Empathy Machines

Before I get to what I really want to write about today, this:

“Reading is an empathy-generating machine.” – Dr. Vivek Murthy

Isn’t this the truth? When we are having conversations, we are typically taking turns waiting to talk. Our conversations have a tendency to veer off-topic. But when you are reading, it’s just you and the words which you are reading. And written words tend to be more soulful, more thought-out, more vulnerable, more honest than everyday conversations. Reading really helps you to understand how someone else feels about their experiences. Empathy is being able to answer the question: “How do you think this makes me feel?” for someone else, other than yourself. Reading gives you time to absorb and to understand the words, and to make conclusions about the words, without getting defensive or argumentive or confused. I absolutely love to read and empathy is a wonderful by-product of reading.

And also before I get to what I really want to write about today, this:

Credit: @woofknight, X

“Oh to have impacted someone so much that they find bits of your soul and hold the memory of you in things and places when you’re not around.” Isn’t this a beautiful part of the human experience? Isn’t it wonderful to have people (and pets) in your life who come to mind often, even when they are not around. And isn’t it also great to be the person who someone is reminded of, when they see or experience certain things? These are the types of aspects of living life, that my soul crushes on, hard.

Okay, finally to what I planned to write about today:

Yesterday, our youngest son called me around 11 am. And my heart fell to the floor. I knew that my son was at work, my kids rarely call me (texting is king), and also, he has epilepsy. Thankfully my son was fine, but he was letting me know that he had just gotten an emailed letter stating that his longtime neurologist/epitologist’s practice was no longer taking my son’s health insurance.

This was the final push, which we have long-known was coming, to force us to go about finding my son a new practioner. His neurologist is getting close to retirement age, he practices in a town three hours from where our son lives, and he is technically a Pediatric Neurologist. Our son turns 24 at the end of the year.

Already I have a lump in my throat, writing this. Our son was 14 when he was diagnosed with epilepsy. He started with the small seizures called “absence seizures” or “petit mal” seizures which had probably been going on longer than we think. I often thought that my son was ignoring me or distracted with daydreaming, which I know is not out of the realm of things that teenage boys do. (he has two older brothers) However, the summer that he was diagnosed with epilepsy, our daughter and I picked him up from a summer camp (where he had gotten very little sleep) and my son’s disjointed, disorganized, “filled with stalls and stares and pauses” stories about the camp made it clear that something just wasn’t right. Later that night, I found some videos of children having absence seizures on “YouTube” and my stomach filled with dread. I took our son to our beloved pediatrician the next day only to have him confirm my fears, and to quickly recommend one of the best pediatric neurologists in town.

It took a long while to see Dr. W. He had quite the waiting list of people from in town, and from out town, who wanted to consult with him. We went to see his younger associate first, and while this young man was fresh out of medical school, and was eager and obviously brilliant, he spoke entirely too fast, and too matter-of-factly, to parents who were quickly coming to terms that life as we had all known it, had come to an end, and a big change was in store for our family. We decided to wait for an appointment with the heralded Dr. W, to see what he had to say about our son’s condition.

I quickly understood why Dr. W was so popular with his patients (and all of the medical staff). He was kind, down-to-Earth, patient to answer all of the questions and challenges that I was peppering him with, and he took a genuine interest in our son, outside of his epilepsy. It turns out that Dr. W had grown up in a farm town, and he took an interest in studying neurology because he had an uncle with epilepsy who chose never to get it treated. (This uncle would often ride around on large tractors, to the dismay of his family.)

Over the years, we have had many ups and downs with our son’s epilepsy. Epilepsy is tricky because it is treated with heavy-duty brain medication, with heavy-duty side effects, and these medications work differently, with each individual and they can stop working as one’s body changes. There is not a “one medication fits all” situation with epilepsy. There are always more questions than answers with any condition involving the brain. Currently, what is thankfully keeping ours son’s seizures at bay, are three different medications, taken two times a day. Some people with epilepsy can never keep their seizures at bay. We are lucky. This I know. I have never been more grateful for anything else in my life. It took us a long time, and a lot of scary moments with our son having many major seizures, to finally get to this combination that currently works for him. And all of the while, Dr W. did everything in his power to support us, but more importantly, to support our son, as we went through this long process of finding meds with the least side effects, that still stopped the seizures. Dr. W cared for our son throughout high school, throughout college, and throughout starting his sales career in his young adulthood. Dr. W has been a constant in our son’s sometimes otherwise unpredictable experiences.

My son was an easy patient. His mother was not. I was a totally desperate, semi-hysterical, pain-in-the-ass, many, many times. (I’m pretty sure that my son and Dr. W probably have some private jokes about his neurotic mother who thinks she knows everything due to her intimate relationship with Dr. Google, and do you know what? I effing love Dr. W for this fact. Dr. W always made our son feel nothing less than a totally normal, awesome guy with an unfortunate affliction which we were going to find a way to control. Usually Dr. W spent the appointments more focused on these sincere questions: “What did our son think about that game last night? Whose our son dating now? How’s school going? Who can I reach out to at the DMV, to let them know that it is now safe for you to drive?”)

When you are going through something tough in life, you are never alone. God sends angels. They are usually in human form. Dr. W will always be one of these “angels on Earth” for me, and for my family. Always. He took “bedside manner” to a down home, yet ethereal form.

So yesterday, with my voice cracking, I told my son that he should reach out to Dr. W for a recommendation of whom he should go to now, for treatment of his epilepsy. The time that we long knew was coming, has now come. Thank you Dr. W, for everything. Thank you. Thank you. Thank you, from the bottom of the deepest wells of my heart. I am a grateful witness and recipient, to you living a well-purposed life.

Are you passing on love or are you passing on pain? Heal your pain and pass on love.

Here is the question of the day from 3000 Questions About Me:

938. What is the most beautiful city in the world?