Diagnosed with cancer

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When I was diagnosed with breast cancer in 001, I did not realize all the changes that were to happen to me in just a short time.

In less than a week after I was diagnosed, a port was surgically placed, and chemo was started. Then soon there were to be side effects. Side effects happen as a result of chemo attacking fast growing cancer cells. Other fast growing cells in my body that were also attacked were in my blood, mouth, nose, intestinal tract, and hair.

I was given medication to help with nausea and vomiting, prer to taking chemo, which helped me greatly. The hair loss started within a week of my first chemo treatment. I remember my grandchildren and myself playing in the living room, something I could still do at that time, when my granddaughter pointed down to her toes and there wrapped up in her toes was some of my hair. Needless to say it was time to go to the beauty shop to have my hair shaved. Luckily for me my hair loss was not as traumatic to me as it was to some of the other women. I chose to wear a cap that my daughter had gotten for me, and inside my home I chose to go bald. I was a real beauty.

Infections were hard for the doctor to fight and diagnose, because the chemo attacked the bone marrow, which produce the white blood cells. My immune cell count was low and I ran a high risk of infections. I had an infection, which took three weeks of taking antibiotics before it cleared up, and the doctor never did know what it was.




The fatigue was something that I could not have comprehended. I was so weak that I could hardly walk without holding on to the furniture. No matter what I did I was out of breath. I could not go outside without someone to help me get back in the house. The steps into my home are only about six inches high and I did not have the strength in my arms or legs to get up them. I still have not regained all my strength back. At times those steps still look and feel like mountains.

Memory loss was a side effect that was hard for me to deal with. The best way for me to describe it would be to say that is sounds a lot like how Alzheimer’s is described to me as. I called it chemo brain. I would see a friend at church whom I have known for years and not remember their name or where I had met them. I could not remember doing things like when I last ate. As a matter of fact, I could not remember most of anything, which was very frustrating. There were times when I would be asked a question and I had to think on how to answer it. I still have a little memory loss, and at times, it is hard for me to concentrate. Like writing this paper because it takes a great deal of thought and concentration. It is very easy for me to lose my train of thought.

The way food tasted after chemo was also hard to get use to. Everything had a metallic taste or tasted bitter. There were many foods that I just could no longer eat because they did not taste good anymore.

When I was taking chemo, it was very hard on my body and there were many side effects. Some of the side effects were irreversible, and others tended to fade away. Those that were irreversible I have learned to live with.





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