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Quest of a dystonic buddhist neuroscientist

Quest of a dystonic buddhist neuroscientist. Thoughts of a graduate student living with mitochondrial disease, the dilemmas of disability, science and consciousness. Wednesday, February 01, 2012. Getting a new service dog! I need your help! The most exciting news I have to report though is that I have been accepted to train with a new service dog through the organization Indiana Canine Assistant Network. Posted by Synaptic Jen @ 12:24 PM. Links to this post. Friday, September 24, 2010. Mattie was a poet ...

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Quest of a dystonic buddhist neuroscientist | neuronswithdystonia.blogspot.com Reviews
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Quest of a dystonic buddhist neuroscientist. Thoughts of a graduate student living with mitochondrial disease, the dilemmas of disability, science and consciousness. Wednesday, February 01, 2012. Getting a new service dog! I need your help! The most exciting news I have to report though is that I have been accepted to train with a new service dog through the organization Indiana Canine Assistant Network. Posted by Synaptic Jen @ 12:24 PM. Links to this post. Friday, September 24, 2010. Mattie was a poet ...
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thank you,jenelle and blitzen,0 comments,matthew,sheridan,eithene,colbie,natalie,heidi and alexandria,rina,sara,and many more,and mito action,jenelle,labels awareness,mito,love and peace,3 comments,4 comments,labels children,dystonia,life,pain,peace,tummy
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Quest of a dystonic buddhist neuroscientist | neuronswithdystonia.blogspot.com Reviews

https://neuronswithdystonia.blogspot.com

Quest of a dystonic buddhist neuroscientist. Thoughts of a graduate student living with mitochondrial disease, the dilemmas of disability, science and consciousness. Wednesday, February 01, 2012. Getting a new service dog! I need your help! The most exciting news I have to report though is that I have been accepted to train with a new service dog through the organization Indiana Canine Assistant Network. Posted by Synaptic Jen @ 12:24 PM. Links to this post. Friday, September 24, 2010. Mattie was a poet ...

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neuronswithdystonia.blogspot.com neuronswithdystonia.blogspot.com
1

Quest of a dystonic buddhist neuroscientist: Identity Theft

http://neuronswithdystonia.blogspot.com/2008/03/identity-theft.html

Quest of a dystonic buddhist neuroscientist. Thoughts of a graduate student living with mitochondrial disease, the dilemmas of disability, science and consciousness. Monday, March 03, 2008. An unfortunate late night phone call from a collections agent alerted me to the fact that I am a victim of identity theft. Here's a good government site about how to protect yourself from identity theft. Http:/ www.ftc.gov/bcp/edu/microsites/idtheft/index.html. Posted by Synaptic Jen @ 9:07 PM. Links to this post.

2

Quest of a dystonic buddhist neuroscientist: Mitochondrial Disease Awareness Week

http://neuronswithdystonia.blogspot.com/2010/09/mitochondrial-disease-awareness-week.html

Quest of a dystonic buddhist neuroscientist. Thoughts of a graduate student living with mitochondrial disease, the dilemmas of disability, science and consciousness. Friday, September 24, 2010. Mitochondrial Disease Awareness Week. Yesterday was an International Day of Peace. This is a day that I always take some time to celebrate in some way. I usually like to remember Mattie Stepanek and read his poem "For Our World" http:/ myhero.com/peace2010. This week is Mitochondrial Disease awareness week and Wed...

3

Quest of a dystonic buddhist neuroscientist: July 2007

http://neuronswithdystonia.blogspot.com/2007_07_01_archive.html

Quest of a dystonic buddhist neuroscientist. Thoughts of a graduate student living with mitochondrial disease, the dilemmas of disability, science and consciousness. Saturday, July 07, 2007. Back to the Big Horns. Our family cabin is near Antelope Butte in the Shell Canyon. Shell Creek and the mountains were as beautiful as I remember, but unfortunately many of the trees have died from the mountain pine beetle. And much of the mountain is being cut down due to the beetle. Posted by Synaptic Jen @ 2:15 PM.

4

Quest of a dystonic buddhist neuroscientist: Some thoughts on life

http://neuronswithdystonia.blogspot.com/2008/09/some-thoughts-on-life.html

Quest of a dystonic buddhist neuroscientist. Thoughts of a graduate student living with mitochondrial disease, the dilemmas of disability, science and consciousness. Wednesday, September 03, 2008. Some thoughts on life. The photo is of my son playing in the surf on our recent summer trip to South Carolina. I loved watching him play in the waves. Posted by Synaptic Jen @ 10:50 PM. Links to this post. I just stumbled upon this blog and found this post beautiful - thanks. Links to this post:.

5

Quest of a dystonic buddhist neuroscientist: Spirituality

http://neuronswithdystonia.blogspot.com/2008/07/spirituality.html

Quest of a dystonic buddhist neuroscientist. Thoughts of a graduate student living with mitochondrial disease, the dilemmas of disability, science and consciousness. Friday, July 18, 2008. Here is my response to a question on the new Wego dystonia bulliten board. I have wondered about the impact of Faith and Spirituality as a way to help cope with Dystonia? What are your thoughts on this? What do you practice? Do you believe Faith has a role in healing? If so, How? Posted by Synaptic Jen @ 10:09 AM.

