Guest guest Posted December 10, 2006 Report Share Posted December 10, 2006 Hi, my name is and I am joining this group to learn ways to help my son, Cordis - almost 3, who is non-verbal. A brief history: Cordis was diagnosed with Infantile Spasms (a severe form of infant epilepsy) at 6.5 mos, though we suspect he began seizing at 4 mos (our doctors thought it was normal when we talked about it, but not when they saw it on video). Anyway, he had uncontrolled seizures (sometimes 100+/day) for about a year and tried 8 meds and the ketogenic diet before he just stopped seizing. We suspect he grew out of the Infantile Spasms. While seizing, his development was at a standstill. He could roll (occasionally) and sit (with some support) but had poor eye contact and was very cognitively delayed. Once the seizures stopped he moved rapidly to crawling, cruising, walking, running. Physically he's pretty typical. Cognitively he is still quite delayed (functioning at between 9-15 mos) and really only makes a couple of sounds ( " bah " , " dada " , and the occasional " mo " ). He does some signing (more, drink, music, chip, cookie, phone) but is not consistent with using the correct sign for what he wants. He's in a non-cat special-ed preschool 5 mornings/week where he gets ST, PT, OT, gets private speech and private OT once a week, and is in ABA/VB therapy 5 days a week for 1 hour/day (though we do not believe he is autistic - we just think it's great therapy). We are also currently doing 40 HBOT dives (we've done 11 so far) and are hearing more sounds (the " dada " just appeared in the last couple of days). We are having his tongue-tie clipped on 1/04/06 because the ear/nose/throat doctor and his speech therapist feel this is just one more obstacle to overcome in a kid with lots of issues. I have a couple of questions re: Vitamin E. Our nutritionist suggested adding Vitamin E to his regimen while on HBOT. She suggested Megafood E 8 or another E with all 8 types. What does this mean? I can't find the Megafood in stores and online it is quite expensive. If it matters, I'll order it but if I could find something similar (with all 8 types of E?) locally that's what I'd rather do. Does anyone know what I should get and where? Also, he's supposed to be on Vitamin C but will not chew up a chewable and doesn't swallow pills. Anyone using a liquid/powdered version and where did you get it? I look forward to learning from the group! , mom to Cordis, almost 3, dx Infantile Spasms @ 6.5 mos, IS resolved, developmental delays Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 10, 2006 Report Share Posted December 10, 2006 Hi , I don't have any wisdom about the Vit. E, but wanted to tell you about powdered Vit. C. NOW Foods makes a highly absorbable form of powdered Vit. C (Sodium ascorbate which is a buffered C - not just ascorbic acid). It is virtually tasteless and you can put it in anything- applesauce, oatmeal, or any liquid that he drinks. We just add it to sippy cups of water. Good luck, Golden [ ] New Here - Intro and question about Vitamin Supplements Hi, my name is and I am joining this group to learn ways to help my son, Cordis - almost 3, who is non-verbal. A brief history: Cordis was diagnosed with Infantile Spasms (a severe form of infant epilepsy) at 6.5 mos, though we suspect he began seizing at 4 mos (our doctors thought it was normal when we talked about it, but not when they saw it on video). Anyway, he had uncontrolled seizures (sometimes 100+/day) for about a year and tried 8 meds and the ketogenic diet before he just stopped seizing. We suspect he grew out of the Infantile Spasms. While seizing, his development was at a standstill. He could roll (occasionally) and sit (with some support) but had poor eye contact and was very cognitively delayed. Once the seizures stopped he moved rapidly to crawling, cruising, walking, running. Physically he's pretty typical. Cognitively he is still quite delayed (functioning at between 9-15 mos) and really only makes a couple of sounds ( " bah " , " dada " , and the occasional " mo " ). He does some signing (more, drink, music, chip, cookie, phone) but is not consistent with using the correct sign for what he wants. He's in a non-cat special-ed preschool 5 mornings/week where he gets ST, PT, OT, gets private speech and private OT once a week, and is in ABA/VB therapy 5 days a week for 1 hour/day (though we do not believe he is autistic - we just think it's great therapy). We are also currently doing 40 HBOT dives (we've done 11 so far) and are hearing more sounds (the " dada " just appeared in the last couple of days). We are having his tongue-tie clipped on 1/04/06 because the ear/nose/throat doctor and his speech therapist feel this is just one more obstacle to overcome in a kid with lots of issues. I have a couple of questions re: Vitamin E. Our nutritionist suggested adding Vitamin E to his regimen while on HBOT. She suggested Megafood E 8 or another E with all 8 types. What does this mean? I can't find the Megafood in stores and online it is quite expensive. If it matters, I'll order it but if I could find something similar (with all 8 types of E?) locally that's what I'd rather do. Does anyone know what I should get and where? Also, he's supposed to be on Vitamin C but will not chew up a chewable and doesn't swallow pills. Anyone using a liquid/powdered version and where did you get it? I look forward to learning from the group! , mom to Cordis, almost 3, dx Infantile Spasms @ 6.5 mos, IS resolved, developmental delays Quote Link to comment Share on other sites More sharing options...
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