Re: Questions on Vit E

[Guest guest]

> >

> > Dear ,

> >

> > I was out of town for a week...its taken days to catch up on

> email,

> > and you can imagine in addition, how many new messages have

posted

> > on this site. I almost missed this one. Anyway, hopefully some

of

> my

> > posts today will answer your questions. You will not find

> anything

> > to read on vitamin E and apraxia, because there is no data. This

> is

> > a totally new observation...and now a growing case series of

> apraxic

> > children who are doing better on vitamin E plus fish oil. But

if

> > you google " Merck manual and vitamin E deficiency " , you will see

a

> > nice table of symptoms of vitamin E deficiency. The symptoms

> overlap

> > those of apraxia/dyspraxia and SID. This is the table that

nearly

> > gave me a coronary back in July, when I first started to look

for

> > info on vitamin E after ph surged when switched to omega 3

> > capsules from liquid, only to start to regress again several

days

> > after switching back to the liquid. The only difference in the

> > liquid and capsules was the vitamin E, and on the high doses of

> > omega we are using...he was getting only 100 IU extra E a day

for

> > about a week, and we saw some amazing and obvious changes that I

> > needed to try to explain. So improvement was seen even with

small

> > addition of vit E, but when I started to supplement him with

> higher

> > doses, that is when we began our road to recovery. But it was

> > reading the Merck manual website that made me suspect that a

> vitamin

> > E deficiency might be playing a role in apraxia...at least in my

> > son's case...a discovery that has changed our lives. -

> >

> >

> >

> >

>