No one claims that Congress decided in its consideration of RFRA whether children could safely consume hoasca or any other drug in a religious ritual under conditions to be specified.  What Congrss decided was that all such issues of conflict between general law and religious practice required individual examination, and that only the courts were equipped to provide that examination, applying a standard enacted by Congress.  The nine days of trial in UDV gave the judge vastly more information about hoasca and its religious use than Congress had about DMT when it put DMT on schedule I, and infinitely more information than Congress had about religious use of hoasca when it put DMT on schedule I.  Congress had literally no information; it had never heard of hoasca when it put DMT on schedule I.
 
In the amendments to the American Indian Religious Freedom Act, Congress authorized religious use of peyote with some exceptions.  The legislative history, and if I recall correctly, the text of the Act as well, are explicit that cases within the exceptions are subject to RFRA.  So in drug applications where Congress thought it had enough information to enact a rule, it enacted a rule, and in applications where it thought it did not have enough information, it enacted RFRA's standard and directed courts to apply that standard.
 
One of the great puzzles of Marci's position, and especially her book, is that she has no confidence in the adversary process of adjudication, and apparently great confidence in the process of legislative hearings and fact finding, which are generally ad hoc and politicized.  Legislatures write bills in general terms, and it is quite common for those bills to apply to facts of which the legislature was totally ignorant.  Most of her horror stories in the book are things legislatures did and that courts would not have done.   Most obviously, there are no cases of courts finding no compelling interest in health care for children; it is legislatures that enacted exemptions to parental duties to provide health care.  So half the book denounces overly generous exemptions granted by legislatures, and the other half says that only legislatures can be trusted in this area; courts should be excluded.
 
Douglas Laycock
University of Texas Law School
727 E. Dean Keeton St.
Austin, TX  78705
   512-232-1341 (phone)
   512-471-6988 (fax)
 


From: [EMAIL PROTECTED] [mailto:[EMAIL PROTECTED] On Behalf Of [EMAIL PROTECTED]
Sent: Friday, February 24, 2006 9:48 AM
To: religionlaw@lists.ucla.edu
Subject: Re: Breaking news in federal RFRA case

Read the legislative history behind RFRA from beginning to end -- the administration of illegal drugs to children by religious groups is not there.  It is a wholesale reconstruction of history to believe that Congress considered the issue in any way, shape, or form.  The vast majority, i.e., over 95%, of the legislative history involves castigating the Supreme Court for Smith.  The practical consequences of RFRA were never approached, because Congress's purpose was to reverse a Supreme Court decision, without any meaningful consideration of what that would accomplish at a policy level.  Now, there are post hoc justifications for RFRA proffered all around, but they do not displace what Congress actually considered and actually knew at the time it was enacted. 
 
As to policy choices, it is my view that RFRA is unsound constitutionally and policy-wise, but the latter does not undermine the former. 
 
And, yes, the placement of a drug on Schedule I does, indeed, end the discussion when the drug is being administered to minors.  The fact the drugs were delivered in a religious context does not change the extraordinary interest of the children.
 
Marci
 
 
In a message dated 2/23/2006 2:36:19 P.M. Eastern Standard Time, [EMAIL PROTECTED] writes:

You assume that the placement of a drug on Schedule I ends the discussion.  I hope that you do not think that it is jesting to suppose that that placement does not end the discussion.  Congress surely must have some sense of the consequences of its decisions (1) to place the drug on Schedule I and (2) to enact RFRA.

 
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