Hello everyone! We wanted to explain a little about the links on the right side of the page. The first one (I think it's the first one anyway) is a link to a website created by parents of children with HLHS. It is a great site for information. There are FAQ, and advise on what questions to ask the dr's, hospital, etc. Check that one out for sure. There is also a link to a hospital for more medical information about HSHS.

The links to Ronald McDonald House and Children's Miracle Network are there because we feel that we will be utilizing these two charities quite a bit through out this ordeal. Jeremy, Myles and I already volunteer at RMH, so that one if near and dear to our hearts anyway.

Soon there will be a link to Paypal. If you wish, you can go there and make donations to an account that has been set up for us. The money will be used for travel expenses, and other things we need while we are away from home and also to help whomever should be taking care of Myles during that time.

On the left side, there is a link to view our profile. We have written a short paragraph about ourselves so check that out if you want.

Right now it's hard to come up with very much to say b/c I haven't had a dr's appointment since the one where we found out. But I have one on Wednesday, so I'll for sure post then. Talk to you later.