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Scott, MD | Living with Muscular Dystrophy.

Living with Muscular Dystrophy. (by Scott)

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Scott, MD | Living with Muscular Dystrophy. | scottmd.wordpress.com Reviews
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Living with Muscular Dystrophy. (by Scott)
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6 disability
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Scott, MD | Living with Muscular Dystrophy. | scottmd.wordpress.com Reviews

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Living with Muscular Dystrophy. (by Scott)

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1

Patient History. | Scott, MD

https://scottmd.wordpress.com/2009/08/29/patient-history

Living with Muscular Dystrophy. Laquo; The Cake Eaters. On TV, you always hear the Docs asking for their patient’s history so they can figure out what’s medically wrong with them. My addiction for medical dramas,. House, M.D. Has influenced me to engage in a little roleplaying as I give my medical history to offer a better understanding of the symptoms of FSHD. (The following is a combined summary taken from my own doctor and therapy sessions, personal notes, and web definitions.). Allergic to any meds?

2

The Ugly Truth | Scott, MD

https://scottmd.wordpress.com/2010/12/24/the-ugly-truth

Living with Muscular Dystrophy. Laquo; The Transition (part 2). When I began the Scott MD blog, I promised to produce an account of all that was true about my muscular dystrophy, no matter how emotional, positive or negative. Explore posts in the same categories:. This entry was posted on December 24, 2010 at 10:13 pm and is filed under Uncategorized. You can subscribe via RSS 2.0. Feed to this post's comments. You can comment below. Or link to this permanent URL. From your own site. It’s a very br...

3

Patient History Follow-Up. | Scott, MD

https://scottmd.wordpress.com/2009/10/11/patient-history-follow-up

Living with Muscular Dystrophy. Laquo; 39 Pounds of Love. There’s an App for me! Patient is reporting new symptoms and continual progression of already weakened muscles. Last Patient History. Evaluation was on 08/29/09. Experiencing more pain going from standing to sitting. Unable to stand for long minutes. New symptoms now include frequent arthritic pain in joints and muscles. Patient can stand in place for a limited time, but can no longer walk. Explore posts in the same categories:. From your own site.

4

There’s an App for me! | Scott, MD

https://scottmd.wordpress.com/2009/10/29/theres-an-app-for-me

Living with Muscular Dystrophy. Laquo; Patient History Follow-Up. The Transition (part 1). There’s an App for me! The iphone has been my lifeline. Since I can’t carry around too many items at a a time, the iphone serves its purpose ten fold. 1 ican call or text people. 2 ican listen to my music. 3 ican read and send my emails. 4 ican surf the web. 5 ican entertain myself with a multitude of simple games. 6 ican watch movies. 7 ican plan and schedule any appointments. 8 ican pay my bills. 2 Comments on &#...

5

The Transition (part 2) | Scott, MD

https://scottmd.wordpress.com/2010/12/17/the-transition-part-2

Living with Muscular Dystrophy. Laquo; The Transition (part 1). The Transition (part 2). It was over a month and the questions started to settle in, “How much longer am I going to be here? 8221; and “Is this my permanent home? 8221; One thing began to ring true, it didn’t look like I was ever going home again. Explore posts in the same categories:. This entry was posted on December 17, 2010 at 6:13 pm and is filed under Disability. You can subscribe via RSS 2.0. Or link to this permanent URL. Create a fr...

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2009 February « This crazy adventure called "Life"

https://livingwithmg.wordpress.com/2009/02

This crazy adventure called Life. Random stories from my life with Myasthenia Gravis. Living with Muscular Dystrophy. Jen on Why me? Kngfisher on Why me? Jen on Following orders. Archive for February, 2009. Coffee or milk…. Posted by Jen on February 20, 2009. Create a free website or blog at WordPress.com.

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2009 October « This crazy adventure called "Life"

https://livingwithmg.wordpress.com/2009/10

This crazy adventure called Life. Random stories from my life with Myasthenia Gravis. Living with Muscular Dystrophy. Jen on Why me? Kngfisher on Why me? Jen on Following orders. Archive for October, 2009. Give me an “I”! Give me a “V”! Give me an “I”! Give me a “g”! What’s that spell? Posted by Jen on October 2, 2009. Or, more acurately, strength! Blog at WordPress.com.

