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Re: NEW Oncotype Dx Roll Call Thread
Hi RomWriter - I just wanted to tell you that I too thought I would just have radiation and be done with it. I had four different drs. tell me that. Turns out because I had one node positive and my tumor turned out to be twice as big as they said it was I ended up having to do chemo. It was quite a shock, but you know at this point (I'm 5 years out) it gives me piece of mind that I did it and have done everything possible to beat this beast. The chemo wasn't as bad as I thought it was going to be. Yes I hated losing my hair, but it's back now and all is good. Hang in there
Nancy
Re: Stage III Cancer Survivors .... 10+ Years and Out
I had to go looking for this thread. Yes, I am posting this a bit early but I wanted to bump the thread back to the top. There are some great stories here.
On November 5th, I will be out ELEVEN years! WoooooHooooo!
That about covers it. I am so thankful for every single day.
Re: Stage III Cancer Survivors........20+ years and out
I'm here too ! 21 year out this past February .Hallelujah !! A lot of changes on these boards since I Iast posted in '24.
I'm continuing to do well with N.E.D. I went off my Aromasin which I've decided that I used as my security blanket after almost 15 years . That was about 3-4 years ago. Although I did really well on that AI ..once off for a period of time I had no idea of it's impact on how I felt. I'm thankful for it but am so glad it is done.
I see a new doc who has made a few changes . I now go every 6 months rather than once a year so as to work in a rotation of Breast MRI and Mammo/US . She is very involved and I feel that she cares for my welfare.
I follow no special diet ,walk about 2 miles most days and probably drink too much wine : ) .
Looking back, never would I think I would be where I am today but an excellent oncologist and breast surgeon and GOD made it happen . Thinking of you all as you make this journey ..there is light at the end of that long dark tunnel !
Re: Poll: How does Breast Cancer Awareness Month make you feel?
Having just recently been diagnosed /w BC and not yet had my biopsy…. I really don't know what to feel. Due to personal reasons, I've kept this from my entire family/household. After Diagnostic Mammogram & Ultrasound I have a mass in my right breast and BI-RADS Category 5 - Highly suggestive of Malignancy. I continue to do research, being careful of where/whom I'm getting my info from. And have a biopsy scheduled Nov. 3rd, 2025. Of course I have more questions than answers, but at least I've tried to look into it all. After seeing all of you that have been through SO much - how did/do you do it?
