Do you STUTTER because of LD?

I have stuttered all my life, long before I got LD. I am a pretty severe stutterer that uses managemt techniques being that there is no cure. I just wonder how much of the severity is due to LD? I am curious to see if anything changes when I start to feel better. I was just wondering how many of you just began to stutter because of LD.  I know that stuttering is neurologically based so I was curious how many peolple with neuro symptoms aquired stuttering as one of their symptoms. I am really interested in this. thanks, amey

Hi,

Stuttering was one of the neuro symptoms that I developed. I was very concerned but with treatment it went away completely. I am not sure if anyone on the board has had your situation but I would think that if you are in treatment in might improve. Keep bumping the question up and lets see if you can get some further responses.

Best wishes,
bcaring

I haven't stuttered but have noticed in my worst times my words slur or I have to stop and think of the word before I say it. While I am much better at this point I haven't noticed this much at all.

i dont stutter but i will mess up on my words and will have to think about the word and it will sometimes come out the wrong way and i will make weird noices cause i messed up on a word....but i have gotten beter with this also sice i have been on cef and doxy together...

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"I will not let Lyme controll my life i will controll my own life"