Hi ladies who are suffering from what I liked to call "rock boob syndrome". I wanted to post this as someone who had tissue expanders in for 8 months, gone through exchange, and seen the other side of it all.
1. I know tissue expanders suck. They are severely uncomfortable and you feel like a weight is on your chest constantly. Sleeping on your side is uncomfortable and sleeping on your stomach is impossible.
I am among the women who was first diagnosed with breast cancer that was Stage 2 with nothing in the sentinel nodes and then 2 1/2 years later found out the breast cancer had spread to bones, liver, lung (Stage 4). The first time I didn't want to know anything about women whose breast cancer had recurred and metastasized. It was too scary. The reality is that many of us (~30%) will have a recurrence.
I find that I get so tired from doing everyday things and can't do a lot 2 days in a row. I am 8 months out of lumpectomy and 4 months out from radiation ? Any helpful hints or ideas. I am on tamoxifen
I recently diagnosed and have surgery scheduled for this Friday. Obviously my immediate family (so now extended family) know; my close friends know; and my employees know. But I'm struggling with whether to tell others... Like my regular customers, other friends I don't see often, etc. On the one hand, I hate the pity I see when I tell people. But on the other hand, I want to shout it out on facebook for all women to check themselves because it can happen to anyone. Thoughts?
I know that we are all supposed to focus on the positive only so if this question is out of line please just disregard or ask Mary to delete it. I know that I personally started to cringe at some of the things "well meaning" friends/family/perfect strangers would say when they found out I had BC. I always tried to temper my outward response by thanking them for their kind thoughts and words because I know cancer makes most people uncomfortable, and most were at a loss as to what to say to begin… read more
Especially at work and with my teenagers. Sometimes I feel depressed. Emotionally its like a bit of Past Tramatic Stress Syndrome combine with a body that will take a year or two to get back to normalish. How do you deal with this?
I know I might ruffle a few feathers but why do people go thru chemo just because doctors say it's part of cancer. I realize there are many of you who absolutely need it but I'm also seeing it being done with women who are stage 1 or 0 or who score low on onco testing. Some are being told right at the time of dx without any further tests being done. It seems so unnecessary for some considering the side affects and long recovery time. I don't mean to anger anyone but does anyone else feel the… read more
Are you receiving advice from people who are well-intentioned, but not helpful?
I have virtual strangers telling me what diet I should be on, what plans I should make, what happened to their mother's cousin's next door neighbor 40 years ago... I know they mean well and are just trying to connect with my diagnosis on some level, but I'm not finding it helpful at all.
Sometimes I just want someone to listen to my story and say, "Wow. It stinks."
Check out this link. Gives you list of foods and meds to avoid while on Tamoxifen and which foods help increase the affect of it.
My onco just told me to stay off herbal supplements that help with hormone inbalance. My meal replacement shake included Maca Root....so I have to make my own shakes now.
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