Pleased to meetcha!
I've been lurking and posting here and there, but haven't yet shared my breast cancer story.
I was diagnosed in July 2015 after my annual mammogram. They said it was a small tumor, the
size of a pea, and I was Stage 1. I opted for the lumpectomy and lo, I went in a Stage 1, and came
out a Stage 3. There were 2 tumors, the pea-sized one that showed up on the mammograms and sonograms
and a second tumor that was 6 cm across. It had also spread to two lymph nodes. It was ER positive
and invasive. I knew radiation and hormones were going to be in the plan, but chemo was added.
So I shook hands with The Red Devil - that's what they called AC and I had the Neulasta shots the next day.
My hands, feet, and nails turned black, as if I had dyed my hair black without wearing gloves. I had gone to
a barbershop and had my hair sheared off the week before I started. I don't know, I think it made me
feel as though I had some control of the situation. It made me feel powerful, but only a little.
I had 4 prescriptions for nausea, so that wasn't a big issue with me. My problem was that my blood count
kept dropping really low. I had 3 blood transfusions by the end of my chemo and I was still exhausted
all the time. Breathing felt like work to me and there were days when I had to force myself to get out
of bed. I actually kept working a full time job, but don't ask me how.
Radiation was easier. I finished two weeks ago. I'm still working on some burns and peeling skin on my underarm
and underbreast areas. I've got lymphedema from the surgery and neuropathy from the chemo. I call them my
cancer scars. Sometimes I'm depressed because I can't move around like I used to and the stinging in my fingers
drives me insane, but I'm still here. I have not yet been declared "NED" (there are nodules in my lung), but I'm
going to take it as it comes and find my little bit powerful where I can.
peony
Comments
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Welcome
Thank you for sharing your story. Your upbeat attitude and strength will inspire many. We are lucky to have such a wonderful community on this board. Many have their family members or close friends as support ( myself included), but being someone who has never known anyone personally who went through treatments, I have found that reading posts here, even if they are old posts, helps me to feel that somewhere there is someone who really does know what I am going through.
may you continue to gain strength, and as discussed on another post, I hope our neuropathy fades away as quickly as it came!
Blessings!
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