NAUGHTY, LAZY EPIGLOTTIS! |
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Looking again at the video from yesterday’s modified barium swallow, something finally caught my eye. Something my wife noticed yesterday when I first played it. (“You never listen to me,” is what I THINK she said, but I don’t think I caught all of it because there was a... |
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Deep Brain Diary
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Adventures in Physical Therapy: Or, “Hey! I Learned Something NEW!” |
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Had my third physical therapy session of the week earlier today. I learned that my sore left shoulder isn’t just a sore left shoulder. It’s called “frozen shoulder syndrome” or “adhesive capsulitis.” Frozen shoulder, also known as periarthritis or adhesive capsulitis, is a syndrome consisting of spontaneous onset of pain and progressive restriction of movement in a shoulder, in the absence of any demonstrable intrinsic joint abnormality. The onset is followed by a chronic phase in which the pain recedes but the shoulder immobility remains marked, and finally by gradual spontaneous resolution. I also learned that it can be caused by Parkinson’s disease. We have found that frozen shoulder is indeed a common complication of Parkinson’s disease, occurring in 12-7% of our patients. The incidence may actually be higher, but we were unable to be certain of the diagnosis in other patients with suggestive histories. Men were affected out of proportion to their numerical majority in our population, contrary to the predominance of women found in other studies of frozen shoulder. So. I learned something new. And that explains why they’re beating the hell out of my shoulder. Deep tendon massage, stretching, bending, twisting, turning. I feel like a Stretch Armstrong toy. "Does it hurt when I do THIS?" Oddly, “frozen shoulder” is commonly the first presenting symptom in PD. But I didn’t get mine until about six months ago. But then, I’ve never been the kind to do things in the typical way. My usual therapist was gone today, so I worked with Karen, who proudly refers to herself as “The Queen of Pain.” After the shoulder workout, we did the balance and walking things. It’s still alarming to me to see how uncoordinated I have become. I’m so used to doing my little shuffle with my arms hanging limp by my side that when I’m told to swing my arms when taking big steps — I have to give it careful thought to accomplish this thing that most folks do all the time without even thinking about it. In fact, Karen had to stop me and start over a few times because I was swinging the left arm and left leg, then right arm and right leg instead of the way YOU walk, which is right arm, left leg, vice versa. We had me take the “big steps” while turning my head side to side. I froze with every second step… usually when turning my head to the left. I was walking like a cheaply made toy robot. Nodding my head while walking is easier, but still challenging and requiring a great deal of thought to accomplish. We did the “stand with one foot in front of the other and turn your head from side to side” thing, too. I was wobbly with my left foot in front of my right leg. I could barely stand with my right foot in front of my left leg. This physical therapy has been a real eye opener. I have at least two more weeks of it. I don’t know if it’s helping anything (other than my shoulder, which does feel looser…) But I’m sure learning stuff. Related articles by Zemanta
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Released May 07, 2010
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Last 5 Posts
And The World Keeps Turning… |
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So, no major exams coming up. I have physical therapy this afternoon and tomorrow morning. I’ll see the speech therapist next Wednesday. And life goes on. Made coffee this morning, then did my exercises, followed by 20-minutes on the bike and a shower. Now, to knuckle down and do some... |
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Consulting the Family Speech Pathologist |
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My genius nephew, Tommy, of whom we all love and his sainted mother would be so proud, had a thing or two to say about the video I posted here earlier today. He’s a grad student, a future speech pathologist. I just had 4 different speech paths look at your MBS. We all agree your epiglottis [... |
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My Lazy, Lazy Epiglottis! |
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Well, we figured out what the problem is. It’s not that I aspirate food and drink on every swallow. But, according to the delightful speech pathologist who fed me barium in various forms and explained the video she shot, there seems to be some weakness around my hyoid bone (the only bone... |
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Time For My Swallowing Test! |
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In about 20 minutes Gail and I will head to the hospital for a modified barium swallowing study. This is what it looks like. (NOTE: This is NOT my study… I’m told, however, that I will be provided with a copy of the film, so watch for it this afternoon!) It’s really quite th... |
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