Guest guest Posted March 13, 2003 Report Share Posted March 13, 2003 I know someone has posted about this, but I can't find the old post. Maybe I didn't look hard enough. lol Anyway I just recieved the liquid ProEFA from Nordic Naturals & it says to give 1/2 teaspoon once a day. My daughter is 2 & weighs about 28 lbs. Is this dosage right for her or should I cut it down some? Wendie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 13, 2003 Report Share Posted March 13, 2003 Wendie: I just got off the phone with nordic naturals. He told me 5ml. per 5 lbs. So if your child weighed 10lbs. you would give 10ml. 2x a day. in Phoenix [ ] ProEFA Dosage > I know someone has posted about this, but I can't find the old post. > Maybe I didn't look hard enough. lol Anyway I just recieved the > liquid ProEFA from Nordic Naturals & it says to give 1/2 teaspoon > once a day. My daughter is 2 & weighs about 28 lbs. Is this dosage > right for her or should I cut it down some? > Wendie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 13, 2003 Report Share Posted March 13, 2003 I would not think that is right. 5 ml = 1 teaspoon. That would mean if your child weighed 25 pounds you would give them 25 ml (5 teaspoons). I would double check with Nordic Naturals, I tried to call them but unfortunately they are closed right now. Their number is 1-800-662-2544. Re: [ ] ProEFA Dosage Wendie: I just got off the phone with nordic naturals. He told me 5ml. per 5 lbs. So if your child weighed 10lbs. you would give 10ml. 2x a day. in Phoenix Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 13, 2003 Report Share Posted March 13, 2003 Thanks , I appreciate that!! Wendie > Wendie: > > I just got off the phone with nordic naturals. He told me 5ml. per 5 lbs. > So if your child weighed 10lbs. you would give 10ml. 2x a day. > > in Phoenix Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 14, 2003 Report Share Posted March 14, 2003 Has anyone checked on this? ..... because that dosage does not sound right to me! IMO, it's best to start off with the 1/2 tsp/once a day (or 1 capsule of Proefa) and then go from there. " Wendie:I just got off the phone with nordic naturals. He told me 5ml. per 5 lbs.So if your child weighed 10lbs. you would give 10ml. 2x a day. in Phoenix " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 14, 2003 Report Share Posted March 14, 2003 Thank you Traci for saying what I've been biting my lip not to say. 5 ml. per 5 pounds?! And I'm 115 pounds so that means...(OK no longer biting my lip -now I'm laughing hysterically) When I talked about drinking glasses of fish oil like water (yuck) that was just (I thought) a joke. Need I remind everyone that Nordic Naturals is a company -a great company -but just a company. Who died and made them the experts when it's our group -CHERAB -and the work that we have done - that has the answers to what has worked for most of our children? Nordic Naturals has no clinical proof to quote since clinical research for our children has not been done yet. We have overwhelming anecdotal results with " one capsule a day -then two when a plateau. Then instead of three -do two ProEFA and one ProEPA " Simple enough. How do we translate that to teaspoons when one capsule isn't anywhere near a teaspoon or even a half a teaspoon -neither is two capsules! In addition to searching past results -which based on overwhelming results you have to take notice of -I myself tend to search for answers from medical doctors and online through reputable sources. I will also not discuss any oil dosage outside of capsules since capsules are the best way to keep track of how much we are giving our children. I knew this pure oil would be a problem outside of the fact that my son Tanner hates the taste of it. I'm sticking to the capsules and have no problem continuing to let you guys know what " most " of us have found to be the best dosage with the capsules. Until hundreds of you give your child the oil and can then months and years later come back again and again to report any positives or negatives on whatever dosages you are using -I'm staying out of this. Good luck! ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 30, 2003 Report Share Posted May 30, 2003 I am new to posting. I have a son, 21 months old who was recently diagnosed with a dev. Delay (two days after I gave birth to our daughter). He appears to be dyspraxic. He is not speaking other than " tic tic " for tickle tickle and he has said bye, done, and again once or twice in the past. He prefers to be carried down the stairs and be fed, although he can do both (backs down the stairs). Mama & dada were rarely used to address us. He has a tendency to get hyperfocused during play and will make this continuous humming noise. His eye contact is usually brief. I recently ordered ProEFA and have been giving him the 1000 mg capsule in his orange juice for less than a week. My question is