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The Anger's

Thursday, September 6, 2012. Grace is enjoying the quiet time at home, and I think it's giving her a chance to express her creativity as well. She loves holding and talking to her baby brother and hearing all of Lilly's Kindergarten stories as well. She is our little sweetheart, but also a three year old, with all of the fun that that entails! We love all of our gifts from God! Monday, August 20, 2012. A Happy Boy Always. Smiling at the nurses. Hungry and getting ready to go back. I had a really good nap!

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The Anger's | protectinghisgifts.blogspot.com Reviews
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Thursday, September 6, 2012. Grace is enjoying the quiet time at home, and I think it's giving her a chance to express her creativity as well. She loves holding and talking to her baby brother and hearing all of Lilly's Kindergarten stories as well. She is our little sweetheart, but also a three year old, with all of the fun that that entails! We love all of our gifts from God! Monday, August 20, 2012. A Happy Boy Always. Smiling at the nurses. Hungry and getting ready to go back. I had a really good nap!
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The Anger's | protectinghisgifts.blogspot.com Reviews

https://protectinghisgifts.blogspot.com

Thursday, September 6, 2012. Grace is enjoying the quiet time at home, and I think it's giving her a chance to express her creativity as well. She loves holding and talking to her baby brother and hearing all of Lilly's Kindergarten stories as well. She is our little sweetheart, but also a three year old, with all of the fun that that entails! We love all of our gifts from God! Monday, August 20, 2012. A Happy Boy Always. Smiling at the nurses. Hungry and getting ready to go back. I had a really good nap!

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protectinghisgifts.blogspot.com protectinghisgifts.blogspot.com
1

The Anger's

http://www.protectinghisgifts.blogspot.com/2012/06/summer-so-far-is-doing-so-well-he-is.html

Wednesday, June 27, 2012. Elijah is doing so well! He is meeting with a infant specialist and a occupational therapist twice a week. We are working on lots of tummy time to get his head nice and strong so he can hold it up! He is doing so good. He is smiling, cooing and laughing! It was just a day trip but he pretty much slept the entire time. So- I would say he enjoyed it. I mean, who doesn't enjoy a vacation where alls you do is sleep? Here are some new photos! He is holding onto is moose toy!

2

The Anger's: May 2012

http://www.protectinghisgifts.blogspot.com/2012_05_01_archive.html

Thursday, May 10, 2012. Settling back in to routine. Subscribe to: Posts (Atom). 160;                                 Settling back in. Watermark template. Powered by Blogger.

3

The Anger's: Home! - or - Life after birth

http://www.protectinghisgifts.blogspot.com/2012/03/home-or-life-after-birth.html

Thursday, March 22, 2012. Or - Life after birth. Elijah - My God is Yahweh! We're home. Where do I start? Dr (luckily my mom and sister were there) she said that the fluid they had pulled from his head was cloudy and they think it may be meningitis. I don't even have words to express how I felt at that moment when she was telling me this. My heart just dropped. I know what meningitis is and I know how deadly it is. How could our baby have this? Subscribe to: Post Comments (Atom). Or - Life after birth.

4

The Anger's: June 2012

http://www.protectinghisgifts.blogspot.com/2012_06_01_archive.html

Wednesday, June 27, 2012. Elijah is doing so well! He is meeting with a infant specialist and a occupational therapist twice a week. We are working on lots of tummy time to get his head nice and strong so he can hold it up! He is doing so good. He is smiling, cooing and laughing! It was just a day trip but he pretty much slept the entire time. So- I would say he enjoyed it. I mean, who doesn't enjoy a vacation where alls you do is sleep? Here are some new photos! He is holding onto is moose toy!

5

The Anger's

http://www.protectinghisgifts.blogspot.com/2012/05/settling-back-in-to-routine-its-been.html

Thursday, May 10, 2012. Settling back in to routine. Subscribe to: Post Comments (Atom). 160;                                 Settling back in. Watermark template. Powered by Blogger.

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theturtlemom.wordpress.com theturtlemom.wordpress.com

My gift to you | theturtlemom

https://theturtlemom.wordpress.com/2013/03/04/my-gift-to-you

The story of our miracle girl, Parker Elizabeth and a little thing called Hydrocephalus…. My gift to you. March 4, 2013. I am a very proud wife and mother. My daughter, Parker was diagnosed at 18 weeks with Hydrocephalus. If you are searching for answers regarding a similar diagnosis, here is our saga. View all posts by theturtlemom ». Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:. Address never made public). Notify me of new comments via email.

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When did she grow up? | theturtlemom

https://theturtlemom.wordpress.com/2013/04/24/when-did-she-grow-up-2

The story of our miracle girl, Parker Elizabeth and a little thing called Hydrocephalus…. When did she grow up? April 24, 2013. Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:. Address never made public). You are commenting using your WordPress.com account. ( Log Out. You are commenting using your Twitter account. ( Log Out. You are commenting using your Facebook account. ( Log Out. You are commenting using your Google account. ( Log Out.

