My first child, who is developmentally typical, slept eight hours at a stretch by the time she was a month old. Having achieved sleep guru status, I declared myself “Supermom,” and assumed that I could solve the problems of every parent and every child for whom sleep didn’t occur so readily. Fast-forward twenty years and… Continue reading When Sleep Is Elusive
I’m a crunchy mama. I make almost all of our meals from scratch, as much as possible from out own chemical-free garden, and I have lavender essential oil on hand at any given moment. I am a smoothie connoisseur, flax seed makes me happy, I take supplements, and prescriptions, side by side. I’m an experienced… Continue reading Research, Experts and Essential Oils
Nike signs its first professional athlete with cerebral palsy and it’s a win for all of us. Parents of children with special needs: the sky's the limit.
When I think of autumn and what the cooler weather means for my disabled son, I worry about what might go wrong. But his adaptability never ceases to amaze.
After my SCI, I was worried I'd no longer be able to enjoy the great outdoors. Thankfully, I was wrong. Our national parks are beautiful and accessible.
For the wheelchair user daunted by challenges in accessing natural sights, rest assured that there are plenty of accessible options to explore in Big Sky.
People seem to see my child’s disability first, him as a human being second. I have a desire to engender understanding on behalf of my child.
If the new disability emoji is the modern world’s equivalent to hieroglyphics, then I'm ready to see my son’s life adequately expressed.
All of a sudden, I’m hearing the term “special needs” questioned, so I did some soul-searching. What's the right way to refer to a child with disability?
"Special needs" may be a controversial term, but for parents of special needs children it denotes the supports and services their children need to thrive.