Guest guest Posted November 17, 2007 Report Share Posted November 17, 2007 Hello, I have been lurking around for the last couple of days but I wanted to come out of the dark and say hi. My son was just diagnosed with autism about 2 weeks ago, he's 3. Though he's very smart, he doen't talk, doesn't socialize with other kids including his siblings, and throws a fit when he's off if his schedule. All i know is that one month he was talking and about 18 months he stopped progressing. I found out that he had a hearing problem, and that was corrected, but he still wasn't picking up on anything I had him tested. The whole time I knew. I have brother and a nephew, even my dad whe was like this. But Like all mothers, I doubted until I had hard facts. There is little to no support here in my side of texas accept for the Center. I'm in Tyler, by the way. It's kind of hard because I don't know what all he needs right now. being that i am a working mother, i can't readily leave my job (Like I want to) and take care of him full time. Right now, He's him school. The PPCD at my child's elementary school is great with the speech therapy, but I don't know what else he would needs. Any pointers or suggestions are greatly appreciated. Thanks. Kalea Simpson 'Truer words were never spoken than those of the written word. " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 17, 2007 Report Share Posted November 17, 2007 I can give you some hope... My son started school when he was 6,,,he is 13 now, he wasnt diagnosed until he was almost 4 and could not speak a word starting school. By the end of the first year at school he was speaking in sentences. Now, he speaks fine, you can still tell he has some sort of speech impairment just by how he speaks, but he speaks very well now. My prayers are with you and your family. Tabitha Muckelrath Leah Vaughn wrote: Hello, I have been lurking around for the last couple of days but I wanted to come out of the dark and say hi. My son was just diagnosed with autism about 2 weeks ago, he's 3. Though he's very smart, he doen't talk, doesn't socialize with other kids including his siblings, and throws a fit when he's off if his schedule. All i know is that one month he was talking and about 18 months he stopped progressing. I found out that he had a hearing problem, and that was corrected, but he still wasn't picking up on anything I had him tested. The whole time I knew. I have brother and a nephew, even my dad whe was like this. But Like all mothers, I doubted until I had hard facts. There is little to no support here in my side of texas accept for the Center. I'm in Tyler, by the way. It's kind of hard because I don't know what all he needs right now. being that i am a working mother, i can't readily leave my job (Like I want to) and take care of him full time. Right now, He's him school. The PPCD at my child's elementary school is great with the speech therapy, but I don't know what else he would needs. Any pointers or suggestions are greatly appreciated. Thanks. Kalea Simpson 'Truer words were never spoken than those of the written word. " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 18, 2007 Report Share Posted November 18, 2007 I would recommend ABA therapy, which made a huge difference developing language and communication skills and improving his behaviors at that early age. Maggie Leah Vaughn wrote: Hello, I have been lurking around for the last couple of days but I wanted to come out of the dark and say hi. My son was just diagnosed with autism about 2 weeks ago, he's 3. Though he's very smart, he doen't talk, doesn't socialize with other kids including his siblings, and throws a fit when he's off if his schedule. All i know is that one month he was talking and about 18 months he stopped progressing. I found out that he had a hearing problem, and that was corrected, but he still wasn't picking up on anything I had him tested. The whole time I knew. I have brother and a nephew, even my dad whe was like this. But Like all mothers, I doubted until I had hard facts. There is little to no support here in my side of texas accept for the Center. I'm in Tyler, by the way. It's kind of hard because I don't know what all he needs right now. being that i am a working mother, i can't readily leave my job (Like I want to) and take care of him full time. Right now, He's him school. The PPCD at my child's elementary school is great with the speech therapy, but I don't know what else he would needs. Any pointers or suggestions are greatly appreciated. Thanks. Kalea Simpson 'Truer words were never spoken than those of the written word. " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 18, 2007 Report Share Posted November 18, 2007 Hi Kalea, my son is doing well. We used ABA for 18 months. I used this mostly to implement intensive dietary intervention. We follow body ecology diet to conquer fungal infection, open pathways for detox, heal digestion (leaky gut), nourish adrenals and all cells/tissue etc.... As his body healed we were able to stop our ABA home program. He now attends 1/2 day specialized preschool and 1/2 day mainstream preschool. He is 4 years old. My suggestion to you is to get a therapy plan started. It sounds like your son would benefit from ABA but more importantly make a plan to get to his healing. Both