Guest guest Posted March 28, 2008 Report Share Posted March 28, 2008 It could be me –but I'd take the opinion of my child's neurodevelopmental medical doctors over the opinion of my child's dance teacher. I mean- other than the dance teacher having a child with some type of CP related issue she can only give you an opinion. And based on what signs in your daughter? (well we know how some dance teachers are... is it because your daughter can't stand on her toes on one foot and stick the other foot over her head with her " toes pointed and leg straight " and hold that while she's spinned around?) You know she has a diagnosis of hypotonia and you are getting appropriate therapy for that. But I can tell this really does bother you –so what signs do you notice if any that would make one suspect hypertonia in her legs? Below I have your last message –and then an archive on this from a parent that was answered by developmental pediatrician Dr. Larry Laveman. The way I believe this came up is because a few years ago –some MDs would give the diagnosis of CP to secure services just like today some give the diagnosis of autism or PDD to secure services whether the child actually has that diagnosis or not. But for CP from what I was told if a child has hypotonia in the body and hypertonia in the extremities that would be a form of CP- but it could be so mild that a parent wouldn't even notice it unless it was pointed out –so on the other hand some MDs didn't give the diagnosis of CP in some cases as they know it can upset the parent – and CP is not degenerative- it is what it is. (those cases would be when it was very mild) So the question is – will the diagnosis of CP make any difference in what you are already doing? Would anyone know if you didn't tell them? Probably not since neurodevelopmental medical doctors didn't know. To add stretching appears to be a good idea –but it's a good idea for anyone who's exercising. Probably even more so if not exercising! http://www.mayoclinic.com/health/stretching/SM00043 The fact that your child is in a dance class tells me that she's at least somewhat coordinated and active. I may not know whether she has hypertonia with her hypotonia or not - but based on the fact you've only been told this by her dance teacher and not any of the professionals if I was a betting 'man' I'd say no. But I do know one thing –your daughter has a mom that is one in a million. It sounds like you always go above and beyond to fight for your child and for all of our children that's what they need. Question the diagnosis- question the therapy –question the progress…because it's our child- and while we only get what's appropriate by the school system -well we only get that if we fight for that too –we all want what is best. None of us has the chance to do things over –so do things in the present so that when you look back down the road you can say with a clear mind no matter what " I did my best " I know you can say this. ~~~~~~~~first a clip of your last message so people know what I'm talking about in regards to the dance teacher- and then the message about this from a parent answered by developmental MD Dr. Larry Laveman: , I am pretty certain that my child had/has (we've been working on it!) hypotonia in her body. No professional has ever mentioned hypertonia to me. However . . .her dance teacher said to me that she noticed that my daughter " had hypertonia in her legs. " She went on to say that she knew about this because her son has some kind of CP related issue. Because no doctor (including our neuro) had ever mentioned this -- I just let it go. But, when I saw this post about CP from the other mom, I began to worry. ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ >My 3 year-old son was diagnosed with what the doctor called at the time > " hypotonia " (and " hypertonia " ) at 1 year old. He's been receiving various >therapies since. He has low tone in the upper body and some high tone in >his >legs/arms. He was 5 weeks premature and only 4lbs. 10oz. He has recently >been diagnosed with Apraxia. >My question is: what is the difference between " hypotonia " and Cerebral >Palsy? My neurologist has told us that hypotonia (and hypertonia, which is >tightness in the muscles) is just another name for Cerebral Palsy (which >has >varying degrees from mild to severe). He said that Cerebral Palsy is a >muscle disorder that is neurologically based. He now refers to my son as >having " mild Cerebral Palsy " and interchanges the term with hypotonia. >Thanks, >Michele Hi Michele: The term " cerebral palsy " , " cerebral paralysis " , etc. are historic terms that describe a nonprogressive disorder of motor control (movement,etc.) of prenatal origen (from before birth). It is vaguely defined and covers a lot of different causes for the problem. Most children with this problem have high tone (hypertonia) which is also called spasticity. Children