Seanan McGuire (seanan_mcguire) wrote,
Seanan McGuire
seanan_mcguire

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Invisible conditions and the hyperkinetic author.

This is National Invisible Chronic Illness Awareness week, which is something I consider to be genuinely important. We're an appearance-based society, to a large extent, and "you don't look sick" is a far-too-common statement. talkstowolves has posted about her experiences living with temporomandibular joint dysfunction (TMJD), as well as a variety of other conditions. It's very eye-opening. Meanwhile, jimhines has posted about the frightening financial realities of diabetes.

I don't have an invisible chronic illness. What I have is an invisible chronic disability. At some point during my early to mid-teens, I managed to severely herniate three disks in my lower lumbar spine (L3-L5, for the morbidly curious). Because I was extremely overweight at the time, every doctor I saw for more than ten years said "lose weight and the pain will go away," and didn't look any deeper to see why a twenty-three year old woman was staggering into their offices screaming whenever she put her foot down and unable to straighten without vomiting.

Because the body learns to cope with things, I eventually recovered enough mobility to decide to do what the doctors were telling me, went on Weight Watchers, and lost over a hundred pounds. This wasn't as hard as it might have been, because I am a) a naturally picky eater and b) naturally really, really, "was walking a mile every morning to the convention center at the San Diego International Comic Convention, because that calmed me down enough to move calmly through the crowds" hyperactive. So "here, eat lettuce and do aerobics," not exactly the most difficult thing I'd ever heard.

Sadly, it turned out that the doctors were wrong. Being severely overweight may have made things worse, but it didn't cause the injury, and a year and a half of hard aerobics definitely made things worse. In the fall of 2007, I began experiencing numbness of my right side, culminating in losing all feeling in my right leg and nearly falling into traffic when I suddenly couldn't walk. That's when a doctor finally slapped me into an MRI machine, went "oh, crap," and started dealing with my actual injuries.

I look totally healthy. I walk quickly. I move sharply. I am 5'7", reasonably young, and apparently able-bodied. But sometimes I sit in the "people with disabilities" seats, because I literally can't stand on the train for the duration of my commute. Sometimes I glaze over while I'm talking to people, because my sciatic nerve has started screaming like my leg is full of fire ants, and I'm trying to figure out a polite way to excuse myself to go take painkillers. Sometimes I keep walking at a crazy death-march pace because I can feel the numbness creeping back, and if I don't get to my destination before I lose the temporary use of my leg, I'm going to be stuck. That's just how life is.

We may eventually pursue surgical solutions—right now, I'm doing physical therapy, restricted forms of exercise, and trying to work out a detente with my own limitations. They aren't bad enough to qualify me for full-time disability, just bad enough to be inconvenient, invisible, and keep me off roller coasters. Sometimes I meet people who blow off my limits as "whining" or "being lazy." They don't stay part of my life for long.

So please, this week, and every week, remember that appearances are deceiving; like books and their covers, you can't judge a person's health by how fast they're moving. They may just be outrunning the collapse.
Tags: contemplation, medical fu, state of the blonde
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  • 165 comments
I was diagnosed with MS at age 26. For the most part, I am lucky enough that I don't allow it to dominate my life; I simply told myself I had too much to do and MS wasn't going to be a part of that. There are times however that my muscles simply won't do anymore and there are times that I am bone-weary exhausted and I know that I need to rest.

In 2007 I herniated my L4-L5 severely. Luckily I found an orthopedic surgeon who didn't want to do surgery. Through a course of intensive physical therapy, I am 90% of the time pain free. When it hits though, it screams at every fiber of my body.

Despite all of this, I continue to teach Jazzercise 3-5 times per week. The strength training of it (particularly core muscle work) only helps with all of it. As an instructor, I have also learned there are certain routines that I will not teach. Anything that involves twisting side to side - pain and dizziness- or weights overhead will not be found in my classes.

For me, the exercise is what keeps me going.

Gentle hugs for you my dear.
The fact that you can teach Jazzercise is actually very, very encouraging to me. I love my Richard Simmons tapes, and I'm trying to ease them back into my daily life. I'm just a happier person when I can do my aerobics.