<?xml version="1.0" encoding="UTF-8" ?>

      <rss version="2.0">		
        <channel>
          <title>WashingtonWatch.com - Comments for P.L. 110-361, The Paul D. Wellstone Muscular Dystrophy Community Assistance, Research, and Education Amendments of 2008</title>
          <link>http://www.washingtonwatch.com/bills</link>
          <description></description>
          <managingEditor>info@washingtonwatch.com</managingEditor>
          <generator>http://www.pjdoland.com/chai/?v=0.1</generator>
          
<item>
<title>Comment by Marie Pichaske (June 28, 2008, 11:28:50)</title>
<link>http://www.washingtonwatch.com/bills/show/110_PL_110-361.html#38435</link>
<description>This bill does for muscular dystrophy what NIH did not do: namely - it funds research - muscle does not have an Institute of its own and NIH treats each of their Institutes like little fifedoms - they protect what is theirs - and fund dieseases they have always funded.  

Until NIH has a more equitable way  of deciding what diseases to fund and how much - this bill is the only hope that that a treatable disease will get a treatment....</description>
<guid isPermaLink="false">38435@http://www.washingtonwatch.com</guid>
<pubDate>Sat, 28 Jun 2008 10:28:50 EDT</pubDate>
</item>
        </channel>
      </rss>
  		