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Life with my Mito kid

Life with my Mito kid. My husband and I have three children. Our youngest, Lex was diagnosed with mitochondrial disease on November 29, 2011. He suffers with hypotonia, sensory processing issues, motor delay, and speech delay. The goal of this blog is to help other families affected by this disease and to raise awareness. Thursday, December 6, 2012. Lexs road to diagnosis. Saturday, November 17, 2012. The Day Our Lives Changed. How did this happen to him? Will he even live to have a future?

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Life with my Mito kid | lifewithmitolex.blogspot.com Reviews
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Life with my Mito kid. My husband and I have three children. Our youngest, Lex was diagnosed with mitochondrial disease on November 29, 2011. He suffers with hypotonia, sensory processing issues, motor delay, and speech delay. The goal of this blog is to help other families affected by this disease and to raise awareness. Thursday, December 6, 2012. Lexs road to diagnosis. Saturday, November 17, 2012. The Day Our Lives Changed. How did this happen to him? Will he even live to have a future?
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Life with my Mito kid | lifewithmitolex.blogspot.com Reviews

https://lifewithmitolex.blogspot.com

Life with my Mito kid. My husband and I have three children. Our youngest, Lex was diagnosed with mitochondrial disease on November 29, 2011. He suffers with hypotonia, sensory processing issues, motor delay, and speech delay. The goal of this blog is to help other families affected by this disease and to raise awareness. Thursday, December 6, 2012. Lexs road to diagnosis. Saturday, November 17, 2012. The Day Our Lives Changed. How did this happen to him? Will he even live to have a future?

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lifewithmitolex.blogspot.com lifewithmitolex.blogspot.com
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Life with my Mito kid: November 2012

http://www.lifewithmitolex.blogspot.com/2012_11_01_archive.html

Life with my Mito kid. My husband and I have three children. Our youngest, Lex was diagnosed with mitochondrial disease on November 29, 2011. He suffers with hypotonia, sensory processing issues, motor delay, and speech delay. The goal of this blog is to help other families affected by this disease and to raise awareness. Saturday, November 17, 2012. The Day Our Lives Changed. How did this happen to him? What does this mean for Lex's future. Our families future? Will he even live to have a future?

2

Life with my Mito kid: December 2012

http://www.lifewithmitolex.blogspot.com/2012_12_01_archive.html

Life with my Mito kid. My husband and I have three children. Our youngest, Lex was diagnosed with mitochondrial disease on November 29, 2011. He suffers with hypotonia, sensory processing issues, motor delay, and speech delay. The goal of this blog is to help other families affected by this disease and to raise awareness. Thursday, December 6, 2012. Lexs road to diagnosis. Subscribe to: Posts (Atom). Lexs road to diagnosis. View my complete profile. Picture Window template. Powered by Blogger.

3

Life with my Mito kid: The Day Our Lives Changed

http://www.lifewithmitolex.blogspot.com/2012/11/the-day-our-lives-changed.html

Life with my Mito kid. My husband and I have three children. Our youngest, Lex was diagnosed with mitochondrial disease on November 29, 2011. He suffers with hypotonia, sensory processing issues, motor delay, and speech delay. The goal of this blog is to help other families affected by this disease and to raise awareness. Saturday, November 17, 2012. The Day Our Lives Changed. How did this happen to him? What does this mean for Lex's future. Our families future? Will he even live to have a future?

4

Life with my Mito kid: Lex's road to diagnosis

http://www.lifewithmitolex.blogspot.com/2012/12/lex-road-to-diagnosis.html

Life with my Mito kid. My husband and I have three children. Our youngest, Lex was diagnosed with mitochondrial disease on November 29, 2011. He suffers with hypotonia, sensory processing issues, motor delay, and speech delay. The goal of this blog is to help other families affected by this disease and to raise awareness. Thursday, December 6, 2012. Lexs road to diagnosis. December 7, 2012 at 12:41 AM. December 7, 2012 at 7:47 AM. December 7, 2012 at 11:12 AM. December 7, 2012 at 11:52 AM. We just went t...

