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	<title> &#187; neurologist</title>
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		<title>&#8216;The Doctors&#8217;&#8230;and the Vagus Nerve Stimulator</title>
		<link>http://www.brainthunders.com/new-posts/the-doctors-and-the-vagus-nerve-stimulator/</link>
		<comments>http://www.brainthunders.com/new-posts/the-doctors-and-the-vagus-nerve-stimulator/#comments</comments>
		<pubDate>Thu, 20 May 2010 14:02:48 +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 Treatments]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[Neurologists]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[Vagus Nerve Stimulator]]></category>
		<category><![CDATA[Epilepsy Surgery]]></category>
		<category><![CDATA[neurologist]]></category>
		<category><![CDATA[Seizures]]></category>
		<category><![CDATA[The Doctors]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=589</guid>
		<description><![CDATA['The Doctors' gave us a great opportunity to explore the option of the Vagus Nerve Stimulator (VNS).]]></description>
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		<slash:comments>1</slash:comments>
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		<title>Cody&#8217;s story&#8230;and her Mom&#8217;s fight to raise Epilepsy awareness</title>
		<link>http://www.brainthunders.com/new-posts/codys-story-and-her-moms-fight-to-raise-epilepsy-awareness/</link>
		<comments>http://www.brainthunders.com/new-posts/codys-story-and-her-moms-fight-to-raise-epilepsy-awareness/#comments</comments>
		<pubDate>Sat, 10 Apr 2010 11:49:18 +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 Drug Side Effects]]></category>
		<category><![CDATA[Epilepsy Medications]]></category>
		<category><![CDATA[Kids and Epilepsy]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[Seizures]]></category>
		<category><![CDATA[anti-seizure medications]]></category>
		<category><![CDATA[epilepsy]]></category>
		<category><![CDATA[Epilepsy advocate]]></category>
		<category><![CDATA[neurologist]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=448</guid>
		<description><![CDATA[Meet an incredible Epilepsy advocate...a Mom who lost a child to Epilepsy.]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/codys-story-and-her-moms-fight-to-raise-epilepsy-awareness/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>
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		<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>6</slash:comments>
		</item>
		<item>
		<title>Chicago-area family dedicated to SUDEP awareness after suffering unbelievable loss</title>
		<link>http://www.brainthunders.com/new-posts/chicago-area-family-dedicated-to-sudep-awareness-after-suffering-unbelievable-loss/</link>
		<comments>http://www.brainthunders.com/new-posts/chicago-area-family-dedicated-to-sudep-awareness-after-suffering-unbelievable-loss/#comments</comments>
		<pubDate>Thu, 25 Mar 2010 11:00:51 +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 Websites]]></category>
		<category><![CDATA[Kids and Epilepsy]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[SUDEP Awareness]]></category>
		<category><![CDATA[Seizures]]></category>
		<category><![CDATA[Talking About Epilepsy]]></category>
		<category><![CDATA[Danny Did Foundation]]></category>
		<category><![CDATA[epilepsy]]></category>
		<category><![CDATA[neurologist]]></category>
		<category><![CDATA[SUDEP]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=402</guid>
		<description><![CDATA[Perhaps one of the greatest mysteries surrounding Epilepsy and seizures is SUDEP or Sudden Unexplained Death in Epilepsy. There is no known cause and like Epilepsy itself, no cure.
]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/chicago-area-family-dedicated-to-sudep-awareness-after-suffering-unbelievable-loss/feed/</wfw:commentRss>
		<slash:comments>6</slash:comments>
		</item>
		<item>
		<title>How to help someone who has been newly diagnosed with Epilepsy&#8230;</title>
		<link>http://www.brainthunders.com/new-posts/how-to-help-someone-who-has-been-newly-diagnosed-with-epilepsy/</link>
		<comments>http://www.brainthunders.com/new-posts/how-to-help-someone-who-has-been-newly-diagnosed-with-epilepsy/#comments</comments>
		<pubDate>Wed, 17 Mar 2010 13:40:39 +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 Surgery]]></category>
		<category><![CDATA[Epilepsy Websites]]></category>
		<category><![CDATA[Epileptologists]]></category>
		<category><![CDATA[Lifestyles]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[Neurologists]]></category>
		<category><![CDATA[New Epilepsy Diagnosis]]></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=385</guid>
		<description><![CDATA[How can you help those who will be diagnosed with Epilepsy just this year? Statistics show 200,000 people will be diagnosed in 2010. Those of us who live with the disease each day know what we are dealing with...but how about those 'newbies' to this life? ]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/how-to-help-someone-who-has-been-newly-diagnosed-with-epilepsy/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Parents with Epilepsy must deliver a message to our children&#8230;</title>
		<link>http://www.brainthunders.com/new-posts/parents-with-epilepsy-must-deliver-a-message-to-our-children/</link>
		<comments>http://www.brainthunders.com/new-posts/parents-with-epilepsy-must-deliver-a-message-to-our-children/#comments</comments>
		<pubDate>Mon, 15 Mar 2010 13:03:48 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Being a Parent with Epilepsy]]></category>