in conjunction I believe will recover our kids. We have more work to do with Tyler, but he is progressing beautifully. > > Hello, > > I have been lurking around for the last couple of days but I wanted to come out of the dark and say hi. My son was just diagnosed with autism about 2 weeks ago, he's 3. Though he's very smart, he doen't talk, doesn't socialize with other kids including his siblings, and throws a fit when he's off if his schedule. All i know is that one month he was talking and about 18 months he stopped progressing. I found out that he had a hearing problem, and that was corrected, but he still wasn't picking up on anything I had him tested. The whole time I knew. I have brother and a nephew, even my dad whe was like this. But Like all mothers, I doubted until I had hard facts. There is little to no support here in my side of texas accept for the Center. I'm in Tyler, by the way. It's kind of hard because I don't know what all he needs right now. being that i am a working mother, i can't readily leave my job (Like I want to) and take care of him full time. > Right now, He's him school. The PPCD at my child's elementary school is great with the speech therapy, but I don't know what else he would needs. Any pointers or suggestions are greatly appreciated. Thanks. > > Kalea Simpson > > 'Truer words were never spoken than those of the written word. " > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 18, 2007 Report Share Posted November 18, 2007 > > Hi there, I just wanted to say I can relate to where you are at....my son was diagnosed at 3 as well. I'd be glad to talk to you one on one if you want to email me. Also, it might be good to contact the Parent Training and Information Center in your area. It would be the PATH Project, and you can find them at www.partnerstx.org. Someone in your region could help support you with educational needs when working with the school. It's a good place to start. I know getting the diagnosis can be difficult, so hang in there! > Hello, > > I have been lurking around for the last couple of days but I wanted to come out of the dark and say hi. My son was just diagnosed with autism about 2 weeks ago, he's 3. Though he's very smart, he doen't talk, doesn't socialize with other kids including his siblings, and throws a fit when he's off if his schedule. All i know is that one month he was talking and about 18 months he stopped progressing. I found out that he had a hearing problem, and that was corrected, but he still wasn't picking up on anything I had him tested. The whole time I knew. I have brother and a nephew, even my dad whe was like this. But Like all mothers, I doubted until I had hard facts. There is little to no support here in my side of texas accept for the Center. I'm in Tyler, by the way. It's kind of hard because I don't know what all he needs right now. being that i am a working mother, i can't readily leave my job (Like I want to) and take care of him full time. > Right now, He's him school. The PPCD at my child's elementary school is great with the speech therapy, but I don't know what else he would needs. Any pointers or suggestions are greatly appreciated. Thanks. > > > Kalea Simpson > > 'Truer words were never spoken than those of the written word. " > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 19, 2007 Report Share Posted November 19, 2007 Kalea, Welcome to the group. I can relate to you in that I am also a working mom. I remember when my son was diagnosed at 2. Soon after my husband was diagnosed with cancer, when I was 8 months pregnant with our 2nd child. It was a very dark time, but we made it through with lots of prayers which were answered, endurance and faith. I did not have a choice to quit work, and I still work. At my last company, I fought for insurance coverage for autism and won. At my new job, I am able to meet many researchers who are working on autism research. I truly believe God puts us where he wants us. I have embraced being a working mom, and I am happy to discuss with you all the resoures available to you. I would highly recommend that you find the best public/private school because you will depend on your child's teachers and therapists more than you can imagine. Also, there are people who can help you--neighbors, friends, church, support groups. My best advice, is to not try to be a super-mom and do it all on your own. You will burn out, and your child needs you. I am sure you will get lots of responses, but I am happy to talk with you anytime. ________________________________________________________________________________\ ____ Be a better pen pal. Text or chat with friends inside Yahoo! Mail. See how. http://overview.mail.yahoo.com/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 3, 2008 Report Share Posted June 3, 2008 HEllo my name is Gus. I live on a 35 head dairy cow farm. My dad wants to retire so we are slowly switching to dairy goats that I can handle by my self. The plan is to get a raw milk permit to sell to local customers. I live in western pa. i hope to meet some good friends here. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 12, 2008 Report Share Posted August 12, 2008 It's not called rambling here. Here we call it reaching out. First, let me introduce myself. My name is Jessie and I am a 30 y/o, um excuse me just had a birthday! 