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10 years since my 3rd cancer

Breast Cancer | Last Active: Jan 3 12:02pm | Replies (6)

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I was diagnosed with stage 1 right breast cancer in 2020. I have a history of very dense small breasts with a history of benign breast tumors and cysts in both breasts. In 2024 I had my yearly Diagnostic mammogram, of my left breast. A cancerous tumor was found. I was given a breast MRI for the first time in my life, to see the extent of the new cancer. It was stage 1, but it is a much worse, fast- growing type than in my right breast. I was told that if I had had a breast MRI in 2023 the cancer would have been found a whole year sooner. But it just isn't part their protocol. It enrages me.
More tumor cells were unleashed into my system during that time. If I had a little more money, I would have a no- contrast, MRI of my trunk area once a year. A person can negotiate a price. Private Open-MRI clinics are supposed to be the cheapest. They rather get your money than not be making any money for 45 minutes. My care is now is either my N.P. or I feel a localized lump on or near my mastectomy sites or nearby lymph nodes, OR I report to them when I have, basically, terminal signs: yellow skin because of liver cancer, pain in my spine because of bone cancer, pain in my lung and breathlessness because it has spread to my lungs. With an MRI once a year, maybe I could find it at stage 3. With the new blood test, RGCC test, which I would have to pay for also, I might have a fighting chance. Please anyone who can afford to pay out-of-pocket less than $2,000 a year, think about adding this to your care. And give input here. I Am Not Cancer Free. No one is, until there are vaccines. vacinecancercoalition.org

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Replies to "I was diagnosed with stage 1 right breast cancer in 2020. I have a history of..."

@colely It Is cancervaccinecoalition.org.

@colely
I’m so sorry your breast cancer is back. I can’t believe they still do not have you getting some type of imaging regularly. Everyone seems to have a different protocol. My recurrent breast cancer came back 3 times as aggressive as the original. I’ve always had regular imaging ordered by my oncologists. I still have a chest CT every 6 months (although I also have neuroendocrine lung cancer). But I also had abdominal and pelvis CTs every 6 months for 4 years until this year they stopped due to radiation exposure. He thinks cancer cells likely got away before the tumor was removed from my chest wall but you know that’s just a wait and see since it takes about a billion cancer cells together to be seen on a scan. I took Kisqali for 5 years and will be on Letrozole for life since my BC is highly hormone driven. I’m glad to be off Kisqali for a few weeks now but it’s also a little scary to go off. It’s hard on the body and it’s nice to see all my blood counts back to normal now. I had a negative breast MRI and negative Signatera test before going off Kisqali. I pray that none of us will see another BC tumor. ❤️