Nicolas has changed me forever. I cannot tell you how with mere words and with the limited space here, but I can tell you for sure that he has.
My blog takes you along our journey as we learn at our 20 week ultrasound that our little boy will be born with a lethal skeletal dysplasia. Follow us through the tough choices, the long days, and ultimately the greatest joy. If you have come here and are faced with similar circumstances I want to give you one thing, something that was stolen from us by doctors, specialists, and even friends, and that is *HOPE*
Showing posts with label special needs. Show all posts
Showing posts with label special needs. Show all posts
Sunday, April 22, 2012
Awareness
Labels:
dwarfism,
family,
moms,
special needs,
trach,
tracheotomy,
vent,
ventilator,
women
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