
That is I will do rads if we can manage to get a setup that will work for me. Rad techs have tried 3 times and the RO doesn't like any of them (flat on back, on back at an angle, and prone) We try again next week. (I have no idea what they think might work? Standing on my head maybe?
I also have no idea what the next step will be if we don't manage to get a rads setup...
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Janie bug- thank you and the MRI turned outnormal. Do I still need to do a mammogram
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Cyborg. Yipeeee!!!!!! I am so happy that your MRI was normal. Im not sure if you need the Mammogram or not.
Cindy it is nice to meet you Congrat!!! on the low oncotype score of 9. Good luck nx week if you have to stand on your head make sure you are not wearing a dress....LOL
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Hello, do I get extra credit for being STAGE 2a twice? I have the uniqueness of having 2 primaries. 2006 and 2012- Both IDC, both ER/PR highly positive, HER2 neg and in mirrored locations in the right and left cleavage quadrants. And as many of my doctors have told me breast cancer does not hop from breast to breast... My original BC had an OncotypeDx of "0"...which is for mets not a new primary.
I have 5 sisters and my mom and her 8 sisters all of whom have never had breast cancer.
I may have isolated a contributing cause as i had midline chest xrays as a 6 week old neonate and xrays ( according to the radition oncologist) just weren't like they are now back in the fifties.
I will be genetic testing and counseling just for family peace of mind.
My anxiety level is much improved since i got good PET scan results and now i await my surgery...
Its not like i don't know what to expect.....
Glad i have found a new home! -
Hello, do I get extra credit for being STAGE 2a twice? I have the uniqueness of having 2 primaries. 2006 and 2012- Both IDC, both ER/PR highly positive, HER2 neg and in mirrored locations in the right and left cleavage quadrants. And as many of my doctors have told me breast cancer does not hop from breast to breast... My original BC had an OncotypeDX of "0".
I have 5 sisters and my mom and her 8 sisters all of whom have never had breast cancer.
I may have isolated a contributing cause as i had midline chest xrays as a 6 week old neonate and xrays ( according to the radition oncologist) just weren't like they are now back in the fifties.
I will be genetic testing and counseling just for family peace of mind.
My anxiety level is much improved since i got good PET scan results and now i await my surgery...
Its not like i don't know what to expect.....
Glad i have found a new home! -
Hi. I haven't posted, because I don't want to discourage anyone who is earlier in the surgery process than I am, but I'm discouraged, so decided it's time to post. I was birads 3 for 1 year, told I had an "architectural distortion"--"nothing to biopsy", "Not to worry". At the end of the year, US and Mammo defined 9mm & 3mm tumor. Had bx and lumpectomy 3/7. Much to everyone's surpise, the tumor was 3.5cm, so chemo was on and radiation followed by aromatase inhibitors. Oncotype done, results coming next week. The problem is, unclear margins. Had re-excision done 3/23. Unclear margins again. This time DCIS, two separate pockets. Now my options are another re-excision, but if margins are unclear, MX, or go directly to MX. My problem is, I do no trust US, Mammo or MRI to screen my breasts, as they did not find tumors, size correctly etc and am having trouble making the decision--don't know if I want to leave breast tissue. Am I thinking clearly about this? I know you have been through lots and heard it all and any thoughts you have would help. Thanks.
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Hi All!
First, so glad to find you all. I feel better already reading the stories and hearing all of your words of encouragement to each other. I feel like I am among family here.
So this is actually my second round with BC. First time was in 1999 - Stage 1 DCIS. This most recent diagnosis was made on 3/22 - Lumpectomy 3/19 -Stage IIa IDC - Sentinel + 1 nodes clear. Waiting to see my MO on 4/9 and waiting on Oncotype results to determine treatment plan.
So I have a weird one for anyone who has a thought. I am post menopausal. Got through that shenanigans over 2 years ago. Did not experience the hot flashes etc...got through it pretty smoothly.
However...in the last 2 days or so, I have felt definite "hot flashes" while sitting or doing nothing of significance. Comes on fast...really hot... then goes away quickly. I haven't started any treatment yet...only thing that is different is the tumor and nodes have been removed. Just seems odd...
Any thoughts??
Again, so glad to find you all! Will not take this ride alone this time.
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Dorrie.. I would find it unlikely that you are having hot flashes due to a lumpectomy... My flashes started on chemo, stopped when chemo stopped and started again when I started Tamoxifen (not as bad though)... Maybe you are pyscho-symmatic?? Or experiencing an untimely menapause SE?
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