When I tell people that I have Multiple Myeloma they say, “I’ve never heard of that cancer before”. So, what is Multiple Myeloma?
Multiple myeloma is a cancer that forms in a type of white blood cell called a plasma cell. Plasma cells help you fight infections by making antibodies that recognize and attack germs.
Multiple myeloma causes cancer cells to accumulate in the bone marrow, where they crowd out healthy blood cells. Rather than produce helpful antibodies, the cancer cells produce abnormal proteins that can cause complications. (1)
Prior to me being diagnosed with Multiple Myeloma, I did not display any symptoms. At least I did not think I did but looking back perhaps I did have some symptoms. I was anemic for years, but it was not low enough to cause any worry (I was always told to take an iron supplement). My white blood count was always normal until I was admitted to the hospital in April 2020.
SYMPTOMS
There are some signs and symptoms to look for however, they vary and if you have any concerns, please consult with your physician.
Low red blood cell count/anemia
Bone pain, bone weakness or bone fractures
Fatigue
Nausea
Infections (frequent colds or sinus infections)
Kidney issues
These are a few signs and symptoms to look for and you can research for additional signs and symptoms at (3).
I rarely had sinus infections and I honestly did not catch colds or the flu. Prior to being diagnosed, I took supplements faithfully. Supplements from turmeric shots (I make my own shots), spirulina, chlorella, ginger shots (I make my own), Vitamin C & D, Probiotics, Omega 3’s and these are just a few supplements that I took. I shared this because I believe my supplements was the reason, I had a strong immune system and if my immune system had been weak, I probably would have had some infections.
The Oncologist that treated me in the ER told me that African Americans are more likely to have multiple myeloma. My Oncologist said Multiple Myeloma tends to show up around the age of 50, welp I had just turned 50, go figure. As far as I know, there is no family history of Multiple Myeloma either.
TESTS & TREATMENTS
A physician can request certain test to diagnosis Multiple Myeloma. I had an MRI and that is when I was told that I had lesions on my spine and later diagnosed with Multiple Myeloma. Other tests include, (these are just a few ways to test).
Blood test
X-rays
Bone marrow aspiration, bone biopsies CT scans and MRI’s
There are several treatments for Multiple Myeloma, and one should consult with their Oncologist about which treatment is best for you. I however did not have an option because I was admitted to the hospital for my back fractures and the Multiple Myeloma.
My treatment started immediately or should I say after the Kyphoplasty (liquid cement to fill the fractures) while in the hospital. My treatment (chemotherapy) was the best option for my Stage III diagnosis. (these are a few treatments, please research for additional treatments even clinical trials)
Chemotherapy
Immunotherapy
Stem Cell Transplant
Radiation Therapy
Hearing the words “you have cancer” scared me but I could not let fear consume me. I was in the fight for my life and I’m still fighting.
“Where the mind goes, the body goes.”
I will leave you with this, always have positive thoughts. It is not easy but do not linger around the negative thoughts. YOUR LIFE DEPENDS ON IT!