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EmilyAnn

Raising a child with a genetic disorder can be very difficult, especially when it is a rare disorder. This blog for my daughter who has 18p- Syndrome, in other words missing the tip on the short arm of her one of her 18th Chromosome. Thursday, September 16, 2010. My brave little girl who has gone through more tests then a lot of adults. I always try to be strong during her appointments and tests. There are tears that flow sometimes, but they are always mine. Tuesday, August 24, 2010. A FRIEND LIKE ME.

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EmilyAnn | emilyanned.blogspot.com Reviews

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Raising a child with a genetic disorder can be very difficult, especially when it is a rare disorder. This blog for my daughter who has 18p- Syndrome, in other words missing the tip on the short arm of her one of her 18th Chromosome. Thursday, September 16, 2010. My brave little girl who has gone through more tests then a lot of adults. I always try to be strong during her appointments and tests. There are tears that flow sometimes, but they are always mine. Tuesday, August 24, 2010. A FRIEND LIKE ME.

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4 always smiling

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EmilyAnn | emilyanned.blogspot.com Reviews

https://emilyanned.blogspot.com

Raising a child with a genetic disorder can be very difficult, especially when it is a rare disorder. This blog for my daughter who has 18p- Syndrome, in other words missing the tip on the short arm of her one of her 18th Chromosome. Thursday, September 16, 2010. My brave little girl who has gone through more tests then a lot of adults. I always try to be strong during her appointments and tests. There are tears that flow sometimes, but they are always mine. Tuesday, August 24, 2010. A FRIEND LIKE ME.

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emilyanned.blogspot.com

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EmilyAnn: August 2010

http://www.emilyanned.blogspot.com/2010_08_01_archive.html

Raising a child with a genetic disorder can be very difficult, especially when it is a rare disorder. This blog for my daughter who has 18p- Syndrome, in other words missing the tip on the short arm of her one of her 18th Chromosome. Tuesday, August 24, 2010. My Beuatiful Baby Girl! Make photo slide shows at www.OneTrueMedia.com. Emily and her Chromosome 18 Friend Julia. A FRIEND LIKE ME. Please don't be afraid of me. I want to be your friend. And if you get to know me. Your rigid thoughts might bend.

2

EmilyAnn: Friendship

http://www.emilyanned.blogspot.com/2010/08/friendship.html

Raising a child with a genetic disorder can be very difficult, especially when it is a rare disorder. This blog for my daughter who has 18p- Syndrome, in other words missing the tip on the short arm of her one of her 18th Chromosome. Tuesday, August 24, 2010. Emily and her Chromosome 18 Friend Julia. A FRIEND LIKE ME. Please don't be afraid of me. I want to be your friend. And if you get to know me. Your rigid thoughts might bend. Thoughts that I am different. From others that you know,. I love that poem!

3

EmilyAnn: A Bunch of Numbers

http://www.emilyanned.blogspot.com/2010/01/bunch-of-numbers.html

Raising a child with a genetic disorder can be very difficult, especially when it is a rare disorder. This blog for my daughter who has 18p- Syndrome, in other words missing the tip on the short arm of her one of her 18th Chromosome. Tuesday, January 12, 2010. A Bunch of Numbers. Emily has 18p- Syndrome and she is missing the top part of the p tip of Chromosome 18 (18p11.32 to be exact). August 8, 2010 at 1:33 PM. Cant wait to read more! Also, I linked your blog on mine :). August 8, 2010 at 5:14 PM.

4

EmilyAnn: January 2010

http://www.emilyanned.blogspot.com/2010_01_01_archive.html

Raising a child with a genetic disorder can be very difficult, especially when it is a rare disorder. This blog for my daughter who has 18p- Syndrome, in other words missing the tip on the short arm of her one of her 18th Chromosome. Tuesday, January 12, 2010. A Bunch of Numbers. Emily has 18p- Syndrome and she is missing the top part of the p tip of Chromosome 18 (18p11.32 to be exact). Subscribe to: Posts (Atom). A Bunch of Numbers. Havre de Grace, Maryland, United States. View my complete profile.

5

EmilyAnn: Always Smiling

http://www.emilyanned.blogspot.com/2010/09/always-smiling.html

Raising a child with a genetic disorder can be very difficult, especially when it is a rare disorder. This blog for my daughter who has 18p- Syndrome, in other words missing the tip on the short arm of her one of her 18th Chromosome. Thursday, September 16, 2010. My brave little girl who has gone through more tests then a lot of adults. I always try to be strong during her appointments and tests. There are tears that flow sometimes, but they are always mine. September 16, 2010 at 12:26 PM.

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Difference in Schools | Different Iz Good™

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Making a Difference for Those With Differences. Skip to primary content. Skip to secondary content. Gift a Voice Application. Gift a Voice Cell Phone Drive. Other Organizations Gifting Apple Devices. Category Archives: Difference in Schools. A Different View: Mainstreaming and Inclusion. March 29, 2012. This gallery contains 1 photo. November 15, 2010. Guest post by Geri Kochis. 8211; Geri blogs at EmilyAnn. Emily is currently educated in a general education classroom and goes to a resource room for spec...

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Raising a child with a genetic disorder can be very difficult, especially when it is a rare disorder. This blog for my daughter who has 18p- Syndrome, in other words missing the tip on the short arm of her one of her 18th Chromosome. Thursday, September 16, 2010. My brave little girl who has gone through more tests then a lot of adults. I always try to be strong during her appointments and tests. There are tears that flow sometimes, but they are always mine. Tuesday, August 24, 2010. A FRIEND LIKE ME.

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WELCOME TO EMILY'S BLOG!!! :)

WELCOME TO EMILY'S BLOG! Baptisms for the dead weekend! I hope u all had a gr8 weekend last weekend! I just wanted to share with u all that last Sat I was able to go with the Singles ward for Baptisms for the dead and it was awesome! It was fun being and goin with everyone and goin to Manti was very pretty with all the fall colors the Temple looked really pretty in the Fall. While bein at the Temple I was able to confirm 20 people! Well thats about it and I hope everyone has a fun and safe Halloween!