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My dad uses thioridazine which essentially makes the PD worse in the
nights, so his tremors and shaking don't wake him.  I believe that this
drug has another, easier to spell name, but this is the name that is on
his med list.  The neuro's initially didn't want to use this - but now
they encourage him to take another at 1 AM if he still can't sleep.

Also - we have found melatonin to be a help.  The archives have a ton of
info on that.

Sara Byron
daughter of Richard 79/28 yrs w/ PD

The following binary file has been uuencoded to ensure successful
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