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Aubrey Margaret Seeman


Photo Album

Aubrey's Photo Page

Total Number of Gifts: 8
Total Value of Gifts: $485.00

Recent Donors in our child's honor

Nawnaw & Pawpaw

Anonymous

Friends & Family of Kevin & Vicki Seeman

Don, Martha, Allison, & Libby

Michael Trainor & Pediatric Care Clinic staff

Charlie Hamby

Mr. and Mrs. Thomas Seeman

Rachel Tyner

View all donors in our child's honor Opens new window.View all donors in our child's honor


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Twinkle Twinkle Little Star

Our daughter Aubrey Margaret was diagnosed with Trisomy 18 at 21 weeks gestation. She was born on 1/12/2009 at 38 weeks and had 2 amazing days with her mom, dad and new family. She became one of God's perfect angels on 1/14/2009. Her memory and the love that we have for her will live on forever.

Seeman Family Website

Please visit our website to view photos and videos of our daughter Aubrey.

http://www.seemanfamilysite.com

Click on the link at the top of the page to access Aubrey's page.

Guest Book

If you would like, you can add your name and a short message to our Guest Book. Thank you.

Sign the Guest Book

Erin Hutchins
Wed, Jan 28, 2009
To Andrea and Aaron, I am so sincerely sorry for your loss of the child that god has blessed you with. The memory of your daughter will live forever in your hearts as well as everyone who has shared this experience with you.

Stacey Spears
Fri, Jan 23, 2009
She is a beautiful angel. I'm so sorry for your loss. She will live on forever in your hearts and in heaven!

Teresa Smith
Wed, Jan 21, 2009
What a beautiful little angel..God Bless your family, as I know what you are going thru. Our little Grace was born 6-29-06 & she went home to be with Jesus on 7-01-06. Just not enough time to spend with her, but she was needed in Heavan more, although we don't understand down here. Keep her memories alive, as they say it gets easier with time, but I have to tell ya, it's going on 3 yrs. and for me it's not any easier. As a Mom, I will be thinking of you.
From another heartbroken T-18 Mom.
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Disclaimer: The content of this page does not reflect the views of the Trisomy 18 Foundation. The Trisomy 18 Foundation offers this space to parents as part of the Support Program. Parents have control over how they tell their child's story as well as which pictures they feel comfortable sharing with the Community.

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