how much should his dosage be and is there any liquid ProEFA available? I don't mind breaking the capsule, but thought the liquid version may be easier. My husband & I both started taking the ProEFA too especially since I'm breastfeeding our 6 week old daughter. My son also tilts his head to the side and rubs his ears a lot. We recently had his ears flushed because he had an ongoing problem with ear wax. He has only had one ear infection. We are in the process of getting him tested for allergies since they run in our family. I'm trying not to get discouraged right now because we are on a waiting list for therapy with early intervention. We are looking into private therapy in a clinic setting until we get some home based therapy. Does anyone have advice or opinions on sensory integration therapy? Some of my son's sensory issues are walking on his tip toes, enjoying deep pressure (crawls under things and enjoys ball pits), lifting heavy things, visual enjoyment from dropping or throwing toys. This is getting a little long so I'll close for now. I appreciate any words of wisdom. We are trying to get involved with a local family support network, but are having a hard time getting them to contact us (which is discouraging when one is looking for advice and understanding). Mom to on, age 21 months w/dev. Delay (dyspraxia ?) and , 6 weeks Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 30, 2003 Report Share Posted May 30, 2003 Hi , You son sounds similar in ways to my 24 month old daughter. As far as expressive language they could be twins. My daughter has repeated 3-4 words but once and has one word now... " up " . I started Georgia on ProEFA 4 weeks ago. 3 weeks in she started using the word UP more than once and last night we heard " ball " . My daughter has no other cognitive issues but does have some muscle weakness attributed to hypotonia - that she is growing out of. knock on wood. I personally think the capsule is the best bet. I have heard continuous posts about liquid store bought EFAs - as a PRECAUTION. Store bought liquid EFAs are ususually rancid - be careful. Oxygen and fish oil don't mix. Nordic Naturals is reputable and you have the assurance of premium quality. Plus you can buy in bulk - they don't go bad. The throwing toys and watching them drop, and the lifting things sounds pretty normal for a 20 month old. Just my oppinion.. But the whole point of my post is that I actually started to see a moderate improvement in my daughter's speech and sounds when I started buying Beechnut's baby food with added DHA. (60 mg.) IN ADDITION TO PROEFA. I have been giving her 1-2 jars a day plus one capsule DHA and that is when we saw the difference. I use it at snack time...their pasta medley or banana creme desert w/DHA. Perhaps she just needed that boost......hope my ideas can help you. Sorry i have no experince w/sensory integration issues..but many group members here do. Hopefully you will hear more info from them. I so know about feeling desperate for outreach and help......it is so important when you are feeling stressed and worried. (I am currently feeling super upset...waiting for test results right now.) I am new too and I don't have much to tell you, but I thought at least acknowledging your post would be helpfull for you. Good luck w/ on & congrats on your new baby. is >From: " & Bracy " <wbracy@...> >Reply- >< > >Subject: RE: [ ] ProEFA dosage >Date: Fri, 30 May 2003 16:13:46 -0400 > >I am new to posting. I have a son, 21 months old who was recently >diagnosed with a dev. Delay (two days after I gave birth to our >daughter). He appears to be dyspraxic. He is not speaking other than > " tic tic " for tickle tickle and he has said bye, done, and again once or >twice in the past. He prefers to be carried down the stairs and be fed, >although he can do both (backs down the stairs). Mama & dada were >rarely used to address us. He has a tendency to get hyperfocused during >play and will make this continuous humming noise. His eye contact is >usually brief. I recently ordered ProEFA and have been giving him the >1000 mg capsule in his orange juice for less than a week. My question >is how much should his dosage be and is there any liquid ProEFA >available? I don't mind breaking the capsule, but thought the liquid >version may be easier. My husband & I both started taking the ProEFA >too especially since I'm breastfeeding our 6 week old daughter. My son >also tilts his head to the side and rubs his ears a lot. We recently >had his ears flushed because he had an ongoing problem with ear wax. He >has only had one ear infection. We are in the process of getting him >tested for allergies since they run in our family. I'm trying not to >get discouraged right now because we are on a waiting list for therapy >with early intervention. We are looking into private therapy in a >clinic setting until we get some home based therapy. Does anyone have >advice or