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Myasthenia Gravis For support and discussions on Myasthenia Gravis, Congenital Myasthenic Syndromes and LEMS. |
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I will be seeing my neurologist on Monday morning. I've been on a high dose of Prednisone for three weeks, and have been tolerating it fairly well. My current level is 60 mg per day, or 1.8mg/kg/day. My normal primary symptoms centered on my face, mouth, tong, and jaw muscles. Speech was very labored or nonexistent by end of the day. Symptoms were much less sever after sleeping. My jaw would drop and I would finding myself aiding it with my hand. I would also assist chewing with my hand. Eating was possible, but it took time, as did drinking. After eating I would have mucus collection in the back of my throat, as I did late into the night around the time I would go to bed.
My neurologist will soon begin to taper the Prednisone down to maintenance levels. After the Prednisone regimen over the last 3 weeks things have markedly improved.
No vision issues. My distance and night vision is excellent. No more double vision since the September severe MG event. After that event, I found that I needed my reading glasses more. I needed them to read the computer screen in the taxicab. I thought this was normal with age. I am using 1.5 strength. After the Prednisone I no longer need the reading glasses to read the taxicab display. But I do have additional symptoms that I did not have before. I know this may be due to the Prednisone, Mestinon, the every changing nature of MG symptoms, or a combination of all three.
Any observations will be appreciated. -Mark- |
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