Guest guest Posted March 2, 2003 Report Share Posted March 2, 2003 hi sherry, i'm sorry to hear about your son.while i don't have personal experience with this, it sounds very similar to what happened to my girlfriend's son. her little boy was talking too and stopped after his shot. she said he was different after his shot. she took him to my naturopath and homeopathy has worked really well for her son. she felt that combined with speech therapy is making a big difference. good luck. mandi -- New here and need some advice Hi. My name is Sherry and here is a brief story : My son will be 3 in July and doesnt seem to want to use language to communicate. I have had him evaluated for all kinds of developmental disorders. They can only tell me that he appears to be perfectly normal with the exception of the speech delay. He will say single words when prompted but is very shy around strangers. He will smile at them and say hi but thats it. The Dr's say they dont see any signs of Autism. I did let them give the MMR shot after months of hesitation. He was saying single words then but stopped shortly after. Of course everyone rolls their eyes at me when I mention this. We are seeing a speech therapist and he will say words for her. I guess I am looking for some input or any suggestions on what might be wrong. We are to see a neurologist next month. I have no clue what to expect there. We just started a mothers morning out program and he loves to go to school. We have only been 3 times so far and I have stayed with him. He has never stayed with anyone else so this will be a little bit of a challenge. I told the director I didnt want him to cry and she said I could stay as long as I wanted. Its ok to me if he cries when I first leave. I understand that there is some mommy seperation going on here too. But I would never let him go more than 10 mins. I will do whatever it takes for his sake. He is very smart and very loving. He likes to play with other kids.....just doesnt talk. Sherri has recommended a homeopath. There is one listed here so I think I will call them tomorrow and just go talk to them to see what they have to say. Any input is greatly appreciated :-) thanks Sherry Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 2, 2003 Report Share Posted March 2, 2003 Sherry, Sounds all too familiar. My son stopped babbling after his first shots and now at 19 months is 6 - 9 months developmentally delayed. He was severely autistic, but thanks to homeopathy and his strict elimination diet, at this point, there are no symptoms of autism. (WOOHHOO!). Just speech and developmental delays. He is catching up quickly on the developmental and OT stuff. But he doesn't really want to make words (I can tell it is difficult or nearly impossible for him to figure out how to make the sounds). He babbles away but it isn't the usual mama, baba, gaga, it's all gobbledygoop. We've done some sign language and he can do four signs (more, all done, mad, and yummy). He was doing mommy and daddy - but he can say both (thank you god!). The reason it sounds so familiar is that I have four friends with babies born the exact same time as my son (July of 2001). EVERY SINGLE ONE of them is speech delayed. Two are completely non-verbal, and two say a few words. All but one is doing speech therapy with good results (the last refuses to believe there is a problem she can't fix on her own - and maybe she can...). In any event, I don't doubt the shots did it for one second. Two had reactions to their shots. The other two moms refuse to discuss it. Oh well... I can only offer info if they want it. So to reassure you, yes, do homeopathy, and yes, I think your son will be perfectly fine doing the speech therapy. He sounds like a great little boy. And yes, it sounds like mom is having a hard time with the separation as well. It gets easier. Truly, a Hi. My name is Sherry and here is a brief story : My son will be 3 in July and doesnt seem to want to use language to communicate. I have had him evaluated for all kinds of developmental disorders. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 2, 2003 Report Share Posted March 2, 2003 Forgot to mention... please, please, please do some serious research before you decide to give your child another booster. He could be a candidate for further regression... Hi. My name is Sherry and here is a brief story : My son will be 3 in July and doesnt seem to want to use language to communicate. I have had him evaluated for all kinds of developmental disorders. