http://www.neurodiversity.com/stuff.html here is a list of stores that celebrate neurodiversity.
Ever since Autism Speaks came out with the movie short Autism Everyday and funded the project for prenatal testing I've been on the net searching for something different something more along the lines of how i feel.
I don't feel my son is damaged, I don't feel he needs "cured" he is not sick or retarded..He is someone who's brain works differently, who sees the world differently.. its not the mercury in the vaccines, its not television..His brain was wired differently...
I look at the puzzle pieces and ribbons...which are wonderful because they make people aware ....but sometimes the message they send is one of hopelessness and pity... don't pity me, don't pity my child... He is special I am in awe of him everyday.
I will admit somedays are difficult and everyones situation is different ... But sometimes, just like everything else in the world stuff worth anything takes time...When he melts down in the middle of a busy parking lot; people stop and stare.... when i finally get him into the car..he says to me "see pumpkins" I laugh to myself ,all he wanted was to see the pumpkins, he just couldn't find the words right away. Our world is so busy we move too fast, he reminds me that sometimes you just need to stop and smell the roses....errr.. the pumpkins.
I know everyone may not agree with me but I cherish who my child is, without his autism he would not be the same child...I do not want him cured of who he is...I want he to be the best he can be.


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Then there was this girl who folded up pizza boxes for a few hours each day at a pizza shop and this one boy who reminded me of my nonverbal son who had his aide there watching as he vacuumed the hallways and rooms at a Holiday Inn or other chain. I liked how they did things based on their interests.
So much emphasis is placed on the newly diagnosed and then those that are in their teens have nothing to assist them later. Luckily here in CA there are things in place for that.
I am planning for high school and beyond for my HFA kid already and never understood how parents whose kids just graduated high school are now asking for resources. They need to plan and make arrangements and visit places. My sister is blind from a brain tumor and has worked with the ARC in NJ for years doing assembly work for Johnson and Johnson.
I saw a news story today how the Easter seals organization brought adults with disabilities to some place that was preparing meals for needy families. That was a good idea.
I am probably the worse parent for a newly dx'd family to contact as I never went through anger or denial and not one to go on and on about the loss of autism. I hear at my website from parents that go on and on about how smart their kid is and they are so worried about what is in store for their kids.
Then you got the ones that want to cure them and tell parents to take a lawyer to their first IEP meeting and to do lots of vitamins, supplements, diets, ABA and all this stuff.
I found some nice stores over at cafepress.com that have shirts and items I want to get. We already get lots of stuff for when going out in public for my son to wear, but these were really nice. BeAware of Autism, celebrate autism, thinking in pictures, understanding autistics.
It is interesting that many adults on the spectrum do not agree or get along with parents of kids. There is no solidarity within the community. Tell someone you do not agree with the vaccine controversy and you get lots of hate mail and stuff, just incredible.
These parents do not realize that their own children on the spectrum will feel the same way as the adults they butt heads with. Or the parents that want to hide the dx from school and family, who does that help?
I could go on, but check out my website for some articles on the topic
http://autismspectrumdisorders.bellaonline.com
I wrote something recently called Holiday Hints and an org sent me an email wanting to reprint it in their newsletter.
I have from here an various other websites come in contact with adults on the spectrum..what an awakening that was! It made me take a look, a good look at how I raise my son so he won't be butting heads (too much) with me later on. I know I will make mistakes as a parent, but one I won't make is to underestimate him. Lord knows, right now I am the one doing the learning.
I think it is very important that his classmates know, kindergarteners love to help and they could and it would be a learning experience for the too.
I'd also like to recommend www.wrongplanet.net.
Cure? We don't need no stinking cure!