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#26
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Oh "they" includes his 2 yr old brother. He talks like a 3.5 yr old and is very imaginative. Very good for Jackson. I call him my sweet baby surprise ![]() |
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#27
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![]() One thing that I had to laugh about was that two weeks ago at DS' IEP, the sped teacher wanted a goal for DS to complete certain patterns--I mentioned that DS already had mastered this goal with his ABA team (his BCBA was there and confirmed this) as well as independently when working with me (with minimal prompting and not even loaded to be self-correcting!) They wanted the goal anyway ![]() So I got a chuckle this week when the SPED teacher saw me after school and said, "You know what, we probed the patterning goal and sure enough, he got them all. I guess we can step it up" mmm-hmmm...I did restrain myself from an 'I told you so' ![]() |
#28
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my youngest who is almost 7 had severe apraxia of speech with almost 4 yrs of speech therapy and 6 months of occupational therapy she is doing fairly well. she doesn't have autism but has some sensory issues and add. she had lack of oxgen from acid reflux at 3 days old which probally caused her speech disorder. she turned blue, dh saved her life with a nasal aspirator. she was over fed by a nursery worker in the hospital who thought she knew it all and that is what caused the acid reflux. 3 hours home from the hospital and she was about to die and if dh wasn't home she probally would had.
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#29
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My soon to be 4 year old son has a severe speech disorder (and prob adhd) is is currently going thru the autism screening. We've had him in speech therapy since before 2 years of age. His genetic panel revealed that he has extremely rare 3q29 microdeletion syndrome. He was born with the cord wrapped around his neck and he was blue and we thought maybe that's what caused apraxia, BUT the genetic doctor I recently saw told me that most babies are born with cord issues and those cord issues don't cause apraxia and it didn't contribute to my son's condition.
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#30
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![]() Wishing health and lots of amazing progress for your DS! |
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#31
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#32
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i just screamed and he took one look at her and yelled suction so i grabbed the nasal aspirator and he cleared the airway. apraxia is either genetic or caused by lack of oxgen and there is nobody anywhere is either family with apraxia. i'm just glad she is now able to talk, it was very hard for everyone when she couldn't.
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#33
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There are two forms of apraxia, CAS or childhood apraxia of speech, which is usually caused by either genetics or a hypoxic event. Then there's developmental apraxia for which there are several possible causes but basically it's neurological. My son has the latter for which he underwent years of speech therapy. In the beginning he had such poor motor control he drooled. He's got a small pt job now, he started working at 15 as a web site developer and now builds games for pocket change (mostly indie stuff). He's such a cliche, but frankly he has a gift with all things computer that's amazing. He's a junior in HS and is the teachers aide in a web design class. If he sees the actual teacher once a week it's a lot! We've started the college search. I'd like him to stay home the first year or so, he wants to flex his wings....there's just not enough Xanax in the world! |
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#34
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My 2 year old is on the spectrum. However, with chelation & diet change we have seen immediate results and I see a bright future for us all. Feel free to FB me, mommies! It's nice to have someone understand you, because people truly can't if they aren't in your shoes. facebook id: xtinathedreamer |
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#35
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here is a link to apraxia speaks that has a pic of my brooke and her story. Apraxia, Dyspraxia and soon to be ADD or AHDH btw hotmama11 a cord around the neck could cause apraxia even though it doesn't cause every one to have apraxia. it would depend on how long was baby without oxgen. brooke was without long enough for the eyes to roll, i will never get that picture out of my mind, i remember as if if were yesterday. her sensory issues were caused by damage to the central nervous system due to lack of oxgen so there is no doubt it caused her apraxia.
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#36
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Does anyone here have teenager with aspergers? My 13 yr old son's behavior has always been pretty bad at times but it seems to be getting worse as he gets older. His meltdowns are above and beyond in my opinion. He can be the most polite, helpful, and intelligent child I've ever seen. BUT When the smallest thing makes him upset or angry all heck breaks loose. Screaming cussing stomping slamming you name it he does it. Does anyone else have the same issue? I can use any advice or support I can get.
