What we live with (not to be confused with familial complaints, of which I have none)

Here’s how it all started. I think.

It was sometime in April, not long after a trip to Centennial Hospital to have my arrhythmia corrected (which it hopefully has been, but that’s another story.) I began to notice very sharp, stabbing, almost electrical pains in my face and mainly my teeth. It was like a really, really severe toothache, only it wasn’t confined to a single tooth; rather, it was first one tooth, then another. The next day, still another. At another time, it might feel like three or four involved at once.

It was frightening for a lot of reasons, and not just the pain. I can’t afford to spend any money on dental care. My heart and lungs have been the expensive things lately. They’re getting better–I hope–but I can’t afford to deal with a couple of thousand dollars worth of fang repair. So I went in to my usual biannual checkup/cleaning a few months later with some reservations.

The surprise was…no surprises. There was nothing wrong with my teeth. X-rays seemed to show this conclusively. I breathed a sigh of relief…kind of. You see, the pain had never gone away, and at times it was quite blinding.

It’s hard to explain this. A toothache, yes, that’s easy to quantify to anyone who’s ever had one. Or a migraine, or a cluster headache. Kidney stones, and God knows I’ve had my share of those. Or a broken tailbone. Yes, that too.

This…this is something different, and what was worse, it was something I couldn’t pin down.

Being the inquisitive sort, I began to do a little research on that Great Fount Of All Information, the Internet. It didn’t take long to find a few hints. But being rational, and having an appointment upcoming with the wonderful Dr. Anna I figured I would just lay everything out to her and see what she had to allow.

Dr. Anna is nothing if not thorough. She asked all of the questions and I gave all of the answers. She examined me every way she could and should, and she sent me to an ENT to rule out issues with my sinuses. I do have occasional issues with my sinuses. But the phrase that kept coming up is trigeminal neuralgia. This wonderful little condition comes with the humorous alternative moniker “suicide disease” because a) it’s so painful (it is) b) no one believes you have it (try and convince someone you’re in blinding pain for no really good reason!) and c) it’s rather difficult to treat, apparently. There are options, but none really offer complete relief, and there’s always the question of money, or lack thereof.

Anyway. My ENT visit was today. And Dr Roth, who is a very nice man, is sending me for a CT scan. More $$$, to be sure, which I am not keen on but I guess I have to do it, then a return visit next week. All the while I keep having to grin and bear it. Last night I shaved, brushed my teeth, and washed my face…and I cannot adequately describe the resulting pain.

No one will ever see these words, probably. But I will post it nonetheless, and continue to do so as this strange journey progresses. Mayhap as time goes on someone will get a little comfort from knowing they’re not alone.

6 Comments

  1. Hey Jim – your old neighbor from Elmer Street in Griffith here…I’ve had trigeminal neuralgia for years and your symptoms do sound familiar! Before I was diagnosed the pain scared me to death…I would be standing still and all of a sudden it felt like I got hit on the side of my head with a hammer (but from the inside of my head). It literally knocked me over one time while I was sitting down. My neurologist prescribed Tegretol which worked very well for me in a short time. I hope you get answers and relief!

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  2. Ooh, chronic pain. I would know nothing about that, she says with sarcasm dripping from her lips…James, finding that one great doctor out of the millions out there is one of the hard parts of the journey. Finding the treatment that works is the hardest part. I wish you all the best, my friend. I hope you find therapy and solace in your new blog. >^..^<

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