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	<title>Muscular Dystrophy News Forums | Barry Glaberman | Activity</title>
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				<title>Barry Glaberman replied to the discussion Being dismissed and mistreated by doctors in the forum Adults​ ​With​ ​Muscular Dystrophy</title>
				<link>https://musculardystrophynews.com/forums/forums/topic/being-dismissed-and-mistreated-by-doctors/#post-15070</link>
				<pubDate>Fri, 21 Feb 2020 06:41:17 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://musculardystrophynews.com/forums/forums/topic/being-dismissed-and-mistreated-by-doctors/#post-15070"><span class="bb-reply-lable">Reply to</span> Being dismissed and mistreated by doctors</a></p> <div class="bb-content-inr-wrap"><p>Even the best doctors don’t have the answers to everything. I don’t agree that they should treat us like it is in our head. With MD alone, being that it rare in the scope of diseases, can have a lot of missed cues. I have been fortunate enough to have a neurologist who could recognize my having MD. However, I haven’t had an answer as to what&hellip;<span class="activity-read-more" id="activity-read-more-4041"><a href="https://musculardystrophynews.com/forums/forums/topic/being-dismissed-and-mistreated-by-doctors/#post-15070" rel="nofollow"> Read more</a></span></p>
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				<title>Barry Glaberman replied to the discussion Shaking due to muscle weakness in the forum Adults​ ​With​ ​Muscular Dystrophy</title>
				<link>https://musculardystrophynews.com/forums/forums/topic/shaking-due-to-muscle-weakness/#post-15045</link>
				<pubDate>Tue, 18 Feb 2020 23:35:52 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://musculardystrophynews.com/forums/forums/topic/shaking-due-to-muscle-weakness/#post-15045"><span class="bb-reply-lable">Reply to</span> Shaking due to muscle weakness</a></p> <div class="bb-content-inr-wrap"><p>I have spasms, not shaking per se, like in Parkinson. Because of this, I no longer drive. I never know when it is going to happen. It can be mild like when you get a chill or it can be violent. My wife refers to it as the bedrock twitch from the Flintstones.   It is bad that I guess we have to make lite of it.  She even says that I spasm when I&hellip;<span class="activity-read-more" id="activity-read-more-4012"><a href="https://musculardystrophynews.com/forums/forums/topic/shaking-due-to-muscle-weakness/#post-15045" rel="nofollow"> Read more</a></span></p>
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				<title>Barry Glaberman replied to the discussion Pain Level in the forum Diagnosis​ ​Info​ ​and​ ​General​ ​Questions</title>
				<link>https://musculardystrophynews.com/forums/forums/topic/pain-level/#post-14959</link>
				<pubDate>Sun, 09 Feb 2020 01:46:39 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://musculardystrophynews.com/forums/forums/topic/pain-level/#post-14959"><span class="bb-reply-lable">Reply to</span> Pain Level</a></p> <div class="bb-content-inr-wrap"><p>I have thought about it, but because of being in the USA, I don’t think it is covered on Medicare. CBD oil didn’t do anything for me.  For the most part, I deal with the pain. When it gets to me, I lie down for a while till my strength builds up.</p>
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				<title>Barry Glaberman changed their profile picture</title>
				<link>https://musculardystrophynews.com/forums/activity/p/3838/</link>
				<pubDate>Sun, 02 Feb 2020 06:38:41 -0600</pubDate>

