[Note: This experience is wildly outside the
realm of the Modified Atkins Diet for Seizures,
as this parent found the opposite to be the solution - namely carb
loading. However, this alternate experience demonstrates that
each person is different, and a parent is always the best advocate!]
My daughter is 8 and started having seizures at 5. Our neurologist
thought that she may have had a glucose transport deficiency. She
would have seizures in the morning, after a lot of exercise, if she
didn't have a snack before bed. The glucose in her CSF was lower
than it should be 2.6 (it should be between 2.8 and 4.4). She had
the genetic test for the glucose transport deficiency and it came
back negative.
I started feeding her every 2-3 hours (lots of carbs) and giving her
cornstarch before bed to keep her glucose levels up over night. She
is now seizure free unless she over exterts herself (more than 2
hours of exercise). We never did the MAD or ketogenic diet. I wonder
how many other
children would respond to the carb loading/frequent
feeding/cornstarch.
Maybe there are a lot of kids with low CSF glucose and don't know
it. The premise behind MAD and the ketogenic diet is to get the
energy to the brain using an alternate pathway (ketones) [note
there are several theories as to why the MAD works. A couple
are discussed here].
We were lucky we had sucess and I would have tried the MAD diet next
if what we did hadn't have worked.
My daughter is also on a gluten/dairy and soy free diet as am I. I
tried re-introducing soy and dairy at one point and she had trouble
swallowing and chewing. Haven't had a problem since the foods have
been permanently eliminated. She had occipital lobe seizures. She
was having 5-10/day two years ago. We never medicated her. She would
not lose consciousness with the seizures. She also had problems with
balance and left sided weakness.
Everything seems to have corrected itself. She's a very happy,
healthy
little girl who does well in school and has lots of friends.
I hope this may help someone.
Susan