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Epilepsy/cerebrial palsy??


Question: my dughter has these 2 diseases and she has been to a half dozen specialist but yet she continues to have seizures daily.she has been to phillys children hospital yet nothing seems to help.they have inplanted a device under her arm that is suppose to stop the seizures but they dont. suggestions pleaseeeeeeeeeee
Answers: Hi.

One thing doctors never seem to think of is thujone

It might be in a muscle ointment, gin, vermouth, mothballs pretty much anything that smells like camphor or cedar or juniper or sage or oregano oil, all of these compounds that are related are mostly accumulative and toxic and can cause seizures. Take a look around your spice rack type the word thujone and spices in the search engines, look around your yard where she plays etc get to know the plant life, once you smell a few things with it in you will recognize the smell, yellow cedar thujone occidentalis has the most in the twiggy branches for potency but it's the other accompanying similar compounds that are with thujone and are less well known terpenes that also do harm. It's slow acting and long lasting the trees generally produce the most into the air in the hottest of summer, but the effects can be quite long lasting all year long.

I think it kinda forms a very hard to dissolve membrane that specific gravity keeps topmost causing the signal along the axon to arc rather than transmit axonally along the sodium /potassium pump as usual, sodium levels may also be involved in this process.

What i suggest to change the polarity a bit altering the ionic environment a bit, in the most safe possible way that may be able to help.

First ingredient

Carbonated ozonated spring water, it might not say ozonated on the main lable but check the ingredient list of the water. (don't add sodium)

This is free radical action, oxydation, it's got a bad rap but it breaks down crap in your brain that your brain cannot break down on its own also , crap it doesn't want or need.

A glass of this from the water section xtr fds with about a quarter gram of citric acid in it. (wine supply store will have or can order it).... a quarter gram tastes better but you can use more up to a gram is the daily requirement of vitamin C which is what it is, personnally i'd go far to get citric acid rather than settle for ascorbic acid . I think citric is better.

The citric acid is an anti-oxydant, vitamin C

however when mixed with the ozonated water it becomes a super-oxydant which scrubbs the brain quickly.

Use only the first glass or two of the ozonated water it should be consumed quickly when opened for best effect.

Wait a half an hour after drinking, then have a glass of pure orange juice with pulp, this is also 250mgs or 1/4 daily dose of vitamin C, drink alone this after the treatment to reprotect the brain with the antioxydantive vitamin C.

Do this once per day for a week, see if it helps the first time or few, one glass or two followed with regular pure orange juice or grape if its pure .

Vitamin C is what THEY call a pre-cursor, but it's used by the brain to make dopamine, which makes further chemicals that the brain likes and uses.

It could be the nerve is obstructed, but, neurology is still learning about the neurotransport system of the sub-arachnoid layers so they can't really figure out if it's blocked when they don't know that it can be blocked.

See my work on cerebrospinal fluid www.Ob1.fcpages.com
try some divine inspirations while drinking the vitamin c water or soon after to speed up the process to get the best effects from it.

Quite often yawning is present when one is comming out of a seizure.

Ob1

(there's a healing hand on my 360)
You may need to do some research of the conditions through the major hospitals that have either held clinical trials or have a good success rate. I wouldn't recommend involving her in any clinical trials but take a look at whats working and what isn't.

It may be that the two conditions or medications are clashing. Whatever the cause, you need to do some strategic research to find out.

I hope and pray that you find the right answers that will greatly improve the quality of your daughter's life.

God Bless you and your family!!!
http://www.cerebralpalsysource.com/About...
I cannot imagine how difficult this must be for you. It is so hard to see your children in pain. I do not know much about cerebral palsy, but I know quite a bit about epilepsy. My husband is epileptic. He gets grand Mal's and partials. (I know there is a bunch of different terms for these, but that is what we have always called them) We have yet to find out why he is epileptic, however, after much trial and error we have been able to control his seizures. It can be tricky to find the right med and the right dosage of the right med. I don't really have any advise, other than to be patient and DILIGENT. Something will work. Doctors admit they know very little about the brain, so many treatments are just a shot in the dark. There was a time I felt like you. Frustrated, hopeless, scared. But now my husband is fully functioning. He has not had a single seizure in over 2 years! I hope that time is soon for you. Good Luck


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