born prematurely, like your child, are at higher risk for CP than the general population. Not all motor tone abnormalities are CP, nor do all children with CP have similar problems with tone. As CVA is associated with problems of motor control of the mouth and pharynx (the back of your throat), it is logical that some children with CP will have problems in this area of motor control as well. The other reason that your doctor may be using the CP term is for enhanced reimbursement from your insurer - they are more willing to pay for a " hard " diagnosis like CP than a " soft " diagnosis of apraxia. Larry Laveman, MD Consultant, CHERAB ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 28, 2008 Report Share Posted March 28, 2008 Em, I personally think that you have your daughter on a wonderful program.... It's my 'dream' program for a youngster with hypotonia.... Go gettm' girl! Janice [sPAM][ ] " High Tone " versus " Low Tone " OK, I officially have two of our doctors rolling their eyes at me today! Oh well. . . This started with someone else's child receiving a CP diagnosis. This reminded me that a dance teacher had told me that my daughter had " tone " in her legs. I thought she was clearly wrong, as the neuro had said my daughter had hypotonia (very mild). However, said today that you could have hypotonia in the trunk and hypertonia in the legs. I spoke with the neuro, who said he only had hypotonia reflected in his file on my daughter. I then spoke twice with our pediatrician. He said that if there were a " significant issue " he would have spoken to me about it. He said it is possible that she could have a minor issue with it that he could have missed during regular check-ups. He allowed me to go through all the physical activities we work on with her, and said he felt that we were covering our bases. He did suggest that we add stretching to her routine, which he said would help with hypertonia if it were an issue. He offered to put us in touch with a physical therapist to suggest appropriate exercises (and do another evaluation if we wanted). However, overall he was very encouraging, and basically said that if there is an issue it is very mild, and said he felt daily stretching would take care of it. (We already do running, weight bearing exercises, and horseback riding.) We did a PT eval a while ago, and we given some exercise suggestions, but never really did PT. We started hippotherapy, but she did so well at it, they removed her from the class and put her in a sports riding class. Have most of your children done PT? As I understand it, my insurance isn't going to cover this -- but we'll do it anyway if it is the right thing to do. Opinions? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 28, 2008 Report Share Posted March 28, 2008 That is so true.... Em.... if your child is capable of taking dance classes.... she is an absolute rock star as far as dyspraxia goes. She would be the first young girl on the boards I have seen to survive the first class! Most dyspraxic kids have a terrible time copying their bodies and need sensory input (ie. touch) to position themselves correctly. I have heard a few tough stories of dyspraxic girls taking dance and bawling hysterically after one class NEVER to return! Dance classes are often so competitive and driven..... Keep doing what you are doing and keep your daughter as happy and full of self-esteem as you can. Janice [sPAM][ ] Re: " High Tone " versus " Low Tone " It could be me -but I'd take the opinion of my child's neurodevelopmental medical doctors over the opinion of my child's dance teacher. I mean- other than the dance teacher having a child with some type of CP related issue she can only give you an opinion. And based on what signs in your daughter? (well we know how some dance teachers are... is it because your daughter can't stand on her toes on one foot and stick the other foot over her head with her " toes pointed and leg straight " and hold that while she's spinned around?) You know she has a diagnosis of hypotonia and you are getting appropriate therapy for that. But I can tell this really does bother you -so what signs do you notice if any that would make one suspect hypertonia in her legs? Below I have your last message -and then an archive on this from a parent that was answered by developmental pediatrician Dr. Larry Laveman. The way I believe this came up is because a few years ago -some MDs would give the diagnosis of CP to secure services just like today some give the diagnosis of autism or PDD to secure services whether the child actually has that diagnosis or not. But for CP from what I was told if a child has hypotonia in the body and hypertonia in the extremities that would be a form of CP- but it could be so mild that a parent wouldn't even notice it unless it was pointed out -so on the other hand some MDs didn't give the diagnosis of CP in some cases as they know it