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

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.