Guest guest Posted June 5, 2009 Report Share Posted June 5, 2009 I just went to an acupuncturist today and she said the first step in treatment is to get an MRI. Our son's doctor also suggested a neurologist. For those of you that have had them done, I was wondering two things: 1. What did the MRI show? 2. What was the suggested treatment? We are on a tight budget and I don't want to get an MRI, " just to know " . If we end up doing this, I want to know if there would be any change in course because of it or are we basically at square one again. I can't afford expensive treatments like neurofeedback, so is there any sense in getting an MRI? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 6, 2009 Report Share Posted June 6, 2009 We just got the MRI done - showed nothing - chromozone study - showed nothing - EEG - showed a wave in the left and right temporal region - but nothing to give DX of apraxia - we got these tests done with a pediatric neurologist.... he would only say developmental - needs extreme speech therapy - would not say apraxia, although I am pretty sure that is what she has - we are seeing remarkable results with the fish oil and continuously going over videos (baby bumblebee, my baby can read) - anything that enforces repeated language - I also have purchased items from super duper publications and I do lots of oral motor activities - I'm at the point that I don't care honestly if she gets the " apraxia " DX as long as she gets the therapy she needs and deserves... we as parents are their greatest advocates/teachers... good luck [ ] If your child had an MRI, what did it show? I just went to an acupuncturist today and she said the first step in treatment is to get an MRI. Our son's doctor also suggested a neurologist. For those of you that have had them done, I was wondering two things: 1. What did the MRI show? 2. What was the suggested treatment? We are on a tight budget and I don't want to get an MRI, " just to know " . If we end up doing this, I want to know if there would be any change in course because of it or are we basically at square one again. I can't afford expensive treatments like neurofeedback, so is there any sense in getting an MRI? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 6, 2009 Report Share Posted June 6, 2009 My son has more reason to believe something would show on an MRI than most because he has a history of head trauma, a R temporal skull fracture. His Chromosome testing was all normal, EEGs have been normal, MRI normal. Due to the insurance we had through most of this the only test I paid for was the recent MRI. Everything else was when we were struggling and had Medicaid. My MRI co-insurance was about $270. It seems over the years that MOST kids on this list have completely normal EEGs and MRIs, but these are still tests than many have had or have at least had recommended. A small number have chromosomal differences, but for most the why part of apraxia remains a mystery. I pursued the EEG and later MRI testing due to my son having both apraxia (which has responded to quality speech therapy) as well as lingering language issues which his therapists think look like aphasia (usually due to damage to the brain.) Yet he still remains a mystery. An EEG or MRI is something you can get at any time. I chose to delay both until we hit a point in therapeutic progress where further testing and explanations again seemed like the prudent thing to do. My son was also older and didn't need to be sedated (or sedated as strongly in the case of EEG - he did some awake, some under sedation) for these procedures and they were less traumatic because of this. Miche Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 6, 2009 Report Share Posted June 6, 2009 My neuro immediately did an MRI, EEG, and bloodwork. The MRI showed very small scars (don't remember where), but she said that with technology now, they're finding more scarring that they didn't see years ago. It was not in a place that could be related to any problems. EEG was perfectly normal, bloodwork showed a slight iron deficiency. To the best of my knowledge, an MRI won't show anything on CAS, only if it was caused by brain damage or if there are other problems. > > I just went to an acupuncturist today and she said the first step in treatment is to get an MRI. Our son's doctor also suggested a neurologist. For those of you that have had them done, I was wondering two things: > > 1. What did the MRI show? > > 2. What was the suggested treatment? > > We are on a tight budget and I don't want to get an MRI, " just to know " . If we end up doing this, I want to know if there would be any change in course because of it or are we basically at square one again. I can't afford expensive treatments like neurofeedback, so is there any sense in getting an MRI? > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 6, 2009 Report Share Posted June 6, 2009 First step in treating what? What condition are you trying to treat or do you/they think