Any 3c survivor stories out there?

Suze 35,The treatment does seem to go on forever.  I think rads especially does because it is every day.  But before you know it, it will be over and that is a little stunning and scary in itself to suddenly be on your own so much.  Yes, there are follow ups but not like the 20 questions before treatment each time.

 Godsgirl-I am a one year TN Stage 3c fluke and hope to keep on flukin.  You must be doing something right.  Any advice?

Hi Suze35, thank you for bumping this. Survivors are out there, just busy living their lives! It is a hard day today, but it will be better. I go for my second ac tomorrow and I think I have a bit of anxiety over that also. I worry that the cancer is not shrinking, even though I have a good feeling about it and my breast seems to be a bit smaller, Never could feel the tumor, but breast did start to look a bit larger right before diagnoses. Are you done with rads? Weren't you doing more chemo after rads? Have you decided which chemo? Hope you are feeling good.

Hey ladies.not Stage 3 but I'm here anyway..with TN...sometimes I wonder if it really matters what stage you are??

Anyway...you guys keep "flukin"...may we all keep "flukin"

I was first diagnosed stage 2b in May of 2008, just passed my 3 year anniversary of a survivor.... But in Nov of 2010 I had a cough and they found the same TN BC in my right lung... I have had 6 tx of Carbo/gems and it seems to be working... I am now Stage 4 but plan on fighting this with all I have in me..

I am newly diagnosed IIIb 5/27/11. Although I have a feeling it is more like IIIc. I do remember reading the initial path report that showed invasion into breast tissue with multiple nodes and skin involvement.  My regular mammo did not show tumor, but it did showed many lymph nodes, so initially they biopsied the a node which showed ER- PR- Her2+. PET showed diffuse right breast CA with 2 small areas behind the nipple. Got a call yesterday that the main tumors that they found on MRI/Ultrasound were TNBC. I started AC last week with lots of nausea day 3/4, and a better nausea plan for next time. I'll find out today if my treatment will change at all. Was going to do ACx4 over 8 weeks, TCHx12 weeks, then surgery/rads, then finish out year with H. This is a roller coaster ride. Thought I had myself in check, but it is so hard. You women are ALL an inspiration for so many. Keep it going we need each and every one of you.

I was 1 year in March.  I am TNBC. 

I had a uni-SIEA reconstruction 2 wks ago.