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Andrew 's Web Page

Welcome to Andrew's Web Page. Little Andrew was diagnosed with Spinal Muscular Atrophy (SMA) Type I when he was seven weeks old. This web page is being provided to keep family and friends updated about our little one. We thank you so much for your love and support.

Journal

Monday, October 14, 2002 at 08:40 PM (CDT)

Many tears, fears, wants, wishes, heartaches, and a few smiles have passed our way since Andrew Richard left us to be at home with his Heavenly Father. This is very had to write and to see the website again. Most days come and go now with passing thoughts of Andrew but there are still many days of darkness when our arms ache to hold him and see his smile again. We miss you terribly, Andrew but we are glad you are happy and can run and play just like other kids.

We want you to know (and you probably already do) that Mommy and Daddy are thinking of trying to have a second baby. Granny thinks that you would be happy - especially since you know that they will be such a good mommy and daddy to your brother or sister. Love forever, Ganny

Look at past journal entries


Guestbook
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Links:

http://www.curesma.com   Please take the time to visit if you can. A cure IS POSSIBLE - but we need your help!


 
 

EmailEmail address  : jannehorton@yahoo.com

 
 


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Note: The foregoing information was authored by the patient, parent or guardian, or other parties who are solely responsible for the content. Such announcements or their content are not necessarily endorsed by CaringBridge, Inc. or any sponsoring agent.  This information does not confirm that anyone is or was actually a patient at any facility.

 
 
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