Category Archives: Personal

The great foot collapse

The pain in my feet and ankles has gotten severely worse over the last few months. I finally got to a podiatrist and got some answers. Due to the unusual structure of my lower legs and ankles, I have always naturally stood and walked with my feet pointing outward at about a 70º angle. Years of doing that, and trying not to do that by forcing my feet to point more forward while walking, have led to increasing stress on my feet until finally, a while back, a series of problems erupted.

My arches now collapse while I walk, causing my ankle to slide inward from the heel of my foot, so that I not only walk flat-footed, but my ankle is not centered over my heel, and my heel is actually twisted so that I’m almost walking on the side of my heel instead of the sole of my foot. The result is enormous stress on my ankles and lower legs.

This also causes my toes—especially my inner toes (the big toes and the one or two next to them)—to lose contact with the ground or the insole of my shoe while I walk, so my feet naturally began to curl my toes under so that they made contact with the floor while walking, since the toes play a crucial role in balance and stride.

But curled under like that, the part of my toes that make contact with the floor aren’t the bottoms like they should be. Instead, the tips of my toes, including the nails, are being pushed into the floor with every step. This causes strain on my metatarsals and the tendons in my feet.

It also means that my toenails and the skin at the tips of my toes are essentially becoming one big callus. It’s hard to see where one ends and the other begins. It’s pretty weird looking.

This may also be damaging nerves in my feet and ankles. And that’s where things get real. Who knows how much permanent harm has been done by all this?

The podiatrist and I are working to gradually increase support under my feet to try to mitigate things and keep my feet from sliding off-center on my heel so much, to try to get my toes back to the floor the way they belong. With luck we will at least reduce the amount of pain I’m in, as well as the various visible problems with my toes themselves.

I’m frustrated that nobody figured this out sooner; it’s not like I haven’t specifically asked my doctors if the unusual structure of my feet and the way I walk might be a problem. Sigh…

The Beginning

Welcome! This is the first post on Neurillogical, my blog about my unpredictable, painful, and so far generally undiagnosed neurological issues. I started this blog to have a place to write down my experiences and feelings, but also to vent, and to share my story with others that might have similar issues.

My pain started in my legs at first, way back in 2000 or 2001. I don’t really remember for sure. It sort of snuck up on me, gradually worsening until I finally was in so much pain at night trying to sleep that I had to see my doctor. Back then, the pain was worst while lying down. My legs would feel like ants were swarming among the fibers of my muscles, and I gradually started to have more and more trouble sleeping as the pain worsened. I haven’t had a solid night of sleep since before this.

I moved to Tennessee with my wife (from California) in 2002, and my first appointment with my primary care physician is recorded in my medical records. The very first sentence is something to the effect of “Patient complains of frequent severe leg pain.” A “just to give it a name” diagnosis of fibromyalgia was applied.

In 2010 or 2011, I suddenly developed terrible, sharp pain that felt like it was deep inside my left ear. After ruling out ear infection, orthodontic problems, migraine, and a number of other issues, the diagnosis was finally trigeminal neuralgia. Not long after that, the pain migrated down into the left side of my neck, and it stayed there for a very long time, despite having a discectomy to correct a minor nerve root compression problem.

Things continued to slowly, steadily worsen. I developed tremors in my arms, and sometimes I would have spasms that would cause an arm, or a leg, or sometimes even my entire body to lurch. At times, I would be working at my desk, using my mouse, and would uncontrollably lift the mouse from my mousepad and slam it back down again.

Then the electric shock sensations started. The feeling that I was being blasted by electric current randomly around my body. Mostly in my arms, sometimes in my legs or face. Those continued to worsen, along with the spasms and uncontrolled movements.

After that came the numbness and tingling. I can no longer feel many of my toes at all, and the entire area below the knee is always numb at best, with some areas extremely so. Everything from my lower back down to there is at least in pins-and-needles territory most of the time, and sometimes it’s even worse.

More and more symptoms crop up, and more and more specialists are stumped. It’s crazy.

We have never successfully diagnosed my condition. It keeps changing, and it is definitely steadily worsening. The pain moves around my body, sometimes in my legs, sometimes in my neck and shoulders, sometimes in my face.

I’m miserable from the pain a lot of the time. I do my best to fake otherwise though, because I don’t want my daughter to know just how bad it is. She’s aware I have pain problems, and that as far as we know they don’t mean anything serious is wrong beside nerves acting out of line, but she doesn’t really know just how much of the time I feel it, and just how bad it is.

My wife and daughter give me a reason to keep fighting for answers.

Anyway, that’s a quick overview. I’ll be talking about various specific incidents, issues, and problems over time in future posts.