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	<title>positive attitude | BBHwithMS</title>
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	<description>******************************* BBH - BOOBS BOOTS &#38; HAIR **************************** Inappropriate MMJ Momma - Living With Multiple Sclerosis and Finding The Reasons to Laugh and Smile</description>
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	<title>positive attitude | BBHwithMS</title>
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	<item>
		<title>Multiple Sclerosis &#038; Cannabis: Traveling With An Invisible Disease</title>
		<link>/multiple-sclerosis-cannabis-traveling-with-an-invisible-disease/</link>
					<comments>/multiple-sclerosis-cannabis-traveling-with-an-invisible-disease/#comments</comments>
		
		<dc:creator><![CDATA[Meg]]></dc:creator>
		<pubDate>Mon, 09 Apr 2018 21:04:30 +0000</pubDate>
				<category><![CDATA[disabled]]></category>
		<category><![CDATA[living with MS]]></category>
		<category><![CDATA[means of mobility]]></category>
		<category><![CDATA[MMJ & Multiple Sclerosis]]></category>
		<category><![CDATA[MS]]></category>
		<category><![CDATA[MS Awareness]]></category>
		<category><![CDATA[Multiple Sclerosis]]></category>
		<category><![CDATA[Multiple Sclerosis & Cannabis]]></category>
		<category><![CDATA[Multiple Sclerosis & Positive Attitude]]></category>
		<category><![CDATA[Multiple Sclerosis & Traveling]]></category>
		<category><![CDATA[positive attitude]]></category>
		<category><![CDATA[Traveling with an Invisible Disease]]></category>
		<category><![CDATA[Traveling with MS]]></category>
		<category><![CDATA[Uncategorized]]></category>
		<category><![CDATA[using a cane]]></category>
		<category><![CDATA[MS & Travel]]></category>
		<category><![CDATA[Multiple Sclerosis & Travel]]></category>
		<category><![CDATA[Multiple Sclerosis and Cannabis]]></category>
		<category><![CDATA[Traveling with an Invisible disease]]></category>
		<guid isPermaLink="false">/?p=3906</guid>

					<description><![CDATA[Smiles and laughter are infectious!  People are drawn to other people that seem genuinely happy, who seem to be loving life.  Because ultimately ALL of us want that, to be happy and to love life. &#160; This past week we traveled to Syracuse New York, which REALLY is not all that impressive, seeing as it [&#8230;]]]></description>
		
					<wfw:commentRss>/multiple-sclerosis-cannabis-traveling-with-an-invisible-disease/feed/</wfw:commentRss>
			<slash:comments>14</slash:comments>
		
		
			</item>
		<item>
		<title>What I Owe To My MS: Continuing To Be Strong &#038; Grateful</title>
		<link>/what-i-owe-to-my-ms-continuing-to-be-strong-grateful/</link>
					<comments>/what-i-owe-to-my-ms-continuing-to-be-strong-grateful/#comments</comments>
		
		<dc:creator><![CDATA[Meg]]></dc:creator>
		<pubDate>Mon, 14 Nov 2016 19:09:35 +0000</pubDate>
				<category><![CDATA[Being Strong with a disease]]></category>
		<category><![CDATA[Gratitude]]></category>
		<category><![CDATA[living with a disease]]></category>
		<category><![CDATA[living with MS]]></category>
		<category><![CDATA[MS]]></category>
		<category><![CDATA[MS & friends]]></category>
		<category><![CDATA[National MS Society]]></category>
		<category><![CDATA[positive attitude]]></category>
		<category><![CDATA[smile & laugh]]></category>
		<category><![CDATA[Strength to cope with MS]]></category>
		<category><![CDATA[Uncategorized]]></category>
		<category><![CDATA[why me?]]></category>
		<guid isPermaLink="false">/?p=2285</guid>

					<description><![CDATA[I had the honor once again to be a guest on the Brain Injury Radio show Mess With MS; hosted by Lisa Dryer on Saturday night.  Although I have yet to sit and listen back to myself (I am sure there are plenty of rambling moments) I did want to share just how much I [&#8230;]]]></description>
		
					<wfw:commentRss>/what-i-owe-to-my-ms-continuing-to-be-strong-grateful/feed/</wfw:commentRss>
			<slash:comments>3</slash:comments>
		
		
			</item>
		<item>
		<title>OH SHIT&#8230;NOT Again!  What Classifies A Fall As A &#8220;Good&#8221; Fall?</title>
		<link>/what-classifies-a-fall-as-a-good-fall/</link>
					<comments>/what-classifies-a-fall-as-a-good-fall/#comments</comments>
		
