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  • Personal Autism Blog

  • Welcome to the personal autism blog at Autism Epicenter. This is a digital online diary (and more) written directly by parents of children with ASD as we deal with the triumphs and challenges of raising children with Autistic Spectrum Disorder. Two people post here, both parents of different families, both dealing with autism.

    With this blog you are gaining access into a whole new world. If you're parenting a child with ASD yourself, then you can relate. If you're not, maybe this will help you gain an understanding of what parents go through. Either way, welcome to our world!

  • September 2010
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Comment from: Beatrice Jones [Visitor]
Thomas stuff is expensive. Your right about that. And our son loves Thomas too. I wish insurance would cover the cost of Thomas the Tank Engine!

:-)
11/07/09 @ 22:49
Comment from: Jess [Visitor]
I meet people all the time who are in some way connected to someone with autism. Its like a giant chain and we're all connected.

Nice post. How come you never use capitals?
11/09/09 @ 16:28
Comment from: sherri [Visitor]
not sure why except that it just seems to save time. i catch myself at work sometimes doing the same thing. lol. i have to rewrite a lot there.
11/09/09 @ 18:14
Comment from: Nadia55 [Visitor]
I'm inclined to agree with you.
12/01/09 @ 07:03
Comment from: Alisa [Visitor] Email
You are so right that someone in power should do something about funding to help autistic children in public school. I was transferring my kids into a new district and they refused to transfer my youngest who is autistic because of funding. I had to use a friends address just to get him into the district. The district we were in didnt provide any services for Caleb and the other district had services but said they can only take and give him services if he was living in the district....So sad when one child is denied because he lives just on the other side of the district line.
12/10/09 @ 02:22
Comment from: Ruben [Visitor]
Thanks for this!
12/10/09 @ 09:32
Comment from: sherri [Visitor]
it is a shame that you have to give out false information to get your child some help! the system is soooo messed up.

when esmond turns three in feburary, we are basically on our own. state helps stops. and of course, most therapies are not covered (pre-existing) or they have a lifetime cap. for example, the last place i worked for would only pay for 80 lifetime hours of speech therapy.
12/14/09 @ 16:19

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