Skip to main content

Looking to the New Year with Concern

Yesterday I had an annual visit with the cardiologist. It was the first time I’d been to the hospital since the breakout of Covid-19.

 I knew I’d need to wear a mask before entering the building, since most businesses have adopted this policy since the virus began to spread.

 Entering the building, I walked to the bank of elevators. Pushing the button, I chose the floor for my doctor’s office. When the doors opened, I saw 4 large blue circles on the floor inside. In each circle, the words social distancing appeared. I was caught off guard, realizing, even in elevators, people weren’t allowed to be close.

 Stepping inside, I obediently stepped on a circle. Right behind me, a man entered. I spoke to him through my mask offering a muffled, “Good Morning.” He did not respond although I knew he heard me. Our eyes locked and his fear was evident as he moved to the far corner of the elevator. I felt like a leper.

 When we reached our destination, we both exited the elevator. I went one way and he the other.

 Walking down the halls, I glanced into glass windowed offices. Inside each were chairs spread apart, many of them numbered. Signs outside office doors notified patients of limited capacity and without an appointment, one could not be seen.  

 I went in to register, my temperature was taken, and I was asked if I’d been exposed to the virus or if I had any symptoms. Answering in the negative, I took my seat.

 When the nurse called my name, I was taken to an exam room where I waited for the doctor. Before he entered, the nurse explained I’d need an EKG. Since I’d never met this particular nurse before, I gave her a heads up. I said, “When you attach the leads, you’ll be surprised.” Her questioning look said it all, that’s when I informed her, I was a “flattie,” a breast cancer victim who’d chosen not to reconstruct. She laughed and said, “I’ve seen everything, honey. Don’t you worry.”

 The EKG only took a few minutes and the doctor came in to perform his exam. I received good news and was told I didn’t need to return for a year. Before he left the room, the doctor and I talked.

 “You know,” he said, “I had Covid-19 for 2 weeks in late March. It was terrible.” Wondering why he was sharing such personal information, I listened as he continued. “Are you going to get the vaccine when it is released?” I gave him an honest reply, “I don’t know.” He said, “You really should, you know. With your compromised immunity, you should be among the first to get it.”

 I was surprised to hear I was considered to have compromised immunity, especially after 6 and ½ years of fighting cancer, but he insisted it was true.

 I left his office feeling conflicted. My doctor was advising I receive the vaccine when it became available but I was concerned. In the first place, the vaccine had barely been tested. In the second place, I had lymphedema, which made receiving inoculations difficult. Instead of being able to receive vaccines in my arms, I needed to receive them in my buttocks. Most nurses gave me a hard time when I tried to explain.

 I wondered if the majority of breast cancer patients were being advised to take the vaccine and if so, how many would comply?

 I also wondered if many women might forego visiting their doctors during COVID-19? Would they skip having suspicious lumps checked for fear associated with catching the virus? And would all of this contribute to an increase in the number of breast cancer cases next year?

 The new year is filled with uncertainty and while we wish we could see COVID-19 completely disappear; it seems it will be around for several more months. Will the vaccine offer hope? Should everyone receive it? The decision is one that must be weighed individually but for those with compromised immunity, like those affected by cancer, it seems a no brainer, especially when doctors recommend it, but I've already made up my mind. I'm not taking it, no matter what. 

The reasons I've decided against taking it are varied, but the main one is due to the lack of time given to trials. There's no hard evidence about potential side effects and I'm not willing to be a human guinea pig. Some may say I'm crazy, and that's okay. Everyone has a right to their own choices concerning immunizations and other medical procedures. I hope you'll take time to weigh yours carefully. 

Stay safe and well.

 

Comments

Popular posts from this blog

Sometimes I just want to pull my hair out

Sometimes I just want to pull my hair out, especially when I read a friend's blog post and I just can't wrap my head around it. This morning, I was reading a post from a fellow breast cancer survivor. She said her cancer has returned and is growing in her spine. As soon as I read the words, I burst into tears. I just didn't understand! We'd been diagnosed with the same type of cancer in the same year. How could it be that her cancer had returned and mine had not? And what made it even more difficult to understand and accept was the fact that she'd chosen to go the traditional treatment route. I'd opted not to do that. She'd endured chemotherapy, radiation, and the anti-hormone therapy afterward. I'd refused chemo, had done 28 rounds of radiation, and had only taken the anti-hormone drugs for a couple of months. It just didn't compute and it certainly didn't seem fair. But that's what sucks about cancer. It doesn't follow the rules.

Cancer the gift that keeps on giving - the high cost of cancer

There's a basket of bills sitting in the corner of my bedroom. I try not to look at it as I enter the room but I know it's there. Its contents spill out onto the floor whenever my husband stuffs another bill into the basket. Usually, when the mail comes, he gets it first so he can filter what I see and what I don't see. Since he's the only one working, he takes care of our financial responsibilities and while I'm thankful for that, I'm not ignorant about our mounting bills. Cancer is expensive. Even if you've reached maintenance phase, it's costly. There are always tests to be run, blood to be taken, doctors to see. It never ends. Just knowing this will be a continual process for the rest of my life frustrates me and the alternative, death, will be my only way out. It would be nice to know that cancer could be a once and done kind of thing but that's only wishful thinking. Everyone knows cancer is a long and very involved illness. I had no id

Annual checkup yields good news!

Yesterday I went to the Cancer Treatment Centers of America for my annual check up. For those unfamiliar with the cancer treatment center, it's an integrative facility that provides services for the body, mind, and spirit. My day began in the survivorship department. While there, I met with the doctor and was asked about how I'd been feeling both physically and emotionally. We talked for about half an hour. The doctor and I had a few laughs and it was probably the most pleasant visit I've ever had. Instead of making me feel that she was the doctor and I was the patient, I felt like we were old friends just having a good chat. It was refreshing and I left her office feeling very optimistic. Next was the port lab where I have my blood drawn. It's always a challenge there because I always have to explain about my lymphedema and why it's necessary to have blood drawn from my hand instead of my arm. You'd think, after 4 years of being a patient there, they'