Special Needs

physiatrist?

DS's PT asked whether we'd seen a physiatrist, and we haven't, but I'm thinking about making an appt.

Has anyone's child seen a physiatrist?  For what purpose, and what did s/he do for your child?  I'd appreciate anyone's input.   

Thanks.

Re: physiatrist?

  • We see one for DS.  he has severe hypertonia.  The dr gave us baclofen and is going to keep an eye on his muscles.  to make sure he never needs a few botox injections to help develop the opposing ones. 
    To my boys:  I will love you for you Not for what you have done or what you will become I will love you for you I will give you the love The love that you never knew
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  • We like ours a lot. They don't diagnose, but they monitor muscle development. Ours always checks for  hyperextension in DS' joints, etc. He is also the one to prescribe his leg braces, etc.

     

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