Guest guest Posted January 1, 2007 Report Share Posted January 1, 2007 I am new to this group. Can someone tell me exact what is ProEFA? My son has not been diagnosed with Apraxia as of yet. He does have CBPS Which is going to be an issue for his speech if there is any at all. He is 17 months and doesn't say too much. We kind of got him to say what I think was " elmo " but not positive, and he hasn't said it again since. He goes to speech therapy 2 x a week among other therapies. I am wondering if there are other ways to help this area. <http://www.babyjellybeans.com/web/do/site?ID=5864> http://www.babyjellybeans.com/web/do/site?ID=5864 _____ From: [mailto: ] On Behalf Of mp8kdh Sent: Monday, January 01, 2007 8:46 PM Subject: [ ] Apraxia , ProEFA and Sleep Disturbances?? I am new to the group and apologize if this issue has already been addressed. I am desperate! My 4 year-old son has Apraxia (verbal). I am thrilled to report that with intense private and public school speech therapy (primarily Kaufman Method) over the last 11 months, he is talking - a lot with a high degree of intelligibility. I started him on ProEFA in August and did notice a difference - his physical movements became more fluid and his articulation improved within 3 weeks after commencement. However, at about the same time his sleep patterns became terrible. He wakes frequently at night and seems wired - wanting to talk, to go downstairs, to go outside, etc. His diet is excellent, he is on no other medication (herbal or otherwise) and his personality is even, not all at hyper. He just can't seem to settle during the night, though we give the supplement in the morning. Going to sleep is not an issue. Since any naps during the day are brief, the child is perpetually exhausted. Has anyone had any similar experience? Also, what happens if you stop the ProEFA, is there regression? My whole family says to choose speech over sleep, but I have to think the lack of sleep is going to be problematic, especially with Kindergarden on the horizon. Any advice is appreciated. Thanks, Kim. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 1, 2007 Report Share Posted January 1, 2007 Kim. Has this been ongoing since you started the efa's back in August? My daughter acts like this when we have increased, or when we restart after runnng out. We recently experienced this. She's been taking them for about a week now, and for the last several nights she wakes up in the middle of the night, but we can get her to go back in her bed and " rest " . And during the day she is very hyper.Constantly on the go. To the point where she is " flapping " her arms and legs- On the go- but staying in the same spot on the rug. know what i mean. How many EFA capsules does he take in the am? Dawn in NJ > > I am new to the group and apologize if this issue has already been > addressed. I am desperate! My 4 year-old son has Apraxia (verbal). I > am thrilled to report that with intense private and public school > speech therapy (primarily Kaufman Method) over the last 11 months, he > is talking - a lot with a high degree of intelligibility. I started > him on ProEFA in August and did notice a difference - his physical > movements became more fluid and his articulation improved within 3 > weeks after commencement. However, at about the same time his sleep > patterns became terrible. He wakes frequently at night and seems > wired - wanting to talk, to go downstairs, to go outside, etc. His > diet is excellent, he is on no other medication (herbal or otherwise) > and his personality is even, not all at hyper. He just can't seem to > settle during the night, though we give the supplement in the morning. > Going to sleep is not an issue. Since any naps during the day are > brief, the child is perpetually exhausted. Has anyone had any similar > experience? Also, what happens if you stop the ProEFA, is there > regression? My whole family says to choose speech over sleep, but I > have to think the lack of sleep is going to be problematic, especially > with Kindergarden on the horizon. Any advice is appreciated. Thanks, > Kim. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 1, 2007 Report Share Posted January 1, 2007 , Pro-EFA, is the " pro " fessional grade of EFA. EFA is essential fatty acids. Omega 3,6, which is fish oil. And Omega 9, from borage oil. Here is the companies website for lots of info. Although this product can be purcahsed elsewhere. And also, there are TONS of archives on the EFA topic. http://www.nordicnaturals.com/ As far as his communication delay, have you thought about using sign language? I can tell you, we used it with my now 5 1/2 year old. It was the best thing I could have done for us. Vist SigningTime.Com for awesome dvd's. Dawn in NJ > > I am new to this group. Can someone tell me exact what is ProEFA? > > My son has not been diagnosed with Apraxia as of yet. He does have CBPS > > Which is going to be an issue for his speech if there is any at all. > > He is 17 months and doesn't say too much. We kind of got him to say what I > think was " elmo " but not positive, and he hasn't said it again since. > > He goes to speech therapy 2 x a week among other therapies. I am wondering > if there are other ways to help this area. > > > > > > <http://www.babyjellybeans.com/web/do/site?ID=5864> > http://www.babyjellybeans.com/web/do/site?ID=5864 > > > > > > _____ > > From: > [mailto: ] On Behalf Of mp8kdh > Sent: Monday, January 01, 2007 8:46 PM > > Subject: [ ] Apraxia , ProEFA and Sleep Disturbances?? > > > > I am new to the group and apologize if this issue has already been > addressed. I am desperate! My 4 year-old son has Apraxia (verbal). I > am thrilled to report that with intense private and public school > speech therapy (primarily Kaufman Method) over the last 11 months, he > is talking - a lot with a high degree of intelligibility. I started > him on ProEFA in August and did notice a difference - his physical > movements became more fluid and his articulation improved within 3 > weeks after commencement. However, at about the same