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	<title> &#187; Seizures</title>
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		<title>Back to Work&#8230;and Back to Life!</title>
		<link>http://www.brainthunders.com/new-posts/1159/</link>
		<comments>http://www.brainthunders.com/new-posts/1159/#comments</comments>
		<pubDate>Sat, 12 Feb 2011 13:07:15 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Being a Parent with Epilepsy]]></category>
		<category><![CDATA[Epilepsy and Marriage]]></category>
		<category><![CDATA[Life Changes and Epilepsy]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[Seizures]]></category>
		<category><![CDATA[Stress and Epilepsy]]></category>
		<category><![CDATA[Talking About Epilepsy]]></category>
		<category><![CDATA[Women and Epilepsy]]></category>
		<category><![CDATA[Working with Epilepsy]]></category>
		<category><![CDATA[managing epilepsy]]></category>
		<category><![CDATA[working and epilepsy]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=1159</guid>
		<description><![CDATA[Heading back to work really got me thinking about ability and how able I am to manage my Epilepsy, manage my household, take care of a 5-year-old and...work.]]></description>
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		<slash:comments>6</slash:comments>
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		<title>Living with Epilepsy&#8230;and Living in Fear</title>
		<link>http://www.brainthunders.com/new-posts/living-with-epilepsy-and-living-in-fear/</link>
		<comments>http://www.brainthunders.com/new-posts/living-with-epilepsy-and-living-in-fear/#comments</comments>
		<pubDate>Sun, 02 Jan 2011 14:13:08 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Being a Parent with Epilepsy]]></category>
		<category><![CDATA[Epilepsy Advocates]]></category>
		<category><![CDATA[Epilepsy Community]]></category>
		<category><![CDATA[Epilepsy Treatments]]></category>
		<category><![CDATA[Kids and Epilepsy]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[Seizures]]></category>
		<category><![CDATA[Talking About Epilepsy]]></category>
		<category><![CDATA[Vagus Nerve Stimulator]]></category>
		<category><![CDATA[Epilepsy and Fear]]></category>
		<category><![CDATA[Epilepsy and Staying Active]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=1148</guid>
		<description><![CDATA[I live in constant fear of when the next seizure will strike; where I'll be when it does strike and who will be with me. I'm not always public with my fears, but they are incredibly distracting and controlling. Many times, it's so easy to keep them bottled up. ]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/living-with-epilepsy-and-living-in-fear/feed/</wfw:commentRss>
		<slash:comments>6</slash:comments>
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		<title>New Year&#8217;s Resolution Time&#8230;What&#8217;s Your Story?</title>
		<link>http://www.brainthunders.com/new-posts/new-years-resolution-time-whats-your-story/</link>
		<comments>http://www.brainthunders.com/new-posts/new-years-resolution-time-whats-your-story/#comments</comments>
		<pubDate>Mon, 27 Dec 2010 16:15:07 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Driving with Epilepsy]]></category>
		<category><![CDATA[Epilepsy Advocates]]></category>
		<category><![CDATA[Epilepsy Causes]]></category>
		<category><![CDATA[Epilepsy Community]]></category>
		<category><![CDATA[Epilepsy Legislation]]></category>
		<category><![CDATA[Epilepsy Medication Switching]]></category>
		<category><![CDATA[Epilepsy Medications]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[Seizure Alert Dogs]]></category>
		<category><![CDATA[Seizures]]></category>
		<category><![CDATA[Stress and Epilepsy]]></category>
		<category><![CDATA[SUDEP Awareness]]></category>
		<category><![CDATA[Supporting Epilepsy Programs]]></category>
		<category><![CDATA[epilepsy awareness]]></category>
		<category><![CDATA[family and epilepsy]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=1144</guid>
		<description><![CDATA[I was thinking this morning, are there some realistic New Year's resolutions that I actually might adhere to? And, can I make sure they not only benefit and define me, but are also epilepsy issues I care so deeply about?]]></description>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>Courage&#8230;and How it Relates to Living Life with Epilepsy</title>
		<link>http://www.brainthunders.com/new-posts/courage-and-how-it-relates-to-living-life-with-epilepsy/</link>
