Rhonda

"This diagnosis has impacted my life tremendously.”
This diagnosis has impacted my life tremendously.
I am still going back in my mind thinking about what could have happened to prevent this second diagnosis. Is it something the doctors DIDN’T do, is it something I was suppose to do OR NOT to do after I was told I was “CANCER FREE”?.... These questions play in my head daily.
I am married with children and grandchildren, and I can’t bear the thought of not being here with them. My PCP asked my husband to inquire from my Oncologist what my prognosis looks like. I told him to not ask that question. If given a timeframe, that would devastate me. I’m still working and living my life the way I did before the diagnosis, but it most certainly is a “new norm.”
In June 2016 I was diagnosed tripple negative breast cancer recurring cancer.r in my brain lungs stage 4
I was originally diagnosed with stage 1 breast cancer in 2011. I made it six years when I noticed pain in what I thought was my kidney (I do have a kidney disorder). My family doctor found nothing, and he sent me to my urologist.
I was a 54-year-old lady when I went for my first mammogram, and it came back positive for estrogen-fed breast cancer. Scans showed it had already gone to my spine, my chest cavity, then it started a mass in my arm.
I was diagnosed in April 2018 at the age of 32. I fully believe a positive outlook and strive to survive are crucial to fight this.
In March 2016, I had DCIS Stage 0. I was treated with a lumpectomy and radiation. Ten months later during my routine mammogram, they found more cancer.
Nine years later, I went back to the doctor with arm pain. I was told it was most likely not breast cancer. I insisted they do a scan, and sure enough, cancer.
There are some days that I feel very upbeat in conquering this disease, but then there's times where my liver might be painful and it drags me down. I know I might not live much longer.
This diagnosis has impacted my life tremendously. I am still going back in my mind thinking about what could have happened to prevent this second diagnosis.
I was transferred to UCC in Chicago on November 13, 2018, and have seen ENT so far. My next appointment will be the December 1 for the gyno team. This is ridiculous and never-ending.
After months of not feeling well, I was finally diagnosed on June 1, 2018. I don't have any family history, and genetic testing was also negative.