can upset the parent - and CP is not degenerative- it is what it is. (those cases would be when it was very mild) So the question is - will the diagnosis of CP make any difference in what you are already doing? Would anyone know if you didn't tell them? Probably not since neurodevelopmental medical doctors didn't know. To add stretching appears to be a good idea -but it's a good idea for anyone who's exercising. Probably even more so if not exercising! http://www.mayoclinic.com/health/stretching/SM00043 The fact that your child is in a dance class tells me that she's at least somewhat coordinated and active. I may not know whether she has hypertonia with her hypotonia or not - but based on the fact you've only been told this by her dance teacher and not any of the professionals if I was a betting 'man' I'd say no. But I do know one thing -your daughter has a mom that is one in a million. It sounds like you always go above and beyond to fight for your child and for all of our children that's what they need. Question the diagnosis- question the therapy -question the progress.because it's our child- and while we only get what's appropriate by the school system -well we only get that if we fight for that too -we all want what is best. None of us has the chance to do things over -so do things in the present so that when you look back down the road you can say with a clear mind no matter what " I did my best " I know you can say this. ~~~~~~~~first a clip of your last message so people know what I'm talking about in regards to the dance teacher- and then the message about this from a parent answered by developmental MD Dr. Larry Laveman: , I am pretty certain that my child had/has (we've been working on it!) hypotonia in her body. No professional has ever mentioned hypertonia to me. However . . .her dance teacher said to me that she noticed that my daughter " had hypertonia in her legs. " She went on to say that she knew about this because her son has some kind of CP related issue. Because no doctor (including our neuro) had ever mentioned this -- I just let it go. But, when I saw this post about CP from the other mom, I began to worry. ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ >My 3 year-old son was diagnosed with what the doctor called at the time > " hypotonia " (and " hypertonia " ) at 1 year old. He's been receiving various >therapies since. He has low tone in the upper body and some high tone in >his >legs/arms. He was 5 weeks premature and only 4lbs. 10oz. He has recently >been diagnosed with Apraxia. >My question is: what is the difference between " hypotonia " and Cerebral >Palsy? My neurologist has told us that hypotonia (and hypertonia, which is >tightness in the muscles) is just another name for Cerebral Palsy (which >has >varying degrees from mild to severe). He said that Cerebral Palsy is a >muscle disorder that is neurologically based. He now refers to my son as >having " mild Cerebral Palsy " and interchanges the term with hypotonia. >Thanks, >Michele Hi Michele: The term " cerebral palsy " , " cerebral paralysis " , etc. are historic terms that describe a nonprogressive disorder of motor control (movement,etc.) of prenatal origen (from before birth). It is vaguely defined and covers a lot of different causes for the problem. Most children with this problem have high tone (hypertonia) which is also called spasticity. Children born prematurely, like your child, are at higher risk for CP than the general population. Not all motor tone abnormalities are CP, nor do all children with CP have similar problems with tone. As CVA is associated with problems of motor control of the mouth and pharynx (the back of your throat), it is logical that some children with CP will have problems in this area of motor control as well. The other reason that your doctor may be using the CP term is for enhanced reimbursement from your insurer - they are more willing to pay for a " hard " diagnosis like CP than a " soft " diagnosis of apraxia. Larry Laveman, MD Consultant, CHERAB ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 28, 2008 Report Share Posted March 28, 2008 HI there, yes my son still has PT. he def has dyspraxia of the body and reading lisa's response I had no idea that hypo and hyper can go together. learn something new everyday!!! He does have both. he is not flexible and very weak with just about everything, throwing, hitting, running, even his posture is bent. he tires very easily. he could do throwing and hitting for awhile or dribble the basketball or run, or walk great but only for short periods of time. I feel bad for him because i know others look at him like he's lazy but he truely is tired. I want to add that he also has some vestibular issues as well. I think its related to the body too. he never had confidence or trusted his own body. he HATES high places, he is just beginning to swing on a swing (he's 8) anything that