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Bringing Luka Home

A blog about our life with a child who has severe craniofacial differences--all the joy that comes with it. Adopted from Poland, home forever.

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Bringing Luka Home | fivekanekids.blogspot.com Reviews
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A blog about our life with a child who has severe craniofacial differences--all the joy that comes with it. Adopted from Poland, home forever.
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4 adoption time line
5 medical update
6 severe sleep apnea
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8 posted by
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Bringing Luka Home | fivekanekids.blogspot.com Reviews

https://fivekanekids.blogspot.com

A blog about our life with a child who has severe craniofacial differences--all the joy that comes with it. Adopted from Poland, home forever.

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1

Bringing Luka Home: November 2014

http://fivekanekids.blogspot.com/2014_11_01_archive.html

The Continued Story of Life with Lukasz. The Continued Story of Life with Lukasz. Our Craniofacial Team at Children's Medical Center- Dallas. Where We Went for Adoption Info. Sunday, November 9, 2014. Chaos is a Friend of Mine. An eventful month that kept me so busy that I have not kept up with my email (sacrilege! So, here is a quick update on all the happenings:. Luckily, the nurses and receptionist were sympathetic and called maintenance. They asked if it was really expensive because they would ha...

2

Bringing Luka Home: November 2012

http://fivekanekids.blogspot.com/2012_11_01_archive.html

The Continued Story of Life with Lukasz. The Continued Story of Life with Lukasz. Our Craniofacial Team at Children's Medical Center- Dallas. Where We Went for Adoption Info. Wednesday, November 7, 2012. Images of a Bare Skull. Especially since he's learned how to sign "eat" and is VERY demanding about it. On Nov. 6, I woke Lukasz up at 5:45 am and fed him. All day I was faced with insistent "eat" signing and pulling on my arms and legs with with pointing to the kitchen. He was "starving"! Trust me, when...

3

Bringing Luka Home: February 2014

http://fivekanekids.blogspot.com/2014_02_01_archive.html

The Continued Story of Life with Lukasz. The Continued Story of Life with Lukasz. Our Craniofacial Team at Children's Medical Center- Dallas. Where We Went for Adoption Info. Tuesday, February 25, 2014. Ever Consider Adopting A Child with Craniofacial Issues? Or, If Not, Maybe Pass this Info On? But, first, "Advocate" is Not the Right Word. Everyone talks about "adovcating" for a child but I really don't think that is the correct word. "To advocate" means " to. So, here is the info on Bode (pass it on):.

4

Bringing Luka Home: Adoption Time Line

http://fivekanekids.blogspot.com/p/adopt.html

The Continued Story of Life with Lukasz. The Continued Story of Life with Lukasz. Our Craniofacial Team at Children's Medical Center- Dallas. Where We Went for Adoption Info. December 29, 2011-Adoption Application Mailed to Children’s House International. January 10, 2012—Accepted by CHI to Poland Program. January 11, 2012 – International Homestudy Interviews by Social Worker. January 13, 2012 – International Homestudy Visit. February 2, 2012 – International Homestudy Completed and Mailed to CHI. June 1,...

5

Bringing Luka Home: Where We Went for Adoption Info

http://fivekanekids.blogspot.com/p/where-we-went-for-information-we.html

The Continued Story of Life with Lukasz. The Continued Story of Life with Lukasz. Our Craniofacial Team at Children's Medical Center- Dallas. Where We Went for Adoption Info. Where We Went for Adoption Info. We started with www.adoption.state.gov. Then I went to the Council on Accreditation’s website ( http:/ coanet.org/programs/hague-accreditation-and-approval/monitoring-and-oversight/. This report lists all substantiated. That is simply not true. Complaints are included ONLY if they are substantiated.

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Coming Down the Home Stretch? | Our Continued Adventure

https://ourcontinuedadventure.wordpress.com/2012/08/07/coming-down-the-home-stretch

Chronicling our adoption journey to Poland to find our daugther. Laquo; We Are Family! Coming Down the Home Stretch? August 7, 2012 by ourcontinuedadventure. Here are some new pics. Hope all is well with everyone back home, and hopefully we will be seeing you soon! On August 8, 2012 at 1:59 am. On August 8, 2012 at 2:00 am. Thinking of you guys – the pictures are precious! On August 8, 2012 at 5:14 am. We are heading that way soon but I think we’ll miss you by days (BOO! Talk to you soon! I feel like you...

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The Continued Story of Life with Lukasz. The Continued Story of Life with Lukasz. Our Craniofacial Team at Children's Medical Center- Dallas. Where We Went for Adoption Info. Sunday, March 27, 2016. The Big Texan on our way. From Las Cruces, NM. The more concerning update is the result of his sleep study in January. Last week, Dr. Mitchell, Lukasz’s ENT told us that Lukasz stops breathing 13 – 15 times an hour. If it is so small now, how much smaller will it get as he gets older? I forgot to ask. CPAP Th...

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