31 y/o college student in early childhood education, with a focus on special education and a strong desire to work directly with children and families on the spectrum. Oh, and I am a high functioning autistic. Welcome to the group. You will find parents, professionals, and those with autism here as well. As far as the potty training goes, I got my niece one of those potty chairs that sits on the regular potty and makes the hole small enough that she could not fall through, she would not use the smaller potty chair. I don't know how you feel about modeling the necessary behavior for her to understand what you are supposed to do when you sit on the potty, but it was all my niece needed to get started. She finally grasped what the potty was really for and stopped flushing everything else down the toilet, yes I do mean everything else! Socks, shoes, barbies, hairbrush, hair accesories, soap: nothing was spared. If it was in the bathroom, down it went, or at the very least it got a swirly. Some positive reinforcent and we were off with the pull ups and on with the big girl panties. A few tips: Make a note of how long after meals it takes her to need to use the bathroom. You can start scheduling potty breaks around meals and drinks to help get her into the bathroom BEFORE she has to go. That way she it THERE when the need arises. My niece was mostly non-verbal at the time and I used to roll up a magazine while she waited and we would play a noise making game. She would not make the noises with out something to funnel it through, like an empty paper towel roll or the like. The effort of making noise actually helped her to go. Getting her to go to the bathroom on her own took a while longer. We had to keep a good schedule for a while and there were some accidents. Be sure that you associate everything to do with potting as a positive experience. If you push to hard or try to force it she will be put off. Also, if she has an accident it is not a big deal. Be sure to say something like, " Oh you had an accident, lets get some clean panties. " Do not under any circumstance put her down or make an accident a bad thing. It is very importaint that she feel that using the bathroom is a good thing. Some parents with children on the spectrum kids' actually refuse to use the bahroom to the point of bladder infections and severe constipation. Are you using the pull ups that give her a cooling sensation when she wets then a little bit? This could be to much sensory input for her and be a reason why she refuses to wear ones that are not " USED UP " yet and only a bit damp. I think they still make them with out the cooling sensation. Another tip is to iniciate bathroom talk with her. When you change her, talk about the number 1 and the number 2 thing so she can diferentiate between the two. The first time my niece went pee on the potty I got so excited I started clapping my hands and " interupted " her mid stream. Luckily she got going again. But I was sure to wait until she was completely done before celebrating. I hope some of this helps you. The biggest tip I can give you is to wait for her to show interest. Taking of wet pull ups is a great sign she is getting ready. Involve her in the routine of going to the potty. Even if she does not go, have a routine of 15 to 20 minutes after meals and snacks going into the bathroom, sitting on the potty for however long she can tolerate at first: ten seconds, one second, doesn't matter. Then wiping, washing hands, ect. Make it a routine. Okay, I think they call that rambling elsewhere, here I hope they call it good advise. http://speakup.today.com Subject: Hello To: Autism_in_Girls Date: Tuesday, August 12, 2008, 10:06 AM Hi thank you for letting me join I am Sandria I have a 3yr(soon to be 4) autistic daughter and a 5(soon to be 6) aspburger son. I am lost most of the time and over whelmed the rest of the time lol I have joined to meet people in my boat so I dont feel so alone. I live in a very rural part of Pa. Right now I am in need of some advice with potty training my daughter this week she has developed a very adamant desire to not have her wet pull up on. Which is fine with me BUT I can not afford to go through a bag of pull ups daily. I bought a potty chair and a small potty seat for our toilet as well. We began yesterday well she looks at me like what are you nuts? If anyone has any advice please do share with me. I have overcome so much with my children by the seat of my pants but now she has begun having temper tantrums that just wont end and gets aggressive as well so I don't want her brother or anyone else to get hurt by her. I am going to be looking into the GFCF diet as soon as I can as well and the metal detox thing with the immunizations if you can also maybe steer me in a good direction for these too. I have done some internet looking but there is so much out there it just gets so confusing that I would rather speak with people that actually have tried these instead of going in blind. I do the best I can with natural and healthy because my son has 12 food allergy's and they both have food texture issues to deal with. Any way enough rambling Thank you Sandria Quote Link to comment Share on other sites More sharing options...
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