		<comments>http://www.brainthunders.com/new-posts/courage-and-how-it-relates-to-living-life-with-epilepsy/#comments</comments>
		<pubDate>Mon, 20 Dec 2010 12:29:45 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Being a Parent with Epilepsy]]></category>
		<category><![CDATA[Epilepsy Advocates]]></category>
		<category><![CDATA[Epilepsy Community]]></category>
		<category><![CDATA[Epilepsy Treatments]]></category>
		<category><![CDATA[Family]]></category>
		<category><![CDATA[Kids and Epilepsy]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[Seizures]]></category>
		<category><![CDATA[Supporting Epilepsy Programs]]></category>
		<category><![CDATA[Talking About Epilepsy]]></category>
		<category><![CDATA[Women and Epilepsy]]></category>
		<category><![CDATA[epilepsy]]></category>
		<category><![CDATA[Epilepsy and Family]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=1137</guid>
		<description><![CDATA[Having the courage to identify yourself with not just the negative, but mainly the positive is a gift. And, it's something I've worked hard to achieve. I'm determined to not be labeled...]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/courage-and-how-it-relates-to-living-life-with-epilepsy/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
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		<title>Living with Memory Loss&#8230;</title>
		<link>http://www.brainthunders.com/new-posts/1127/</link>
		<comments>http://www.brainthunders.com/new-posts/1127/#comments</comments>
		<pubDate>Thu, 02 Dec 2010 14:36:26 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Epilepsy Advocates]]></category>
		<category><![CDATA[Epilepsy Community]]></category>
		<category><![CDATA[Friendships and Epilepsy]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[Memory Loss and Epilepsy]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[Seizures]]></category>
		<category><![CDATA[Talking About Epilepsy]]></category>
		<category><![CDATA[Memory and Epilepsy]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=1127</guid>
		<description><![CDATA[Memory loss due to my seizures is something I know I will always struggle with, and the fact that it will most likely worsen is quite daunting, but I'm thankful for my close friends and family who can tolerate and console me.]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/1127/feed/</wfw:commentRss>
		<slash:comments>5</slash:comments>
		</item>
		<item>
		<title>Even Caregivers to those with Epilepsy Need Support and Friendship&#8230;</title>
		<link>http://www.brainthunders.com/new-posts/even-caregivers-to-those-with-epilepsy-need-support-and-friendship/</link>
		<comments>http://www.brainthunders.com/new-posts/even-caregivers-to-those-with-epilepsy-need-support-and-friendship/#comments</comments>
		<pubDate>Tue, 16 Nov 2010 15:02:51 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Being a Parent with Epilepsy]]></category>
		<category><![CDATA[Driving with Epilepsy]]></category>
		<category><![CDATA[Epilepsy Advocates]]></category>
		<category><![CDATA[Epilepsy and Marriage]]></category>
		<category><![CDATA[Epilepsy Caregivers]]></category>
		<category><![CDATA[Epilepsy Community]]></category>
		<category><![CDATA[Epilepsy Medications]]></category>
		<category><![CDATA[Epilepsy Treatments]]></category>
		<category><![CDATA[Family]]></category>
		<category><![CDATA[Kids and Epilepsy]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[Supporting Epilepsy Programs]]></category>
		<category><![CDATA[The Stigma of Epilepsy]]></category>
		<category><![CDATA[epilepsy awareness]]></category>
		<category><![CDATA[Seizures]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=1113</guid>
		<description><![CDATA[In nearly 8 years of my living with Epilepsy, my husband has never really spoken at length to anyone who walks in his shoes. His wife lives with a chronic neurological condition called Epilepsy and he is healthy. ]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/even-caregivers-to-those-with-epilepsy-need-support-and-friendship/feed/</wfw:commentRss>
		<slash:comments>2</slash:comments>
		</item>
		<item>
		<title>Defying the Law&#8230;and the Obvious</title>
		<link>http://www.brainthunders.com/new-posts/defying-the-law-and-the-obvious/</link>
		<comments>http://www.brainthunders.com/new-posts/defying-the-law-and-the-obvious/#comments</comments>
		<pubDate>Wed, 10 Nov 2010 11:45:08 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Auras]]></category>
		<category><![CDATA[Driving with Epilepsy]]></category>