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#37
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My son is 17, he has Aspergers. The meltdowns seemed to get worse as he was heading into puberty. Once he got over that hump things calmed down. One thing we did was every day after school he came in and spent an hour alone in his room, spinning on his chair and decompressing from the day. He needed that time to "clean the day off" as he used to say. Then he was usually good for the rest of the night. So I guess time is the answer ![]() |
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#38
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#39
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Autism awareness month is here. I try and post a tip a day on my FB and Twitter for the folks not yet touched by autism. For instance, today's tip was if you see a mom struggling with an "unruly" child, please don't judge, he may have autism. Stores and parking lots were hell for us. I had a lady call 911 on us in a Walmart parking lot. I told her to tell the cops to meet us at home. An hour later they showed up. Ugh! Trying to save other parents the problems ![]() |
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#40
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Mommyslh: Your daughter is beautiful! My DS7 has ADD as well. Best of luck to you! |
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#41
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Such a great idea, Lubbock! I need to find a few activities for the month. I plan to begin organizing our walk team for Autism Speaks walk in October also. I've just been so tired...feel asleep in my wet bath towel with lights and TV on last night! Now that's pooped.
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#42
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My son I have posted about on here with aspergers has been flown to children's hospital and is in surgery for a brain tumor. Last night they put shunt in for the pressure. If we would've missed it for one more day he wouldn't have made til morning. He would've passed because pressure so high. I'm telling everyone this because my son (13) never said anything to anyone about symptoms he was having because his brain functions differently then ours. He was having headaches dizziness double vision at distances n many other things. He never said anything except for "sinus headache " from allergies. So please anyone who has a child with brain issues like aspergers or anything else please ask questions about vision headaches etc no matter how silly u think it may be. My son will have a lot of hospital time surgeries 6 hr long MRI CT scans etc because I never knew he was having any problems. Not to mention I was one night away from losing him.
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#43
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You brought up a really important point to query kids when they seem sick. I think it is a concern for many parents, especially those with children with communication issues--I have often thought that my DS would not know to complain of pain (say if his appendix burst for example) or know how to express it. It is scary and I thank you for the reminder. Hugs to you and your son ![]() |
#44
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I am so sorry to hear about your son, hoping he comes through it just fine! It's a great point tho, they feel and describe pain very differently. My DS was drinking out of a glass one day and it just imploded in his hand! Luckily I heard the glass breaking, he was calmly cleaning up, glass in his hand, blood gushing, I nearly fainted! He was calm and fine with everything, even the lidocaine injection and stitches. A few months later he got stung by a bee on the back patio, you'd think he'd been shot the way he was screaming. Just a whole different perception. |
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#45
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If anyone is in NE Ohio or knows someone in NE Ohio we have a great program called Cops 4 Kids with Autism. Cops 4 Kids With*Autism "Since June 2006 the Cops 4 Kids with Autism program has brought awareness to local authorities in Summit, Medina, Cuyahoga, Lorain, and Huron counties, about families in their community who have an autistic child living with them. Our program puts together baskets annually for the families of these children and the local police officers then deliver the baskets to the families which in turn have a profound positive impact." One of my dearest friends is the director and she is a cop who has a kid with autism.
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#46
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#47
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AChiodini, Thanks for the update, I can imagine that with helping your son it's hard for you to find time to get online! I am so glad they were able to remove most of the tumor, and pray that he tolerates the rest of the treatments well and that they are able to vanquish the rest of the tumor. My thoughts are definitely with you and your son. Sending e-hugs!! ![]() |
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#48
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My 10 year old autistic son gets to come with me for Take Your Child to Work Day on April 26. It will just be half a day, since I don't think he could handle a whole day. I'm excited!
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#49
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#50
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A mother's worries never end! |
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