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	<title>using a cane | 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>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>Multiple Sclerosis &#038; Cannabis &#8211; Traveling With An Invisible Illness</title>
		<link>/multiple-sclerosis-cannabis-traveling-with-an-invisible-illness/</link>
					<comments>/multiple-sclerosis-cannabis-traveling-with-an-invisible-illness/#comments</comments>
		
		<dc:creator><![CDATA[Meg]]></dc:creator>
		<pubDate>Mon, 05 Feb 2018 20:35:03 +0000</pubDate>
				<category><![CDATA[Chronic Illness & Cannabis]]></category>
		<category><![CDATA[Living with Chronic Illness]]></category>
		<category><![CDATA[Medical Marijuana & MS]]></category>
		<category><![CDATA[MS & Traveling]]></category>
		<category><![CDATA[Multiple Sclerosis & Cannabis]]></category>
		<category><![CDATA[Multiple Sclerosis & Traveling]]></category>
		<category><![CDATA[Multiple Sclerosis & vision problems]]></category>
		<category><![CDATA[Traveling with a chronic illness]]></category>
		<category><![CDATA[Uncategorized]]></category>
		<category><![CDATA[using a cane]]></category>
		<guid isPermaLink="false">/?p=3745</guid>

					<description><![CDATA[“You should come to the Expo in Denver this weekend.”  That one simple message I received from an IG user would have a much larger impact on me than he could ever know.  What he was proposing was bigger than anything I have done since shooting babies out for my vagina.  He was suggesting that [&#8230;]]]></description>
		
					<wfw:commentRss>/multiple-sclerosis-cannabis-traveling-with-an-invisible-illness/feed/</wfw:commentRss>
			<slash:comments>10</slash:comments>
		
		
			</item>
		<item>
		<title>Multiple Sclerosis and Exercise: Happy To Be Moving Again</title>
		<link>/multiple-sclerosis-exercise-happy-moving/</link>
					<comments>/multiple-sclerosis-exercise-happy-moving/#comments</comments>
		
		<dc:creator><![CDATA[Meg]]></dc:creator>
		<pubDate>Tue, 18 Jul 2017 02:00:04 +0000</pubDate>
				<category><![CDATA[Being Strong with a disease]]></category>
		<category><![CDATA[Chronic pain]]></category>
		<category><![CDATA[Chronic Pain & Cannabis]]></category>
		<category><![CDATA[divorce]]></category>
		<category><![CDATA[Exercise and MS]]></category>
		<category><![CDATA[living with MS]]></category>
		<category><![CDATA[Multiple Sclerosis & Exercise]]></category>
		<category><![CDATA[single parent]]></category>
		<category><![CDATA[using a cane]]></category>
		<category><![CDATA[chronic illness and exercise]]></category>
		<category><![CDATA[Multiple Sclerosis and exercise]]></category>
		<guid isPermaLink="false">/?p=3247</guid>

					<description><![CDATA[Exercise and keeping your body moving can help counter the effects of Multiple Sclerosis, increase energy and balance, ease symptoms and even help with cognitive issues.  I think we can all agree that this is known and accepted information?  No false news in that assertion.  Just truth.  But&#8230;the truth is, knowing that exercise can help, [&#8230;]]]></description>
		
					<wfw:commentRss>/multiple-sclerosis-exercise-happy-moving/feed/</wfw:commentRss>
			<slash:comments>8</slash:comments>
		
		
			</item>
		<item>
		<title>Coming Out&#8230;How the World Found Out I was &#8220;Damaged Goods&#8221;</title>
		<link>/coming-out/</link>
					<comments>/coming-out/#comments</comments>
		
		<dc:creator><![CDATA[Meg]]></dc:creator>
		<pubDate>Fri, 30 Aug 2013 23:05:00 +0000</pubDate>
				<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[Uncategorized]]></category>
		<category><![CDATA[using a cane]]></category>
		<guid isPermaLink="false">/?p=1202</guid>

					<description><![CDATA[When I was given the FINAL diagnosis of having MS and my response was an immediate &#8220;oh fuck&#8221; my neurologist at the time argued with me that it was an &#8220;oh damn&#8221; moment, and now, years later, I agree, but at the time, I thought he was a nut job.  After all, how would HE [&#8230;]]]></description>
		
					<wfw:commentRss>/coming-out/feed/</wfw:commentRss>
			<slash:comments>19</slash:comments>
		
		
			</item>
		<item>
		<title>The Story of New Feet &#038; Tecfidera Update</title>
		<link>/the-story-of-new-feet-tecfidera-update/</link>
					<comments>/the-story-of-new-feet-tecfidera-update/#comments</comments>
		
		<dc:creator><![CDATA[Meg]]></dc:creator>
		<pubDate>Fri, 28 Jun 2013 22:50:57 +0000</pubDate>
				<category><![CDATA[Biogen]]></category>
		<category><![CDATA[dealing with disease]]></category>
		<category><![CDATA[disease modidying drug]]></category>
		<category><![CDATA[disease modifying drug]]></category>
		<category><![CDATA[DMD]]></category>
		<category><![CDATA[living with a disease]]></category>
		<category><![CDATA[living with MS]]></category>
		<category><![CDATA[MS drugs]]></category>
		<category><![CDATA[reasons to laugh and smile]]></category>
		<category><![CDATA[Tysabri]]></category>
		<category><![CDATA[using a cane]]></category>
		<category><![CDATA[n]]></category>
		<guid isPermaLink="false">/?p=1093</guid>

					<description><![CDATA[This story is from quite a few years ago, shortly after I was diagnosed.  We had spent our month back East with my family and begrudgingly had returned to the life and chaos that hits every September, with the kids going back to school.   It was about 7:30 in the morning and the three [&#8230;]]]></description>
		
					<wfw:commentRss>/the-story-of-new-feet-tecfidera-update/feed/</wfw:commentRss>
			<slash:comments>6</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>I Am Not a MeSs&#8230;.</title>
		<link>/i-am-not-a-mess/</link>
					<comments>/i-am-not-a-mess/#comments</comments>
		
		<dc:creator><![CDATA[Meg]]></dc:creator>
		<pubDate>Fri, 24 May 2013 20:57:08 +0000</pubDate>
				<category><![CDATA[Book]]></category>
		<category><![CDATA[dealing with disease]]></category>
		<category><![CDATA[living with MS]]></category>
		<category><![CDATA[Multiple Sclerosis]]></category>
		<category><![CDATA[smile & laugh]]></category>
		<category><![CDATA[using a cane]]></category>
		<guid isPermaLink="false">/?p=714</guid>

					<description><![CDATA[I had been &#8220;advised&#8221; to NOT blog a few years ago, not until I moved forward with getting my book published&#8230;.the thought being that if I put EVERYTHING (all my stories and funny thoughts) out on the internet, people would be a lot less motivated to buy it (why pay for something that you can [&#8230;]]]></description>
		
					<wfw:commentRss>/i-am-not-a-mess/feed/</wfw:commentRss>
			<slash:comments>5</slash:comments>
		
		
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