requires him to take his feet off the ground terrifies him. I think his body issues contribute to his anxiety, a lot.... He looooves baseball and basketball but he is always a step behind and thank god it does not borther him that he is a step behind. he is such a trooper in these sports. he has a long way to go and i guess i just can't give up. sometimes i feel i push him too much and yes i get embarrased(i hate to admit that). until he says no more he and I will endure. thanks for bringing up this topic I forgot that him that trusting his own body contributes to soooo much of his behavior as well. Somehow if all else fails we always have our physical selfs to count on but what if you didn't, that would certainly not make ME trust the world... my poor guy. he is amazing how my boy continues on. thanks for bringing this up and i hope it helps chris [ ] " High Tone " versus " Low Tone " OK, I officially have two of our doctors rolling their eyes at me today! Oh well. . . This started with someone else's child receiving a CP diagnosis. This reminded me that a dance teacher had told me that my daughter had " tone " in her legs. I thought she was clearly wrong, as the neuro had said my daughter had hypotonia (very mild). However, said today that you could have hypotonia in the trunk and hypertonia in the legs. I spoke with the neuro, who said he only had hypotonia reflected in his file on my daughter. I then spoke twice with our pediatrician. He said that if there were a " significant issue " he would have spoken to me about it. He said it is possible that she could have a minor issue with it that he could have missed during regular check-ups. He allowed me to go through all the physical activities we work on with her, and said he felt that we were covering our bases. He did suggest that we add stretching to her routine, which he said would help with hypertonia if it were an issue. He offered to put us in touch with a physical therapist to suggest appropriate exercises (and do another evaluation if we wanted). However, overall he was very encouraging, and basically said that if there is an issue it is very mild, and said he felt daily stretching would take care of it. (We already do running, weight bearing exercises, and horseback riding.) We did a PT eval a while ago, and we given some exercise suggestions, but never really did PT. We started hippotherapy, but she did so well at it, they removed her from the class and put her in a sports riding class. Have most of your children done PT? As I understand it, my insurance isn't going to cover this -- but we'll do it anyway if it is the right thing to do. Opinions? ________________________________________________________________________________\ ____ Be a better friend, newshound, and know-it-all with Mobile. Try it now. http://mobile./;_ylt=Ahu06i62sR8HDtDypao8Wcj9tAcJ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 28, 2008 Report Share Posted March 28, 2008 , Sorry -- I should clarify. She was evaluated, and put in a class. As it turned out, she sat very tall in the saddle and did not " slump " at all, and she turned out to have excellent balance. After a couple of lessons in this class, they moved her to a private class. After a couple of session there, they suggested that she move out of hippotherapy and into the sports riding class. They said that typically they reserved the hippotherapy for children working at a lower level (their words, not mine). I did speak up and tell them that it is important to me that her tone improve. The PT said that the sports riding class would work on all of the issues that needed to be worked on (tone (posture) and balance) -- and she would get the additional benefit of learning to direct the horse (which they thought would be really good for her self-confidence). I have only been to one place for this, so I have no idea if this is " typical " or not. But I could see how she differed from another little girl that was in her class. My daughter was able to " sit up " in the saddle, and move, even at a trot, without concerns that she would fall off. I revisited the decision with them a couple of times -- in the hippotherapy, there were more of the activities you list. Her class now is (to my very untrained eye) much like horseback riding lessons. They were right on one thing, however -- this has truly helped her self confidence, so I've let it go. She is 7 years old, so her age may have influenced their decision as well. > > > > OK, I officially have two of our doctors rolling their eyes at me > today! Oh well. . . > > > > This started with someone else's child receiving a CP diagnosis. > This reminded me that a > > dance teacher had told me that my daughter had " tone " in her legs. > I thought she was > > clearly wrong, as the neuro had said my daughter had hypotonia > (very mild). However, > > said today that you could have hypotonia in the trunk and > hypertonia