Guest guest Posted September 9, 2010 Report Share Posted September 9, 2010 This makes sense. If we can talk about it without sounding like one side is the devil and the other is not,then that is helpful. Standardized disgnostic and treatment protocols are scary. Esp when you nationalize them.. see this in homeschooling and in education. Federal laws to procect rights and diversity are diff, but we are now seeing in lymeland that after much effort to create fed protection laws and guidelines (as a homeschooler, the fed guidelines part concerns me), it looks like coming at this from a state level is paying off faster. Several to a handful of states now have doctor protection laws.. lyem doc can diagnose and prescribe without fear of retrobution. its easier for smaller less powerful groups to act on a more local level and we have also seen this with lyme awareness. This wil lead to a more favorable climiate for state level legislation. In homeschool land.. i learned if you have nationally defined rules and regs implemented across the board to all states, we are stuck with a system that is much larger to " deal " with if one can at all unless backed by powerful and rich interests. State and local level advocacy and legislation allows for diversity which in this case if not a bad thing. Not sure how this applies to mold related politics.. Robin > > > > obama care just expanded their oligopoly! sue > > > > Quote Link to comment Share on other sites More sharing options...
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