tag:blogger.com,1999:blog-14649024.post3512867256376236197..comments2024-02-13T13:47:56.739-08:00Comments on David McNally - Wiskott Aldrich Syndrome, Bone Marrow Transplant, and Graft-vs-Host Disease: +828 Pictures of our Trip to Jekyll Island Georgia, and Disney World (in October 2008)Aimeehttp://www.blogger.com/profile/13851001723699650438noreply@blogger.comBlogger2125tag:blogger.com,1999:blog-14649024.post-49794811409767786782008-11-30T15:47:00.000-08:002008-11-30T15:47:00.000-08:00Thanks for responding! I hope you don't mind that...Thanks for responding! I hope you don't mind that I put the link to your blog on mine. These blogs have been SO helpful and encouraging that if anyone finds mine, I want them to be able to find others relatively easily as well. It's so great to read about babies and little boys doing at least fairly well after a BMT. It's a little terrifying being on this side of it. I really appreciate you helping me get in touch with other people. It seems like everyone else I talk to has a different experience, but so far, they've all been mostly positive.<BR/><BR/>Thanks again! Your family is beautiful, by the way. :-)Paigehttps://www.blogger.com/profile/14600919321398579141noreply@blogger.comtag:blogger.com,1999:blog-14649024.post-71547372352183951232008-11-29T05:48:00.000-08:002008-11-29T05:48:00.000-08:00Hi! My name is Paige Robins and my 4 1/2 month ol...Hi! My name is Paige Robins and my 4 1/2 month old son was diagnosed with WAS about a month and 1/2 ago. I've been putting updates on Facebook, but to make them more easily accessible, I just started a blog (www.weloveayden.blogspot.com). Thank you for writing about your experience. It's really helpful to read about it.Paigehttps://www.blogger.com/profile/14600919321398579141noreply@blogger.com