Alicia Reed

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Welcome to our Child's Web Page. It has been provided to keep people updated about our Child.Alicia Reed was born with a terminal genetic disorder they call Fanconi Anemia. She will sooner or later need a bone marrow transplant, But this still won't save her precious life.

Journal

Sunday, June 29, 2008 10:45 AM CDT

Hello Everyone!

Alicia's website has been moved to a new place. She now has a blog.

Click here for Alicia's New Website

If that link doesn't work for some reason, here is the exactly website address that you can copy/paste:

http://aliciaslifewithfa.blogspot.com/

For those who are new to leaving comments on blogs, it's very easy. Once you read the entry, you'll see down at the very bottom of the entry that there is a little link that says "Comments", click on that link, and it'll take you to a new page where you leave comments.

You can choose to sign in anonymously (by selecting that option below the comment box) or if you have a sign in name, you can use that. You type in your comment in the comment box and then click "Publish Your Comment". Your comment will then appear off to the left, and it will also be emailed directly to Alicia's family.

Alicia's family really would love everyone to keep following them at their new website. They need all the love and encouragement that they can get during this difficult time. Hope to see you there!

Thanks,
Teresa
(writing on behalf of Michelle...)

Read Journal History

Hospital Information:

Patient Room: A-519

Cincinnati Children's
3333 Burnet
Cincinnati, OH
1-513-636-1519

Links:

E-mail Author: g_mamichelle@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.