in the legs. > > > > I spoke with the neuro, who said he only had hypotonia reflected in > his file on my > > daughter. I then spoke twice with our pediatrician. He said that > if there were a > > " significant issue " he would have spoken to me about it. He said > it is possible that she > > could have a minor issue with it that he could have missed during > regular check-ups. > > > > He allowed me to go through all the physical activities we work on > with her, and said he > > felt that we were covering our bases. He did suggest that we add > stretching to her > > routine, which he said would help with hypertonia if it were an > issue. He offered to put us > > in touch with a physical therapist to suggest appropriate exercises > (and do another > > evaluation if we wanted). However, overall he was very > encouraging, and basically said > > that if there is an issue it is very mild, and said he felt daily > stretching would take care of > > it. (We already do running, weight bearing exercises, and horseback > riding.) > > > > We did a PT eval a while ago, and we given some exercise > suggestions, but never really > > did PT. We started hippotherapy, but she did so well at it, they > removed her from the > > class and put her in a sports riding class. Have most of your > children done PT? As I > > understand it, my insurance isn't going to cover this -- but we'll > do it anyway if it is the > > right thing to do. Opinions? > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 28, 2008 Report Share Posted March 28, 2008 and Janice -- Thank you both for your suggestions and kind words of encouragement! I really needed support yesterday, and so appreciate you taking time to respond to me. After objectively assessing our situation, I do feel we are doing all we can right now. I think as your child gets older, you start to feel there is a time crunch to " fix " everything before it is too late! Don't get me wrong -- my daughter has made amazing progress -- but we still have a way to go. > > , Sorry -- I should clarify. She was evaluated, and put in a class. As it turned out, > she sat very tall in the saddle and did not " slump " at all, and she turned out to have > excellent balance. After a couple of lessons in this class, they moved her to a private > class. After a couple of session there, they suggested that she move out of hippotherapy > and into the sports riding class. They said that typically they reserved the hippotherapy > for children working at a lower level (their words, not mine). I did speak up and tell them > that it is important to me that her tone improve. The PT said that the sports riding class > would work on all of the issues that needed to be worked on (tone (posture) and balance) > -- and she would get the additional benefit of learning to direct the horse (which they > thought would be really good for her self-confidence). I have only been to one place for > this, so I have no idea if this is " typical " or not. But I could see how she differed from > another little girl that was in her class. My daughter was able to " sit up " in the saddle, and > move, even at a trot, without concerns that she would fall off. I revisited the decision with > them a couple of times -- in the hippotherapy, there were more of the activities you list. > Her class now is (to my very untrained eye) much like horseback riding lessons. They were > right on one thing, however -- this has truly helped her self confidence, so I've let it go. > She is 7 years old, so her age may have influenced their decision as well. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 29, 2008 Report Share Posted March 29, 2008 Em, If she is working the body everyday... you are doing it.... it IS happening and she will slowly get stronger. Core body tone takes a long time but just do it in the most pleasant and funnest of ways so that she will keep it up for years and years. And there definately is a time crunch with the older kids as the schoolyard is not a kind place. But you are working the body nicely.... how about those hands..... they can be an aweful problem. Janice Mother of Mark, 13 [sPAM][ ] Re: " High Tone " versus " Low Tone " and Janice -- Thank you both for your suggestions and kind words of encouragement! I really needed support yesterday, and so appreciate you taking time to respond to me. After objectively assessing our situation, I do feel we are doing all we can right now. I think as your child gets older, you start to feel there is a time crunch to " fix " everything before it is too late! Don't get me wrong -- my daughter has made amazing progress -- but we still have a way to go. > > , Sorry -- I should clarify. She was evaluated, and put in a class. As it turned out, > she sat very tall in the saddle and did not " slump " at all, and she turned out to have > excellent balance. After a couple of lessons in this class, they moved her to a private > class. After a couple of session there, they suggested that she move out of hippotherapy > and into the sports riding class. They said that typically they reserved the hippotherapy > for children working at a lower level (their words, not mine). I did speak up and tell them > that it is important to me that her tone improve. The PT said that the sports riding class > would work on all of the issues that needed to be worked on (tone (posture) and balance) > -- and she would get the additional benefit of learning to direct the horse (which they > thought would be really good for her self-confidence). I have only been to one place for > this, so I have no idea if this is " typical " or not. But I could see how she differed from > another little girl that was in her class. My daughter was able to " sit up " in the saddle, and > move, even at a trot, without concerns that she would fall off. I revisited the decision with > them a couple of times -- in the hippotherapy, there were more of the activities you list. > Her class now is (to my very untrained eye) much like horseback riding lessons. They were > right on one thing, however -- this has truly helped her self confidence, so I've let it go. > She is 7 years old, so her age may have influenced their decision as well. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 29, 2008 Report Share Posted March 29, 2008 It sounds like your daughter is a " rock star " as Janice says and that you ask great questions and have a good doc responding to your inquiries. > > > > , Sorry -- I should clarify. She was evaluated, and put in a class. As it turned out, > > she sat very tall in the saddle and did not " slump " at all, and she turned out to have > > excellent balance. After a couple of lessons in this class, they moved her to a private > > class. After a couple of session there, they suggested that she move out of > hippotherapy > > and into the sports riding class. They said that typically they reserved the hippotherapy > > for children working at a lower level (their words, not mine). I did speak up and tell > them > > that it is important to me that her tone improve. The PT said that the sports riding class > > would work on all of the issues that needed to be worked on (tone (posture) and > balance) > > -- and she would get the additional benefit of learning to direct the horse (which they > > thought would be really good for her self-confidence). I have only been to one place for > > this, so I have no idea if this is " typical " or not. But I could see how she differed from > > another little girl that was in her class. My daughter was able to " sit up " in the saddle, > and > > move, even at a trot, without concerns that she would fall off. I revisited the decision > with > > them a couple of times -- in the hippotherapy, there were more of the activities you > list. > > Her class now is (to my very untrained eye) much like horseback riding lessons. They > were > > right on one thing, however -- this has truly helped her self confidence, so I've let it go. > > She is 7 years old, so her age may have influenced their decision as well. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 29, 2008 Report Share Posted March 29, 2008 Sounds like she is doing well.. now sit back and relax and smile. ) > > and Janice -- Thank you both for your suggestions and kind words of > encouragement! I really needed support yesterday, and so appreciate you taking time to > respond to me. After objectively assessing our situation, I do feel we are doing all we can > right now. I think as your child gets older, you start to feel there is a time crunch to " fix " > everything before it is too late! Don't get me wrong -- my daughter has made amazing > progress -- but we still have a way to go. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 29, 2008 Report Share Posted March 29, 2008 Again, thanks to all who responded! I *had* to smile when my daughter was referred to as a rock star! But it did make me realize how far she has come. Although when we started, I was sure she had pure apraxia, I now know that she also has some dyspraxia in her body too. She loves to dance. Last year, she was crushed because the teacher told me she shouldn't take jazz because it simply went too fast for my dear child to keep up. But she kept doing ballet and tap, and this this year, she started jazz too (and has actually been keeping up!). It is nice to have some activities she can do that aren't " therapy " because we do a lot of therapy. > > > > and Janice -- Thank you both for your suggestions and kind words of > > encouragement! I really needed support yesterday, and so appreciate you taking time to > > respond to me. After objectively assessing our situation, I do feel we are doing all we can > > right now. I think as your child gets older, you start to feel there is a time crunch to " fix " > > everything before it is too late! Don't get me wrong -- my daughter has made amazing > > progress -- but we still have a way to go. