Do you STUTTER because of LD?

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Regular Member

Date Joined Jul 2007
Total Posts : 478
   Posted 1/6/2009 11:23 PM (GMT -6)   
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

Regular Member

Date Joined Feb 2006
Total Posts : 346
   Posted 1/7/2009 1:13 PM (GMT -6)   

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,

Regular Member

Date Joined Apr 2008
Total Posts : 266
   Posted 1/7/2009 3:17 PM (GMT -6)   
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.

Regular Member

Date Joined Sep 2008
Total Posts : 293
   Posted 1/7/2009 6:28 PM (GMT -6)   
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...
"I will not let Lyme controll my life i will controll my own life"
lyme since June 08
meds-zithromax 500mg one a day/ 1  month // Plaquenil 200mg twice a day/ 1 month
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