The wonderful news for families who have children diagnosed with Agenesis of the Corpus Callosum, cortical visual impairments, cerebral palsy, developmental delays, polymicrogyria, and autism right is right HERE in this article. The back story here is that Elisabeth's DNA and many of her DDX3X sisters and brothers have been used in this research after we gave the lab permission 3 years ago so we are thrilled to hear that they finally isolated the location.
When the milestones, the charts, and the sequence in development are not there for our children, parents and caregivers like us set out on our own pathway. Elisabeth's story is about searching for the X factor. The X factor that was discovered only in hindsight beginning with an emotional bond and a fleeting but tangible smile to mean "yes" and a flinch in eyebrows to mean "no."
Ranked "Top 30" in parenting blogs to follow!
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