thetarwaterclan.blogspot.com
The Story of Us: October 2008
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The Story of Us. Friday, October 31, 2008. We hope everyone had a very Happy Halloween. Nathan dressed up as Captain Jack Sparrow and Addie was a sock-hop girl. They both looked great! Monday, October 20, 2008. Tuesday, October 14, 2008. Photo and video editing at www.OneTrueMedia.com. Tuesday, October 7, 2008. Make photo slide shows at www.OneTrueMedia.com. The weather in DC has been wonderful! Hope you all enjoy the fall weather. Subscribe to: Posts (Atom). CCAI - Chinese Adoptions. A Family is Forever.
thetarwaterclan.blogspot.com
The Story of Us: May 2011
http://thetarwaterclan.blogspot.com/2011_05_01_archive.html
The Story of Us. Sunday, May 1, 2011. Subscribe to: Posts (Atom). STOMP - Special Need info for military families. CCAI - Chinese Adoptions. Unique - Rare Chromosome Disorders. CDO - Rare Chromosome Disorders. A Family is Forever. Digging A hole to China. Bilbo's Random Thought Collection. I am a stay at home mom with two kids. Our son was born with a rare chromosome disorder and our daughter was adopted from China. My husband is active duty military. This blog is the story of us. View my complete profile.
thetarwaterclan.blogspot.com
The Story of Us: September 2008
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The Story of Us. Sunday, September 28, 2008. A couple of weekends ago we took the kids to the zoo. Addison has been there a couple of times since we brought her home, but she never really seemed interested. This time she LOVED it! At first she was a little scared, but we told her it wasn't scary and she was okay with it. She loved seeing the elephants and monkeys! Saturday, September 13, 2008. You would have thought I would have learned to use spellcheck by now! Addison's First Day of School. Addison had...
thetarwaterclan.blogspot.com
The Story of Us: March 2009
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The Story of Us. Wednesday, March 4, 2009. Everyone is home from the hospital! We flew my mom out on Saturday to help us out. She has been keeping Addie busy - or more like Addie has been keeping my mom busy:-) They are having a great time together, but Addie's energy level is a little higher than my mom's even though she is keeping up pretty good. Thanks for all your prayers and well wishes. We certainly believe that they helped! Subscribe to: Posts (Atom). STOMP - Special Need info for military families.
thetarwaterclan.blogspot.com
The Story of Us: February 2011
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The Story of Us. Saturday, February 26, 2011. Since we accepted Lui Jun Jie's referral, Bob and I couldn't agree on a name. Two weeks ago our agency needed his new name so that we could complete some of the necessary papers in order to get a visa. After much discussion we finally agreed upon a name - Caden Dean Junjie Tarwater. Caden was born 12/10/09 and is currently 14 months old. We received these updated pics of him at the beginning of Jan. Our return to China. Here are his referral pics -. When Jun ...
thetarwaterclan.blogspot.com
The Story of Us: June 2009
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The Story of Us. Friday, June 12, 2009. The Last Few Months. The kids are doing well. Right after we got here, Addison said she missed her old house, but now all she says is that she LOVES her new house. I think she is so happy to have more room to run around in. This house is about twice the size of our other one and Addie will stand at one end of the house yelling, "Mama, where are you? Make an on-line slideshow at www.OneTrueMedia.com. I made a short video of the past few months.I hope you enjoy.
theolerudproject.blogspot.com
Supporting the Jordan Fund: January 2006
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Supporting the Jordan Fund. To raise awareness of Gene Deletion Disorders and the work The Jordan Fund does as well as to raise money for the Fund, Started by Red Sox 1st baseman John Olerud and his wife, Kelly to help others with these and many other disorders, John and Kelly's daughter Jordan has a gene deletion disorder and that is who the foundation is named after. Anything Helps! Sunday, January 29, 2006. Posted by Justyna and Aly at 4:18 PM. Wilmington and Hyde Park, MA. View my complete profile.
justjamesinfo.wordpress.com
Rare Chromosome Disorders | Just James
https://justjamesinfo.wordpress.com/rare-chromosome-disorders
Helping and supporting parents of children with Nystagmus and rare chromosome disorders, particularly chromosome 18 disorders. Welcome to Just James. Blog, Facebook, and Twitter. All of the information you read below is taken from Chromosome Disorder Outreach. Focuses on Chromosome 18 disorders. However, before you can understand Chromosome 18 disorders, it is helpful to know about Chromosomes and Chromosome disorders in general. How are Chromosome Disorders Diagnosed Methods of Cytogenetic Investigation.
pksonline1.tripod.com
Welcome to PKS Support!
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PKS Online Support Group. PKS Information and Conversation. Early Intervention Resources Page. Know of other good resources for caregivers? Click here and send us an email! Help us educate the world about PKS,. The families that are dealing with this. And support them with all they require. To care for their child:. No part of this website may be reproduced without expressed written consent from the owners. To inquire about this, send an email to.
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