opinions on sensory integration therapy? Some of my son's >sensory issues are walking on his tip toes, enjoying deep pressure >(crawls under things and enjoys ball pits), lifting heavy things, visual >enjoyment from dropping or throwing toys. This is getting a little long >so I'll close for now. I appreciate any words of wisdom. We are trying >to get involved with a local family support network, but are having a >hard time getting them to contact us (which is discouraging when one is >looking for advice and understanding). > >Mom to on, age 21 months w/dev. Delay (dyspraxia ?) >and , 6 weeks > > > > > > > > _________________________________________________________________ MSN 8 with e-mail virus protection service: 2 months FREE* http://join.msn.com/?page=features/virus Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 30, 2003 Report Share Posted May 30, 2003 Hello . My name is Kim. My son was 13 months old when my daughter was born so I can relate to all of the emotions you are experiencing with zero sleep. An Occupational Therapist can provide therapy for Sensory Integration issues and can give you more information on the disorder as well as some things you could probably do at home with and for your son. There are many websites with information on the subject as well as the book, The Out of Synch Child, by Carol Stock Kranowitz, M.A. among others. You're really in a good position to be getting such a good head start with your son's therapy. Early Intervention makes a huge difference in most cases. My son only said a hand full of words at 21 months. The only word he said with any consistency was " Mama " . He began Speech Therapy (speech delay) and Occupational Therapy (Sensory Integration Issues) at 27 months old. He probably said 10-12 words at that time. Today he is 34 1/2 months old and has 225+ words. We're seeing a Ped. Neurologist in July. He still has a speech delay (possible apraxia?) and he still exhibits many sensory integration dysfunction symptoms. We started on the Pro-EFA April 10th and have seen amazing results! I applaud you for taking the Pro-EFA while breastfeeding. I wish I had known about it long b/4 I ever got pregnant for the 1st time myself. My son walks on his tip toes sometimes too and prefers to eat with his fingers rather than with his fork or spoon. I could go on and on as well. I just wanted to reach out to you and let you know I'm here if you need to talk. Feel free to e-mail me privately as well. This is a good group and I've learned a great deal from all of the people who post here. RE: [ ] ProEFA dosage I am new to posting. I have a son, 21 months old who was recently diagnosed with a dev. Delay (two days after I gave birth to our daughter). He appears to be dyspraxic. He is not speaking other than " tic tic " for tickle tickle and he has said bye, done, and again once or twice in the past. He prefers to be carried down the stairs and be fed, although he can do both (backs down the stairs). Mama & dada were rarely used to address us. He has a tendency to get hyperfocused during play and will make this continuous humming noise. His eye contact is usually brief. I recently ordered ProEFA and have been giving him the 1000 mg capsule in his orange juice for less than a week. My question is how much should his dosage be and is there any liquid ProEFA available? I don't mind breaking the capsule, but thought the liquid version may be easier. My husband & I both started taking the ProEFA too especially since I'm breastfeeding our 6 week old daughter. My son also tilts his head to the side and rubs his ears a lot. We recently had his ears flushed because he had an ongoing problem with ear wax. He has only had one ear infection. We are in the process of getting him tested for allergies since they run in our family. I'm trying not to get discouraged right now because we are on a waiting list for therapy with early intervention. We are looking into private therapy in a clinic setting until we get some home based therapy. Does anyone have advice or opinions on sensory integration therapy? Some of my son's sensory issues are walking on his tip toes, enjoying deep pressure (crawls under things and enjoys ball pits), lifting heavy things, visual enjoyment from dropping or throwing toys. This is getting a little long so I'll close for now. I appreciate any words of wisdom. We are trying to get involved with a local family support network, but are having a hard time getting them to contact us (which is discouraging when one is looking for advice and understanding). Mom to on, age 21 months w/dev. Delay (dyspraxia ?) and , 6 weeks Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2003 Report Share Posted June 2, 2003 is, Thanks for writing back and for the info. You shared. It is exciting to hear about Georgia's progress! I am actually an O.T., but don't have a lot of experience with SI or apraxia. on has been on the ProEFA