Guest guest Posted October 13, 2006 Report Share Posted October 13, 2006 Squeezing the oil from the capsule is probably better than the liquid, since the liquid is a bit unstable over time. There is DHA in the EFA. I would go with what the group has seen as working with the apraxic kids. We started out with pure DHA and has some problems with it. Start with 2 capsule EFA and 1 capsule EPA (which is the uquivalent of 3/4 tsp) and give this twice a day. Its similar to what your ped is recommending, but more catered to apraxia (all anecdotal info though). You ped is open-minded and has read the literature on benefits of omega 3 in developing brains etc...but the focus in the literatur has been DHA and not EPA...it is only recently that EPA is thought to maybe be as important if not more important than DHA. The vitamin E at 400 - 800 IU is totally safe. Just use the natural (alpha d-tocophorol, not " dl " ) Worth trying. > hi, > > my 2.5 yr.old son has ASD and verbal apraxia. i mentioned to our > neuro-dev.pediatrician that we were interested in trying supplements > such as ProEFA. She recommended that we give Ian 1/2 tsp-1 tsp of > Nordic Naturals Children's DHA and 1/2 tsp-1 tsp of ProEFA. I > noticed that a lot of people have been giving something like: 2 > ProEFA capsules, 1 EPA, and 400 IU vitamin E... haven't heard too > much about the DHA here so I was wondering if I should just do what > everyone else is doing and not follow what the pediatrician is > suggesting...why is she suggesting DHA? doesn't the ProEFA already > have DHA anyways? also, does it make a difference whether i use the > liquid or capsule form of ProEFA? the doctor doesn't seem too keen > on the vitamin E idea either, but we are really wanting to try it > since reading all the positive responses here... > > anyways, if anyone has any suggestions/info., please help! i would > really appreciate it. > > thanks so much, > ingrid > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 13, 2006 Report Share Posted October 13, 2006 Why not offer to share this discussion group with your ped? We all learn new things in various ways. You could give her the links, or maybe even go into the archives and print out a comprehensive journal of sorts. Look, we've all had it beat into our skulls that Dr.'s word is basically " God " . They are just people with a bank of knowledge. They are largely influenced by the drug companies. They have busy lives and most of them actually do believe they are God. This discussion group is the front line. If I've leaned one thing, it's I am totally in charge of working this problem and to listen to my instincts. It's hard sometimes because we just want to be lead by the hand in face of such uncertainty...our childs' future. If a Dr. is not giving you the warm and fuzzies...doesn't seem to be open or up to date. Just move on. For this problem, we need open minded professionals dedicated to the complexities of our kids. That's it. > > hi, > > my 2.5 yr.old son has ASD and verbal apraxia. i mentioned to our > neuro-dev.pediatrician that we were interested in trying supplements > such as ProEFA. She recommended that we give Ian 1/2 tsp-1 tsp of > Nordic Naturals Children's DHA and 1/2 tsp-1 tsp of ProEFA. I > noticed that a lot of people have been giving something like: 2 > ProEFA capsules, 1 EPA, and 400 IU vitamin E... haven't heard too > much about the DHA here so I was wondering if I should just do what > everyone else is doing and not follow what the pediatrician is > suggesting...why is she suggesting DHA? doesn't the ProEFA already > have DHA anyways? also, does it make a difference whether i use the > liquid or capsule form of ProEFA? the doctor doesn't seem too keen > on the vitamin E idea either, but we are really wanting to try it > since reading all the positive responses here... > > anyways, if anyone has any suggestions/info., please help! i would > really appreciate it. > > thanks so much, > ingrid > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 13, 2006 Report Share Posted October 13, 2006 Squeezing the oil from the capsule is probably better than the liquid, since the liquid is a bit unstable over time. There is DHA in the EFA. I would go with what the group has seen as working with the apraxic kids. We started out with pure DHA and has some problems with it. Start with 2 capsule EFA and 1 capsule EPA (which is the uquivalent of 3/4 tsp) and give this twice a day. Its similar to what your ped is recommending, but more catered to apraxia (all anecdotal info though). You ped is open-minded and has read the literature on benefits of omega 3 in developing brains etc...but the focus in the literatur has been DHA and not EPA...it is only recently that EPA is thought to maybe be as important if not more important than DHA. The vitamin E at 400 - 800 IU is totally safe. Just use the natural (alpha d-tocophorol, not " dl " ) Worth trying. > hi, > > my 2.5 yr.old son has ASD and verbal apraxia. i mentioned to our > neuro-dev.pediatrician that we were interested in trying supplements > such as ProEFA. She recommended that we give Ian 1/2 tsp-1 tsp of > Nordic Naturals Children's DHA and 1/2 tsp-1 tsp of ProEFA. I > noticed that a lot of people have been giving something like: 2 > ProEFA capsules, 1 EPA, and 400 IU vitamin E... haven't heard too > much about the DHA here so I was wondering if I should just do what > everyone else is doing and not follow what the pediatrician is > suggesting...why is she suggesting DHA? doesn't the ProEFA already > have DHA anyways? also, does it make a difference whether i use the > liquid or capsule form of ProEFA? the doctor doesn't seem too keen > on the vitamin E idea either, but we are really wanting to try it > since reading all the positive responses here... > > anyways, if anyone has any suggestions/info., please help! i would > really appreciate it. > > thanks so much, > ingrid > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 13, 2006 Report Share Posted October 13, 2006 Why not offer to share this discussion group with your ped? We all learn new things in various ways. You could give her the links, or maybe even go into the archives and print out a comprehensive journal of sorts. Look, we've all had it beat into our skulls that Dr.'s word is basically " God " . They are just people with a bank of knowledge. They are largely influenced by the drug companies. They have busy lives and most of them actually do believe they are God. This discussion group is the front line. If I've leaned one thing, it's I am totally in charge of working this problem and to listen to my instincts. It's hard sometimes because we just want to be lead by the hand in face of such uncertainty...our childs' future. If a Dr. is not giving you the warm and fuzzies...doesn't seem to be open or up to date. Just move on. For this problem, we need open minded professionals dedicated to the complexities of our kids. That's it. > > hi, > > my 2.5 yr.old son has ASD and verbal apraxia. i mentioned to our > neuro-dev.pediatrician that we were interested in trying supplements > such as ProEFA. She recommended that we give Ian 1/2 tsp-1 tsp of > Nordic Naturals Children's DHA and 1/2 tsp-1 tsp of ProEFA. I > noticed that a lot of people have been giving something like: 2 > ProEFA capsules, 1 EPA, and 400 IU vitamin E... haven't heard too > much about the DHA here so I was wondering if I should just do what > everyone else is doing and not follow what the pediatrician is > suggesting...why is she suggesting DHA? doesn't the ProEFA already > have DHA anyways? also, does it make a difference whether i use the > liquid or capsule form of ProEFA? the doctor doesn't seem too keen > on the vitamin E idea either, but we are really wanting to try it > since reading all the positive responses here... > > anyways, if anyone has any suggestions/info., please help! i would > really appreciate it. > > thanks so much, > ingrid > Quote Link to comment Share on other sites More sharing options...
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