		<dc:creator><![CDATA[Meg]]></dc:creator>
		<pubDate>Wed, 16 Mar 2016 17:09:47 +0000</pubDate>
				<category><![CDATA[Being Strong with a disease]]></category>
		<category><![CDATA[confidence]]></category>
		<category><![CDATA[disabled]]></category>
		<category><![CDATA[Exercise and MS]]></category>
		<category><![CDATA[Falling down with MS]]></category>
		<category><![CDATA[I have fallen and can't get up]]></category>
		<category><![CDATA[living with a disease]]></category>
		<category><![CDATA[living with MS]]></category>
		<category><![CDATA[means of mobility]]></category>
		<category><![CDATA[MS]]></category>
		<category><![CDATA[Multiple Sclerosis]]></category>
		<category><![CDATA[Pain]]></category>
		<category><![CDATA[positive attitude]]></category>
		<guid isPermaLink="false">/?p=1792</guid>

					<description><![CDATA[Hey all&#8230;back from my &#8220;winter break with the kids/parents visiting from out of town visit&#8221; hiatus.  I have good news and bad news.  The BAD NEWS is that I had a pretty bad fall.  Knees and palms were pretty shredded up, I may have a fucked up wrist -it hurts like hell to &#8220;move it like [&#8230;]]]></description>
		
					<wfw:commentRss>/what-classifies-a-fall-as-a-good-fall/feed/</wfw:commentRss>
			<slash:comments>16</slash:comments>
		
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			</item>
		<item>
		<title>Another Year with MS &#8211; Being A Strong Motherfucker &#038; Living Out My Dream</title>
		<link>/2016-a-year-of-dreams/</link>
					<comments>/2016-a-year-of-dreams/#comments</comments>
		
		<dc:creator><![CDATA[Meg]]></dc:creator>
		<pubDate>Mon, 04 Jan 2016 20:02:07 +0000</pubDate>
				<category><![CDATA[Being Strong with a disease]]></category>
		<category><![CDATA[dealing with disease]]></category>
		<category><![CDATA[Doctor]]></category>
		<category><![CDATA[Dreams]]></category>
		<category><![CDATA[living with a disease]]></category>
		<category><![CDATA[living with MS]]></category>
		<category><![CDATA[MS]]></category>
		<category><![CDATA[MS & friends]]></category>
		<category><![CDATA[Multiple Sclerosis]]></category>
		<category><![CDATA[positive attitude]]></category>
		<category><![CDATA[reasons to laugh and smile]]></category>
		<category><![CDATA[smile & laugh]]></category>
		<category><![CDATA[Strength to cope with MS]]></category>
		<category><![CDATA[Uncategorized]]></category>
		<category><![CDATA[writing]]></category>
		<guid isPermaLink="false">/?p=1570</guid>

					<description><![CDATA[My life has changed SO much in the past 10 years, when I sit down and spend any time thinking about it, it really is mind blowing. When I was first diagnosed with MS &#8211; I was blessed to have a doctor that seems to have understood who I am and how I deal with [&#8230;]]]></description>
		
					<wfw:commentRss>/2016-a-year-of-dreams/feed/</wfw:commentRss>
			<slash:comments>14</slash:comments>
		
		
			</item>
		<item>
		<title>FUCK!  I&#8217;ve Fallen &#038; I&#8217;m Not Sure I Want To Get Up!</title>
		<link>/help-i-have-fallen-and-i-cant-get-up/</link>
					<comments>/help-i-have-fallen-and-i-cant-get-up/#comments</comments>
		
		<dc:creator><![CDATA[Meg]]></dc:creator>
		<pubDate>Fri, 13 Dec 2013 03:38:38 +0000</pubDate>
				<category><![CDATA[Being Strong with a disease]]></category>
		<category><![CDATA[children's self image]]></category>
		<category><![CDATA[dealing with disease]]></category>
		<category><![CDATA[embarrassing moments]]></category>
		<category><![CDATA[Falling down with MS]]></category>
		<category><![CDATA[I have fallen and can't get up]]></category>
		<category><![CDATA[living with a disease]]></category>
		<category><![CDATA[living with MS]]></category>
		<category><![CDATA[MRI scan for MS]]></category>
		<category><![CDATA[MS]]></category>
		<category><![CDATA[MS and spinal patch]]></category>
		<category><![CDATA[MS and spinal tap]]></category>
		<category><![CDATA[Multiple Sclerosis]]></category>
		<category><![CDATA[parenting]]></category>
		<category><![CDATA[positive attitude]]></category>
		<category><![CDATA[reasons to laugh and smile]]></category>
		<category><![CDATA[reducing stress]]></category>
		<category><![CDATA[smile & laugh]]></category>
		<category><![CDATA[Strength to cope with MS]]></category>
		<category><![CDATA[stress]]></category>
		<category><![CDATA[Uncategorized]]></category>
		<guid isPermaLink="false">/?p=1317</guid>

