My Name's Maggie!

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Dear Friends,

Being so far away from my brother and Wyndy has made it difficult to help them in the ways we would like to - baby sitting here or there, a word of encouragement, or a simple hug.

This page is a small contribution to the support Paul and Wyndy have recieved from all of you. It's very important to them that you be able to see how special Miss Maggie Wyn is. We're glad we could help in this regard.

Jon & Sara

PS - This may take a few minutes to load. I'm not a big fan of thumbnails here.

Here I am at one week old taking a little nap...

We felt this is the best way to share the special beauty of our Maggie Wyn with all of you out there thinking and praying for us. Here is a gathering of images from June, 1998 that express how incredible Maggie is, and how much we love her.

Paul

Fast forward five months...

 

I just got out of the bath...

As I'm sure most of you know Maggie has Spinal Muscular Atrophy, an untreatable (except with love) neurological disorder. For more information go to the families of SMA web site.

My blue period...

 

Proud Papa...

Go girl...

I like it outside...

My cousin Anna doesn't like the Simpsons. She doesn't know what she's missing...

Here's my crib and my special parents.

 

Bless them.

Thanks for stopping by.