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Being human Medicine Reflections on Life, Being Human, and Medicine

Mentors

I met him when I was a 4th year medical student. My military scholarship allowed me to do an elective each year at a military hospital. I had chosen to do pulmonary medicine at the Naval Medical Center Portsmouth, VA. 

I met him on my first day in the pulmonary medicine clinic. Dr. C was a Captain in the U.S. Navy. He was a specialist in pulmonary medicine. He was a southerner, complete with the soft, lazy sounding accent. I was a young medical student. We both wore the working uniform of the day which were Navy Khakis made of CNT (Certified Navy Twill). He was a Captain. I wore the single bar of an Ensign. 

We went to see a patient with asthma. Perhaps it was the pollen or the flowers in the Virginia area that were causing her problems. They always had such beautiful Azaleas each year in Virginia Beach. Regardless of the cause she had been having multiple flares of her asthma. Each episode brought her to sick call or to the medical urgent care clinic. With the flares she would get a brief course of prednisone and would improve. She had accumulated enough of these that she was in danger of being pushed out of the military.

In order to serve in the United States Navy, everyone had to have a physical examination each year. The primary reason for the physical examination is to determine if you are, “fit for all duty at sea and on foreign shores.” That is the standard for the Navy. Unlike some of the other branches of the military, the Navy feels that based on their mission, if you cannot be fit to do everything, then you are not fit for service.  If you are not fit for service then you receive a “medical board”. A medical board removes you from the military. 

Our asthma patient was being sent to us to see if she should have a medical board. She was 16 years into her Navy career. She could retire in 4 years. With the 20 years, she would have lifelong medical benefits and a lifelong pension. A medical board before that time might give her some disability payment or not depending on whether the board determined if her condition “existed prior to enlistment (EPTE).” Either way she would lose her pension.

Captain C listened to her and examined her. He asked her if she wanted to remain in the Navy. She shook her head yes vigorously. She had committed 16 years of her life to her career. She really wanted to at least get to the 20 years to get her pension. 

Captain C took me out to the charting area. We looked through her record. Charts were paper then. They travelled with every sailor from duty station to duty station. We could see every medical interaction she had ever had. We could see her initial entry into the military, every physical examination, and every clinic visit. He pointed out that she did not have any hospitalizations. Each of her asthma flares had improved with outpatient treatment. 

“Do you know what she needs?” he asked me.

“What does she need sir?” I replied.

“She needs a big jar of prednisone and to be taught how to stay away from us.”  

I can still hear his southern drawl as he said it and that expression, “a big jar…” 

Captain C took a blank consult sheet and started writing on it. His writing wasn’t neat or pretty but it was legible. On one side of the paper, he drew a picture of her chest x-ray. That was his trademark. He always did that. When he was finished writing, we went back into our patient’s room.

“I am going to try to help you finish your career. But you need to promise me that you will work with me.” He then went through a process of teaching her how to use occasional courses of prednisone to counter her asthma flares. He made her promise to not use them too frequently and to call him if the flares became too frequent. He then wrote a prescription for a “big jar of prednisone” and gave it to her.  He set her up for a follow up visit to monitor her progress.

I learned a lot in that first hour in clinic. I don’t know whether he realized it but he was teaching me in ways that went far beyond just lung disease.  

You could always recognize one of Captain C’s notes. On every note he would draw a picture of the chest x-ray. A picture is worth a thousand words. From Captain C I learned that there is a lot more that you can communicate than just the words you write. You should create a full picture of who the patient is and what you thought was going on. For a chest physician looking at the chest x-ray is key. It often means so much more than just reading a sentence about what someone thought the x-ray showed. 

In future years I found myself looking in the charts for Captain C’s notes. I would flip through the pages looking for the rough drawing of the patient’s chest x-ray. A quick look at his note would tell me a lot.  The sketch was always valuable, but I looked for his notes for reasons that went beyond the sketch.

Captain C’s words themselves were about creating a picture of who the patient was and what was going on. His words were honest and plain and to the point. They were important. When you finished reading his note, you could see in your mind and really understand what was going on.  Reading his notes, I could always hear his southern accent in my mind. He wrote exactly like he spoke which was exactly like he thought. He would even put, “I think” in the notes. 

These notes had immense value. They were not some generic worthless writing of the same stuff over and over again. The notes gave you a valuable opinion, insights and a plan for each patient. They contained the thoughts of an expert. 

We get lost today in the world of electronic notes. It is easy to use the computer to generate enormous and lengthy notes that say nothing. I get so frustrated when I see notes that require several minutes to scroll through only to find no expression of human thought anywhere in the note. I would rather have only 1 sentence that showed what the physician thought than 20 pages of computer-generated meaningless data.

