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	<title> &#187; Epilepsy Community</title>
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		<title>2011 Summer Stroll for Epilepsy Season&#8230;in the Books!</title>
		<link>http://www.brainthunders.com/new-posts/2011-summer-stroll-for-epilepsy-season-in-the-books/</link>
		<comments>http://www.brainthunders.com/new-posts/2011-summer-stroll-for-epilepsy-season-in-the-books/#comments</comments>
		<pubDate>Mon, 27 Jun 2011 16:29:46 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Being a Parent with Epilepsy]]></category>
		<category><![CDATA[Epilepsy Advocates]]></category>
		<category><![CDATA[Epilepsy Causes]]></category>
		<category><![CDATA[Epilepsy Community]]></category>
		<category><![CDATA[Epilepsy organizations]]></category>
		<category><![CDATA[Family]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[epilepsy]]></category>
		<category><![CDATA[epilepsy advocacy]]></category>
		<category><![CDATA[Epilepsy advocate]]></category>
		<category><![CDATA[epilepsy awareness]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=1174</guid>
		<description><![CDATA[Thanks to the Epilepsy Foundation of Michigan for a wonderful Summer Stroll season!]]></description>
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		<slash:comments>1</slash:comments>
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		<title>Donation Envy&#8230;What&#8217;s In It for Us?</title>
		<link>http://www.brainthunders.com/new-posts/donation-envy-whats-in-it-for-us/</link>
		<comments>http://www.brainthunders.com/new-posts/donation-envy-whats-in-it-for-us/#comments</comments>
		<pubDate>Wed, 01 Jun 2011 15:07:52 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Epilepsy Advocates]]></category>
		<category><![CDATA[Epilepsy Causes]]></category>
		<category><![CDATA[Epilepsy Community]]></category>
		<category><![CDATA[Epilepsy organizations]]></category>
		<category><![CDATA[Family]]></category>
		<category><![CDATA[Friendships and Epilepsy]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[Supporting Epilepsy Programs]]></category>
		<category><![CDATA[Talking About Epilepsy]]></category>
		<category><![CDATA[The Stigma of Epilepsy]]></category>
		<category><![CDATA[epilepsy]]></category>
		<category><![CDATA[epilepsy advocacy]]></category>
		<category><![CDATA[Epilepsy advocates]]></category>
		<category><![CDATA[epilepsy awareness]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=1167</guid>
		<description><![CDATA[We as epilepsy advocates can't be discouraged when we don't get the help or the support we want. We have to work for it, and work hard. NOT EVERYONE UNDERSTANDS EPILEPSY OR EVEN KNOWS WHAT IT IS! So, it's our job to teach them what the needs are and what programs are available.]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/donation-envy-whats-in-it-for-us/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
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		<title>Caregivers and Epilepsy&#8230;it Takes All Kinds!</title>
		<link>http://www.brainthunders.com/new-posts/caregivers-and-epilepsy-it-takes-all-kinds/</link>
		<comments>http://www.brainthunders.com/new-posts/caregivers-and-epilepsy-it-takes-all-kinds/#comments</comments>
		<pubDate>Tue, 04 Jan 2011 10:57:22 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Being a Parent with Epilepsy]]></category>
		<category><![CDATA[Epilepsy Caregivers]]></category>
		<category><![CDATA[Epilepsy Community]]></category>
		<category><![CDATA[Kids and Epilepsy]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[Talking About Epilepsy]]></category>
		<category><![CDATA[Caregivers and Epilepsy]]></category>
		<category><![CDATA[epilepsy]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=1156</guid>
		<description><![CDATA[Being a caregiver, whether you are talking about Epilepsy or anything else, is one of the toughest jobs on the planet. Really.]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/caregivers-and-epilepsy-it-takes-all-kinds/feed/</wfw:commentRss>
		<slash:comments>1</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>
		</item>
		<item>
		<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>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/new-years-resolution-time-whats-your-story/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<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>
		<item>
		<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>Wrestling with Ignorance&#8230;or Understanding the Choices Others Make?</title>
		<link>http://www.brainthunders.com/new-posts/wrestling-with-ignorance-or-understanding-the-choices-others-make/</link>
		<comments>http://www.brainthunders.com/new-posts/wrestling-with-ignorance-or-understanding-the-choices-others-make/#comments</comments>
		<pubDate>Sun, 21 Nov 2010 12:28:33 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Being a Parent with Epilepsy]]></category>
		<category><![CDATA[Epilepsy Advocates]]></category>
		<category><![CDATA[Epilepsy and Facebook]]></category>
		<category><![CDATA[Epilepsy Causes]]></category>
		<category><![CDATA[Epilepsy Community]]></category>
		<category><![CDATA[Epilepsy organizations]]></category>
		<category><![CDATA[Epilepsy Websites]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[Purple for Epilepsy]]></category>
		<category><![CDATA[Supporting Epilepsy Programs]]></category>
		<category><![CDATA[Talking About Epilepsy]]></category>
		<category><![CDATA[The Stigma of Epilepsy]]></category>
		<category><![CDATA[Epilepsy advocates]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=1118</guid>
		<description><![CDATA[You all...or WE...should be very proud of our efforts to promote Epilepsy awareness. And, I know it's not over yet. As someone who is always watching the process, I have to wonder: how successful have we been in moving the needle?]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/wrestling-with-ignorance-or-understanding-the-choices-others-make/feed/</wfw:commentRss>
		<slash:comments>3</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>
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