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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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2009
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November
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- Day +67 (Brief ...)
- Day +63 (Thankful for a cure ...)
- Day +62 (Two months and one day ...)
- Day +56 (More of the same ...)
- Day +53 (No news is good news, right?)
- Day +50 (Half way home ...?)
- Day +47 (Routine ...)
- Day +44 ("Boring is good ...")
- Day +42 (Wet, wet, wet ...)
- Day +40 (A lull ...)
- Day +38 (Nurses ...)
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November
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Les phots sont magnifiques : il semble en pleine(s) forme(s), littéralement...
ReplyDeleteJ'espère que son problème de hanche sera vite résolu et ne sera qu'une péripétie supplémentaire sur la voie de la guérison.
On vous embrasse,
Sylvie et les garçons
Fabulous pictures - I want to squeeze his cheeks! Please give Hunter a big smooch from me! And big hug to you and Rhea and Harper :-)
ReplyDeleteHi Rhea,
ReplyDeleteGreat to hear about the platelets going up towards the normal. What a relief that must be!
Hope that his gait and activities get back on track reall soon.
With Best Wishes,
Sumathi
What a happy and handsome boy you are....Go Hunter GO! xx
ReplyDelete