Little Miss Ellie
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Ännu en resa till Mallis. Så underbart! Varje år tänker vi att det kanske är den sista. Kul att vi är på väg igen. Avgjutning av mina fina små fötter. Det är dags för nytt ståskal och vi ska den här gången prova att göra skräddarsydda specialstöd för fötterna.
The content might sometimes get a little heavy. People who are grieving may write sad or difficult things and bring you down. This blog may not be for the faint of stomach or of heart. Read with caution and at your own risk. Well, I sort of hop.
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Mummy and Daddy wanted me to share my life with people who care about me. I was born on the 4th of September 2010. On March the 3rd 2011 at six months old I died, because of a rare genetic disorder called Zellweggers Syndrome. I have lived because of my parents who loved me more than anything else in the whole world. This is my lifestory.CONTENT
This web page littlemissellieprince.blogspot.com states the following, "Mummy and Daddy wanted me to share my life with people who care about me." We saw that the webpage said " I was born on the 4th of September 2010." It also said " On March the 3rd 2011 at six months old I died, because of a rare genetic disorder called Zellweggers Syndrome. I have lived because of my parents who loved me more than anything else in the whole world. How to get the best out of this blog. Thank You for reading - every new reader shows that she has met another person and in her short life made such an impact."SEEK SIMILAR DOMAINS
I really feel blessed to have such a caring husband. Here are some pictures from our trip. I have the BEST group of friends! Some are married some are single ,.
This is the place where you can personalize your profile! By moving, adding and personalizing widgets. You can drag and drop to rearrange. You can edit widgets to customize them.
Beijing Bound! Sunday, July 05, 2015. So excited to see the Zhang family and the kids! Plus, we had two translation apps that were really helpful. Luckily the local English teacher came over to help us later in the evening, which was a nice addition to our group.
Chiari Malformation, Syringromyelia, Platybasia, Basilar Invagination. Friday, December 23, 2011. Emma had another MRI and x-rays. Muhonen today and he is pleased with her progress. He wants to see x-rays in 6 months. She is doing good and happy. Hope you all have a Merry Christmas. Monday, October 17, 2011. Saturday, September 17, 2011. Child Cervical Halo is GONE! THE HALO IS GONE! Wednesday, August 10, 2011. Wednesday, July 13, 2011.