					<description><![CDATA[&#160; &#160; I’m lying in the pouring rain, covered in shattered glass, wine and blood; unable to get up because my legs have gone paralyzed.  All I can do is laugh; the body shaking, eyes watering up type of laughter.  As hard as I try, I cannot get back up.  I keep thinking of the [&#8230;]]]></description>
		
					<wfw:commentRss>/help-i-have-fallen-and-i-cant-get-up/feed/</wfw:commentRss>
			<slash:comments>11</slash:comments>
		
		
			</item>
		<item>
		<title>THANKFUL For That Which Makes Me Strong &#8211; How MS Made Me Stronger</title>
		<link>/thankful-for-that-which-makes-me-strong-how-ms-made-me-stronger/</link>
					<comments>/thankful-for-that-which-makes-me-strong-how-ms-made-me-stronger/#comments</comments>
		
		<dc:creator><![CDATA[Meg]]></dc:creator>
		<pubDate>Fri, 29 Nov 2013 20:38:45 +0000</pubDate>
				<category><![CDATA[Being Strong with a disease]]></category>
		<category><![CDATA[dealing with disease]]></category>
		<category><![CDATA[divorce]]></category>
		<category><![CDATA[living with a disease]]></category>
		<category><![CDATA[living with MS]]></category>
		<category><![CDATA[MS]]></category>
		<category><![CDATA[Multiple Sclerosis]]></category>
		<category><![CDATA[positive attitude]]></category>
		<category><![CDATA[Strength to cope with MS]]></category>
		<category><![CDATA[Uncategorized]]></category>
		<category><![CDATA[why me?]]></category>
		<guid isPermaLink="false">/?p=1135</guid>

					<description><![CDATA[I AM STRONG!  &#160; Always have been, and hopefully always will be.   I didn&#8217;t choose to get this disease; I&#8217;m pretty sure no one did (or any other disease for that matter.)  When I was confronted with the truth, for the real reason that first my foot felt like it was chronically asleep, then the leg, then [&#8230;]]]></description>
		
					<wfw:commentRss>/thankful-for-that-which-makes-me-strong-how-ms-made-me-stronger/feed/</wfw:commentRss>
			<slash:comments>4</slash:comments>
		
		
			</item>
		<item>
		<title>Confessions of a Potty-Sleeper</title>
		<link>/confessions-of-a-potty-sleeper/</link>
					<comments>/confessions-of-a-potty-sleeper/#comments</comments>
		
		<dc:creator><![CDATA[Meg]]></dc:creator>
		<pubDate>Fri, 14 Jun 2013 15:35:48 +0000</pubDate>
				<category><![CDATA[dealing with disease]]></category>
		<category><![CDATA[divorce]]></category>
		<category><![CDATA[living with a disease]]></category>
		<category><![CDATA[MS]]></category>
		<category><![CDATA[Multiple Sclerosis]]></category>
		<category><![CDATA[positive attitude]]></category>
		<category><![CDATA[reasons to laugh and smile]]></category>
		<category><![CDATA[smile & laugh]]></category>
		<category><![CDATA[Uncategorized]]></category>
		<guid isPermaLink="false">/?p=1032</guid>

					<description><![CDATA[I have something that I need to get off my chest&#8230;.to confess to all of you wonderful readers out there.  I&#8217;m not sure what the reaction to this confession will be, if I will risk loosing some of you, but I can&#8217;t NOT say anything, because at the end of the day, it is there, [&#8230;]]]></description>
		
					<wfw:commentRss>/confessions-of-a-potty-sleeper/feed/</wfw:commentRss>
			<slash:comments>12</slash:comments>
		
		
			</item>
		<item>
		<title>Not an &#8220;Oh Fuck&#8221; moment with MS&#8230;.and update on Biogen -Tecfidera</title>
		<link>/not-an-oh-fuck-moment-with-ms-and-update-on-biogen-tecfidera/</link>
					<comments>/not-an-oh-fuck-moment-with-ms-and-update-on-biogen-tecfidera/#comments</comments>
		