time his sleep > patterns became terrible. He wakes frequently at night and seems > wired - wanting to talk, to go downstairs, to go outside, etc. His > diet is excellent, he is on no other medication (herbal or otherwise) > and his personality is even, not all at hyper. He just can't seem to > settle during the night, though we give the supplement in the morning. > Going to sleep is not an issue. Since any naps during the day are > brief, the child is perpetually exhausted. Has anyone had any similar > experience? Also, what happens if you stop the ProEFA, is there > regression? My whole family says to choose speech over sleep, but I > have to think the lack of sleep is going to be problematic, especially > with Kindergarden on the horizon. Any advice is appreciated. Thanks, > Kim. > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 1, 2007 Report Share Posted January 1, 2007 Kim and Dawn, When I read, " To the point where she is " flapping " her arms and legs- On the go- but staying in the same spot on the rug. know what i mean. " --it reminded me of my son. I don't know if either of your kids have sensory issues or not, but I'm remembering from past posts that EFAs can induce sensory behaviors. This has been our experience as well. I could not use Pro-EFA alone on my son as his sensory seeking behaviors worsened. It wasn't until we began using 800IUs of Vitamin E daily that I could add the Pro-EFA. On 200 IUs and 400 IUs the completely resolved sensory-seeking behavior would fully return even if I gave him just one capsule. I'm giving him 2 Pro-EFAs per day now and even on 800IUs I am seeing occasional, mild sensory-seeking behavior that was not there at all before the Pro EFA. But nothing that would cause me to stop the EFAs. EFAs oxidize Vitamin E, so if you are not using Vitamin E, the EFAs could be depleting the child's Vitamin E stores and inducing sensory issues that were not previously there. I mention this because when my son's proprioceptive-seeking behaviors were at their peak it would take forever to get him to sleep as he was constantly " on the move " - day and night. Even as an infant in his Baby Bjorn he would kick his arms and legs constantly and HAD to be held if you expected him to sleep at all (he needed the deep pressure sensation). Before I knew about sensory integration I would leave his room complaining that he was " doing everything to keep from falling asleep " . He had very restless limbs, needing to kick and push against his bed rails (or me). Now I know that his body was just craving that type of sensory input, poor little guy. He normally slept through the night, however. But when I first began EFA supplementation and things got worse, he began waking in the night with the restless legs. We were on a brushing/compression program through OT. He would wake and I could tell from his movements that he needed to be brushed, so I brushed him and he would fall back to sleep immediately. I stopped the EFA, began the Vitamin E one day and then literally overnight all proprioceptive-seeking behaviors stopped. Just thought I'd share as it sounds a lot like what we experienced. > > > > I am new to the group and apologize if this issue has already been > > addressed. I am desperate! My 4 year-old son has Apraxia > (verbal). I > > am thrilled to report that with intense private and public school > > speech therapy (primarily Kaufman Method) over the last 11 months, > he > > is talking - a lot with a high degree of intelligibility. I > started > > him on ProEFA in August and did notice a difference - his physical > > movements became more fluid and his articulation improved within 3 > > weeks after commencement. However, at about the same time his > sleep > > patterns became terrible. He wakes frequently at night and seems > > wired - wanting to talk, to go downstairs, to go outside, etc. > His > > diet is excellent, he is on no other medication (herbal or > otherwise) > > and his personality is even, not all at hyper. He just can't seem > to > > settle during the night, though we give the supplement in the > morning. > > Going to sleep is not an issue. Since any naps during the day are > > brief, the child is perpetually exhausted. Has anyone had any > similar > > experience? Also, what happens if you stop the ProEFA, is there > > regression? My whole family says to choose speech over sleep, but > I > > have to think the lack of sleep is going to be problematic, > especially > > with Kindergarden on the horizon. Any advice is appreciated. > Thanks, > > Kim. > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 1, 2007 Report Share Posted January 1, 2007 Thanks for the reply. I will look into that. He recoginizes about 5 signs that we do to him all the time. (Eat, drink, mom, dad, more) But because of his condition, he doesn't use his arms or hands much so signing is out for now. I was hoping that would be his form of communication but I was told we should look into other things. You're right signing time videos are awesome. We watch them all the time! _____ From: [mailto: ] On Behalf Of jerzmomof4 Sent: Monday, January 01, 2007 10:20 PM Subject: [ ] Re: Apraxia , ProEFA and Sleep Disturbances?? , Pro-EFA, is the " pro " fessional grade of EFA. EFA is essential fatty acids. Omega 3,6, which is fish oil. And Omega 9, from borage oil. Here is the companies website for lots of info. Although this product can be purcahsed elsewhere. And also, there are TONS of archives on the EFA topic. http://www.nordicna <http://www.nordicnaturals.com/> turals.com/ As far as his communication delay, have you thought about using sign language? I can tell you, we used it with my now 5 1/2 year old. It was the best thing I could have done for us. Vist SigningTime.Com for awesome dvd's. Dawn in NJ > > I am new to this group. Can someone tell me exact what is ProEFA? > > My son has not been diagnosed with Apraxia as of yet. He does have CBPS > > Which is going to be an issue for his speech if there is any at all. > > He is 17 months and doesn't say too much. We kind of got him to