				
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				<title>Barry Glaberman replied to the discussion Pain Level in the forum Diagnosis​ ​Info​ ​and​ ​General​ ​Questions</title>
				<link>https://musculardystrophynews.com/forums/forums/topic/pain-level/#post-14910</link>
				<pubDate>Sun, 02 Feb 2020 06:31:25 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://musculardystrophynews.com/forums/forums/topic/pain-level/#post-14910"><span class="bb-reply-lable">Reply to</span> Pain Level</a></p> <div class="bb-content-inr-wrap"><p>What doctors do say is that muscular dystrophy has no pain. BS! There is a lot of pain associated with muscular dystrophy! Much is due to the fact that muscles are atrophying. As the get weaker and smaller, they are causing strain on the bones and joints that they are attached to. Since pain is subjective, mine can be anywhere from a five to&hellip;<span class="activity-read-more" id="activity-read-more-3837"><a href="https://musculardystrophynews.com/forums/forums/topic/pain-level/#post-14910" rel="nofollow"> Read more</a></span></p>
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				<title>Barry Glaberman replied to the discussion Businesses Creating More Inclusive Products in the forum Mobility Aids and Medical Equipment</title>
				<link>https://musculardystrophynews.com/forums/forums/topic/businesses-creating-more-inclusive-products/#post-12560</link>
				<pubDate>Wed, 15 May 2019 21:30:52 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://musculardystrophynews.com/forums/forums/topic/businesses-creating-more-inclusive-products/#post-12560"><span class="bb-reply-lable">Reply to</span> Businesses Creating More Inclusive Products</a></p> <div class="bb-content-inr-wrap"><p>This is true. However, going back to the late seventies and early eighties, there was a lot of things that had to be incorporated into the start of the ADA way before the government got to vote on it. Unfortunately with the government creating a negative aura, we have to fight with our negative to create a positive. In other words, the&hellip;<span class="activity-read-more" id="activity-read-more-1633"><a href="https://musculardystrophynews.com/forums/forums/topic/businesses-creating-more-inclusive-products/#post-12560" rel="nofollow"> Read more</a></span></p>
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				<title>Barry Glaberman replied to the discussion Businesses Creating More Inclusive Products in the forum Mobility Aids and Medical Equipment</title>
				<link>https://musculardystrophynews.com/forums/forums/topic/businesses-creating-more-inclusive-products/#post-12552</link>
				<pubDate>Wed, 15 May 2019 17:25:25 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://musculardystrophynews.com/forums/forums/topic/businesses-creating-more-inclusive-products/#post-12552"><span class="bb-reply-lable">Reply to</span> Businesses Creating More Inclusive Products</a></p> <div class="bb-content-inr-wrap"><p>I think we have a better chance of witnessing a world miracle before the Industry makes our life easier! If they can rip off our medical providers and us because of need, they will. The main reason is the cost of supply and demand. economics folks.</p>
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				<title>Barry Glaberman replied to the discussion Current Job in the forum Adults​ ​With​ ​Muscular Dystrophy</title>
				<link>https://musculardystrophynews.com/forums/forums/topic/current-job/#post-11874</link>
				<pubDate>Fri, 22 Mar 2019 01:01:35 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://musculardystrophynews.com/forums/forums/topic/current-job/#post-11874"><span class="bb-reply-lable">Reply to</span> Current Job</a></p> <div class="bb-content-inr-wrap"><p>I no longer work because of the MD as well as several other illnesses. My last job was a manager of a hotel. I have worked in retail, wholesale, entrepreneur, janitor, technician, DJ, and delivery. It is important to discuss your illnesses face to face allowing a potential employer to see your capabilities.</p>
<p>Talking about your disability is&hellip;<span class="activity-read-more" id="activity-read-more-1133"><a href="https://musculardystrophynews.com/forums/forums/topic/current-job/#post-11874" rel="nofollow"> Read more</a></span></p>
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				<title>Barry Glaberman replied to the discussion Current Job in the forum Adults​ ​With​ ​Muscular Dystrophy</title>
				<link>https://musculardystrophynews.com/forums/forums/topic/current-job/#post-11872</link>
				<pubDate>Thu, 21 Mar 2019 16:36:27 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://musculardystrophynews.com/forums/forums/topic/current-job/#post-11872"><span class="bb-reply-lable">Reply to</span> Current Job</a></p> <div class="bb-content-inr-wrap"><p>I let my resume speak for itself. I did not mention any disability in my letter of intent either. I  just showed up for my interview with my adaptive equipment for my interview. I focused on my abilities and strengths. There were questions about my disability, however, I tried to refocus on the job at hand. If I needed reasonable&hellip;<span class="activity-read-more" id="activity-read-more-1123"><a href="https://musculardystrophynews.com/forums/forums/topic/current-job/#post-11872" rel="nofollow"> Read more</a></span></p>
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				<title>Barry Glaberman replied to the discussion Adaptive Clothing for MD in the forum Young Adults With ​MD</title>
				<link>https://musculardystrophynews.com/forums/forums/topic/11172/#post-11514</link>
				<pubDate>Fri, 22 Feb 2019 20:08:57 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://musculardystrophynews.com/forums/forums/topic/11172/#post-11514"><span class="bb-reply-lable">Reply to</span> Adaptive Clothing for MD</a></p> <div class="bb-content-inr-wrap"><p>Although Tommy Hilfiger has a line of clothes, it would be great if it were affordable or at least covered by medical insurance. I personally couldn’t afford $65.00 for a shirt or more for pants. Another case of taking advantage of us.</p>
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				<title>Barry Glaberman replied to the discussion How do you deal with healthcare costs? in the forum Adults​ ​With​ ​Muscular Dystrophy</title>
				<link>https://musculardystrophynews.com/forums/forums/topic/how-do-you-deal-with-healthcare-costs/#post-11481</link>
				<pubDate>Thu, 21 Feb 2019 13:55:14 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://musculardystrophynews.com/forums/forums/topic/how-do-you-deal-with-healthcare-costs/#post-11481"><span class="bb-reply-lable">Reply to</span> How do you deal with healthcare costs?</a></p> <div class="bb-content-inr-wrap"><p>It is insane the cost of healthcare especially for cronic and and rare diseases with no cures. It is also disastrous if you have cancer. We have a school health plan that is state controlled, but they are not taking advantage of bulk purchasing. I mean each department ment in the state negotiates their own policy. My wife gets reduced cost for&hellip;<span class="activity-read-more" id="activity-read-more-747"><a href="https://musculardystrophynews.com/forums/forums/topic/how-do-you-deal-with-healthcare-costs/#post-11481" rel="nofollow"> Read more</a></span></p>
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				<title>Barry Glaberman changed their profile picture</title>
				<link>https://musculardystrophynews.com/forums/activity/p/556/</link>
				<pubDate>Mon, 11 Feb 2019 19:43:39 -0600</pubDate>

