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@waterboy

jmb... I also have ETs, but they seem to be milder than yours. Mine seem to be worse when trying to do more precise things...like writing, typing ect. I can carry a glass, or cup. I was evaluated at Mayo, Rochester for DEEP BRAIN STIMULATION, OR PRECISE ULTRASONIC ABLATION. However, I was declined for multiple reasons... age, severe COPD, PEs, Alpha 1, and stage of condition. DBS is where they implant electrodes in your brain (like having a pace maker), the PUA is where they use ultrasound to ablate part of the control center of your brain (you can spend 2 to 3 hours going in and out of an MRI machine.)

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Replies to "jmb... I also have ETs, but they seem to be milder than yours. Mine seem to..."

Because of my other medical problems they have me on Clonzepam.

Just had semi annual visit with my movement disorder doctor. I gave run the gammet of drugs for ET and none of them helped. I’ve been on Gabapentin for several years including the maximum recommended dosage (2700 of mg) without relief. Chose not to have ultrasound therapy or the implant. I’m going to try a very small dose of Valium only when crafting and sewing as those are impossible to do with tremors. Has anyone tried Valium?