Quote:
Originally Posted by soccertese
johnt,
this thread was by a new poster advocated stopping C/L and trying an unproven cocktail of drugs which he supposedly had just started. what could be more dangerous than that? i would never post anything about an alternative therapy i tried that improved symptoms until i had tried it for 6 months, where's the value except just self-indulgence? did you consider this protocol?
let me ask you this, if the outcome had been positive, with no independent proof of anything, even if the poster has pd, would you try the protocol? i sure wouldn't.
if you want to lump my posts in with his go ahead.
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They would have to find a doctor to prescribe them......No? Therefore no real danger here. I also take flexeril and ibuprofin. My DBS is working too well and am getting dystonia in my shoulder. Slowly turning the stimulator down, but in the meantime these meds have helped my PD as well. My doctor said no to the cogentin (sp?) but instead recommended botox.
HTH!