		<category><![CDATA[Epilepsy Community]]></category>
		<category><![CDATA[Kids and Epilepsy]]></category>
		<category><![CDATA[Life Changes and Epilepsy]]></category>
		<category><![CDATA[Lifestyles]]></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[Vagus Nerve Stimulator]]></category>
		<category><![CDATA[epilepsy]]></category>
		<category><![CDATA[neurologist]]></category>
		<category><![CDATA[Parents with Epilepsy]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=379</guid>
		<description><![CDATA[Those of us who live with Epilepsy, or those who care for someone living with Epilepsy view parenthood in a unique way. ]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/parents-with-epilepsy-must-deliver-a-message-to-our-children/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>To switch or not to switch&#8230;taking care of your Epilepsy might mean making a tough decision about your doctor</title>
		<link>http://www.brainthunders.com/new-posts/to-switch-or-not-to-switch-taking-care-of-your-epilepsy-might-mean-making-a-tough-decision-about-your-doctor/</link>
		<comments>http://www.brainthunders.com/new-posts/to-switch-or-not-to-switch-taking-care-of-your-epilepsy-might-mean-making-a-tough-decision-about-your-doctor/#comments</comments>
		<pubDate>Wed, 10 Mar 2010 15:32:20 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Epilepsy Community]]></category>
		<category><![CDATA[Epilepsy Medications]]></category>
		<category><![CDATA[Epilepsy Surgery]]></category>
		<category><![CDATA[Epilepsy Treatments]]></category>
		<category><![CDATA[Epileptologists]]></category>
		<category><![CDATA[Life Changes and Epilepsy]]></category>
		<category><![CDATA[Lifestyles]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[Neurologists]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[Seizures]]></category>
		<category><![CDATA[Switching Neurologists]]></category>
		<category><![CDATA[epilepsy]]></category>
		<category><![CDATA[epileptologist]]></category>
		<category><![CDATA[neurologist]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=371</guid>
		<description><![CDATA[Switching doctors...or even getting a second opinion shouldn't be something you fear. It's a necessary part of your care.]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/to-switch-or-not-to-switch-taking-care-of-your-epilepsy-might-mean-making-a-tough-decision-about-your-doctor/feed/</wfw:commentRss>
		<slash:comments>2</slash:comments>
		</item>
		<item>
		<title>The opinions of others matter when it comes to making decisions about Epilepsy care&#8230;but use caution</title>
		<link>http://www.brainthunders.com/new-posts/the-opinions-of-others-matter-when-it-comes-to-making-decisions-about-epilepsy-care-but-use-caution/</link>
		<comments>http://www.brainthunders.com/new-posts/the-opinions-of-others-matter-when-it-comes-to-making-decisions-about-epilepsy-care-but-use-caution/#comments</comments>
		<pubDate>Mon, 08 Mar 2010 14:26:31 +0000</pubDate>
		<dc:creator>Alysse</dc:creator>
				<category><![CDATA[Epilepsy Community]]></category>
		<category><![CDATA[Epilepsy Medications]]></category>
		<category><![CDATA[Epilepsy Treatments]]></category>
		<category><![CDATA[Epilepsy Websites]]></category>
		<category><![CDATA[Lifestyles]]></category>
		<category><![CDATA[Living with Epilepsy]]></category>
		<category><![CDATA[Neurologists]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[Seizures]]></category>
		<category><![CDATA[anti-seizure medication]]></category>
		<category><![CDATA[epilepsy]]></category>
		<category><![CDATA[neurologist]]></category>
		<category><![CDATA[Vimpat]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=362</guid>
		<description><![CDATA[If you're like me, when it comes to your illness--in this case Epilepsy, if it's time to try something new, whether it's an anti-seizure medication, a test, a new doctor, treatment center or alternative therapy, the research floodgates are opened. My computer becomes my best friend. ]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/the-opinions-of-others-matter-when-it-comes-to-making-decisions-about-epilepsy-care-but-use-caution/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>The power of Connection can provide strength when living with Epilepsy</title>
		<link>http://www.brainthunders.com/new-posts/the-power-of-connection-can-provide-strength-when-living-with-epilepsy/</link>
		<comments>http://www.brainthunders.com/new-posts/the-power-of-connection-can-provide-strength-when-living-with-epilepsy/#comments</comments>
		<pubDate>Thu, 04 Mar 2010 11:55:01 +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 Websites]]></category>
		<category><![CDATA[New Posts]]></category>
		<category><![CDATA[Talking About Epilepsy]]></category>
		<category><![CDATA[epilepsy]]></category>
		<category><![CDATA[Epilepsy-related websites]]></category>
		<category><![CDATA[neurologist]]></category>
		<category><![CDATA[Seizures]]></category>

		<guid isPermaLink="false">http://www.brainthunders.com/?p=358</guid>
		<description><![CDATA[As someone living with Epilepsy, I never truly understood what connection meant or how much it could do in terms of outreach and support until I experienced it.]]></description>
		<wfw:commentRss>http://www.brainthunders.com/new-posts/the-power-of-connection-can-provide-strength-when-living-with-epilepsy/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
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