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Our son, Hunter, was diagnosed with a rare immuno-deficiency disease, Wiskott-Aldrich Syndrome, in August of 2008. He was almost 14 months old at the time of his diagnosis. This blog will follow Hunter's journey as he negotiates the ups and downs of his testing, potential procedures and future outlook.
Hunter
Hunter
Hunter
Hunter aura bientôt autant de cheveux que Harper !
ReplyDeleteBises à tous,
Sylvie et ses hommes
They are so beautiful! Hunter looks awesome!! So we have some good news... We get to go HOME! in two weeks. We are having a teleconference with Docs and home so that they know exactly what to do with Henry. I can't hardly believe it I'm so nervous excited. If I start going crazy and freaking out at home I'll call you guys!
ReplyDeleteHope life is treating you very well. Sending Hugs your way.
Hello from Seattle! So glad you guys made it back home to LA and are able to be together as a family. It definitely takes time to settle back in and being home and keeping everyone healthy isn't easy, but it sure is wonderful.
ReplyDeleteMia's doing well. We are up in Seattle still a few times a month for treatment, but overall things are good.
I hope you guys are doing well.
Take Care,
Lani Benavente
(360)790-2798