We have no nativity to attend this year. It is the first year in a decade that we have not attended a nativity. Our little Carys is now too grown up to be in a nativity. She will… Read More
Posted on 16th Dec 2015 by Ali Isaac
Life With A Special Needs Child
Cardiofaciocutaneous Syndrome, Carys, CFC, deep pressure massage, disability, disabled, motherhood, mothering, oral stimulation, OT, rare syndrome, sensory processing disorder, special needs, the Sensory Diet, Wilbargar Brushing Protocol
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