		<dc:creator><![CDATA[Meg]]></dc:creator>
		<pubDate>Tue, 11 Jun 2013 17:26:59 +0000</pubDate>
				<category><![CDATA[Biogen]]></category>
		<category><![CDATA[dealing with disease]]></category>
		<category><![CDATA[disease modidying drug]]></category>
		<category><![CDATA[DMD]]></category>
		<category><![CDATA[living with a disease]]></category>
		<category><![CDATA[living with MS]]></category>
		<category><![CDATA[means of mobility]]></category>
		<category><![CDATA[MS]]></category>
		<category><![CDATA[MS doctor]]></category>
		<category><![CDATA[MS drugs]]></category>
		<category><![CDATA[Multiple Sclerosis]]></category>
		<category><![CDATA[Neurologist]]></category>
		<category><![CDATA[positive attitude]]></category>
		<category><![CDATA[segway]]></category>
		<category><![CDATA[Tecfidera]]></category>
		<category><![CDATA[using a cane]]></category>
		<guid isPermaLink="false">/?p=1014</guid>

					<description><![CDATA[I have said that I will keep you updated on what is happening with my latest and greatest med &#8211; Biogen&#8217;s Tecfidera, and I will, but first wanted to share my story about &#8220;OH FUCK.&#8221; I was diagnosed with MS in December of 2007, Merry Christmas to me!  The symptoms began in June, first a [&#8230;]]]></description>
		
					<wfw:commentRss>/not-an-oh-fuck-moment-with-ms-and-update-on-biogen-tecfidera/feed/</wfw:commentRss>
			<slash:comments>13</slash:comments>
		
		
			</item>
		<item>
		<title>Biogen Tecfidera &#8211; One week in&#8230;</title>
		<link>/biogen-tecfidera-one-week-in/</link>
					<comments>/biogen-tecfidera-one-week-in/#comments</comments>
		
		<dc:creator><![CDATA[Meg]]></dc:creator>
		<pubDate>Wed, 05 Jun 2013 17:30:01 +0000</pubDate>
				<category><![CDATA[Biogen]]></category>
		<category><![CDATA[dealing with disease]]></category>
		<category><![CDATA[disease modidying drug]]></category>
		<category><![CDATA[DMD]]></category>
		<category><![CDATA[living with MS]]></category>
		<category><![CDATA[MRI scan for MS]]></category>
		<category><![CDATA[MS]]></category>
		<category><![CDATA[MS drugs]]></category>
		<category><![CDATA[Multiple Sclerosis]]></category>
		<category><![CDATA[positive attitude]]></category>
		<category><![CDATA[smile & laugh]]></category>
		<category><![CDATA[Tecfidera]]></category>
		<category><![CDATA[using a cane]]></category>
		<guid isPermaLink="false">/?p=986</guid>

					<description><![CDATA[For those of you that may be following my experience with Tecfidera a disease modifying drug (DMD) for the MS, I wanted to give a quick update.  I have been taking it for just over a week.  I took a half dose for seven days and yesterday bumped up to the full dose.  As for side-effects, [&#8230;]]]></description>
		
					<wfw:commentRss>/biogen-tecfidera-one-week-in/feed/</wfw:commentRss>
			<slash:comments>3</slash:comments>
		
		
			</item>
		<item>
		<title>Today I was diagnosed with MS</title>
		<link>/today-i-was-diagnosed-with-ms/</link>
					<comments>/today-i-was-diagnosed-with-ms/#comments</comments>
		
		<dc:creator><![CDATA[Meg]]></dc:creator>
		<pubDate>Thu, 30 May 2013 03:02:19 +0000</pubDate>
				<category><![CDATA[dealing with disease]]></category>
		<category><![CDATA[disease modifying drug]]></category>
		<category><![CDATA[living with MS]]></category>
		<category><![CDATA[MS]]></category>
		<category><![CDATA[Multiple Sclerosis]]></category>
		<category><![CDATA[positive attitude]]></category>
		<category><![CDATA[reasons to laugh and smile]]></category>
		<category><![CDATA[smile & laugh]]></category>
		<category><![CDATA[Tecfidera]]></category>
		<guid isPermaLink="false">/?p=913</guid>

					<description><![CDATA[Well ok, not really, but in some ways it feels like it.  Even though I have had MS since 2007,  I have never spent time on-line looking for anything regarding the disease.  Not information, not symptoms, not medicine and certainly not others that have MS (or MS-BFFs as my daughter would call them.)  I think [&#8230;]]]></description>
		
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			<slash:comments>4</slash:comments>
		
		
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