say what I > think was " elmo " but not positive, and he hasn't said it again since. > > He goes to speech therapy 2 x a week among other therapies. I am wondering > if there are other ways to help this area. > > > > > > <http://www.babyjell <http://www.babyjellybeans.com/web/do/site?ID=5864> ybeans.com/web/do/site?ID=5864> > http://www.babyjell <http://www.babyjellybeans.com/web/do/site?ID=5864> ybeans.com/web/do/site?ID=5864 > > > > > > _____ > > From: <mailto: %40> > [mailto: <mailto: %40> ] On Behalf Of mp8kdh > Sent: Monday, January 01, 2007 8:46 PM > <mailto: %40> > Subject: [ ] Apraxia , ProEFA and Sleep Disturbances?? > > > > I am new to the group and apologize if this issue has already been > addressed. I am desperate! My 4 year-old son has Apraxia (verbal). I > am thrilled to report that with intense private and public school > speech therapy (primarily Kaufman Method) over the last 11 months, he > is talking - a lot with a high degree of intelligibility. I started > him on ProEFA in August and did notice a difference - his physical > movements became more fluid and his articulation improved within 3 > weeks after commencement. However, at about the same time his sleep > patterns became terrible. He wakes frequently at night and seems > wired - wanting to talk, to go downstairs, to go outside, etc. His > diet is excellent, he is on no other medication (herbal or otherwise) > and his personality is even, not all at hyper. He just can't seem to > settle during the night, though we give the supplement in the morning. > Going to sleep is not an issue. Since any naps during the day are > brief, the child is perpetually exhausted. Has anyone had any similar > experience? Also, what happens if you stop the ProEFA, is there > regression? My whole family says to choose speech over sleep, but I > have to think the lack of sleep is going to be problematic, especially > with Kindergarden on the horizon. Any advice is appreciated. Thanks, > Kim. > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2007 Report Share Posted January 2, 2007 I am new to this group. Can someone tell me exact what is ProEFA? My son has not been diagnosed with Apraxia as of yet. He does have CBPS Which is going to be an issue for his speech if there is any at all. He is 17 months and doesn't say too much. We kind of got him to say what I think was " elmo " but not positive, and he hasn't said it again since. He goes to speech therapy 2 x a week among other therapies. I am wondering if there are other ways to help this area. <http://www.babyjellybeans.com/web/do/site?ID=5864> http://www.babyjellybeans.com/web/do/site?ID=5864 _____ From: [mailto: ] On Behalf Of mp8kdh Sent: Monday, January 01, 2007 8:46 PM Subject: [ ] Apraxia , ProEFA and Sleep Disturbances?? I am new to the group and apologize if this issue has already been addressed. I am desperate! My 4 year-old son has Apraxia (verbal). I am thrilled to report that with intense private and public school speech therapy (primarily Kaufman Method) over the last 11 months, he is talking - a lot with a high degree of intelligibility. I started him on ProEFA in August and did notice a difference - his physical movements became more fluid and his articulation improved within 3 weeks after commencement. However, at about the same time his sleep patterns became terrible. He wakes frequently at night and seems wired - wanting to talk, to go downstairs, to go outside, etc. His diet is excellent, he is on no other medication (herbal or otherwise) and his personality is even, not all at hyper. He just can't seem to settle during the night, though we give the supplement in the morning. Going to sleep is not an issue. Since any naps during the day are brief, the child is perpetually exhausted. Has anyone had any similar experience? Also, what happens if you stop the ProEFA, is there regression? My whole family says to choose speech over sleep, but I have to think the lack of sleep is going to be problematic, especially with Kindergarden on the horizon. Any advice is appreciated. Thanks, Kim. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2007 Report Share Posted January 2, 2007 Kim. Has this been ongoing since you started the efa's back in August? My daughter acts like this when we have increased, or when we restart after runnng out. We recently experienced this. She's been taking them for about a week now, and for the last several nights she wakes up in the middle of the night, but we can get her to go back in her bed and " rest " . And during the day she is very hyper.Constantly on the go. To the point where she is " flapping " her arms and legs- On the go- but staying in the same spot on the rug. know what i mean. How many EFA capsules does he take in the am? Dawn in NJ > > I am new to the group and apologize if this issue has already been > addressed. I am desperate! My 4 year-old son has Apraxia (verbal). I > am thrilled to report that with intense private and public school > speech therapy (primarily Kaufman Method) over the last 11 months, he > is talking - a lot with a high degree of intelligibility. I started > him on ProEFA in August and did notice a difference - his physical > movements became more fluid and his articulation improved within 3 > weeks after commencement. However, at about the same time his sleep > patterns became terrible. He wakes frequently at night and seems > wired - wanting to talk, to go downstairs, to go outside, etc. His > diet is excellent, he is on no other medication (herbal or otherwise) > and his personality is even, not all at hyper. He just can't seem to > settle during the night, though we give the supplement in the morning. > Going to sleep is not an issue. Since any naps during the day are > brief, the child is perpetually exhausted. Has anyone had any similar > experience? Also, what happens if you stop the ProEFA, is there > regression? My whole family says to choose speech over sleep, but I > have to think the lack of sleep is going to be problematic, especially > with Kindergarden on the horizon. Any advice is appreciated. Thanks, > Kim. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2007 Report Share Posted January 2, 2007 , Pro-EFA, is the " pro " fessional grade of EFA. EFA is essential fatty acids. Omega 3,6, which is fish oil. And Omega 9, from borage oil. Here is the companies website for lots of info. Although this product can be purcahsed elsewhere. And also, there are TONS of archives on the EFA topic. http://www.nordicnaturals.com/ As far as his communication delay, have you thought about using sign language? I can tell you, we used it with my now 5 1/2 year old. It was the best thing I could have done for us. Vist SigningTime.Com for awesome dvd's. Dawn in NJ > > I am new to this group. Can someone tell me exact what is ProEFA? > > My son has not been diagnosed with Apraxia as of yet. He does have CBPS > > Which is going to be an issue for his speech if there is any at all. > > He is 17 months and doesn't say too much. We kind of got him to say what I > think was " elmo " but not positive, and he hasn't said it again since. > > He goes to speech therapy 2 x a week among other therapies. I am wondering > if there are other ways to help this area. > > > > > > <http://www.babyjellybeans.com/web/do/site?ID=5864> > http://www.babyjellybeans.com/web/do/site?ID=5864 > > > > > > _____ > > From: > [mailto: ] On Behalf Of mp8kdh > Sent: Monday, January 01, 2007 8:46 PM > > Subject: [ ] Apraxia , ProEFA and Sleep Disturbances?? > > > > I am new to the group and apologize if this issue has already been > addressed. I am desperate! My 4 year-old son has Apraxia (verbal). I > am thrilled to report that with intense private and public school > speech therapy (primarily Kaufman Method) over the last 11 months, he > is talking - a lot with a high degree of intelligibility. I started > him on ProEFA in August and did notice a difference - his physical > movements became more fluid and his articulation improved within 3 > weeks after commencement. However, at about the same time his sleep > patterns became terrible. He wakes frequently at night and seems > wired - wanting to talk, to go downstairs, to go outside, etc. His > diet is excellent, he is on no other medication (herbal or otherwise) > and his personality is even, not all at hyper. He just can't seem to > settle during the night, though we give the supplement in the morning. > Going to sleep is not an issue. Since any naps during the day are > brief, the child is perpetually exhausted. Has anyone had any similar > experience? Also, what happens if you stop the ProEFA, is there > regression? My whole family says to choose speech over sleep, but I > have to think the lack of sleep is going to be problematic, especially > with Kindergarden on the horizon. Any advice is appreciated. Thanks, > Kim. > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2007 Report Share Posted January 2, 2007 Kim and Dawn, When I read, " To the point where she is " flapping " her arms and legs- On the go- but staying in the same spot on the rug. know what i mean. " --it reminded me of my son. I don't know if either of your kids have sensory issues or not, but I'm remembering from past posts that EFAs can induce sensory behaviors. This has been our experience as well. I could not use Pro-EFA alone on my son as his sensory seeking behaviors worsened. It wasn't until we began using 800IUs of Vitamin E daily that I could add the Pro-EFA. On 200 IUs and 400 IUs the completely resolved sensory-seeking behavior would fully return even if I gave him just one capsule. I'm giving him 2 Pro-EFAs per day now and even on 800IUs I am seeing occasional, mild sensory-seeking behavior that was not there at all before the Pro EFA. But nothing that would cause me to stop the EFAs. EFAs oxidize Vitamin E, so if you are not using Vitamin E, the EFAs could be depleting the child's Vitamin E stores and inducing sensory issues that were not previously there. I mention this because when my son's proprioceptive-seeking behaviors were at their peak it would take forever to get him to sleep as he was constantly " on the move " - day and night. Even as an infant in his Baby Bjorn he would kick his arms and legs constantly and HAD to be held if you expected him to sleep at all (he needed the deep pressure sensation). Before I knew about sensory integration I would leave his room complaining that he was " doing everything to keep from falling asleep " . He had very restless limbs, needing to kick and push against his bed rails (or me). Now I know that his body was just craving that type of sensory input, poor little guy. He normally slept through the night, however. But when I first began EFA supplementation and things got worse, he began waking in the night with the restless legs. We were on a brushing/compression program through OT. He would wake and I could tell from his movements that he needed to be brushed, so I brushed him and he would fall back to sleep immediately. I stopped the EFA, began the Vitamin E one day and then literally overnight all proprioceptive-seeking behaviors stopped. Just thought I'd share as it sounds a lot like what we experienced. > > > > I am new to the group and apologize if this issue has already been > > addressed. I am desperate! My 4 year-old son has Apraxia > (verbal). I > > am thrilled to report that with intense private and public school > > speech therapy (primarily Kaufman Method) over the last 11 months, > he > > is talking - a lot with a high degree of intelligibility. I > started > > him on ProEFA in August and did notice a difference - his physical > > movements became more fluid and his articulation improved within 3 > > weeks after commencement. However, at about the same time his > sleep > > patterns became terrible. He wakes frequently at night and seems > > wired - wanting to talk, to go downstairs, to go outside, etc. > His > > diet is excellent, he is on no other medication (herbal or > otherwise) > > and his personality is even, not all at hyper. He just can't seem > to > > settle during the night, though we give the supplement in the > morning. > > Going to sleep is not an issue. Since any naps during the day are > > brief, the child is perpetually exhausted. Has anyone had any > similar > > experience? Also, what happens if you stop the ProEFA, is there > > regression? My whole family says to choose speech over sleep, but > I > > have to think the lack of sleep is going to be problematic, > especially > > with Kindergarden on the horizon. Any advice is appreciated. > Thanks, > > Kim. > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2007 Report Share Posted January 2, 2007 Thanks for the reply. I will look into that. He recoginizes about 5 signs that we do to him all the time. (Eat, drink, mom, dad, more) But because of his condition, he doesn't use his arms or hands much so signing is out for now. I was hoping that would be his form of communication but I was told we should look into other things. You're right signing time videos are awesome. We watch them all the time! _____ From: [mailto: ] On Behalf Of jerzmomof4 Sent: Monday, January 01, 2007 10:20 PM Subject: [ ] Re: Apraxia , ProEFA and Sleep Disturbances?? , Pro-EFA, is the " pro " fessional grade of EFA. EFA is essential fatty acids. Omega 3,6, which is fish oil. And Omega 9, from borage oil. Here is the companies website for lots of info. Although this product can be purcahsed elsewhere. And also, there are TONS of archives on the EFA topic. http://www.nordicna <http://www.nordicnaturals.com/> turals.com/ As far as his communication delay, have you thought about using sign language? I can tell you, we used it with my now 5 1/2 year old. It was the best thing I could have done for us. Vist SigningTime.Com for awesome dvd's. Dawn in NJ > > I am new to this group. Can someone tell me exact what is ProEFA? > > My son has not been diagnosed with Apraxia as of yet. He does have CBPS > > Which is going to be an issue for his speech if there is any at all. > > He is 17 months and doesn't say too much. We kind of got him to say what I > think was " elmo " but not positive, and he hasn't said it again since. > > He goes to speech therapy 2 x a week among other therapies. I am wondering > if there are other ways to help this area. > > > > > > <http://www.babyjell <http://www.babyjellybeans.com/web/do/site?ID=5864> ybeans.com/web/do/site?ID=5864> > http://www.babyjell <http://www.babyjellybeans.com/web/do/site?ID=5864> ybeans.com/web/do/site?ID=5864 > > > > > > _____ > > From: <mailto: %40> > [mailto: <mailto: %40> ] On Behalf Of mp8kdh > Sent: Monday, January 01, 2007 8:46 PM > <mailto: %40> > Subject: [ ] Apraxia , ProEFA and Sleep Disturbances?? > > > > I am new to the group and apologize if this issue has already been > addressed. I am desperate! My 4 year-old son has Apraxia (verbal). I > am thrilled to report that with intense private and public school > speech therapy (primarily Kaufman Method) over the last 11 months, he > is talking - a lot with a high degree of intelligibility. I started > him on ProEFA in August and did notice a difference - his physical > movements became more fluid and his articulation improved within 3 > weeks after commencement. However, at about the same time his sleep > patterns became terrible. He wakes frequently at night and seems > wired - wanting to talk, to go downstairs, to go outside, etc. His > diet is excellent, he is on no other medication (herbal or otherwise) > and his personality is even, not all at hyper. He just can't seem to > settle during the night, though we give the supplement in the morning. > Going to sleep is not an issue. Since any naps during the day are > brief, the child is perpetually exhausted. Has anyone had any similar > experience? Also, what happens if you stop the ProEFA, is there > regression? My whole family says to choose speech over sleep, but I > have to think the lack of sleep is going to be problematic, especially > with Kindergarden on the horizon. Any advice is appreciated. Thanks, > Kim. > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2007 Report Share Posted January 2, 2007 > > > > > > I am new to the group and apologize if this issue has already > been > > > addressed. I am desperate! My 4 year-old son has Apraxia > > (verbal). I > > > am thrilled to report that with intense private and public school > > > speech therapy (primarily Kaufman Method) over the last 11 > months, > > he > > > is talking - a lot with a high degree of intelligibility. I > > started > > > him on ProEFA in August and did notice a difference - his > physical > > > movements became more fluid and his articulation improved within > 3 > > > weeks after commencement. However, at about the same time his > > sleep > > > patterns became terrible. He wakes frequently at night and seems > > > wired - wanting to talk, to go downstairs, to go outside, etc. > > His > > > diet is excellent, he is on no other medication (herbal or > > otherwise) > > > and his personality is even, not all at hyper. He just can't seem > > to > > > settle during the night, though we give the supplement in the > > morning. > > > Going to sleep is not an issue. Since any naps during the day > are > > > brief, the child is perpetually exhausted. Has anyone had any > > similar > > > experience? Also, what happens if you stop the ProEFA, is there > > > regression? My whole family says to choose speech over sleep, > but > > I > > > have to think the lack of sleep is going to be problematic, > > especially > > > with Kindergarden on the horizon. Any advice is appreciated. > > Thanks, > > > Kim. > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2007 Report Share Posted January 2, 2007 , Kim, and , and everyone else... I've alway thought Abby was exhibiting " ADHD " Type behaviors, rather then sensory seeking/sensory avoidance behaviors. The " flapping " of her arms/legs (constant motion) I perceived it to be hyperactiveness/impulsivity. Where maybe it was sensory seeking. She used to do the same thing(s) in bed, and in my arms as in infant- pusing against me, or the side of the rails, etc. However, then, I knew NOTHING of apraxia, or SID. I thought maybe it was gas, or pure restlessness. (Duhh huh) And now OMG- I am having such " light bulb " moments. She used to gag all the time on her food- she would over stuff her mouth and then gag on her food. One time, she sat in her high chair crying so hard- she was so hungry, she had food (pieces of a sandwhich I put in front of her) on her tongue, but yet couldn't feel it. I remember sitting there in total bewilderment not understanding this. (She was about 12- 13 months at the time) My point is...I just started the EFA/EPA supplements, and low and behold, she is gagging again. So my thinking is she has a lack of feeling in her oral cavity. Now, I've been giving her Vitamin E. I have " Source Natural's " Vitamin E, with 67 mg of mixed tocopherols. 