				
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				<title>Barry Glaberman changed their profile picture</title>
				<link>https://musculardystrophynews.com/forums/activity/p/550/</link>
				<pubDate>Mon, 11 Feb 2019 19:27:49 -0600</pubDate>

				
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				<title>Barry Glaberman posted a new activity comment</title>
				<link>https://musculardystrophynews.com/forums/activity/p/354/</link>
				<pubDate>Sat, 09 Feb 2019 13:03:59 -0600</pubDate>

									<content:encoded><![CDATA[<p><span>I was diagnosed with, EMG, muscle biopsy (2), and several blood tests and genetic testing. Although genetic is relatively new it was not conclusive. Even now if you look at my body you can see how my limbs and all are getting smaller. At least theyare not saying it is in my head. The doctors also had approved me fo a power chair several years&hellip;</span><span class="activity-read-more" id="activity-read-more-354"><a href="https://musculardystrophynews.com/forums/activity/p/354/" rel="nofollow"> Read more</a></span></p>
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				<title>Barry Glaberman posted a new activity comment</title>
				<link>https://musculardystrophynews.com/forums/activity/p/262/</link>
				<pubDate>Fri, 08 Feb 2019 21:23:48 -0600</pubDate>

									<content:encoded><![CDATA[<p><span>Being 63 and not knowing what form of MD I have, makes life more difficult. I have been to two clinics and one SSA doctor. One doctor only specialized in one form of MD therefore he couldn’t be bothered. SSA doctor confirms MD but doesn’t know what kind either. Third doct justs wants a wait and see attitude, but agrees with MD. I<br />
Am on SSDI&hellip;</span><span class="activity-read-more" id="activity-read-more-262"><a href="https://musculardystrophynews.com/forums/activity/p/262/" rel="nofollow"> Read more</a></span></p>
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				<title>Barry Glaberman posted a new activity comment</title>
				<link>https://musculardystrophynews.com/forums/activity/p/191/</link>
				<pubDate>Fri, 08 Feb 2019 18:50:20 -0600</pubDate>

									<content:encoded><![CDATA[<p><span>I have undiagnosed Type MD with a possible EDMD. I am disabled because of this and can’t find answers especially from the MDA clinic. I have muscle atrophy and uncontrollable muscle spasms with no difinitive answers. Maybe someone can help.</span></p>
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				<title>Barry Glaberman became a registered member</title>
				<link>https://musculardystrophynews.com/forums/activity/p/178/</link>
				<pubDate>Fri, 08 Feb 2019 18:34:09 -0600</pubDate>

				
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