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 2, 2003 Report Share Posted March 2, 2003 Dear Sherry, Welcome. Sheri is the one to talk to about homeopathic approaches. I just started learning about classical homeopathic approaches and am new to this arena, but I can tell you about some of the educational and/or therapeutic approaches I used with my son. His name is and he was non-verbal at age three. He had what was called a total communication approach in his IEP (Individualized Educational Plan). Everyone that worked with my son, including me, used many avenues of communication, i.e. sign language, pictures, pictures (icons) with the word(s), communication devices that he could push a button or touch a screen and it would speak for him, modeling, written word--I labeled a lot of things in the house, etc. When my son's team knew he could read, we tapped into that avenue for communication and speech. Today is seven and talks, but is NOT conversational. Most of his speech is requesting something and/or repetitive speech. He does know and sings a lot of nursery rhymes, reads out loud and can quote some of his favorite stories off by heart and can recall word for word many Mother Goose rhymes. Another thing we did and still do with , is Greenspan's floortime play. I have some info. on this and I could mail it to you if you would like. Greenspan basically involves the parent, teacher, therapist, etc. to allow the child to take the lead in an activity. Once the child is engaged, you work toward circles of communication. I remember one of the first things I did with . He wanted me to push him in the wheelburrow--he climbed in and gave me non-verbal cues. But, instead of just giving in to his non-verbal cues I gave him an anticipatory set-- " Ready, get set________ " And then after a little wait, JJ would say " GO! " Kind of a fill in the blank thing. I will never forget it. Today, if he is really into something, like swinging and needs a push, he will generally come up with the entire sentence on his own with a " Ready, get set go! " Or we might get a " Blast off , solar systems, stars! " Yea, he is missing a bit in that sentence, but it is great to hear him speak! His syntax is not age appropiate (for example he will say " I want a drink juice " ), but his speech therapist thinks that will come in time. We are just elated that he is finally trying to string words together. So, hang in there and remember that it might be baby steps or you son may develop speech quickly. You know him best and need to set up a program that best meets his needs. I hope I have helped in some way. Lynda New here and need some advice Hi. My name is Sherry and here is a brief story : Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 3, 2003 Report Share Posted March 3, 2003 >> Sherri has recommended a homeopath. There is one listed here so I >> think I will call them tomorrow and just go talk to them to see >what >> they have to say. >> Any input is greatly appreciated :-) >> thanks >> Sherry Who is that you found on my list? Sheri -------------------------------------------------------- Sheri Nakken, R.N., MA, Classical Homeopath Vaccination Information & Choice Network, Nevada City CA & Wales UK $$ Donations to help in the work - accepted by Paypal account vaccineinfo@... voicemail US 530-740-0561 (go to http://www.paypal.com) or by mail Vaccines - http://www.nccn.net/~wwithin/vaccine.htm Homeopathy course - http://www.nccn.net/~wwithin/homeo.htm ANY INFO OBTAINED HERE NOT TO BE CONSTRUED AS MEDICAL OR LEGAL ADVICE. THE DECISION TO VACCINATE IS YOURS AND YOURS ALONE. ****** " Just look at us. Everything is backwards; everything is upside down. Doctors destroy health, lawyers destroy justice, universities destroy knowledge, governments destroy freedom, the major media destroy information and religions destroy spirituality " .... Ellner Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 3, 2003 Report Share Posted March 3, 2003 a, my son is 18 months old, completely unvaxxed, and doesn't speak a word either! Sometimes they are just slow to speak. He used to say Dada, bye-bye, horses, fish, meow, yum-yum, and a few other things, and he just stopped. He knows exactly what he wants and what he wants to say, but he just points and " eh, eh " , and shakes his head yes and no. He's been so busy with his motor skills that the verbal skills just aren't a top priority for him right now. I didn't know that they even did speach therapy for an 18 month old! www.ChestnutHillCurlies.com Re: New here and need some advice > Sherry, Sounds all too familiar. My son stopped babbling after his first shots and now at 19 months is 6 - 9 months developmentally delayed. He was severely autistic, but thanks to homeopathy and his strict elimination diet, at this point, there are no symptoms of autism. (WOOHHOO!). Just speech and developmental delays. He is catching up quickly on the developmental and OT stuff. But he doesn't really want to make words (I can tell it is difficult or nearly impossible for him to figure out how to make the sounds). He babbles away but it isn't the usual mama, baba, gaga, it's all gobbledygoop. We've done some sign language and he can do four signs (more, all done, mad, and yummy). He was doing mommy and daddy - but he can say both (thank you god!). > > The reason it sounds so familiar is that I have four friends with babies born the exact same time as my son (July of 2001). EVERY SINGLE ONE of them is speech delayed. Two are completely non-verbal, and two say a few words. All but one is doing speech therapy with good results (the last refuses to believe there is a problem she can't fix on her own - and maybe she can...). > > In any event, I don't doubt the shots did it for one second. Two had reactions to their shots. The other two moms refuse to discuss it. Oh well... I can only offer info if they want it. > > So to reassure you, yes, do homeopathy, and yes, I think your son will be perfectly fine doing the speech therapy. He sounds like a great little boy. And yes, it sounds like mom is having a hard time with the separation as well. It gets easier. > > Truly, > a > Hi. My name is Sherry and here is a brief story : > > My son will be 3 in July and doesnt seem to want to use language to > communicate. I have had him evaluated for all kinds of developmental > disorders. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 3, 2003 Report Share Posted March 3, 2003 .. > I did let them give the MMR shot after months of hesitation. He was > saying single words then but stopped shortly after. Of course > everyone rolls their eyes at me when I mention this. Hi Sherry, Just wanted to say that my son lost the ability to speak after the MMR and had what we now know were probably subtle seizures (eyes rolling back for a few seconds). We have been trying to find experts/researchers on language regression in the absence of autism and it has been very difficult. Where are you located? We are in KY. Our ped at the time also rolled her eyes at us and said, " there is no relationship between vaccines and your son's speech problems. " We stopped all shots nonetheless - ( he has both exemptions) and of course we stopped taking our son to her. Email me off list and we can " talk " more about this. Best, Sandy > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 3, 2003 Report Share Posted March 3, 2003 My son was like that, too, pointing and grunting for the longest time. He was well past 3 before he could easily be understood by people outside our family. I think 18 months would be a bit early to be labeling a child (especially a boy) speech delayed. The other thing was dd (who is 20 months older than my ds) did plenty of talking for the both of them, so I think he was content with that and didn't even try (maybe he figured he couldn't get a word in edgewise anyway if he did try!) : ) Kay a, my son is 18 months old, completely unvaxxed, and doesn't speak a word either! Sometimes they are just slow to speak. He used to say Dada, bye-bye, horses, fish, meow, yum-yum, and a few other things, and he just stopped. He knows exactly what he wants and what he wants to say, but he just points and " eh, eh " , and shakes his head yes and no. He's been so busy with his motor skills that the verbal skills just aren't a top priority for him right now. I didn't know that they even did speach therapy for an 18 month old! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 3, 2003 Report Share Posted March 3, 2003 , Interesting! I realize some children are just late talkers. It's when they have been vaxed and there was a reaction that a red flag should go up. (The CDC itself reports an increase in speech delays for vaxed kids.) My son has other developmental delays so speech isn't the only one. He also has motor coordination, and hypotomia. But my other two friends' kids only have the speech delays and the speech therapy is helping tremendously. I'm sure there are many kids that will just start talking one day when they are good and ready without any therapy. I also know that many toddlers will stop doing new skills they have acquired while they learn something else. It's when the original skills don't return that there may be an issue. Of course, I'm no expert... just sharing my experiences. Truly, a Re: New here and need some advice a, my son is 18 months old, completely unvaxxed, and doesn't speak a word either! Sometimes they are just slow to speak. He used to say Dada, bye-bye, horses, fish, meow, yum-yum, and a few other things, and he just stopped. He knows exactly what he wants and what he wants to say, but he just points and " eh, eh " , and shakes his head yes and no. He's been so busy with his motor skills that the verbal skills just aren't a top priority for him right now. I didn't know that they even did speach therapy for an 18 month old! www.ChestnutHillCurlies.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 4, 2003 Report Share Posted March 4, 2003 I felt like you were describing my son to a T at that age. I also see a connection with vaccines. I just had my 2nd child and got the eyes rolling when the pedi nurse (who comes to your home here for the first visit) was informed we will not be vaxing and why. As for ds, he was diagnosed with a " unique " but normal personality. So we just stopped vaxing him, but didn't think of trying homopathy until recently. Since ds never really gets sick it was never a worry. He is now 9 and started takling around 4 - 5 years, yet it started with him describing. Sometimes I still have to explain what he means to people who aren't use to him. Cyn~ New here and need some advice > Hi. My name is Sherry and here is a brief story : > > My son will be 3 in July and doesnt seem to want to use language to > communicate. I have had him evaluated for all kinds of developmental > disorders. > They can only tell me that he appears to be perfectly normal with the > exception of the speech delay. He will say single words when > prompted but is very shy around strangers. He will smile at them and > say hi but thats it. > The Dr's say they dont see any signs of Autism. > I did let them give the MMR shot after months of hesitation. He was > saying single words then but stopped shortly after. Of course > everyone rolls their eyes at me when I mention this. > We are seeing a speech therapist and he will say words for her. > I guess I am looking for some