400 iu. I give her one a day. I suppose I need to change her daily regiment of vit.E FYI- with the EFA/EPA came yet another surge. Today she clearly asked, " mom, who where are we going? " when i answered she said, " Oh ok, I just wondering " . And no that wasn't a typo.. she still confused her " WH " questions. For example the other day she asked, " Who are we eating for dinner? " My husband jokingly replied with a sick sense of humor, " no one, my little jeffrey dahmer " Of course she meant to say, " what is for dinner? " Dawn in NJ > > > > > > > > I am new to the group and apologize if this issue has already > > been > > > > addressed. I am desperate! My 4 year-old son has Apraxia > > > (verbal). I > > > > am thrilled to report that with intense private and public > school > > > > speech therapy (primarily Kaufman Method) over the last 11 > > months, > > > he > > > > is talking - a lot with a high degree of intelligibility. I > > > started > > > > him on ProEFA in August and did notice a difference - his > > physical > > > > movements became more fluid and his articulation improved > within > > 3 > > > > weeks after commencement. However, at about the same time his > > > sleep > > > > patterns became terrible. He wakes frequently at night and > seems > > > > wired - wanting to talk, to go downstairs, to go outside, > etc. > > > His > > > > diet is excellent, he is on no other medication (herbal or > > > otherwise) > > > > and his personality is even, not all at hyper. He just can't > seem > > > to > > > > settle during the night, though we give the supplement in the > > > morning. > > > > Going to sleep is not an issue. Since any naps during the day > > are > > > > brief, the child is perpetually exhausted. Has anyone had any > > > similar > > > > experience? Also, what happens if you stop the ProEFA, is > there > > > > regression? My whole family says to choose speech over sleep, > > but > > > I > > > > have to think the lack of sleep is going to be problematic, > > > especially > > > > with Kindergarden on the horizon. Any advice is appreciated. > > > Thanks, > > > > Kim. > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2007 Report Share Posted January 2, 2007 Yep - we are already giving Vit K (Life Extension Super K, the brand you use) squeezing out a scant capsule-full once a week. Our appointment with Dr. Agin is on Tuesday and I will definitely be discussing doses above 800IUs with her. I agree that he will probably benefit from more - his response with each increase has been phenomenal and I still see room for improvement. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2007 Report Share Posted January 2, 2007 > Your husband has my sort of warped sense of humor. Thanks for the chuckly. - When ph was still making errors...tr was pronounced " f " . So when he anounced that he want a big " Truck " for his birthday...it was not exactly taken well by the babysitter. - > , Kim, and , and everyone else... > > > I've alway thought Abby was exhibiting " ADHD " Type behaviors, rather > then sensory seeking/sensory avoidance behaviors. > > The " flapping " of her arms/legs (constant motion) I perceived it to > be hyperactiveness/impulsivity. Where maybe it was sensory seeking. > > She used to do the same thing(s) in bed, and in my arms as in infant- > pusing against me, or the side of the rails, etc. However, then, I > knew NOTHING of apraxia, or SID. I thought maybe it was gas, or pure > restlessness. (Duhh huh) > > And now OMG- I am having such " light bulb " moments. She used to gag > all the time on her food- she would over stuff her mouth and then gag > on her food. One time, she sat in her high chair crying so hard- she > was so hungry, she had food (pieces of a sandwhich I put in front of > her) on her tongue, but yet couldn't feel it. I remember sitting > there in total bewilderment not understanding this. (She was about 12- > 13 months at the time) > > My point is...I just started the EFA/EPA supplements, and low and > behold, she is gagging again. So my thinking is she has a lack of > feeling in her oral cavity. > > Now, I've been giving her Vitamin E. I have " Source Natural's " > Vitamin E, with 67 mg of mixed tocopherols. 400 iu. I give her one a > day. I suppose I need to change her daily regiment of vit.E > > > FYI- with the EFA/EPA came yet another surge. Today she clearly > asked, " mom, who where are we going? " when i answered she said, " Oh > ok, I just wondering " . > > And no that wasn't a typo.. she still confused her " WH " questions. > For example the other day she asked, " Who are we eating for dinner? " > My husband jokingly replied with a sick sense of humor, " no one, my little jeffrey dahmer " > Of course she meant to say, " what is for dinner? " > > > Dawn in NJ > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2007 Report Share Posted January 2, 2007 > > > > > > I am new to the group and apologize if this issue has already > been > > > addressed. I am desperate! My 4 year-old son has Apraxia > > (verbal). I > > > am thrilled to report that with intense private and public school > > > speech therapy (primarily Kaufman Method) over the last 11 > months, > > he > > > is talking - a lot with a high degree of intelligibility. I > > started > > > him on ProEFA in August and did notice a