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Seizure meds?

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We've had our son (Gregor, 8) on the SCD diet for a week now. He'd

been on the ketogenic diet for a year, without noticeable improvements

except for when we weaned Epilim/Depakote, and is SO enjoying all the

new foods! Elaine Gottschall's delicious recipes are going down a

treat.

So far he has been more 'stimmy' than usual - his diagnosis is Landau

Kleffner syndrome which has many similarities to autism, and the

stimmy behaviour has only emerged in the last 6 months. He also seems

pretty tired and is sleeping very well, which is great! Gregor lost

all communication 2 years ago but is very alert and physically quick,

so we have to be vigilant to keep him from cheating but we're used to

that after keto. We thought the diet worth a try as his stomach is

always bloated although he's otherwise quite thin. He doesn't have

noticeable bowel problems otherwise, but was on huge amounts of

antibiotics during chemo for cancer when he was 3. Speech loss

started soon after.

He's on Ethosuximide/Zarontin which is full of nasty stuff -

saccharin, E211, sucrose... I know this is not helpful to the diet at

all. We would love to have him drug free but would need to see an

improved EEG before considering a wean. His seizures are subclinical

during sleep.

Has anyone else started the diet while on AED's? I'm trying to get an

idea of how much they interfere - not enough to completely stop the

diet from helping, I hope?! Any thoughts appreciated,

UK

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