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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
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Blog Archive
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2009
(95)
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October
(23)
- Day +36 (Halloween party at the hospital ...)
- Day +34 (The first twenty-four hours ...)
- Day +32/+33 (Discharged ...)
- Day +30/+31 (6 weeks ...)
- Day +29 Part 2 (Early results ...)
- Day +28/+29 (The outside world ...)
- Day +27 (Daylight ...)
- Day +25/+26 (Field trip ...)
- Day +23/+24 (Status quo ...)
- Day +21/+22 (Improvement ...)
- Day +19/+20 (Like a newborn ...)
- Day +18 (The 5 major requirements to be discharged...
- Day +17 (Today's News...)
- Day +16 (Top ten ...)
- Day +15 (Back to the Transplant Unit ...)
- Day +14 (Hunter is where he needs to be...)
- Day +13 (The good and the bad ...)
- Day +12
- Day +11 (It's back ...)
- Day +10 (Isolation ...)
- Day +9
- Day +8
- Day +7 (One week later ...)
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October
(23)
Hourrah !!!
ReplyDeleteça se fête : nous débouchons une bonne bouteille avec les parents, en l'honneur d'Hunter le héros !!!
Mille bisous marseillais de
Sylvie et les garçons, Marie-France, Jean-Claude
Congratulations! That is great news! Keep going Hunter.
ReplyDeleteSumathi
That is truely wonderful news! I am so happy for you all. Hope the good new keeps on coming....x
ReplyDeleteCongratulations Baba! You're the strongest baby in the world !!
ReplyDeleteCongratulations too the three of you!! That is so awesome!! Keep strong Hunter...we love you!
ReplyDeleteYeaaaaah! Praise God! I'm so happy for you all. Keep strong and keep the faith.
ReplyDeleteLove Val T.
YAAAYYYYYY! I cannot possibly express how happy I am for Hunter and you all. Love you guys! ~Renee
ReplyDelete