for less than a week, but we did see something encouraging the other day. He tried to imitate another boy at the playground and hop on one foot. We haven't noticed any changes in his speech yet, but we realize it can take some time. I did get some Beech Nut baby food to try and I will definitely consider that when my daughter starts eating solids. Did you get the test results back that you mentioned? I hope everything is o.k. We are finally going to be starting therapy next week! Thanks again for the encouragement. RE: [ ] ProEFA dosage Hi , You son sounds similar in ways to my 24 month old daughter. As far as expressive language they could be twins. My daughter has repeated 3-4 words but once and has one word now... " up " . I started Georgia on ProEFA 4 weeks ago. 3 weeks in she started using the word UP more than once and last night we heard " ball " . My daughter has no other cognitive issues but does have some muscle weakness attributed to hypotonia - that she is growing out of. knock on wood. I personally think the capsule is the best bet. I have heard continuous posts about liquid store bought EFAs - as a PRECAUTION. Store bought liquid EFAs are ususually rancid - be careful. Oxygen and fish oil don't mix. Nordic Naturals is reputable and you have the assurance of premium quality. Plus you can buy in bulk - they don't go bad. The throwing toys and watching them drop, and the lifting things sounds pretty normal for a 20 month old. Just my oppinion.. But the whole point of my post is that I actually started to see a moderate improvement in my daughter's speech and sounds when I started buying Beechnut's baby food with added DHA. (60 mg.) IN ADDITION TO PROEFA. I have been giving her 1-2 jars a day plus one capsule DHA and that is when we saw the difference. I use it at snack time...their pasta medley or banana creme desert w/DHA. Perhaps she just needed that boost......hope my ideas can help you. Sorry i have no experince w/sensory integration issues..but many group members here do. Hopefully you will hear more info from them. I so know about feeling desperate for outreach and help......it is so important when you are feeling stressed and worried. (I am currently feeling super upset...waiting for test results right now.) I am new too and I don't have much to tell you, but I thought at least acknowledging your post would be helpfull for you. Good luck w/ on & congrats on your new baby. is Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2003 Report Share Posted June 2, 2003 Hi , , That's great about starting therapy next week - we are still waiting for the blood tests and we have an MRI scheduled for next month. I have been reasured that everything will most likely show up normal - Georgia has mild hypotonia - do you have experince working as an OT with hypotonic children? We have not been referred to an OT, only a PT. Feel free to email me personally if you want to swap questions, share info and support... is alexisryan@... >From: " & Bracy " <wbracy@...> >Reply- >< > >Subject: RE: [ ] ProEFA dosage >Date: Mon, 2 Jun 2003 12:43:19 -0400 > >is, >Thanks for writing back and for the info. You shared. It is exciting to >hear about Georgia's progress! I am actually an O.T., but don't have a >lot of experience with SI or apraxia. on has been on the ProEFA >for less than a week, but we did see something encouraging the other >day. He tried to imitate another boy at the playground and hop on one >foot. We haven't noticed any changes in his speech yet, but we realize >it can take some time. I did get some Beech Nut baby food to try and I >will definitely consider that when my daughter starts eating solids. >Did you get the test results back that you mentioned? I hope everything >is o.k. We are finally going to be starting therapy next week! Thanks >again for the encouragement. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 16, 2005 Report Share Posted January 16, 2005 Sorry...I forget you all don't know Ben! He's about 30 pounds and has only been on ProEFA for two full weeks. I give him one capsule of ProEFA daily and have given a ProEPA about 3-4 different times later in the day (so he'd be getting a total of two capsules on those days). I read in the Late Talker (p. 111) that a boy was getting 3000-mg Omega-3 so I thought giving Ben two capsules/day would be ok. That's why he gets one ProEFA daily and, on occassion, I add a ProEPA. I'd like to give both each day but don't want to overwhelm his system- if that's possible. I'm always a bit cautious giving my kids new " stuff " so I decided to post to get some " advice " . Thank you for replying! Cheryl > > > Can anyone give me some insight on how to know the accurate dosage > of ProEFA to give my son?? I give him one ProEFA daily and have, on > occasion, given him a ProEPA also. > > Cheryl > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
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