Once more, I’ve been thinking. You’ll notice I do that, every day, forever. The past few days I’ve had many thoughts on the simplification of life, the world, the events of the world, our societies, our economies, and how everything, everywhere, works. Mostly, none of the thoughts have been good.
It’s a complicated process to explain, this simplification of life that backfires, and results in life not working at all. But it’s all tied to an innate need people have to feel in control of their lives, and their worlds, and to feel safe.
To understand the depth, width, and scale of this topic, I need to provide many examples. It will take a while to illustrate this, so this will not be the only time I speak of this overly simplified world people insist on making.
Since this topic is observable across every aspect of life on this planet, I can start with pretty much any aspect of life, and illustrate the process. Where to start? How about here?
I have several friends who have chronic physical illnesses. These range from ME/CFS through EDS, IBS, Crohn’s Disease, and an entire book of names. I’ll start with ME/CFS, just because it works as well as any of the rest of them.
ME/CFS is, typically, not considered a disease by many people. It’s considered, “laziness”, and “a play for disability benefits”. This is the case because there’s not a precise definition for ME/CFS. In other words, it has no physically documented causes. You can’t run a blood test for it. You can’t see it in an MRI scan of the patient. You can’t see it in CAT scans. Or X-Rays. Or EKGs.
Conventional medical testing used to identify the conditions people are dealing with never identify ME/CFS. This is because ME/CFS is not typical. And therein lies the problem, and the chaos that overly simplified thinking produces.
The best understanding I’ve found, to date, of ME/CFS is difficult for most people to understand. It’s something that happens at the cellular level of the human body, where the body’s cells enter into a constant, unending, self preservation state, similar to when the body is at risk of starving, freezing, or other traumatic situations. The cells go into a mode of conserving energy. They stop producing energy. They shut down.
The result is, the ME/CFS patient has no energy. It hurts to move. It hurts to breathe. It hurts to listen to the heating and cooling systems in their house. It hurts to turn on a light in the room. It hurts to pull the covers of the bed on. It hurts to take them off.
With the cells of their bodies effectively shut down, and not producing energy for use, movement becomes limited. No energy in the body, no energy produced by the cells of one’s muscles, means no movement. Movement burns what energy does exist. Movement is contrary to survival, at the cellular level. Movement shuts down. When these people do move, they end up burning what little energy they have, and can remain nearly motionless, and in intense pain, for days afterward. Sometimes, even for weeks.
Food does not solve the problem. Exercise does not solve the problem. Therapy does not solve the problem. The problem is at the cellular level of the body. Until the cells can be reset to function normally, instead of in an emergency state to conserve energy, and maintain life at all cost, the problem continues to exist.
These symptoms, this cellular condition, is something that medical testing procedures don’t address, and don’t identify. The result is the lament, “ME/CFS doesn’t exist.” With ME/CFS victims being informed there is nothing wrong with them.
Welcome to overly simplified medicine. Where medicine as practiced assumes we know everything, and test for everything, and can identify everything, and can solve everything. And anything that we can’t identify, can’t fix, can’t test, simply doesn’t exist.
We have no problem with physical conditions like broken bones. Those are easy to observe, and identify. We also have methods of solving the conditions of broken bones. Bone replacement. Bone mending. Bone reconstruction. We know how to fix broken bones, such as broken legs, and fingers.
ME/CFS? We can’t even identify its causes. So it doesn’t exist. We don’t know how it works, so it doesn’t exist. We can’t correct the problem, so it doesn’t exist.
It comes down to black and white, as a staggeringly simplified view of the world, and of diseases, and of how the human body works, and interacts with the environment we all live in. It comes down to a desperate, ingrained need to feel in control of ourselves. Of our environments. To feel safe.
For ME/CFS to exist, we have to admit we don’t know what it is, we don’t know who can or can’t get it, we don’t know how to treat it, we don’t know how it works. We have to admit we are not in control, we don’t know everything, and we aren’t nearly as safe as we want to be.
As a result, to maintain that image of safety, security, stability, and control, many people have concluded ME/CFS doesn’t exist. It can’t exist within their framework of reality. They don’t know anyone who lives with it. They don’t know anyone who knows what it is, or how it works. They know that ME/CFS victims apply for disability benefits, when medical testing shows there is nothing wrong with them.
It all adds up to an overly simplified view of life. A view limited to the perspective, and experience of the individual, and the individual’s need to feel safe, and secure, in their life.
The result? ME/CFS spreads, slowly, within a segment of the population of the world, and most people don’t even admit it exists.
It’s life. Overly simplified. In the names of security, safety, and comfort.
I’ll speak more about this overly simplified life in additional posts. As I’ve said already. I see this over simplification of reality in virtually every aspect of society. There is much more to say about it.