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My special needs son

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I am the mom of a severely brain injured little boy who is now 8 years

old. He has epilepsy (5 different types of seizures), cortical

blindness, spastic quad CP, reflux with high risk for aspiration

pneumonia, feeding tube, etc...

He has been on the ketogenic diet for 4 years (he was weaned from it 3

years ago)and has been tried and failed on all available seizure

medications. He has 30-150 seizures a day.

I finally got the help of our neurologist and dietician to work with

me to give him some real food pureed through his tube. He is still on

some formula. It is called Neocate Junior.

I am interested in getting him on the SCD but wondering if there is

anyone else here that has a child with similar issues?

Thanks so much for any help or comments that you could share.

Sincerely, Tammy

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