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I was wondering if anyone has any advise on which way of life I should lead with

my son. About 2 weeks ago I was in the hospital and they taught my son how to

chew and swallow which was great but about 3-4 days after he started the food he

started up with watery stools between 6-10 times a day which kept going on . My

pediatrician said stop with the food and just nurse (he is 2) and see if there

is a difference so I did . His stools were less times but if I would give him

any food it would be very watery and he would make more . Someone advised me to

speak to the doctors from the hospital I was at and get there advise so I did

today and he said don't worry he doesn't have what your daughter has it is not

something catchy just give all solid foods and don't look at what comes out from

the bottom. Now I am confused go along with my pediattrician and keep him off

food till the diareah goes away then start him with chicken (even though he

doesn't like it) because he believes it is a good possibility he is starting

what Miriam has ( this is how Miriam started all her problems aftr we started

her on solids she started with the diareah till today. or to follow the othe r

doctor. If some one can give me advise on which doctor to follow and what is the

likely hood he has EG like my daughter has.

Now Miriam she is down with the prednisone to 5 mg every other days (she has

been on the prednisone for 7 weeks already) She waws making everyones life

miserable for a while and she finally said to me the other day " mommy do you

know why I am always crying ( which was 80% of the day) why because my tummy

hurts alot alot " so I took out of her diet most things except chicken and rice

and she is a different child she is back to her sweet self. Does that mean the

steroids aren't working.

Shana ( mom to Miriam 3 1/2 EG,food allergies, Yisroel 2 asthma food allergies

, Tehilla 7)

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