input or any suggestions on what might > be wrong. We are to see a neurologist next month. I have no clue > what to expect there. > We just started a mothers morning out program and he loves to go to > school. We have only been 3 times so far and I have stayed with > him. He has never stayed with anyone else so this will be a little > bit of a challenge. I told the director I didnt want him to cry and > she said I could stay as long as I wanted. Its ok to me if he cries > when I first leave. I understand that there is some mommy seperation > going on here too. But I would never let him go more than 10 mins. > I will do whatever it takes for his sake. > He is very smart and very loving. He likes to play with other > kids.....just doesnt talk. > Sherri has recommended a homeopath. There is one listed here so I > think I will call them tomorrow and just go talk to them to see what > they have to say. > Any input is greatly appreciated :-) > thanks > Sherry > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 8, 2003 Report Share Posted July 8, 2003 my almost 5 y/o son 7/18 has me baffled and distraught. since attending regular pre-k i have noticed his motor skills are behind others his own age. difficulty catching ball, poor coordination. poor upper body strength, strong legs, i think he has overcompensated for weak upprer arm strength. i know this is a speech disorder message board, but maybe he has a mild form of the speech with more motor difficultie. he was speech delayed, had him tested by EIP but he wasn't delayed enough. he would pronounce begining sound and end of word but leave out the middle. that is the most vivid memory of his patterns that i can recall.spoke like he had mouth full of marbles at times. he starts regular kindergarten is sept. a 6.5 hour day which scares the heck out of me. he has started to state he can't he wont try new things because he can't do them. i spoke to new schools psycologist about having him re-evaluated, she said she would have him done in sept. they don't do them over the summer. she suggested i have a private pt evaluation on my own to see where he stands.i did that and he is in the 19th percentile 12% is the cutoff for services.she said in two of the areas he tested at 3.8 years but in one area he tested in above a 5 yo range.i think one skill put him over to a higher percentile. she said he had mildly tight hamstrings, poor muscle development upper arms.he can't skip, jumps but falls most times when he lands.he is very bright, knows all his letters can count up to 30-35, after doing some net surfing i came upon dyspraxia, but also cerebal palsy. as far as cerebral palsy goes, both are very similar in symptoms, the mild form of cp. anyone here have any idea how to differntiate between the two. my pediatrician said falling within the 19th percentile is still ok, within normal, my ped is a glass is half full type of guy, while i am a half empty person.he appreciated my concerns and suggested a neurolgy consult to put my mind at ease he said.my son just asked me the other day, why can't i make my body ride my bike faster? (training wheel bike of course)he is slow and deliberate. so is his writing, he can write ok, but this little guy has been writing his letters almost daily since january. he has finally gotten the proper pencil grasp , but only for about 2 weeks now.he also has a defeatist attitude lately, he says i can't or refuses to try new things without tremendous encouragement.also is saying i'm stupid now, that is what is scaring me. what will he do when he gets to school and i am not there to push him. he is quiet by nature, kind and goes with the flow, i think he will get eaten up in school.any one know anything about motor dyspraxia versus cerebra palsy? is the only way by brain scan or mri? his neurology appointment isn't until august 8th and i am losing my mind trying to get him up to speed for september.PLEASE someone give me some ideas or suggestions for him. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 8, 2003 Report Share Posted July 8, 2003 Hi, First of all, I would put your request in writing with the school to have a full OT, PT and speech evaluation and request an IEP meeting. Confirm that this was promised the first week of school. They are already playing games by telling you to get your own PT eval. OT can also help with gross motor skills you describe. PT Is difficult to get in a school environement b/c it is more medical and as long a child functions in the class, does stairs, walks across the room with a tray can get up from a seated position they are off the hook. So focis on the OT. Make sure they use a test that tests connected speech and not isolated words. That is where apraxic children who are speaking break down the most. Look into a gymnastics type class. This did wonders for my now 5 year old. Also take advantage of the summer and do lots of swimming. Second find an advocate so when you have an IEP meeting you have someone who knows your rights at your side. It fascinates me how cooperative schools are when their attempts to not service our kids are under scrutiny. Good luck, and stay in touch on the board. You will learn tons here! Mom to 5 and 3 > my almost 5 y/o son 7/18 has me baffled and distraught. since > attending regular pre-k i have noticed his