Elias!: What it’s all about!

Pages

What is FA?
Video Archive
Medical Dx and Anomalies
Main Page

Monday, November 9, 2009

What it’s all about!

Email This BlogThis!Share to Twitter Share to Facebook Share to Pinterest

1 comment:

Lolita BreckenridgeNovember 10, 2009 at 1:18 PM
Thanks for the smile! Lovely!
ReplyDelete
Replies

Add comment

Share your thoughts or questions

Newer Post Older Post Home

Subscribe to: Post Comments (Atom)

We appreciate you reading and following Elias' journey.

Welcome & thank you for visiting

We appreciate your time and interest in our amazing little boy. There is a handy tool bar at the bottom right hand corner. This allows easy access to Elias' YouTube channel and to the Facebook page (Hope for Elias) which was setup and is maintained by our friends, Stace & Jessica. Finally there are simple ways for you to search and share the site and posts. This helps spread awareness for this horrible disease, Fanconi Anemia

About Our Son Elias!

Elias!: Elias was born on May 1, 2008 @ 2:41 am. He spent five and a half months in the Neonatal Intensive Care Unit. On October 9, 2008 Elias was diagnosed with Fanconi Anemia, a rare genetic disease that often leads to bone marrow failure, leukemia, and higher risk for other types of cancer. We are blessed to have Elias home with us now as of October 15, 2008. He is such a happy baby that melts everyone's hearts. Welcome to our struggles and celebrations for life with Elias

View my complete profile