The Cancer Survivors Network (CSN) is a peer support community for cancer patients, survivors, caregivers, families, and friends! CSN is a safe place to connect with others who share your interests and experiences.
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
-
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!
-
Discussion Boards
- All Discussion Boards
- 6 Cancer Survivors Network Information
- 6 Welcome to CSN
- 122.5K Cancer specific
- 2.8K Anal Cancer
- 455 Bladder Cancer
- 311 Bone Cancers
- 1.6K Brain Cancer
- 28.6K Breast Cancer
- 407 Childhood Cancers
- 27.9K Colorectal Cancer
- 4.6K Esophageal Cancer
- 1.2K Gynecological Cancers (other than ovarian and uterine)
- 13K Head and Neck Cancer
- 6.4K Kidney Cancer
- 681 Leukemia
- 802 Liver Cancer
- 4.2K Lung Cancer
- 5.1K Lymphoma (Hodgkin and Non-Hodgkin)
- 242 Multiple Myeloma
- 7.2K Ovarian Cancer
- 69 Pancreatic Cancer
- 493 Peritoneal Cancer
- 5.6K Prostate Cancer
- 1.2K Rare and Other Cancers
- 544 Sarcoma
- 743 Skin Cancer
- 659 Stomach Cancer
- 192 Testicular Cancer
- 1.5K Thyroid Cancer
- 5.9K Uterine/Endometrial Cancer
- 6.4K Lifestyle Discussion Boards