<?xml version="1.0" encoding="UTF-8"?>
<rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:wfw="http://wellformedweb.org/CommentAPI/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	xmlns:slash="http://purl.org/rss/1.0/modules/slash/"
	>

<channel>
	<title> &#187; Epilepsy Foundation of Michigan</title>
	<atom:link href="http://www.brainthunders.com/tag/epilepsy-foundation-of-michigan/feed/" rel="self" type="application/rss+xml" />
	<link>http://www.brainthunders.com</link>
	<description></description>
	<lastBuildDate>Mon, 27 Jun 2011 16:29:46 +0000</lastBuildDate>
	<language>en</language>
	<sy:updatePeriod>hourly</sy:updatePeriod>
	<sy:updateFrequency>1</sy:updateFrequency>
	<generator>http://wordpress.org/?v=3.1.3</generator>
		<item>
		<title>Time to Think about Camp&#8230;and Yes, your Child with Epilepsy does have the Opportunity to Attend Camp!</title>
		<link>http://www.brainthunders.com/new-posts/time-to-think-about-camp-and-yes-your-child-with-epilepsy-does-have-the-opportunity-to-attend-camp/</link>
		<comments>http://www.brainthunders.com/new-posts/time-to-think-about-camp-and-yes-your-child-with-epilepsy-does-have-the-opportunity-to-attend-camp/#comments</comments>
		<pubDate>Sun, 18 Apr 2010 12:56:32 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Being a Parent with Epilepsy]]></category>
		<category><![CDATA[Epilepsy Camps]]></category>
		<category><![CDATA[Epilepsy Community]]></category>
		<category><![CDATA[Epilepsy Websites]]></category>
		<category><![CDATA[Kids and Epilepsy]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[epilepsy]]></category>
		<category><![CDATA[Epilepsy Camp]]></category>
		<category><![CDATA[Epilepsy Foundation of Michigan]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=474</guid>
		<description><![CDATA[If you are the parent of a child with Epilepsy, there's great opportunity for you to experience summer programs all around the country. How about camp?]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/time-to-think-about-camp-and-yes-your-child-with-epilepsy-does-have-the-opportunity-to-attend-camp/feed/</wfw:commentRss>
		<slash:comments>1</slash:comments>
		</item>
		<item>
		<title>Local Epilepsy Foundations&#8230;Reach out to Them and Know you are Not Alone in your Journey!</title>
		<link>http://www.brainthunders.com/new-posts/local-epilepsy-foundations-reach-out-to-them-and-know-you-are-not-alone-in-your-journey/</link>
		<comments>http://www.brainthunders.com/new-posts/local-epilepsy-foundations-reach-out-to-them-and-know-you-are-not-alone-in-your-journey/#comments</comments>
		<pubDate>Fri, 16 Apr 2010 12:04:58 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Epilepsy Advocates]]></category>
		<category><![CDATA[Epilepsy Community]]></category>
		<category><![CDATA[Epilepsy Websites]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[Talking About Epilepsy]]></category>
		<category><![CDATA[epilepsy]]></category>
		<category><![CDATA[epilepsy advocacy]]></category>
		<category><![CDATA[Epilepsy Foundation of Michigan]]></category>
		<category><![CDATA[epilepsy fundraisers]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=468</guid>
		<description><![CDATA[For those of you around the world, if you've never participated in a gathering or fundraiser for your local Epilepsy Foundation, I highly suggest it! It's very easy to do, and not only will your Epilepsy Foundation benefit, but you stand to gain so much! ]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/local-epilepsy-foundations-reach-out-to-them-and-know-you-are-not-alone-in-your-journey/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Should my child&#8217;s school be aware of MY epilepsy?</title>
		<link>http://www.brainthunders.com/new-posts/should-my-childs-school-be-aware-of-my-epilepsy/</link>
		<comments>http://www.brainthunders.com/new-posts/should-my-childs-school-be-aware-of-my-epilepsy/#comments</comments>
		<pubDate>Wed, 02 Dec 2009 11:55:03 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Lifestyles]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[Seizures]]></category>
		<category><![CDATA[epilepsy]]></category>
		<category><![CDATA[Epilepsy Foundation of Michigan]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=69</guid>
		<description><![CDATA[If you--the parent--are the one with seizures, and not your child, how much information do you really owe to your child's school and/or his teachers?
]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/should-my-childs-school-be-aware-of-my-epilepsy/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
	</channel>
</rss>

