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	<title> &#187; Epilepsy Treatments</title>
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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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		<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>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>Teaching and Informing the Very Young&#8230;when They are the Ones with Epilepsy</title>
		<link>http://www.brainthunders.com/new-posts/teaching-and-informing-the-very-young-when-they-are-the-ones-with-epilepsy/</link>
		<comments>http://www.brainthunders.com/new-posts/teaching-and-informing-the-very-young-when-they-are-the-ones-with-epilepsy/#comments</comments>
		<pubDate>Sat, 16 Oct 2010 11:56:29 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Being a Parent with Epilepsy]]></category>
		<category><![CDATA[Epilepsy Advocates]]></category>
		<category><![CDATA[Epilepsy Caregivers]]></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[Talking About Epilepsy]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=1069</guid>
		<description><![CDATA[When exactly do you tell a child about his or her epilepsy and everything that comes along with it? Granted he knows when he's not feeling well, but as a young child, can he understand what it is that's making him sick? ]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/teaching-and-informing-the-very-young-when-they-are-the-ones-with-epilepsy/feed/</wfw:commentRss>
		<slash:comments>1</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>One Mom&#8217;s Journey with Epilepsy and her Determination to Help Her Daughter&#8230;</title>
		<link>http://www.brainthunders.com/new-posts/one-moms-journey-with-epilepsy-and-her-determination-to-help-her-daughter/</link>
		<comments>http://www.brainthunders.com/new-posts/one-moms-journey-with-epilepsy-and-her-determination-to-help-her-daughter/#comments</comments>
		<pubDate>Mon, 16 Aug 2010 12:42:10 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Alternative Therapies for Epilepsy]]></category>
		<category><![CDATA[Epilepsy Advocates]]></category>
		<category><![CDATA[Epilepsy and Health Care Reform]]></category>
		<category><![CDATA[Epilepsy Community]]></category>
		<category><![CDATA[Epilepsy Medications]]></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[The Ketogenic Diet for Epilepsy]]></category>
		<category><![CDATA[Epilepsy advocates]]></category>
		<category><![CDATA[ketogenic diet]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=954</guid>
		<description><![CDATA[Paulette George is a wife, mother and author. She penned the book, Good Morning Beautiful, about her daughter Christina's journey with Epilepsy and Autism. Suffering more than 100 seizures each day, Paulette and her husband eventually discovered the Ketogenic Diet and they began implementing the diet for Christina. Brainthunders spoke to her.]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/one-moms-journey-with-epilepsy-and-her-determination-to-help-her-daughter/feed/</wfw:commentRss>
		<slash:comments>3</slash:comments>
		</item>
		<item>
		<title>When One of Your Personal Advocates Falls Ill&#8230;</title>
		<link>http://www.brainthunders.com/new-posts/when-one-of-your-personal-advocates-falls-ill/</link>
		<comments>http://www.brainthunders.com/new-posts/when-one-of-your-personal-advocates-falls-ill/#comments</comments>
		<pubDate>Wed, 11 Aug 2010 13:57:49 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Animals and Epilepsy]]></category>
		<category><![CDATA[Auras]]></category>
		<category><![CDATA[Epilepsy Advocates]]></category>
		<category><![CDATA[Epilepsy Treatments]]></category>
		<category><![CDATA[Family]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[Seizures]]></category>
		<category><![CDATA[Talking About Epilepsy]]></category>
		<category><![CDATA[epilepsy]]></category>
		<category><![CDATA[seizure alert dogs]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=942</guid>
		<description><![CDATA[Tucket was Andrew's dog, through and through, but in January 2003, when I became sick and began this journey called Epilepsy, Tucket really became 'my' dog. We always marveled at how he could sense seizures. He was not trained to be a seizure alert dog, but he has this amazing quality. He climbs into my lap when my auras begin, sometimes even tugging at my clothes so I know to sit down on a piece of furniture if I'm standing.]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/when-one-of-your-personal-advocates-falls-ill/feed/</wfw:commentRss>
		<slash:comments>9</slash:comments>
		</item>
		<item>
		<title>A Comment Worth Commenting on&#8230;</title>
		<link>http://www.brainthunders.com/new-posts/a-comment-worth-commenting-on/</link>
		<comments>http://www.brainthunders.com/new-posts/a-comment-worth-commenting-on/#comments</comments>
		<pubDate>Mon, 09 Aug 2010 13:37:12 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Being a Parent with Epilepsy]]></category>
		<category><![CDATA[Childcare]]></category>
		<category><![CDATA[Epilepsy Advocates]]></category>
		<category><![CDATA[Epilepsy and Pregnancy]]></category>
		<category><![CDATA[Epilepsy Research Studies]]></category>
		<category><![CDATA[Epilepsy Treatments]]></category>
		<category><![CDATA[Family]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[epilepsy and children]]></category>
		<category><![CDATA[Parents with Epilepsy]]></category>
		<category><![CDATA[Seizures]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=920</guid>
		<description><![CDATA[As for my child, I pride myself on the fact that she has just as normal a life as her friends and classmates, and I work very hard at this. Does her mother have seizures? Yes, but she is cognizant of that and she knows how to react. I surround myself with people who understand and care, from my husband to my very, very close friends. So, I never worry that she is deprived of love and attention.]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/a-comment-worth-commenting-on/feed/</wfw:commentRss>
		<slash:comments>9</slash:comments>
		</item>
		<item>
		<title>Scary Story of Doctor Accused of Misdiagnosing Kids Carries Lessons</title>
		<link>http://www.brainthunders.com/new-posts/scary-story-of-doctor-accused-of-misdiagnosing-kids-carries-lessons/</link>
		<comments>http://www.brainthunders.com/new-posts/scary-story-of-doctor-accused-of-misdiagnosing-kids-carries-lessons/#comments</comments>
		<pubDate>Fri, 06 Aug 2010 18:50:42 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Epilepsy Drug Side Effects]]></category>
		<category><![CDATA[Epilepsy Medications]]></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[Diagnosing Epilepsy]]></category>
		<category><![CDATA[Neurologists]]></category>
		<category><![CDATA[Pediatric Neurologists]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=915</guid>
		<description><![CDATA[A neurologist in Detroit is accused of misdiagnosing hundreds of children...telling them they had Epilepsy. It turns out, they don't. He prescribed medication for virtually all of them, brutal and terrifying anti-seizure medications. ]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/scary-story-of-doctor-accused-of-misdiagnosing-kids-carries-lessons/feed/</wfw:commentRss>
		<slash:comments>1</slash:comments>
		</item>
		<item>
		<title>Reaction&#8230;and Action</title>
		<link>http://www.brainthunders.com/new-posts/reaction-and-action/</link>
		<comments>http://www.brainthunders.com/new-posts/reaction-and-action/#comments</comments>
		<pubDate>Mon, 02 Aug 2010 12:03:45 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Epilepsy Advocates]]></category>
		<category><![CDATA[Epilepsy and Facebook]]></category>
		<category><![CDATA[Epilepsy Community]]></category>
		<category><![CDATA[Epilepsy Medications]]></category>
		<category><![CDATA[Epilepsy Treatments]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[SUDEP Awareness]]></category>
		<category><![CDATA[epilepsy advocacy]]></category>
		<category><![CDATA[Epilepsy Websites]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=909</guid>
		<description><![CDATA[Regarding the aolhealth.com post last week, I heard from SO many readers, both new and old...and your compliments were very encouraging, not to mention, welcome! I also received lots of advice, questions and words of encouragement. It's why I'm doing what I'm doing with this blog!]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/reaction-and-action/feed/</wfw:commentRss>
		<slash:comments>1</slash:comments>
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