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My son is 9 and new to the diet. How we got here--my aunt was

diagnosed with celiac disease. I had my son's blood tests done

through alletess. Casein was 5000+ and gluten was 4500+. His IGG

(?) to gluten and casein were both 2+. Does any of this sound

familiar? Does this mean he has leaky gut? My son is high

functioning autistic/PDD also suspect he is dyslexic. He is

mainstreamed in school but has an aide. I suspect my younger son is

ADHD-he is having blood test this week. I am also going to request

to be screened for celiac. I must say all of this is overwhelming,

but has been much easier to know there are people in my situation out

there. I have laughed with you, cried with you, and appreciated each

and everyone of the posts (I have been reading the past couple of

weeks). I wish I had a dr standing along side of me telling me I was

doing everything right!! I have placed that in God's hands. We have

been CF for about 2 weeks. I just started packing lunch this week

and as we use us " bad " food I am trying to replace with " good " food.

Cereal has been refused this week -- Doesn't like the new milk. Also

stomach ache (I never know if this is true) and the " run " started

yesterday. Is this a good thing? Thanks to all of you!

Bernie (Gabe - autistic), (Zach and --don't know what the other

initials stand for)

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