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May | 2013 | theturtlemom

https://theturtlemom.wordpress.com/2013/05

The story of our miracle girl, Parker Elizabeth and a little thing called Hydrocephalus…. Monthly Archives: May 2013. May 25, 2013. Cure International Hospital for Hydrocephalus – Uganda. Owen Higgins (My Hydrocephalus Bible). The Spohrs Are Multiplying. September is Hydrocephalus Awareness Month! Create a free website or blog at WordPress.com. Blog at WordPress.com.

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Mat Man | theturtlemom

https://theturtlemom.wordpress.com/2013/08/03/mat-man

The story of our miracle girl, Parker Elizabeth and a little thing called Hydrocephalus…. August 3, 2013. Parker has little interest in drawing. I’m not sure if its because she isn’t very good at it or why. But, this summer she has had one on one OT at Special Care and I love the results! In just several weeks, she drew this. I’ve never seen her draw a figure that actually looks like a person. I’m hopeful this momentum continues into the school year. And tagged Fine Motor Skills. One response ». Septembe...

theturtlemom.wordpress.com theturtlemom.wordpress.com

April | 2013 | theturtlemom

https://theturtlemom.wordpress.com/2013/04

The story of our miracle girl, Parker Elizabeth and a little thing called Hydrocephalus…. Monthly Archives: April 2013. When did she grow up? April 24, 2013. Cure International Hospital for Hydrocephalus – Uganda. Owen Higgins (My Hydrocephalus Bible). The Spohrs Are Multiplying. September is Hydrocephalus Awareness Month! Create a free website or blog at WordPress.com. Blog at WordPress.com.

theturtlemom.wordpress.com theturtlemom.wordpress.com

August | 2013 | theturtlemom

https://theturtlemom.wordpress.com/2013/08

The story of our miracle girl, Parker Elizabeth and a little thing called Hydrocephalus…. Monthly Archives: August 2013. August 27, 2013. It’s hard to articulate how much one little girl can change your world. I wonder what would have happened if Parker had not been diagnosed with Hydrocephalus? Yesterday was Parker’s 5th Birthday. It brings tears to my eyes to think of how much love I have for that little girl. You are my sunshine, Parker Elizabeth, when skies are grey. August 3, 2013. Create a free web...

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Turtles | theturtlemom

https://theturtlemom.wordpress.com/2013/05/25/turtles

The story of our miracle girl, Parker Elizabeth and a little thing called Hydrocephalus…. May 25, 2013. I am a very proud wife and mother. My daughter, Parker was diagnosed at 18 weeks with Hydrocephalus. If you are searching for answers regarding a similar diagnosis, here is our saga. View all posts by theturtlemom ». 2 responses ». June 13, 2013 at 9:49 am. Dear Turtle Mom,. I hope you can be so kind to help us out on this life-and-death issue…. June 13, 2013 at 12:02 pm. Leave a Reply Cancel reply.

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My American Girl | theturtlemom

https://theturtlemom.wordpress.com/2013/07/24/my-american-girl

The story of our miracle girl, Parker Elizabeth and a little thing called Hydrocephalus…. July 24, 2013. We had a family vacation planned to Breckenridge this week. Last Friday, Parker became ill with a bug she picked up at daycare. It became obvious the illness she had was contagious and she wouldn’t be able to travel😦. Sadly, we cancelled our tickets and got antibiotics. So, what was a sour and sad family trip wound up with a sunny side. View all posts by theturtlemom ». One response ». Loved reading ...

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theturtlemom | theturtlemom

https://theturtlemom.wordpress.com/author/theturtlemom

The story of our miracle girl, Parker Elizabeth and a little thing called Hydrocephalus…. I am a very proud wife and mother. My daughter, Parker was diagnosed at 18 weeks with Hydrocephalus. If you are searching for answers regarding a similar diagnosis, here is our saga. September is Hydrocephalus Awareness Month! September 19, 2016. July 31, 2016. The exposure would be beyond anything I’ve ever seen. And, here is a press release from The Hydrocephalus Association:. March 6, 2016. It is easy to forget t...

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The Anger's

Thursday, September 6, 2012. Grace is enjoying the quiet time at home, and I think it's giving her a chance to express her creativity as well. She loves holding and talking to her baby brother and hearing all of Lilly's Kindergarten stories as well. She is our little sweetheart, but also a three year old, with all of the fun that that entails! We love all of our gifts from God! Monday, August 20, 2012. A Happy Boy Always. Smiling at the nurses. Hungry and getting ready to go back. I had a really good nap!

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