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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

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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

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