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#1 | ||
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My Navy buddy, who said he got laid out on the floor, even on a small dose, never did say what his "small" dose was. I just figured that 90 - 100mg pills with upping the dose every other day would run you. When you get to your second dose of 100mg, make sure you've spaced it out in the day. When you get to 4 pills & more, daily, probably work your way around the "route". My Nero started me on 4-100mg daily & that sure wasn't enough. On that first prescription of 120 caps, I moved up to 600mg daily & then 900mg daily, without the desired effect on my "folded sock" behind the toes. I'm at 600x3 daily now & I really could use a 4th dose, and probably 300mg would do it. Half another pill. (600's are scored hard oval pills). I really don't want to give you any personal recommendations if you need to go beyond 300x3, but by that time, jumping 300mg a day shouldn't knock you on your butt, after your body gets used to the stuff. You might get a bit light headed for a short time, but not too bad.
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#2 | ||
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When my son was home last year he had an attack of post-herpetic neuralgia, he had shingles on his face as a child. I know that this is an on-label use for gabapentin, so I gave him one. It worked like a charm, but knocked him out. Evidently much lower dosages than the 600 mg. I gave him would have been better. He is a very tall man, and a heavy drinker, so I was surprised. He also has CMT, but no pain yet.
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#3 | ||
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Quote:
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#4 | ||
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I am on Gabapentin since October 2011. I started at 300mg 3x/day. I had difficulty adjusting to this dosage. I experienced all sorts of side effects -- light headedness, sleepiness, brain fogginess/memory lapses -- and the worst was the negative thoughts. The negative thoughts have long been gone but I still have all the rest. At one time, I was washing dishes, unknowingly, I dropped it because I fell asleep. I wanted to stop the medication but the pain was the big motivator for me to continue using it. My neuro offered no alternative medicines except an additional Nortriptyline (not as a substitute) but I refused for personal reason.
The 300mg did not work for me. I played around with my dosage trying to find the most minimum dosage that will work. I was concerned of increasing it too early as I realized this is for the long haul. Little by little I increased it to where I am now -- 600mg 3x/day. My neuro said that when you find hte right dosage, you will stay there for a long time (that was a consolation!). Everytime I increase my dosage, the light headedness is more pronounced, but after awhile, my body gets adjusted, but the somnolence and memory lapses still remain. The Gabapentin, for me, only weans off some of the symptoms like - zapping, electric jolts but not the pain in hte feet and legs. I can tolerate walking but not standing (strange). |
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