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LIVING with multiple system atrophy (msa) | Paul's blog about living with Multiple System Atrophy – MSA is neuro-degenerative brain disease, sometimes called11 an atypical Parkinson disorder, but is much rarer and progresses much faster. I was d

Paul's blog about living with Multiple System Atrophy - MSA is neuro-degenerative brain disease, sometimes called11 an atypical Parkinson disorder, but is much rarer and progresses much faster. I was diagnosed in June 2008, but onset was likely Fall 2004. Most MSA patients die within 10 years. I intend to beat the odds. (by Paul)

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LIVING with multiple system atrophy (msa) | Paul's blog about living with Multiple System Atrophy – MSA is neuro-degenerative brain disease, sometimes called11 an atypical Parkinson disorder, but is much rarer and progresses much faster. I was d | livingwithmsa.com Reviews
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LIVING with multiple system atrophy (msa) | Paul's blog about living with Multiple System Atrophy – MSA is neuro-degenerative brain disease, sometimes called11 an atypical Parkinson disorder, but is much rarer and progresses much faster. I was d | livingwithmsa.com Reviews

https://livingwithmsa.com

Paul's blog about living with Multiple System Atrophy - MSA is neuro-degenerative brain disease, sometimes called11 an atypical Parkinson disorder, but is much rarer and progresses much faster. I was diagnosed in June 2008, but onset was likely Fall 2004. Most MSA patients die within 10 years. I intend to beat the odds. (by Paul)

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Uncategorized | LIVING with multiple system atrophy (msa)

http://livingwithmsa.com/category/uncategorized

LIVING with multiple system atrophy (msa). December 6, 2012 · 10:18 pm. Aix-en-provence, July 2008, on a father/son romp around Paul’s favourite grape-growing region. As many of you know, Paul died peacefully at the end of July 2012, in the midst of a vacation with his family at a cottage in Haliburton, where he could sit on the deck and watch his three granddaughters play by the lake. As his wife (my mother) Valerie wrote in the days following,. May 21, 2011 · 1:42 pm. Last weekend, my son Kevin came to...

2

Travel | LIVING with multiple system atrophy (msa)

http://livingwithmsa.com/category/travel

LIVING with multiple system atrophy (msa). October 2, 2011 · 9:43 am. My Summer was a Roller Coaster Ride – Part 2. Published September 12, I wrote that my wild roller coaster ride this summer came from four intense, parallel experiences. I addressed the first two in Part 1. Coping with MSA Symptom Changes. September 12, 2011 · 9:05 am. My Summer was a Roller Coaster Ride – Part 1. I was lamenting that I hadn’t posted since May. The failing health of my Mom, still living in her own condominium at 93.

3

Symptoms | LIVING with multiple system atrophy (msa)

http://livingwithmsa.com/category/symptoms

LIVING with multiple system atrophy (msa). January 22, 2012 · 10:00 pm. Every Culture has its Own Swear Words. Is the MSA Support Community a ‘culture’? Two definitions — ‘the behaviors and beliefs characteristic of a particular social. Ethnic, or age group’. 8212; and — ‘the quality that arises from a pursuit of excellence’ — seem to support a ‘yes’ response. What criteria should you use to select swear words for the MSA Support culture? Take a deep breath and let all that pent-up emotion run wild!

4

Socialize | LIVING with multiple system atrophy (msa)

http://livingwithmsa.com/category/socialize

LIVING with multiple system atrophy (msa). January 31, 2012 · 9:20 am. My Terrible, Horrible, No Good, Very Bad Day! I wrote this post in September 2010, saved it in draft, and promptly forgot about it. So here it is —-. You may know that I’ve borrowed this title from a children’s story we loved to read to our kids “. Alexander and the Terrible, Horrible, No Good, Very Bad Day! Continue reading →. May 21, 2011 · 1:42 pm. On Dec. 28, 2010, I posted ‘ All My Vehicles. On the way there and the way back, Kev...

5

My Summer was a Roller Coaster Ride – Part 1 | LIVING with multiple system atrophy (msa)

http://livingwithmsa.com/2011/09/12/my-summer-was-a-roller-coaster-ride-part-1

LIVING with multiple system atrophy (msa). My Summer was a Roller Coaster Ride – Part 2 →. September 12, 2011 · 9:05 am. My Summer was a Roller Coaster Ride – Part 1. I was lamenting that I hadn’t posted since May. But I quickly realized that a lot had happened in my life June through August, with many highs and some intense lows. You might say that i was on a wild roller coaster ride. That ride came from four intense, parallel experiences:. A big push to get a communication circle website up and running.

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world-msa-day.org world-msa-day.org

MSA SUPPORT GROUPS

http://www.world-msa-day.org/World-MSA-Day/LINKS_WWW.html

Http:/ www.emsa-sg.org/. Http:/ www.rarediseasecommunities.org/en/community/multiple-system-atrophy. Http:/ www.msa-ams.be. Http:/ www.msa-danmark.dk. Http:/ asso.orpha.net/ARAMISE/cgi-bin/index.php? Http:/ asso.orpha.net/ARAMISE/cgi-bin/index.php? Http:/ neuroligue.over-blog.com/article-journee-mondiale-a-m-s-lundi-03-octobre-2011-85661235.html. Http:/ www.msatrust.org.uk. Or www.msatrust.org.uk. Contact number: 020 7940 4666. Simon Roodhouse and his new companion - MSA. Is Sonja’s Afrikaans blog. Bob M...

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One Day at a Time ~ Brenda's Journey with MSA: Friends ~Their Journey

http://msaonedayatatime.blogspot.com/p/friends-their-journey.html

One Day at a Time Brenda's Journey with MSA. Multiple System Atrophy (MSA) - My journey and interesting tidbits. Helping Hands Where To Get It. Http:/ myfamilyandmsa.wordpress.com. Http:/ www.karenolsonblog.com/. Http:/ sonjasegriffels.blogspot.com/. MSA in South Africa. Http:/ msainsouthafricawithsonja.blogspot.com/. Http:/ findingprettyagain.blogspot.com/. Https:/ www.facebook.com/profile.php? Denns and Lori Jankeway. Https:/ www.facebook.com/ljakeway. Simon Roodhouse and his new companion-MSA. Awesome...

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LIVING with multiple system atrophy (msa) | Paul's blog about living with Multiple System Atrophy – MSA is neuro-degenerative brain disease, sometimes called11 an atypical Parkinson disorder, but is much rarer and progresses much faster. I was d

LIVING with multiple system atrophy (msa). December 6, 2012 · 10:18 pm. Aix-en-provence, July 2008, on a father/son romp around Paul’s favourite grape-growing region. As many of you know, Paul died peacefully at the end of July 2012, in the midst of a vacation with his family at a cottage in Haliburton, where he could sit on the deck and watch his three granddaughters play by the lake. As his wife (my mother) Valerie wrote in the days following,. June 16, 2012 · 12:00 pm. 8216;There and Back Again’!

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Living With MS and PCOs. Saturday, March 3, 2012. Just existing and watching time go by. I do have to have another treatment of solumedrol because she thinks my face and bladder issues are due to some inflammation. If that's the case, if it's a home infusion at least I can watch TV or something while they do it. Look at everything I've been through! That's all that I have to say because my life has become boring and mundane and sometimes stressful. Friday, January 27, 2012. Tuesday, November 8, 2011.

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