msajourney blogspot.com

My MSA Journey

Multiple System Atrophy I Have This Disease - It Doesn39;t Have Me

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LINKS TO WEB SITE

Watch this, Mom!

Watch this, Mom! Sunday, August 7, 2016. See them here on flickr. Wednesday, July 27, 2016. This batch is now up here. Sunday, July 24, 2016. Tuesday, July 19, 2016. Monday, July 18, 2016. And lily cleaning sneakers in the shower.

Marikos MSA InfoShare

Stem Cell Therapy for neurological degenerative diseases. Sunday, February 13, 2011. I hope the above information hs been helpful, though I realize it may not have been what you were hoping to hear. Please feel free to either write or call if you would like additional information. We are always willing to share whatever information we might have. Wednesday, February 10, 2010. Nevertheless, there are stem cell treatments being offered in variou.

One Day at a Time Brendas Journey with MSA

Helping Hands Where To Get It. Friday, June 7, 2013. Last Week of Fall Camp. The last week of fall camp started with a party and ended with a party. Nd took lots of pictures of the fortress. Some of oldest rocks are there.

Skeets Journey

Thursday, January 21, 2010. Stem Cells Transplanted in ALS Patient in U. Watching CNN this morning, I saw a brief mention of this in the ticker at the bottom of the screen. Wednesday, January 20, 2010.

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My MSA Journey

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Multiple System Atrophy I Have This Disease - It Doesn39;t Have Me

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This web page msajourney.blogspot.com states the following, "Multiple System Atrophy I Have This Disease - It Doesnt Have Me." We saw that the webpage said " Sunday, February 1, 2015." It also said " Hi, this is Steves daughter Deb writing. It was very important to my dad to donate his brain for research. He also wanted us to have a definitive diagnosis MSA is not typically hereditary, unlike some very similar diseases. He would have been relieved to know that the brain autopsy results indicated a definite diagnosis of MSA. Here is the statement we received from the University of Miami Brain Endowment Bank."

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