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The Climb « This crazy adventure called "Life"

https://livingwithmg.wordpress.com/2009/11/15/the-climb

This crazy adventure called Life. Random stories from my life with Myasthenia Gravis. Living with Muscular Dystrophy. Jen on Why me? Kngfisher on Why me? Jen on Following orders. Laquo; Give me an “I”! Give me a “V”! Give me an “I”! Give me a “g”! What’s that spell? Posted by Jen on November 15, 2009. What keeps us up and moving? So many times it’s easier to quit. And, as the lyrics above so wisely point out, sometimes we will lose, whether that loss comes in the form of a failed dream, the los...You are...

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2009 November « This crazy adventure called "Life"

https://livingwithmg.wordpress.com/2009/11

This crazy adventure called Life. Random stories from my life with Myasthenia Gravis. Living with Muscular Dystrophy. Jen on Why me? Kngfisher on Why me? Jen on Following orders. Archive for November, 2009. Posted by Jen on November 15, 2009. What keeps us up and moving? So many times it’s easier to quit. And, as the lyrics above so wisely point out, sometimes we will lose, whether that loss comes in the form of a failed dream, the loss of a loved one, or something else . And yet, the major...

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Why me? « This crazy adventure called "Life"

https://livingwithmg.wordpress.com/2010/02/28/why-me

This crazy adventure called Life. Random stories from my life with Myasthenia Gravis. Living with Muscular Dystrophy. Jen on Why me? Kngfisher on Why me? Jen on Following orders. Laquo; The Energizer Bunny. Posted by Jen on February 28, 2010. I seem to be asking myself that question a lot lately. but I’m not asking it in the traditional sense of looking at the bad and the negative in my life, and wondering why did I end up with Myasthenia. Instead, I’m asking why is my life so blessed? From your own site.

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2010 January « This crazy adventure called "Life"

https://livingwithmg.wordpress.com/2010/01

This crazy adventure called Life. Random stories from my life with Myasthenia Gravis. Living with Muscular Dystrophy. Jen on Why me? Kngfisher on Why me? Jen on Following orders. Archive for January, 2010. Posted by Jen on January 3, 2010. Blog at WordPress.com.

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Treatment options « This crazy adventure called "Life"

https://livingwithmg.wordpress.com/2009/09/26/treatment-options

This crazy adventure called Life. Random stories from my life with Myasthenia Gravis. Living with Muscular Dystrophy. Jen on Why me? Kngfisher on Why me? Jen on Following orders. Laquo; What’s your Mountain? Give me an “I”! Give me a “V”! Give me an “I”! Give me a “g”! What’s that spell? Posted by Jen on September 26, 2009. I had one of those “ah ha! This entry was posted on September 26, 2009 at 12:15 pm and is filed under Uncategorized. You can follow any responses to this entry through the RSS 2.0.

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2009 May « This crazy adventure called "Life"

https://livingwithmg.wordpress.com/2009/05

This crazy adventure called Life. Random stories from my life with Myasthenia Gravis. Living with Muscular Dystrophy. Jen on Why me? Kngfisher on Why me? Jen on Following orders. Archive for May, 2009. Posted by Jen on May 11, 2009. Create a free website or blog at WordPress.com.

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2008 December « This crazy adventure called "Life"

https://livingwithmg.wordpress.com/2008/12

This crazy adventure called Life. Random stories from my life with Myasthenia Gravis. Living with Muscular Dystrophy. Jen on Why me? Kngfisher on Why me? Jen on Following orders. Archive for December, 2008. Posted by Jen on December 18, 2008. Create a free website or blog at WordPress.com.

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2009 March « This crazy adventure called "Life"

https://livingwithmg.wordpress.com/2009/03

This crazy adventure called Life. Random stories from my life with Myasthenia Gravis. Living with Muscular Dystrophy. Jen on Why me? Kngfisher on Why me? Jen on Following orders. Archive for March, 2009. A trip to the neurologist. Posted by Jen on March 30, 2009. Posted by Jen on March 17, 2009. Well….in less than 24 hours I’ve already eaten 4 (of the 6) packs in the box. Why not? The goal for today:. Posted by Jen on March 16, 2009. Breathe. Isn’t that an ambitious goal? Posted by Jen on March 4, 2009.

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Scott, MD | Living with Muscular Dystrophy.

Living with Muscular Dystrophy. Posted December 24, 2010 by Scott. When I began the Scott MD blog, I promised to produce an account of all that was true about my muscular dystrophy, no matter how emotional, positive or negative. The Transition (part 2). Posted December 17, 2010 by Scott. It was over a month and the questions started to settle in, “How much longer am I going to be here? 8221; and “Is this my permanent home? So that’s that. The transition was indeed an emotional one. As I hin...Being conne...

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