		<category><![CDATA[Epilepsy and Facebook]]></category>
		<category><![CDATA[Epilepsy Community]]></category>
		<category><![CDATA[Family]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[Neurologists]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[Seizure First Aid]]></category>
		<category><![CDATA[Seizures]]></category>
		<category><![CDATA[Talking About Epilepsy]]></category>
		<category><![CDATA[driving and epilepsy]]></category>
		<category><![CDATA[Epilepsy and Family]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=1098</guid>
		<description><![CDATA[The fact of the matter is, every state has a law that applies to drivers who have seizures. It's up to our doctors to make sure we are abiding those laws, but it's also up to those of us who live with Epilepsy to adhere to them.]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/defying-the-law-and-the-obvious/feed/</wfw:commentRss>
		<slash:comments>8</slash:comments>
		</item>
		<item>
		<title>Face it&#8230;Memory Loss Is and Will Always be Part of this Journey</title>
		<link>http://www.brainthunders.com/new-posts/face-it-memory-loss-is-and-will-always-be-part-of-this-journey/</link>
		<comments>http://www.brainthunders.com/new-posts/face-it-memory-loss-is-and-will-always-be-part-of-this-journey/#comments</comments>
		<pubDate>Sun, 26 Sep 2010 13:19:56 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Epilepsy Community]]></category>
		<category><![CDATA[Epilepsy Treatments]]></category>
		<category><![CDATA[Friendships and Epilepsy]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[Memory Loss and Epilepsy]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[Seizures]]></category>
		<category><![CDATA[Memory and Epilepsy]]></category>
		<category><![CDATA[Memory loss with Epilepsy]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=1030</guid>
		<description><![CDATA[Memory issues with Epilepsy absolutely stink!]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/face-it-memory-loss-is-and-will-always-be-part-of-this-journey/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Tragedy in Texas&#8230;Lessons Can Be Learned</title>
		<link>http://www.brainthunders.com/new-posts/tragedy-in-texas-lessons-can-be-learned/</link>
		<comments>http://www.brainthunders.com/new-posts/tragedy-in-texas-lessons-can-be-learned/#comments</comments>
		<pubDate>Sun, 19 Sep 2010 13:05:59 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Epilepsy Advocates]]></category>
		<category><![CDATA[Epilepsy Caregivers]]></category>
		<category><![CDATA[Epilepsy Community]]></category>
		<category><![CDATA[Family]]></category>
		<category><![CDATA[Kids and Epilepsy]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[Seizure First Aid]]></category>
		<category><![CDATA[Seizures]]></category>
		<category><![CDATA[Talking About Epilepsy]]></category>
		<category><![CDATA[epilepsy awareness]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=1022</guid>
		<description><![CDATA[A high school football player in Texas collapsed  and died Saturday, reportedly after suffering a seizure. He was the star quarterback, had just thrown his second touchdown of the game, was an A student, and had a history of seizures. ]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/tragedy-in-texas-lessons-can-be-learned/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Friendship and Life with Epilepsy</title>
		<link>http://www.brainthunders.com/new-posts/friendship-and-life-with-epilepsy/</link>
		<comments>http://www.brainthunders.com/new-posts/friendship-and-life-with-epilepsy/#comments</comments>
		<pubDate>Mon, 13 Sep 2010 09:55:07 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Being a Parent with Epilepsy]]></category>
		<category><![CDATA[Epilepsy Advocates]]></category>
		<category><![CDATA[Friendships and Epilepsy]]></category>
		<category><![CDATA[Kids and Epilepsy]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[Seizures]]></category>
		<category><![CDATA[Women and Epilepsy]]></category>
		<category><![CDATA[epilepsy]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=1008</guid>
		<description><![CDATA[Still, with weekly, and most of the time daily seizures...it's pretty special when you can lose yourself in something, with someone, and for the moment you don't have to think about 'the E word'.]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/friendship-and-life-with-epilepsy/feed/</wfw:commentRss>
		<slash:comments>3</slash:comments>
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