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i was just made aware about 3 weeks ago that my son may be autistic. he's 23 mos. i've taken him to be evaluated by his pediatrician (incredible doc), a speech therapist and a friend of mine who is a nurse and also has an autistic son. all agree that there are red flags for autism with my son. i think the hardest thing for me is realizing that i may never have the relational ability with him that i anticipated. you know, you expect to read books with your kid, conversate, sign songs together, etc. but my son doesn't do those things- he plays alone most of the time, doesn't talk hardly at all, moves away often when i try to play/interact with him. it's hard to be around other kids his age because it makes me mourn my expectations for my relationship with him. i don't think all is lost; i do believe that with therapy, he will get better, and he has some. my nurse friend suggested dietary changes such as filtered water, no dairy, taking cod liver oil (nasty), etc. anyone have experiences to share about dietary stuff with an autistic child?
:) ~sommer
www.SavvySmallFry.com (fyi, my website- if you like unique kids' stuff) |
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would like to know more
hi . absolutely. one flag is not talking, and especially if a child talks and then stops, which is what my son has done, though he's starting to talk a little more lately- probably due to speech therapy he's been in for a few weeks now. i really jumped to it with evaluation and assistance because i've read and been told that the sooner you act, the better. some kids with autism, if caught early enough, can function completely "normally" by the time they're school-age. another flag is lack of awareness of their place in the space around them. my son will run into things/people will little reaction or fear of injury to himself/others or fear of hurting others' feelings or getting a reaction out of them. another flag is not making eye contact. my son will babble but look the other way, or come up to me/my husband and point at us, but look the other way. another flag is sensory intergration problems. like my son will run with his head to the side- obviously looking for the sensory effect of things moving while he does or staying still while he passes. he will play with the pattern of paint on a wall or shadows, or he will study the outline of objects and run his hand along them over and over and over. or he will put a toy on the table and sit in front of it or lay on the floor with a toy, and move it back and forth toward his face/past his face, getting sensory stimulation from the changing perspective. let me add an aside here- some kids have sensory integration issues and aren't autistic, but all autistic kids have sensory integration issues- that's what his speech therapist told me, because we're not totally sure that my son is autistic, but we've identified the SI issue definitely. another flag is lack of imitation. another is ignoring people when they try to interact with them. there are lots. and some "normal" kids do some of these things, but i think that when your child is doing multiple, you should pay attention. another aside- autism is a spectrum in that some kids are highly-functioning autistic, and it goes across the spectrum in intensity. there are many websites to check out, such as www.sensoryresources.com, www.autism-society.org, etc. i've been told that a great book is The Out-of-Sync Child and i plan to get it. i would advise that if you have concerns, get it checked out. but a lot of older docs have old-school training on the subject, so if you can, find a younger doc, because so much has been discovered about autism in recent years and the younger docs are better-versed. even if your pediatrician poo-poos your concern, go with your gut feeling and see a speech therapist. the next step is to see an occupational therapist. no one is going to look out for your baby but you, so don't fear offending docs or ignoring their advice if you really feel concerned. my nurse friend has told me that she's talked to sooo many parents who didn't act when they knew they should've, out of fear/whatever, but it's so detrimental to children to deny their needs being addressed, no matter how scared you may be or embarrassed that it's happening (yes, that's a normal feeling, though not the most fun to talk about).
anyway, if anyone wants to ask me anything at any time, feel free- i'm a very open person and love to help. also, i live in grapevine, tx, so if anyone is close and wants a good reference for pediatrician, speech therapist or occupational therapist, i'll give you the info i have. my pediatrician is a God-send. my son had Croup last fall and he rocked my son in his office, and gave me his cell & home phone #s and pager # in case i needed anything at any hour. INCREDIBLE. he really cares about his patients and their families.
y'all be blessed 
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