motor skills are behind > others his own age. difficulty catching ball, poor coordination. poor > upper body strength, strong legs, i think he has overcompensated for > weak upprer arm strength. i know this is a speech disorder message > board, but maybe he has a mild form of the speech with more motor > difficultie. he was speech delayed, had him tested by EIP but he > wasn't delayed enough. he would pronounce begining sound and end of > word but leave out the middle. that is the most vivid memory of his > patterns that i can recall.spoke like he had mouth full of marbles at > times. he starts regular kindergarten is sept. a 6.5 hour day which > scares the heck out of me. he has started to state he can't he wont > try new things because he can't do them. i spoke to new schools > psycologist about having him re-evaluated, she said she would have > him done in sept. they don't do them over the summer. she suggested > i have a private pt evaluation on my own to see where he stands.i did > that and he is in the 19th percentile 12% is the cutoff for > services.she said in two of the areas he tested at 3.8 years but in > one area he tested in above a 5 yo range.i think one skill put him > over to a higher percentile. she said he had mildly tight hamstrings, > poor muscle development upper arms.he can't skip, jumps but falls > most times when he lands.he is very bright, knows all his letters can > count up to 30-35, after doing some net surfing i came upon > dyspraxia, but also cerebal palsy. as far as cerebral palsy goes, > both are very similar in symptoms, the mild form of cp. anyone here > have any idea how to differntiate between the two. my pediatrician > said falling within the 19th percentile is still ok, within normal, > my ped is a glass is half full type of guy, while i am a half empty > person.he appreciated my concerns and suggested a neurolgy consult to > put my mind at ease he said.my son just asked me the other day, why > can't i make my body ride my bike faster? (training wheel bike of > course)he is slow and deliberate. so is his writing, he can write ok, > but this little guy has been writing his letters almost daily since > january. he has finally gotten the proper pencil grasp , but only for > about 2 weeks now.he also has a defeatist attitude lately, he says i > can't or refuses to try new things without tremendous > encouragement.also is saying i'm stupid now, that is what is scaring > me. what will he do when he gets to school and i am not there to > push him. he is quiet by nature, kind and goes with the flow, i think > he will get eaten up in school.any one know anything about motor > dyspraxia versus cerebra palsy? is the only way by brain scan or mri? > his neurology appointment isn't until august 8th and i am losing my > mind trying to get him up to speed for september.PLEASE someone give > me some ideas or suggestions for him. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 19, 2005 Report Share Posted November 19, 2005 Thanks Notan and Ann for your advice, that relly helps, but I'm still so sad.. this past months were soo good that I thought I was cured, I eat what I liked, I slept perfect (unless my son wakes me up) I didn't even had heartburn. And now thinking back how bad I was before the surgery.. oh please I don't want that again...I hope. I'm from Mexico but I have been living in Minnesota for almost 8 years. Beautiful place where you live Ann I wish I could visit again! Tace care and thanks again. Hilda lilac_blossom_lady <lilac_blossom_lady@...> wrote: Hello Hilda, Welcome to the Group. Don't panic darlin'. I think that what you are describing has happened to quite a few people. From what I have read, some people need a dilation a few months after surgery. You would think that having the surgery would be a permanent answer wouldn't you? But it doesn't seem to be like that. As for the blood, join the club! As long as it doesn't happen regularly the Doctors don't seem to be too concerned about it. I had some a couple of weeks ago and did exactly the same as you,panicked, straight onto email to talk to my friend . A couple of hours later I was feeling a lot calmer when I could be a bit more logical. Our oesophaguses (oesophagi ? - Oh blimey!) become quite vulnerable, misshapen, sore - you name it, they are it, and sometimes they complain. I assume you will be seeing you Doc quite soon so that he can arrange a check-up for you. Meanwhile try not to worry too much. Just have a chat to us lot if it is getting you down. There is a lot of caring in this Group. Lots of love from Ann in England (Where are you Hilda?) XXX >> Hi everyone, > I'm new here and I was diagnosed with achalasia a little over 3 years > ago, i went through a terrible pregnancy, right after my son was born I > had a botox shot which helped for about 4 months then I had the heller > myotomy (last april) and I thought I was cured.. but I'm starting to > get food stuck and today I threw up for the first time, it was very > hard and painful, and I could see some blood in there.> I'm very scared, Please! has this happened to any of you too?> Thanks in advance> Hilda> FareChase - Search multiple travel sites in one click. Quote Link to comment Share on other sites More sharing options...
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