We get lost in our communication with each other also. Whenever I blog I find that I write too many words. I have to go back and simplify. I delete words. I shorten sentences. I delete entire sentences or paragraphs that do not add value. The goal is to communicate. If we do that well we create a picture that others can see and understand. 

Often I fill my interactions with others with a flurry of words but only narrowly communicate. Oddly, I am worse at this when it is really important. It feels safer to bury what is really important under too many unimportant words.  I think I fear being blunt, open and honest. 

But from Captain C I learned to say what I think.  In medicine, and in life, when someone is able to do that, as humans we hungrily gravitate toward it. It is like digging through the chart looking for the rough sketch of the chest x-ray that will indicate a Captain C note. We seek it out because there we find reality and truth.

That afternoon we went to the lung cancer tumor board. This is where a group of experts get together to review cases of patients diagnosed with or suspected of having lung cancer. We talk about options and what would be the best care of the patient. 

One patient’s case was presented. He had advanced lung cancer.  Captain C spoke up, 

 “Do you know what this man needs?” He paused for effect and looked around the room.  “He needs a big jar of morphine and a fishing pole.” It truly was the best option for that patient. At that time there was really no effective treatment for him. Any attempts to treat him would just make him feel worse and were not going to help to improve his survival.

I hear people talk about their mentors. Sometimes I feel left out. 

When I hear about a mentor I imagine someone selecting me and then investing hours and hours of focused attention on me. I can’t say that I have ever really had that.

If I am honest, however, I realize that while I haven’t had one specific mentor, I have had dozens. I cherish all of them and what I learned from them. Most of them never realized how they were teaching and molding me. They likely had no idea what a dramatic impact they would have on my life and who I am.

To this day I can still hear Captain C’s voice in my head. Late at night when I am sitting at my computer trying to finish my day’s notes it comes back to me. What should we do for this patient? Should we put in an LVAD? Should we try to push to get him to transplant? Is there anything else? I read the written interpretations of the echocardiograms and the heart catheterizations. The words are empty and lack enough substance to guide my decision making. 

I open up the software and start viewing all of the images myself. As I do I start to get a feeling for what I really think is best. I could have just typed the quick note. Press F2 and select the standard language. Maybe type, “Continue current inotropes. Evaluation in progress.” 

Instead, my memory of Captain C pushes me. I push myself to put a real opinion. I hope that I can be the expert that guides the care to the best options. I start writing what I really think. I hope that will help me the next time I see the patient. Maybe it will help others who also will see the patient?

I saw another patient in the office. He was elderly and frail. He was failing. His heart failure was causing more and more problems for him. The easy path would be to put him in the hospital. I worried that if I did so he would never go home. Being in the hospital is hard on people. We do all sorts of tests on them. With each test we make them “npo” (not able to eat). They come back from the tests exhausted. As hard as we try to keep the wards quiet, there are noises in the night. They never sleep well in the hospital. I have seen so many patients get admitted and then not go home or go home just a shadow of who they were before.

“Do you know what you need? You need to not let me hurt you by putting you in the hospital.” The patient doesn’t know but in the back of my head I can hear a familiar voice complete with his southern accent,  “Let’s come up with a plan to keep you away from the emergency room and the hospital.” 

After we come out the exam room, I explain to the student who is with me that there is some data showing improved survival duration with hospice. “What this patient needs is a big jar of torsemide (a diuretic) and to be home with their family!” 

I try not to say it with an accent, but in my head is Captain C’s voice, southern accent and all. 

I hope he would be proud of me. 

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Being human Medicine Reflections on Life, Being Human, and Medicine Updates on my health

A COVID 19 Diary: What Was It Like For Us?

My Apple Watch vibrated my wrist. We were at home at dinner, but I looked anyway. A new MyChart result was available. I pulled out my phone and clicked on the alert and the app opened. I was nervous. I waited for what I had thought would be reassurance.

COVID 19 PCR: Detected.

You have got to be kidding me. Really? 

Now what? This led to a whole cascade of thoughts and events. But let’s go back a few days.  

On the weekend before I felt good. I was busy and active. Sarah was feeling sore and achy. She had however had a good workout via her trainer (virtually over zoom) on Friday. Sometimes she pushes it too hard and she can feel it for a few days.

