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Simon Roodhouse and his new companion - MSA

My story of living with Multiple Systems Atrophy (MSA). Through this blog I want to raise the profile of MSA and share experiences with others. My aim is to create a record of what it is like living with this disease mainly through photographic images.

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Simon Roodhouse and his new companion - MSA | livingwithmsa.blogspot.com Reviews
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My story of living with Multiple Systems Atrophy (MSA). Through this blog I want to raise the profile of MSA and share experiences with others. My aim is to create a record of what it is like living with this disease mainly through photographic images.
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Simon Roodhouse and his new companion - MSA | livingwithmsa.blogspot.com Reviews

https://livingwithmsa.blogspot.com

My story of living with Multiple Systems Atrophy (MSA). Through this blog I want to raise the profile of MSA and share experiences with others. My aim is to create a record of what it is like living with this disease mainly through photographic images.

INTERNAL PAGES

livingwithmsa.blogspot.com livingwithmsa.blogspot.com
1

Simon Roodhouse and his new companion - MSA: December 2012

http://livingwithmsa.blogspot.com/2012_12_01_archive.html

Simon Roodhouse and his new companion - MSA. My story of living with Multiple Systems Atrophy (MSA). Through this blog I want to raise the profile of MSA and share experiences with others. My aim is to create a record of what it is like living with this disease mainly through photographic images. Sunday, 23 December 2012. The Advent candle is lit, most of my cards are now up, I have a roaring fire, just two sleeps until Jesus’ birthday and it’s not raining! What more could a girl want? I’ve just li...

2

Simon Roodhouse and his new companion - MSA: May 2013

http://livingwithmsa.blogspot.com/2013_05_01_archive.html

Simon Roodhouse and his new companion - MSA. My story of living with Multiple Systems Atrophy (MSA). Through this blog I want to raise the profile of MSA and share experiences with others. My aim is to create a record of what it is like living with this disease mainly through photographic images. Saturday, 4 May 2013. The only UK charity dedicated to providing specialist support to all those who like Simon are affected by MSA; a life-limiting neurodegenerative brain disease . In Grace’s own words:.

3

Simon Roodhouse and his new companion - MSA

http://livingwithmsa.blogspot.com/2013/05/i-have-decided-that-with-graces.html

Simon Roodhouse and his new companion - MSA. My story of living with Multiple Systems Atrophy (MSA). Through this blog I want to raise the profile of MSA and share experiences with others. My aim is to create a record of what it is like living with this disease mainly through photographic images. Saturday, 4 May 2013. The only UK charity dedicated to providing specialist support to all those who like Simon are affected by MSA; a life-limiting neurodegenerative brain disease . In Grace’s own words:. This ...

4

Simon Roodhouse and his new companion - MSA: January 2013

http://livingwithmsa.blogspot.com/2013_01_01_archive.html

Simon Roodhouse and his new companion - MSA. My story of living with Multiple Systems Atrophy (MSA). Through this blog I want to raise the profile of MSA and share experiences with others. My aim is to create a record of what it is like living with this disease mainly through photographic images. Sunday, 6 January 2013. It would have been Simon’s 65. Continuing the theme of walking, here’s a challenge for all the females and males too maybe. It’s called Walk in Her Shoes. I’m hoping to. Picture Window te...

5

Simon Roodhouse and his new companion - MSA: Challenges

http://livingwithmsa.blogspot.com/2012/11/challenges.html

Simon Roodhouse and his new companion - MSA. My story of living with Multiple Systems Atrophy (MSA). Through this blog I want to raise the profile of MSA and share experiences with others. My aim is to create a record of what it is like living with this disease mainly through photographic images. Friday, 16 November 2012. What a lovely week we’ve had weather wise in Yorkshire. What's it been like for you? Subscribe to: Post Comments (Atom). Picture Window template. Powered by Blogger.

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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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Simon Roodhouse and his new companion - MSA

Simon Roodhouse and his new companion - MSA. My story of living with Multiple Systems Atrophy (MSA). Through this blog I want to raise the profile of MSA and share experiences with others. My aim is to create a record of what it is like living with this disease mainly through photographic images. Saturday, 4 May 2013. The only UK charity dedicated to providing specialist support to all those who like Simon are affected by MSA; a life-limiting neurodegenerative brain disease . In Grace’s own words:. Mark ...

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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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