he has? Doing the test depends upon what your trying to find out. It may not be needed..depends. > > I just went to an acupuncturist today and she said the first step in treatment is to get an MRI. Our son's doctor also suggested a neurologist. For those of you that have had them done, I was wondering three things: > > 1. What did the MRI show? > > 2. What was the suggested treatment? > > 3. Does your child have a speech/language disorder? > > We are on a tight budget and I don't want to get an MRI, " just to know " . If we end up doing this, I want to know if there would be any change in course because of it or are we basically at square one again? > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 6, 2009 Report Share Posted June 6, 2009 --Thank you for the info on your MRI. We wanted to get our daughter an MRI as well to see what might be amis... Fish oil? please explain further.. Winter - In , " Lora " <katanna@...> wrote: > > We just got the MRI done - showed nothing - chromozone study - showed > nothing - EEG - showed a wave in the left and right temporal region - but > nothing to give DX of apraxia - we got these tests done with a pediatric > neurologist.... he would only say developmental - needs extreme speech > therapy - would not say apraxia, although I am pretty sure that is what > she has - we are seeing remarkable results with the fish oil and continuously > going over videos (baby bumblebee, my baby can read) - anything that > enforces repeated language - I also have purchased items from super > duper publications and I do lots of oral motor activities - I'm at the point > that I don't care honestly if she gets the " apraxia " DX as long as she gets > the therapy she needs and deserves... we as parents are their greatest > advocates/teachers... > > good luck > > [ ] If your child had an MRI, what did it show? > > > > > > I just went to an acupuncturist today and she said the first step in treatment is to get an MRI. Our son's doctor also suggested a neurologist. For those of you that have had them done, I was wondering two things: > > 1. What did the MRI show? > > 2. What was the suggested treatment? > > We are on a tight budget and I don't want to get an MRI, " just to know " . If we end up doing this, I want to know if there would be any change in course because of it or are we basically at square one again. I can't afford expensive treatments like neurofeedback, so is there any sense in getting an MRI? > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 6, 2009 Report Share Posted June 6, 2009 He is having trouble pronouncing things, his speech is hard to understand. > > > > I just went to an acupuncturist today and she said the first step in treatment is to get an MRI. Our son's doctor also suggested a neurologist. For those of you that have had them done, I was wondering three things: > > > > 1. What did the MRI show? > > > > 2. What was the suggested treatment? > > > > 3. Does your child have a speech/language disorder? > > > > We are on a tight budget and I don't want to get an MRI, " just to know " . If we end up doing this, I want to know if there would be any change in course because of it or are we basically at square one again? > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 7, 2009 Report Share Posted June 7, 2009 Is this speech trouble new? A regression? Then RUSH to get a 24 hour EEG. He may have Landau Kleffner Syndrome and he will keep regressing til you treat. Suzanne -- In , " " <elizabethsoliday@...> wrote: > > He is having trouble pronouncing things, his speech is hard to understand. > > > > > > > > I just went to an acupuncturist today and she said the first step in treatment is to get an MRI. Our son's doctor also suggested a neurologist. For those of you that have had them done, I was wondering three things: > > > > > > 1. What did the MRI show? > > > > > > 2. What was the suggested treatment? > > > > > > 3. Does your child have a speech/language disorder? > > > > > > We are on a tight budget and I don't want to get an MRI, " just to know " . If we end up doing this, I want to know if there would be any change in course because of it or are we basically at square one again? > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 8, 2009 Report Share Posted June 8, 2009 My 7dd has had many MRI's for Hydrocephalus. they've never been ordered because of her Apraxia. If you find a good Ped Neuro--they can order an CT or MRI and it will be covered by insurance if the doctor orders it. Just talking to the Ped Neuro might get some answers without going thru that kind of testing. > > I just went to an acupuncturist today and she said the first step in treatment is to get an MRI. Our son's doctor also suggested a neurologist. For those of you that have had them done, I was wondering two things: > > 1. What did the MRI show? > > 2. What was the suggested treatment? > > Quote Link to comment Share on other sites More sharing options...
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