[epilepsy] Re: Shaking.

 

You could see results or a difference in a few weeks, but you really need to give it at least 3 months to see a difference. A Dr Shealy did do a small study with transdermal magnesium to prove if it worked or not, and in six weeks there was a significant increase in magnesium levels - at least for those test subjects. But as Dr Shealy says, those "subjects were carefully picked". Stress uses up a lot of magnesium - all kinds of stress which includes emotional, physical as well as mental. This is because adrenalin causes a lot of magnesium to be used up. And so therefore any kind of illness does cause a lot of magnesium to be used up. So how quickly a person's magnesium levels can be increased depends on the amount of stress they have as well as how low the levels are to begin with, so this is very individual. A convulsion will cause a lot of magnesium to be used, for example. Do not expect all seizues to be stopped for at least a year - this is using the transdermal magnesium everyday. I also had Multiple Chemical Sensitivities as well as ME - and associated issues so it was not a unusual that it took so long for me to be sure of not haveing any seizures. For me, there was a need for a lot of magnesium for several issues, not only seizures.
Just start with lower amounts then the instuctions say for the first week or two, until the body adjusts. Magnesium causes people to detox, and your child does not need that complication plus some of the symptoms of detoxing can be painful....

If you have any questions , feel free to email me offlist.
Good luck!
many blessings
Shan

You might want to look into the nebulizing obtion for getting magnesium into the body and absorbed too.

--- In epilepsy@yahoogroups.com, "mlauchner" <oldstuff4me@...> wrote:
>
> Shan --
>
> Thanks for reposting this info. I too did not save it the last time you put it out there. I'm going to check out the website and when the budge allows, (in a week or so hopefully) I'm going to order some of this mag. I figure I won't know what you're talking about until I try it. On my son that is. So I will certainly report back and let everyone know what happens!
>
> BTW, my son has been drinking the Kangen water for over a month now and unfortunately we don't see any improvement in the seizures. I know others have, but I guess it's just not for him.
>
> Blessings to all and have a great weekend!
> Michelle
>
>
> >
>

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