Technology has progressed at light years compared to when I was helping my son with speech and language delays associated with Aspberger's Syndrome (an ASD). In recent years iPad Applications (apps) for children with speech delays have become necessary tools in classrooms and for those treating autism spectrum children. Now, you don't even have to be a professional to help children with speech delays or language learning difficulties. More Here...
Pica ~ An eating disorder characterized by the consumption of non-food items for more than a month.
PICA AND AUTISM, our history...
I used to ask myself, "How can she eat TOILET PAPER, CARDBOARD, FOIL, PAINT CHIPS (and more) and not eat the meals I carefully and lovingly prepare for her????
No one had an answer to this question..... some offered judgmental expressions; as if my mothering her wasn't up to snuff. And yet the contempt in others' voices was present, as they questioned how she got the object or substance in her mouth in the first place. More Here...
Guest post by health services researcher David Mandell, Sc.D., of the University of Pennsylvania’s Center for Mental Health Policy and Services Research and the Center for Autism Research at The Children’s Hospital of Philadelphia.
[Editor’s note: This past weekend, Dr. Mandell and his colleagues presented the early results of “Estimating the Economic Costs of Autism,” a study funded by Autism Speaks with guidance and technical assistance from the World Health Organization. You can read our related news story here.]
We knew we’d grab attention with our updated estimate of autism’s economic costs: $126 billion annually in the United States. Our comprehensive analysis, supported by an Autism Speaks research grant, included indirect costs such as lost income and care giving, as well as direct costs in healthcare, education and adult services.More Here...

“Nobody realizes that some people expend tremendous energy merely
to be normal.”
Albert Camus
More Here...



I found out about GAPS via a mom at the OT office . Two years a
go, there wasn't much about this, but since then, it seems to
have blossomed. I just wanted to share two great sites that has
helped my kids. I wasn't that stick. We already ate bone broths,
and I already cooked everything homemade. I did have to switch to
making GF breads vs other breads that I made. I did have to
switch noodles. Also, I took a year to make the switch. My
kids were so finicky about foods, that I couldn't change it all
at once. I had to give them a chance to adapt. So while this is a
great diet for kids and adults who deal with autism, it also
isn't smart to make radical changes quickly. While change
is necessary, you must give them time to change and it will not
happen over night. More Here...

When your child gets diagnosed with a disability, they give you
some antidepressants and a copy of Emily Perl Kingsley's "Welcome
to Holland." She's a mother of a child with Down syndrome who, by
all accounts, is the shiznit. I'd go into detail, but then you'd
compare me to her, and I'd hate for someone as well known for
being awesome to be taken down a notch or two because of my own
awesomeness. You understand.
Anyways. This little metaphor is PERFECT for when your child gets diagnosed with Down syndrome. PERFECT. It's short, so I'm going to paste it here:
More Here...

I've had my preconceived notions when my son initially didn't
respond as was expected.
Sure he was developing ok physically, but mentally and emotionally it was like something was missing.
He tries to talk to me, but starts crying, as if his voice was taken away.
I can see it in his hitting of the walls and furniture, and sometimes even my wife and I.
He wants so desperately to share something with us, but struggles at times to get even a word or two out.
It's like he's a foreigner visiting a country where their is no english translation.