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hypotonicworld.blogspot.com hypotonicworld.blogspot.com

Sunshine in a Hypotonic World: Rae's Book Review: You Are Special

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Sunshine in a Hypotonic World. Living in the world of Rett Syndrome, celebrating all the little victories, taking life one day at a time and trying to keep a sense of humor about it all. What is Rett Syndrome? Thursday, December 6, 2012. Rae's Book Review: You Are Special. Awhile back, I ventured into my local Lifeway Christian Bookstore and while perusing the children's books, I came across the story of Punchinello, a Wemmick ( think Pinocchio after he came to life, but before he became a "real boy".

hypotonicworld.blogspot.com hypotonicworld.blogspot.com

Sunshine in a Hypotonic World: January 2015

http://hypotonicworld.blogspot.com/2015_01_01_archive.html

Sunshine in a Hypotonic World. Living in the world of Rett Syndrome, celebrating all the little victories, taking life one day at a time and trying to keep a sense of humor about it all. What is Rett Syndrome? Tuesday, January 6, 2015. When There Are No Words. It seems weird to write a post about there being no words, but more often than not I find that there just aren't adequate words to express my sorrows and empathy to members of our Rett community. Nothing I can think of feels right. These are the on...

hypotonicworld.blogspot.com hypotonicworld.blogspot.com

Sunshine in a Hypotonic World: April 2015

http://hypotonicworld.blogspot.com/2015_04_01_archive.html

Sunshine in a Hypotonic World. Living in the world of Rett Syndrome, celebrating all the little victories, taking life one day at a time and trying to keep a sense of humor about it all. What is Rett Syndrome? Tuesday, April 7, 2015. Accepting the Answer Given. A few weeks ago, when I managed to pull myself together, I attended church. I just sat there with my hands in my lap. Trapped in my own thoughts. Not focused on the sermon. I can't even tell you where my mind drifted off to during ...The message c...

hypotonicworld.blogspot.com hypotonicworld.blogspot.com

Sunshine in a Hypotonic World: Accepting the Answer Given

http://hypotonicworld.blogspot.com/2015/04/accepting-answer-given.html

Sunshine in a Hypotonic World. Living in the world of Rett Syndrome, celebrating all the little victories, taking life one day at a time and trying to keep a sense of humor about it all. What is Rett Syndrome? Tuesday, April 7, 2015. Accepting the Answer Given. A few weeks ago, when I managed to pull myself together, I attended church. I just sat there with my hands in my lap. Trapped in my own thoughts. Not focused on the sermon. I can't even tell you where my mind drifted off to during ...The message c...

hypotonicworld.blogspot.com hypotonicworld.blogspot.com

Sunshine in a Hypotonic World: When There Are No Words

http://hypotonicworld.blogspot.com/2015/01/when-there-are-no-words.html

Sunshine in a Hypotonic World. Living in the world of Rett Syndrome, celebrating all the little victories, taking life one day at a time and trying to keep a sense of humor about it all. What is Rett Syndrome? Tuesday, January 6, 2015. When There Are No Words. It seems weird to write a post about there being no words, but more often than not I find that there just aren't adequate words to express my sorrows and empathy to members of our Rett community. Nothing I can think of feels right. These are the on...

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Life with my Mito kid

Life with my Mito kid. My husband and I have three children. Our youngest, Lex was diagnosed with mitochondrial disease on November 29, 2011. He suffers with hypotonia, sensory processing issues, motor delay, and speech delay. The goal of this blog is to help other families affected by this disease and to raise awareness. Thursday, December 6, 2012. Lexs road to diagnosis. Saturday, November 17, 2012. The Day Our Lives Changed. How did this happen to him? Will he even live to have a future?

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