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	<title> &#187; Epilepsy Websites</title>
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		<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>
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		<title>Speak up and Speak out about Living Life with Epilepsy!</title>
		<link>http://www.brainthunders.com/new-posts/speak-up-and-speak-out-about-living-life-with-epilepsy/</link>
		<comments>http://www.brainthunders.com/new-posts/speak-up-and-speak-out-about-living-life-with-epilepsy/#comments</comments>
		<pubDate>Wed, 07 Jul 2010 13:28:47 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Epilepsy Advocates]]></category>
		<category><![CDATA[Epilepsy and Facebook]]></category>
		<category><![CDATA[Epilepsy Websites]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[Seizures]]></category>
		<category><![CDATA[SUDEP Awareness]]></category>
		<category><![CDATA[SUDEP]]></category>
		<category><![CDATA[Talking About Epilepsy]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=680</guid>
		<description><![CDATA[Speaking up and speaking out CAN help. With 3 million people in the U.S. living with Epilepsy and nearly 50 million people around the world, we can stand up and be noticed!]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/speak-up-and-speak-out-about-living-life-with-epilepsy/feed/</wfw:commentRss>
		<slash:comments>1</slash:comments>
		</item>
		<item>
		<title>Understanding the Fear and Stigma of Epilepsy</title>
		<link>http://www.brainthunders.com/new-posts/understanding-the-fear-and-stigma-of-epilepsy/</link>
		<comments>http://www.brainthunders.com/new-posts/understanding-the-fear-and-stigma-of-epilepsy/#comments</comments>
		<pubDate>Fri, 25 Jun 2010 11:33:58 +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 Community]]></category>
		<category><![CDATA[Epilepsy Websites]]></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[epilepsy advocacy]]></category>
		<category><![CDATA[Parents with Epilepsy]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=647</guid>
		<description><![CDATA[I was told that one of my daughter's friends will not be able to come over to our house for a play date because of my 'situation' as it was termed. The mother does not want to expose her child to 'anything scary', i.e. a seizure. ]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/understanding-the-fear-and-stigma-of-epilepsy/feed/</wfw:commentRss>
		<slash:comments>2</slash:comments>
		</item>
		<item>
		<title>Get in the Game&#8230;to promote Epilepsy Advocacy</title>
		<link>http://www.brainthunders.com/new-posts/get-in-the-game-to-promote-epilepsy-advocacy/</link>
		<comments>http://www.brainthunders.com/new-posts/get-in-the-game-to-promote-epilepsy-advocacy/#comments</comments>
		<pubDate>Mon, 21 Jun 2010 16:13:19 +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 Legislation]]></category>
		<category><![CDATA[Epilepsy Websites]]></category>
		<category><![CDATA[Kids and Epilepsy]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[SUDEP Awareness]]></category>
		<category><![CDATA[epilepsy advocacy]]></category>
		<category><![CDATA[epilepsy funding]]></category>
		<category><![CDATA[parenting]]></category>
		<category><![CDATA[SUDEP]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=640</guid>
		<description><![CDATA[Epilepsy and SUDEP has become their mission with the Danny Did Foundation. And, they are doing a fantastic job. Their spirit and their drive to raise awareness and try to teach more people about Epilepsy and SUDEP in particular has truly inspired thousands of us!]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/get-in-the-game-to-promote-epilepsy-advocacy/feed/</wfw:commentRss>
		<slash:comments>2</slash:comments>
		</item>
		<item>
		<title>Your Seizure Log can help All of us&#8230;</title>
		<link>http://www.brainthunders.com/new-posts/your-seizure-log-can-help-all-of-us/</link>
		<comments>http://www.brainthunders.com/new-posts/your-seizure-log-can-help-all-of-us/#comments</comments>
		<pubDate>Tue, 11 May 2010 13:26:23 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Epilepsy Advocates]]></category>
		<category><![CDATA[Epilepsy Community]]></category>
		<category><![CDATA[Epilepsy Medications]]></category>
		<category><![CDATA[Epilepsy Websites]]></category>
		<category><![CDATA[Epileptologists]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[Seizures]]></category>
		<category><![CDATA[Tracking Seizures]]></category>
		<category><![CDATA[caregivers]]></category>
		<category><![CDATA[epilepsy]]></category>
