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TMJ/MS

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Dan,

Sorry, can't help much there as because I had neither TMJ or MS itself

it was something I never pursued, You are certainly right about

resources on the Internet! 10 years ago after my PLS diagnosis I could

find virtually nothing out about it, but nowadays there is lots to be

found, especially through PLS-FRIENDS which is another group like

this one.

Guess the best thing to do is hit Google with TMJ and MS and see where

it leads.

Cheers,

Glines wrote:

,

No, I was just wondering if there were any resources on the

Internet. It has grown so much in the last 10 years. Based on my

experience the theory is correct, but there is no proof only my opinion.

Dan

-- .

,-._|\ Covington / Oz \ \_,--.x/ v

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