difference - his > physical > > > movements became more fluid and his articulation improved within > 3 > > > weeks after commencement. However, at about the same time his > > sleep > > > patterns became terrible. He wakes frequently at night and seems > > > wired - wanting to talk, to go downstairs, to go outside, etc. > > His > > > diet is excellent, he is on no other medication (herbal or > > otherwise) > > > and his personality is even, not all at hyper. He just can't seem > > to > > > settle during the night, though we give the supplement in the > > morning. > > > Going to sleep is not an issue. Since any naps during the day > are > > > brief, the child is perpetually exhausted. Has anyone had any > > similar > > > experience? Also, what happens if you stop the ProEFA, is there > > > regression? My whole family says to choose speech over sleep, > but > > I > > > have to think the lack of sleep is going to be problematic, > > especially > > > with Kindergarden on the horizon. Any advice is appreciated. > > Thanks, > > > Kim. > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2007 Report Share Posted January 2, 2007 Your welcome. And we enjoyed reading phs' birthday wish. I think we all need a good laugh every now and again. Dawn > > > Your husband has my sort of warped sense of humor. Thanks for the > chuckly. - > > When ph was still making errors...tr was pronounced " f " . > > So when he anounced that he want a big " Truck " for his birthday...it > was not exactly taken well by the babysitter. - > > > , Kim, and , and everyone else... > > > > > > I've alway thought Abby was exhibiting " ADHD " Type behaviors, > rather > > then sensory seeking/sensory avoidance behaviors. > > > > The " flapping " of her arms/legs (constant motion) I perceived it to > > be hyperactiveness/impulsivity. Where maybe it was sensory seeking. > > > > She used to do the same thing(s) in bed, and in my arms as in > infant- > > pusing against me, or the side of the rails, etc. However, then, I > > knew NOTHING of apraxia, or SID. I thought maybe it was gas, or > pure > > restlessness. (Duhh huh) > > > > And now OMG- I am having such " light bulb " moments. She used to gag > > all the time on her food- she would over stuff her mouth and then > gag > > on her food. One time, she sat in her high chair crying so hard- > she > > was so hungry, she had food (pieces of a sandwhich I put in front > of > > her) on her tongue, but yet couldn't feel it. I remember sitting > > there in total bewilderment not understanding this. (She was about > 12- > > 13 months at the time) > > > > My point is...I just started the EFA/EPA supplements, and low and > > behold, she is gagging again. So my thinking is she has a lack of > > feeling in her oral cavity. > > > > Now, I've been giving her Vitamin E. I have " Source Natural's " > > Vitamin E, with 67 mg of mixed tocopherols. 400 iu. I give her one > a > > day. I suppose I need to change her daily regiment of vit.E > > > > > > FYI- with the EFA/EPA came yet another surge. Today she clearly > > asked, " mom, who where are we going? " when i answered she said, " Oh > > ok, I just wondering " . > > > > And no that wasn't a typo.. she still confused her " WH " questions. > > For example the other day she asked, " Who are we eating for > dinner? " > > My husband jokingly replied with a sick sense of humor, " no one, > my little jeffrey dahmer " > > Of course she meant to say, " what is for dinner? " > > > > > > Dawn in NJ > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 3, 2007 Report Share Posted January 3, 2007 , Kim, and , and everyone else... I've alway thought Abby was exhibiting " ADHD " Type behaviors, rather then sensory seeking/sensory avoidance behaviors. The " flapping " of her arms/legs (constant motion) I perceived it to be hyperactiveness/impulsivity. Where maybe it was sensory seeking. She used to do the same thing(s) in bed, and in my arms as in infant- pusing against me, or the side of the rails, etc. However, then, I knew NOTHING of apraxia, or SID. I thought maybe it was gas, or pure restlessness. (Duhh huh) And now OMG- I am having such " light bulb " moments. She used to gag all the time on her food- she would over stuff her mouth and then gag on her food. One time, she sat in her high chair crying so hard- she was so hungry, she had food (pieces of a sandwhich I put in front of her) on her tongue, but yet couldn't feel it. I remember sitting there in total bewilderment not understanding this. (She was about 12- 13 months at the time) My point is...I just started the EFA/EPA supplements, and low and behold, she is gagging again. So my thinking is she has a lack of feeling in her oral cavity. Now, I've been giving her Vitamin E. I have " Source Natural's " Vitamin E, with 67 mg of mixed tocopherols. 400 iu. I give her one a day. I suppose I need to change her daily regiment of vit.E FYI- with the EFA/EPA came yet another surge. Today she clearly asked, " mom, who where are we going? " when i answered she said, " Oh ok, I just wondering " . And no that wasn't a typo.. she still confused her " WH " questions. For example the other day she asked, " Who are we eating for dinner? " My husband jokingly replied with a sick sense of humor, " no one, my little jeffrey dahmer " Of course she meant to say, " what is for dinner? " Dawn in NJ > > > > > > > > I am new to the group and apologize if this issue has already > > been > > > > addressed. I am desperate! My 4 year-old son has Apraxia > > > (verbal). I > > > > am thrilled to report that with intense private and public > school > > > > speech therapy (primarily Kaufman Method) over the last 11 > > months, > > > he > > > > is talking - a lot with a high degree of intelligibility. I > > > started > > > > him on ProEFA in August and did notice a difference - his > > physical > > > > movements became more fluid and his articulation improved > within > > 3 > > > > weeks after commencement. However, at about the same time his > > > sleep > > > > patterns became terrible. He wakes frequently at night and > seems > > > > wired - wanting to talk, to go downstairs, to go outside, > etc. > > > His > > > > diet is excellent, he is on no other medication (herbal or > > > otherwise) > > > > and his personality is even, not all at hyper. He just can't > seem > > > to > > > > settle during the night, though we give the supplement in the > > > morning. > > > > Going to sleep is not an issue. Since any naps during the day > > are > > > > brief, the child is perpetually exhausted. Has anyone had any > > > similar > > > > experience? Also, what happens if you stop the ProEFA, is > there > > > > regression? My whole family says to choose speech over sleep, > > but > > > I > > > > have to think the lack of sleep is going to be problematic, > > > especially > > > > with Kindergarden on the horizon. Any advice is appreciated. > > > Thanks, > > > > Kim. > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 3, 2007 Report Share Posted January 3, 2007 Yep - we are already giving Vit K (Life Extension Super K, the brand you use) squeezing out a scant capsule-full once a week. Our appointment with Dr. Agin is on Tuesday and I will definitely be discussing doses above 800IUs with her. I agree that he will probably benefit from more - his response with each increase has been phenomenal and I still see room for improvement. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 3, 2007 Report Share Posted January 3, 2007 > Your husband has my sort of warped sense of humor. Thanks for the chuckly. - When ph was still making errors...tr was pronounced " f " . So when he anounced that he want a big " Truck " for his birthday...it was not exactly taken well by the babysitter. - > , Kim, and , and everyone else... > > > I've alway thought Abby was exhibiting " ADHD " Type behaviors, rather > then sensory seeking/sensory avoidance behaviors. > > The " flapping " of her arms/legs (constant motion) I perceived it to > be hyperactiveness/impulsivity. Where maybe it was sensory seeking. > > She used to do the same thing(s) in bed, and in my arms as in infant- > pusing against me, or the side of the rails, etc. However, then, I > knew NOTHING of apraxia, or SID. I thought maybe it was gas, or pure > restlessness. (Duhh huh) > > And now OMG- I am having such " light bulb " moments. She used to gag > all the time on her food- she would over stuff her mouth and then gag > on her food. One time, she sat in her high chair crying so hard- she > was so hungry, she had food (pieces of a sandwhich I put in front of > her) on her tongue, but yet couldn't feel it. I remember sitting > there in total bewilderment not understanding this. (She was about 12- > 13 months at the time) > > My point is...I just started the EFA/EPA supplements, and low and > behold, she is gagging again. So my thinking is she has a lack of > feeling in her oral cavity. > > Now, I've been giving her Vitamin E. I have " Source Natural's " > Vitamin E, with 67 mg of mixed tocopherols. 400 iu. I give her one a > day. I suppose I need to change her daily regiment of vit.E > > > FYI- with the EFA/EPA came yet another surge. Today she clearly > asked, " mom, who where are we going? " when i answered she said, " Oh > ok, I just wondering " . > > And no that wasn't a typo.. she still confused her " WH " questions. > For example the other day she asked, " Who are we eating for dinner? " > My husband jokingly replied with a sick sense of humor, " no one, my little jeffrey dahmer " > Of course she meant to say, " what is for dinner? " > > > Dawn in NJ > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 3, 2007 Report Share Posted January 3, 2007 Your welcome. And we enjoyed reading phs' birthday wish. I think we all need a good laugh every now and again. Dawn > > > Your husband has my sort of warped sense of humor. Thanks for the > chuckly. - > > When ph was still making errors...tr was pronounced " f " . > > So when he anounced that he want a big " Truck " for his birthday...it > was not exactly taken well by the babysitter. - > > > , Kim, and , and everyone else... > > > > > > I've alway thought Abby was exhibiting " ADHD " Type behaviors, > rather > > then sensory seeking/sensory avoidance behaviors. > > > > The " flapping " of her arms/legs (constant motion) I perceived it to > > be hyperactiveness/impulsivity. Where maybe it was sensory seeking. > > > > She used to do the same thing(s) in bed, and in my arms as in > infant- > > pusing against me, or the side of the rails, etc. However, then, I > > knew NOTHING of apraxia, or SID. I thought maybe it was gas, or > pure > > restlessness. (Duhh huh) > > > > And now OMG- I am having such " light bulb " moments. She used to gag > > all the time on her food- she would over stuff her mouth and then > gag > > on her food. One time, she sat in her high chair crying so hard- > she > > was so hungry, she had food (pieces of a sandwhich I put in front > of > > her) on her tongue, but yet couldn't feel it. I remember sitting > > there in total bewilderment not understanding this. (She was about > 12- > > 13 months at the time) > > > > My point is...I just started the EFA/EPA supplements, and low and > > behold, she is gagging again. So my thinking is she has a lack of > > feeling in her oral cavity. > > > > Now, I've been giving her Vitamin E. I have " Source Natural's " > > Vitamin E, with 67 mg of mixed tocopherols. 400 iu. I give her one > a > > day. I suppose I need to change her daily regiment of vit.E > > > > > > FYI- with the EFA/EPA came yet another surge. Today she clearly > > asked, " mom, who where are we going? " when i answered she said, " Oh > > ok, I just wondering " . > > > > And no that wasn't a typo.. she still confused her " WH " questions. > > For example the other day she asked, " Who are we eating for > dinner? " > > My husband jokingly replied with a sick sense of humor, " no one, > my little jeffrey dahmer " > > Of course she meant to say, " what is for dinner? " > > > > > > Dawn in NJ > > > > > Quote Link to comment Share on other sites More sharing options...
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