		<category><![CDATA[Seizure Logs]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=553</guid>
		<description><![CDATA[The overall goal of tracking seizures is to find a pattern, the seizure triggers and the length and severity of seizures to make sure you are being treated properly.]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/your-seizure-log-can-help-all-of-us/feed/</wfw:commentRss>
		<slash:comments>1</slash:comments>
		</item>
		<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>A Great Film we can All Learn From&#8230;and a Great Family Talking about Living with Epilepsy</title>
		<link>http://www.brainthunders.com/new-posts/a-great-film-we-can-all-learn-from-and-a-great-family-talking-about-living-with-epilepsy/</link>
		<comments>http://www.brainthunders.com/new-posts/a-great-film-we-can-all-learn-from-and-a-great-family-talking-about-living-with-epilepsy/#comments</comments>
		<pubDate>Wed, 14 Apr 2010 13:37:05 +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[Epilepsy Websites]]></category>
		<category><![CDATA[Kids and Epilepsy]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[Seizures]]></category>
		<category><![CDATA[epilepsy]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=464</guid>
		<description><![CDATA[A film done to honor Evan Moss and his life with Epilepsy, just won the top prize at the Neuro Film fest and the Fan Favorite Award.]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/a-great-film-we-can-all-learn-from-and-a-great-family-talking-about-living-with-epilepsy/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Spend a day seeking out some real facts about Epilepsy!</title>
		<link>http://www.brainthunders.com/new-posts/spend-a-day-seeking-out-some-real-facts-about-epilepsy/</link>
		<comments>http://www.brainthunders.com/new-posts/spend-a-day-seeking-out-some-real-facts-about-epilepsy/#comments</comments>
		<pubDate>Tue, 06 Apr 2010 14:21:19 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Epilepsy Advocates]]></category>
		<category><![CDATA[Epilepsy Chat Rooms]]></category>
		<category><![CDATA[Epilepsy Community]]></category>
		<category><![CDATA[Epilepsy Medications]]></category>
		<category><![CDATA[Epilepsy Research Studies]]></category>
		<category><![CDATA[Epilepsy Treatments]]></category>
		<category><![CDATA[Epilepsy Websites]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[Neurologists]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[Seizures]]></category>
		<category><![CDATA[Talking About Epilepsy]]></category>
		<category><![CDATA[epilepsy]]></category>
		<category><![CDATA[epilepsy news]]></category>
		<category><![CDATA[neurologist]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=444</guid>
		<description><![CDATA[So often, we all get wrapped up in communicating through social media outlets and spreading the word about Epilepsy via chatrooms. Are we caught up on the news about the disease?]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/spend-a-day-seeking-out-some-real-facts-about-epilepsy/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Is the VNS (Vagus Nerve Stimulator) the right solution for your Epilepsy? Here&#8217;s my story&#8230;</title>
		<link>http://www.brainthunders.com/new-posts/is-the-vns-vagus-nerve-stimulator-the-right-solution-for-your-epilepsy-heres-my-story/</link>
		<comments>http://www.brainthunders.com/new-posts/is-the-vns-vagus-nerve-stimulator-the-right-solution-for-your-epilepsy-heres-my-story/#comments</comments>
		<pubDate>Fri, 02 Apr 2010 11:17:36 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Alternative Therapies for Epilepsy]]></category>
		<category><![CDATA[Epilepsy Medications]]></category>
		<category><![CDATA[Epilepsy Surgery]]></category>
		<category><![CDATA[Epilepsy Treatments]]></category>
		<category><![CDATA[Epilepsy Websites]]></category>
		<category><![CDATA[Epileptologists]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[Neurologists]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[Seizures]]></category>
		<category><![CDATA[Vagus Nerve Stimulator]]></category>
		<category><![CDATA[epilepsy]]></category>
		<category><![CDATA[neurologist]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=428</guid>
		<description><![CDATA[Once you get the 'NO' on surgery and you've experimented with multiple meds, is there anything left that will help you take back your life from a life of seizures?]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/is-the-vns-vagus-nerve-stimulator-the-right-solution-for-your-epilepsy-heres-my-story/feed/</wfw:commentRss>
		<slash:comments>9</slash:comments>
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