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 29, 2008 Report Share Posted March 29, 2008 Janice, Sorry I missed your earlier question about fine motor. I am always looking for things to work her hands, so if you have ideas, please, please send them our way!!!! Your therapy ideas are amazing (I have been using your oral motor ideas for her " L " and she's almost got it!! A major, major improvement!!) We started with OT -- lots of theraputty squishing (and we did that exercise that talked about where you pull little beads out of the clay!) to strengthen the fingers. We also did a lot of finger isometrics so that each finger was able to move independently. We then moved on to handwriting, which was a little difficult. We used an OT for the Handwriting without Tears program. There were no tears with that program, but honestly, she didn't make a lot of progress with it. I think perhaps she needed more " basic training. " After more " basics, " I worked with her on a program by Dianne Craft (Brain Integration Therapy) which basically had her drawing a sideways 8 (to cross the midline) and then writing each letter of the alphabet on this " lazy 8. " It took about 10-15 minutes a day and we did it for about 12 weeks. At the end, I still thought her handwriting needed work, but we needed a break, so we stopped. A month or so after that, with no further anything, her handwriting suddenly improved. I think maybe all the work just needed some time to click. Now she takes piano lessons. Practicing really works her fingers, and again, she doesn't think of it as therapy because so many of her little friends take piano as well. Having a girl with fine motor issues is a double-edged sword (in my opinion). I honestly believe teachers expect more from the girls (better handwriting, better coloring, etc.). I have some boys of my own, so I can say that has been our case anyway. On the other side, my daughter enjoys fine motor activities more than her brothers. So, I can get her to work on Perler beads (those little beads you put on a plastic form and iron), or do Shrinky Dinks (which involve tracing, coloring, cutting), or string tiny beads for necklaces. When she was a little younger, she loved the " Chicken Socks " books by Klutz -- each book was kind of a do-it-yourself activity, involving cutting, tying, etc. I am also looking for new ideas! Please send them my way!!! > > > > > > and Janice -- Thank you both for your suggestions and kind words of > > > encouragement! I really needed support yesterday, and so appreciate you taking time > to > > > respond to me. After objectively assessing our situation, I do feel we are doing all we > can > > > right now. I think as your child gets older, you start to feel there is a time crunch to > " fix " > > > everything before it is too late! Don't get me wrong -- my daughter has made > amazing > > > progress -- but we still have a way to go. > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 29, 2008 Report Share Posted March 29, 2008 Let me tell you.... that dance is therapy! WOW! If she can do dance, I would not consider her to have many motor planning issues in the gross motor area anymore! Congrats! You beat it! She is a Rock Star! That is the key.... to slowly transfer from therapy to skill sets and Normal skill building like other kids. Again..... how are her hands. That is the toughest and the last to truly be identified..... the hands..... would be a shame for us to miss it if she struggles with her hands. Janice [sPAM][ ] Re: " High Tone " versus " Low Tone " Again, thanks to all who responded! I *had* to smile when my daughter was referred to as a rock star! But it did make me realize how far she has come. Although when we started, I was sure she had pure apraxia, I now know that she also has some dyspraxia in her body too. She loves to dance. Last year, she was crushed because the teacher told me she shouldn't take jazz because it simply went too fast for my dear child to keep up. But she kept doing ballet and tap, and this this year, she started jazz too (and has actually been keeping up!). It is nice to have some activities she can do that aren't " therapy " because we do a lot of therapy. > > > > and Janice -- Thank you both for your suggestions and kind words of > > encouragement! I really needed support yesterday, and so appreciate you taking time to > > respond to me. After objectively assessing our situation, I do feel we are doing all we can > > right now. I think as your child gets older, you start to feel there is a time crunch to " fix " > > everything before it is too late! Don't get me wrong -- my daughter has made amazing > > progress -- but we still have a way to go. > Quote Link to comment Share on other sites More sharing options...
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