Monday evening the temperature outside dropped. It felt chilly in the house. That is not unusual with a sudden shift in the temperature. I put on a sweatshirt. When I went to bed I still felt a bit chilled. I was happy to be under the covers. I slept fitfully but that also is not unusual with my adrenal insufficiency. In the morning I pulled out our thermometer and checked my temperature.  98.0 on my forehead and 98.6 in the ear.   I was fine.  I completed my hospital questionnaire. Muscle aches = not new, usual. Fatigue = not new, usual. No fever. All was good.  I was careful to distance myself from others. As usual I used hand cleaner on my hands obsessively all day. I was also careful to not have close exposure to patients. I of course wore a surgical mask all day.

Tuesday night I got the same sweatshirt out of the closet and put it on. At bedtime again I felt chills (this time worse) and pulled the covers up to my chin. Could this be COVID? Or was this just a minor cold virus or even just my adrenal insufficiency? In bed I grabbed my phone and scheduled a COVID test for the next morning. That next morning, I felt about the same. My temperature was 98.6 on my forehead and 99.0 in my ear. The questionnaire again: Green checkmark (good to go to work). This time I wore an N-95 mask plus a surgical mask over the top. I did even more obsessive handwashing and use of hand cleaner and efforts to distance myself. I left the hospital briefly to drive to the testing location to get my COVID test and then returned to work. When I had the option, I closed myself away in a private office space, just for an added level of safety.

One of the hard parts of this pandemic is the constant worry. 

Minor symptoms suddenly made me worry that I could have the virus. Could I be the one to transmit it to others? Every cough caught my attention. Should I get tested? Or was I wasting resources getting the test done? Or should I have had the test done the day before (after the first night of feeling chilled? Should I be at work? The questionnaire told me I was ok. But what if I really did have COVID?

My biometric tracker (Oura) told me that I should be taking it easy. It had noted that my average temperature while sleeping was 2.1 degrees above normal. It still did not meet the criteria (temperature 100 degrees or greater) from the screening questionnaire from work. 

That afternoon, I called to check on my mother. My father had died the week before after a long fight with cancer (not COVID related). I wanted to see how she was doing. She told me that my niece who had come for the funeral had been having chills and feeling feverish. She was being kept in isolation in one of the upstairs bedrooms in the farm house where I grew up. I reassured her. Our symptoms seemed pretty minor. I told her that I had been tested that morning and I would let her know as soon as I had a result.

This was actually my 3rd COVID test. I had been through this routine. I knew how it went. 1. Anxiety and questions and decision to get tested. 2. Waiting for the result. 3. The vibration on my Apple Watch or my phone and then 4. The feeling of relief when the test was negative.

But not this time.

Really? Really?

I spoke with Margaret and Sarah. They too were having symptoms (achy, tired, not sleeping well, and some minor cold like symptoms).  Probably all 3 of us had it.

What next?

  1. Notifications: Openness and honesty is always the best policy. We systematically notified everyone we had been in contact with over the past few days, even if those contacts were “safe” (both of us masked and at a distance.)  That included notifying my division chief and those responsible for finding people to cover for me at work plus everyone I had worked with.
  2. Where? Obviously we began trying to figure out where, when and from whom we contracted the virus. This is not easy. The true answer is that we will never know. We did not have any high-risk exposures that we were aware of. We had thought we were being careful. Maybe my father’s visitation or funeral?
  3. What next? This is of course a bit scary. Were we going to have mild cases? Or would we get very ill? I got on Amazon. I thought someone would have put together a COVID kit. Here is what I would put in a COVID kit: Thermometer, pulse oximeter, Zinc, Vitamin D, and maybe some Vitamin C and an incentive spirometer? I didn’t find any COVID kits. I ordered a pulse oximeter. I am not trying to give advice on this, but our approach was: Rest, trying to get up and walk around regularly, Tylenol or naproxen as needed for fevers and myalgias, monitored pulse oximetry on all of us and consider: Vitamin D, Zinc, aspirin. I called my mother and sister and gave them the news. Ultimately we decided that my niece very likely had COVID. The smartest thing then would be to bring her to our house so that she could isolate with us rather than exposing my mother and sister and brother who were staying at my mother’s house. 

The next day we all felt worse. Every muscle in my body hurt. I was exhausted. It was a challenge to get off of the sofa. Each time one of the dogs wanted to go outside or come in, it was an event. We would decide which of us would take the energy to open the door. Sarah and Margaret did put together a wonderful Thanksgiving dinner for us. While the turkey cooked we remarked how wonderful it smelled. Sarah suddenly couldn’t smell it. She went to the oven and opened the door. The heat and steam from the turkey hit her in the face. She still couldn’t smell the turkey. Fortunately, she said that she could still taste it when we ate but over the next few days she noted things either not tasting or tasting, “off.” 

