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Kiefer Family Adventures: Surgery Tomorrow

http://kieferfam.blogspot.com/2010/07/surgery-tomorrow.html

Raising a Preemie with Achondroplasia. Wednesday, July 21, 2010. Sorry it's been so long again! Olivia will be having her tonsils and adenoids removed tomorrow. She will be staying in the PICU at least one night after. We'll keep everyone posted as best we can. We will be thinking of you guys! Big hugs to sweet Olivia! July 21, 2010 at 8:39 PM. Hope all goes well! July 22, 2010 at 9:17 AM. Praying for you Olivia! July 22, 2010 at 10:10 AM. Subscribe to: Post Comments (Atom). View my complete profile.

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Kiefer Family Adventures: July 2010

http://kieferfam.blogspot.com/2010_07_01_archive.html

Raising a Preemie with Achondroplasia. Friday, July 23, 2010. They sent us home this morning! Olivia had a great night. She was on slightly lower oxygen than normal, and did better than normal! They sent us home on her normal oxygen though. She already wanted to play outside when we got home this morning! Thursday, July 22, 2010. I have to go now though because they just said we have to move to the hall because there is a tornado warning. We'll keep you posted! Wednesday, July 21, 2010. Nathan's World- L...

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Kiefer Family Adventures: January 2010

http://kieferfam.blogspot.com/2010_01_01_archive.html

Raising a Preemie with Achondroplasia. Sunday, January 10, 2010. Sorry it’s been so long since I have posted! Olivia is doing great! She is cruising along furniture and walls, and sits very well on her own. She is more interested in food now, but still doesn’t want to swallow. We are supposed to go see a feeding therapist soon to work on that issue. She is still on the same amount of oxygen that she’s been on for over a year now. Olivia had a renal ultrasound recently also. Her nurses love her and she lo...

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Kiefer Family Adventures: June 2009

http://kieferfam.blogspot.com/2009_06_01_archive.html

Raising a Preemie with Achondroplasia. Wednesday, June 17, 2009. Sorry I’ve been a slacker with the updates again. We’ve been busy with graduations, end of the school year, birthdays, doctor appts, etc. We’ve been having fun though so it’s ok. We also saw the pulmonologist. He decided that it was best not to mess with Olivia’s oxygen for right now, because of the vomiting issue we are currently battling. Otherwise he thought Olivia was doing well. We have had of my nieces for a couple of days each. I...

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Kiefer Family Adventures: November 2008

http://kieferfam.blogspot.com/2008_11_01_archive.html

Raising a Preemie with Achondroplasia. Wednesday, November 26, 2008. What are you thankful for? Here are a few things I am thankful for this Thanksgiving:. An amazing little girl who makes my heart smile! My supportive husband who is a great father. Wonderful Family and Friends. This year has not always been easy on us, but we’ve had more support than we could ever have imagined. All of you who have become another extended family. I love reading your stories, and hearing your comments about ours! Anyway,...

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Kiefer Family Adventures: October 2008

http://kieferfam.blogspot.com/2008_10_01_archive.html

Raising a Preemie with Achondroplasia. Friday, October 24, 2008. Nine Month Check-up and I'm it! Sorry that I’ve been such a slacker with the updates lately! Now I’ll bombard you with tons of info though! Little Miss Olivia is now officially a member of Little People of America! We went for Olivia’s nine-month check-up today. Dr. Keil said that Olivia looks great, especially considering her rough start. Her lungs still sound good and clear! What a tough little cookie! Her favorite toy is her tube though!

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Kiefer Family Adventures: Yippee! Yahoo!

http://kieferfam.blogspot.com/2010/07/yippee-yahoo.html

Raising a Preemie with Achondroplasia. Friday, July 23, 2010. They sent us home this morning! Olivia had a great night. She was on slightly lower oxygen than normal, and did better than normal! They sent us home on her normal oxygen though. She already wanted to play outside when we got home this morning! Glad to hear that Olivia is home doing well after her surgery! What a trooper, beautiful little angel! Thank you for the update! We are sending our best thoughts and prayers to all your family!

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Kiefer Family Adventures: April 2009

http://kieferfam.blogspot.com/2009_04_01_archive.html

Raising a Preemie with Achondroplasia. Tuesday, April 28, 2009. Something very exciting happened while we were waiting between appointments! We met another family with a 17 month old boy named Caden, who also has achondroplasia. While his mom and I sat and talked he climbed up in my lap. It was the sweetest thing, and he is absolutely adorable! It was really nice to meet someone so close by, who sees some of the same doctors that we do. These magazines are neat! I love to read! Wednesday, April 15, 2009.

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Kiefer Family Adventures: February 2009

http://kieferfam.blogspot.com/2009_02_01_archive.html

Raising a Preemie with Achondroplasia. Friday, February 27, 2009. Olivia has had quite a week. She got her first tooth on Tuesday, another on Wednesday, and has two more ready to come through! In addition to that she has started trying to crawl. Yay for me, I finally figured out how to add video! Sohere is a short video of Olivia trying to get to the remote control! I didn't get the video camera until she was half way there. Sorry for the incredibly shaky video job! Wednesday, February 25, 2009. The doct...

kieferfam.blogspot.com kieferfam.blogspot.com

Kiefer Family Adventures: December 2008

http://kieferfam.blogspot.com/2008_12_01_archive.html

Raising a Preemie with Achondroplasia. Monday, December 29, 2008. We hope everyone had a wonderful Christmas! Our first Christmas with Olivia was a busy one, but a really great one! We spent Christmas Eve at my grandparents’ house, Christmas day at my parents’ house, and had a final Christmas celebration yesterday. Olivia got completely spoiled, but she loves all the gifts she got! Olivia wasn’t entirely sure what to do with the gifts, but she did like to pull on and eat the paper. Can you believe it?

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Joe Kiefer Index

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