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dystoniadiary.blogspot.com dystoniadiary.blogspot.com

Dystonia Diary: May 2006

http://dystoniadiary.blogspot.com/2006_05_01_archive.html

This is what it's like to have cervical dystonia - the good, the bad, and the ugly. Actually, there's nothing good about it. Saturday, May 20, 2006. Since my 16 Botox shots, I expected to have great pain relief. And I expected to be able to hold my head more-or-less straight while walking, without having to use my hand. I also expected to get a good night's sleep. Well, about a month later, I have great pain relief. Posted by I go by many names. @ 2:27 PM. Links to this post. I go by many names.

dystoniadiary.blogspot.com dystoniadiary.blogspot.com

Dystonia Diary: July 2006

http://dystoniadiary.blogspot.com/2006_07_01_archive.html

This is what it's like to have cervical dystonia - the good, the bad, and the ugly. Actually, there's nothing good about it. Friday, July 14, 2006. Since I stopped drinking my favorite Starbucks drink - the one that had caffeine but they told me it didn't - the Zanaflex is working better. The Tizanidine is still pretty ineffective though, but since I don't have much more of it, it's not a problem. Posted by I go by many names. @ 9:13 PM. Links to this post. Sunday, July 09, 2006. So far, so good - mostly.

dystoniadiary.blogspot.com dystoniadiary.blogspot.com

Dystonia Diary: March 2006

http://dystoniadiary.blogspot.com/2006_03_01_archive.html

This is what it's like to have cervical dystonia - the good, the bad, and the ugly. Actually, there's nothing good about it. Wednesday, March 22, 2006. So far, I slept pretty well last Tuesday through Friday, badly Sat and Sun, better Mon, and badly last night. I wish I knew why my sleep hasn't been consistant. I take my meds exactly as prescribed, and I don't drink any caffeine. It's intensely frustrating. Maybe my doctor will have some idea when I see him next month. Links to this post. He also noticed...

dystoniadiary.blogspot.com dystoniadiary.blogspot.com

Dystonia Diary: June 2006

http://dystoniadiary.blogspot.com/2006_06_01_archive.html

This is what it's like to have cervical dystonia - the good, the bad, and the ugly. Actually, there's nothing good about it. Wednesday, June 14, 2006. Posted by I go by many names. @ 8:28 PM. Links to this post. I go by many names. California, United States. View my complete profile. Follow me on Twitter. Dystonia Medical Research Foundation. National Spasmodic Torticollis Association. ADDER - Fighting Dystonia (click on FAQ). The European Dystonia Portal. Dystonia Information Page (NIND).

dystoniadiary.blogspot.com dystoniadiary.blogspot.com

Dystonia Diary: February 2006

http://dystoniadiary.blogspot.com/2006_02_01_archive.html

This is what it's like to have cervical dystonia - the good, the bad, and the ugly. Actually, there's nothing good about it. Saturday, February 25, 2006. New insurance adjuster (6 in 2 years), I don't know if he'll agree to authorise more Botox - or anything else - as needed. Guess I'll find out when my doctor asks for more. The good news is that now that my cold is finally gone, I can finally sleep at night. Posted by I go by many names. @ 3:25 PM. Links to this post. Wednesday, February 15, 2006. Dysto...

dystoniadiary.blogspot.com dystoniadiary.blogspot.com

Dystonia Diary: January 2006

http://dystoniadiary.blogspot.com/2006_01_01_archive.html

This is what it's like to have cervical dystonia - the good, the bad, and the ugly. Actually, there's nothing good about it. Saturday, January 28, 2006. Maybe by 2 weeks I'll notice more of a difference. If not, it's going to be a long. 4 months until my next shots. Good news is that I got some extra pay (a "floating holiday" I never took), and I have 4 days off in a row! I can catch up on my sleep, and prune my roses - before it's too late. Posted by I go by many names. @ 12:23 AM. Links to this post.

dystoniadiary.blogspot.com dystoniadiary.blogspot.com

Dystonia Diary: November 2005

http://dystoniadiary.blogspot.com/2005_11_01_archive.html

This is what it's like to have cervical dystonia - the good, the bad, and the ugly. Actually, there's nothing good about it. Wednesday, November 30, 2005. At my doctor's appointment yesterday, I was hoping to get more Botox, but the doctor said he was going to just watch me for a while. The last shots are still working to a degree, but the pain is getting a little worse. That's probably partly due to the extra holiday work. Posted by I go by many names. @ 4:18 PM. Links to this post. Links to this post.

dystoniadiary.blogspot.com dystoniadiary.blogspot.com

Dystonia Diary: December 2005

http://dystoniadiary.blogspot.com/2005_12_01_archive.html

This is what it's like to have cervical dystonia - the good, the bad, and the ugly. Actually, there's nothing good about it. Sunday, December 11, 2005. I'm still waiting for another Botox treatment. Hopefully I'll get it this month, but the Dr may wait to see how I'm doing. It's been almost 4 months since my last treatment, and I'm surprised (and glad) that it's lasted this long. Posted by I go by many names. @ 3:11 PM. Links to this post. I go by many names. California, United States.

dystoniadiary.blogspot.com dystoniadiary.blogspot.com

Dystonia Diary: April 2006

http://dystoniadiary.blogspot.com/2006_04_01_archive.html

This is what it's like to have cervical dystonia - the good, the bad, and the ugly. Actually, there's nothing good about it. Tuesday, April 18, 2006. I had 16 shots of Botox today, and I can't believe how sore I was later! The shots were around 7:20am, and it's a little after 8:30pm, and I still. Ache That's unusual, but I did. Have a lot of shots, and a little more Botox than usual. I actually had to take aspirin! Posted by I go by many names. @ 8:37 PM. Links to this post. Friday, April 14, 2006. I go ...

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Quest of a dystonic buddhist neuroscientist

Quest of a dystonic buddhist neuroscientist. Thoughts of a graduate student living with mitochondrial disease, the dilemmas of disability, science and consciousness. Wednesday, February 01, 2012. Getting a new service dog! I need your help! The most exciting news I have to report though is that I have been accepted to train with a new service dog through the organization Indiana Canine Assistant Network. Posted by Synaptic Jen @ 12:24 PM. Links to this post. Friday, September 24, 2010. Mattie was a poet ...

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