My Oura ring told me I had fevers for a full 10 days after that. I was in isolation at home. The next week I did virtual visits (computer office visits with patients) from home. Fortunately, the schedule was light. I would see a patient and then lay on the sofa and nap. I went back to the office 2 weeks after the start of my symptoms. I had never truly had a fever (nothing above 99 degrees). My Oura ring indicated that my temperature was back to normal for at least 48 hours before I saw any patients. 

For me the worst of it lasted for a total of about 3 weeks. My first week back at work I was still very tired. I napped before work, at noon and immediately after work. I went to bed early. By the following weekend I was feeling better. Oddly, I have been doing reasonably well since, at least compared to my chronic adrenal insufficiency symptoms. I have sometimes wondered if the COVID made my right adrenal gland finally wake up? I continue to take my usual steroid replacement doses but have been functioning fairly well over the past several weeks now.

Sarah still is not herself. Her sense of smell has not yet returned. Her sleep patterns are disturbed. She wakes frequently and struggles to get a good night’s sleep. She is trying to be busy and active but finds herself getting tired very quickly. She is still achy. They talk about “long COVID.” This is apparently the observation that for many people recovery can take weeks to months. We continue to pray that she (and Margaret) would return back to normal.

I have had some benefits from having had COVID. It is reassuring to think that at least for a few months I am likely immune. This is not absolute, but I have told people that at least for now I am probably the safest physician at work. I am very unlikely to get COVID or transmit COVID to anyone. I of course still wear all the PPE. It is however reassuring when I am in an exam room with a patient and their mask inevitably drifts down onto their chin that I am not likely at risk. It also seems inevitable that patients will wait to mention COVID like symptoms until the end of their visit (after I have been in the exam room with them for 20+ minutes). It is also nice when I feel the familiar adrenal insufficiency symptoms of diffuse muscle aches and fatigue. At least for now, I am reassured and don’t feel like I need to go and get a 4th, 5th or 6th COVID test. 

I got my COVID vaccine on December 22. I wondered whether or not I should get it. I tried to research it. Most experts say that the protection from the vaccine (because it is against the spike protein) is probably better than the protection that I have because of having had COVID. I asked if I should wait at least 3 months. Some health systems are doing that. I also wondered if others should be a higher priority than me. I was told that our health system’s policy is that I should be vaccinated now. I got the vaccine. I had a sore arm for a couple of days (kind of like after a tetanus shot). On Christmas eve, after a very long day and pushing harder than I should have, I felt chilled. I was fine the next morning. 

I have asked myself, what are the lessons I have learned? What would I do if I had it to do all over again?

  1. COVID fear: I now recognize how this has been hanging over all of us. It is a huge burden. It has multiple aspects to it. We are afraid that we might get COVID and get very ill or die. It is also however the fear that we may be a person who spreads it to others. Do I need to get tested? Is this COVID or is it allergies or something else? Being human means that we have a variety of respiratory symptoms and aches and pains and tiredness from time to time. This past year has been an added burden because we cannot just shrug it off and assume it is nothing. I don’t have an answer for the multifaceted COVID fear other than to acknowledge it. Maybe that makes it a little bit better?
  2. Testing: In retrospect I should have gotten tested that 1st morning after my night of feeling chilled. Clearly I was concerned. The fact that I got out my thermometer and checked my temperature (this was before it was required for us to do so) should have been enough of a clue that I was concerned. 
  3. PPE / social distancing: I thought I was being careful. With my family for my father’s funeral, I thought that I was one of the “safe” ones. While many of my family members wore N-95 masks I wore a standard surgical mask. I have heard so many people talk about how they don’t know where or how they caught COVID. In retrospect I could have and should have been even more careful. With the spread of the new, more infectious strain, this is even more important.
  4. It is real: I have never doubted this, but it bears repeating. While for many COVID might be an asymptomatic or minor disease process, for a lot of people it is really nasty. Those 3 weeks (and for Sarah and Margaret the ongoing symptoms) are no fun. If you can get vaccinated and never get COVID that would be a very good thing.

As usual, this blog is written to share my personal experiences and thoughts. Many have had different experiences. For those of you who have suffered loss and for whom this has been even worse, please know that you have my compassion and (if I am aware of you) my prayers.

Having been through it, I would say:

  • Avoid it if you can. It is no fun.
  • I am happy to have survived it and be doing ok now.
  • Be safe.
  • Get vaccinated if you can.
  • The vaccine is a light at the end of the tunnel for us. Brighter days are ahead!