My name is Sherri. My husband Matt and I are so proud of our 2 great kids who joined our family through the blessing of adoption.

Micayla is our oldest and she has DiGeorge Syndrome. She was diagnosed before birth. She had her first heart surgery at 9 days old. It's been rough at times but she is doing great!!

I created this blog as a place where families dealing with VCFS can link together to share our trials, triumphs, fears and dreams.

Along the left hand side here you will see a list of families/kids that are dealing with VCFS, if you would like to be linked there please comment with your link or email sherriwj@msn.com If there is something that you would like to post please let me know.

Tuesday, November 17, 2009

National Conference

Hey I was so excited to get an email for the VCFS Educational Foundation yesterday. They have a new website and are also on Facebook now!

SUPER exciting news for me is that the conference is in Salt Lake City in July 2010!! Yeah!

Just in case you didn't get the email here it is:

We are excited to share our new, improved web site with you. Be sure to take a look at www.vcfsef.org. Thank you to our new webmaster, Kevin Greek.

While online, join us on Facebook (there is a link from the homepage of our website to take you right there).

Don't forget to save the date:

The 17th Annual International Scientific Meeting of the VCFS Educational Foundation
July 16-18, 2010
Salt Lake City, Utah

The Abstract submission form is on our website!

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