Younger brother has stomach issues

[Guest guest]

Hi Everybody,

My almost-4 year old, has been SCD for 3.5 months. He was diagnosed

as PDD and our DAN doctor recommended he go on the diet. We never

thought he had stomach issues, but results from colonoscopy/endoscopy

from Dr.Krigsman confirmed he had colitis and something with the

esophagus as well. My younger son, who is 1-and-a-half, has had a

terrible stomach since birth. He is neuro-typical. Dr.Krigsman said

he has found that many siblings of PDD patients have similar stomach

issues as well. My question is, how do I go about getting a proper

diagnosis for my younger son? Do I see a regular pediatric GI doctor?

Would he know anything about the connection with SCD/PDD etc.? I

would love to go back to Dr.Krigsman, but he doesn't accept any

insurance and we can't afford to send another child there, so I need

to keep to doctors on my network. I have had the baby on SCD for

about a month with very little results. A side point, the baby has

very strong cravings for fruits. He goes bonkers every time he sees a

banana, date, apple, pear. He has such cravings it actually makes me

think something isn't right. I have thrown a lot out there, but if

anyone has NT siblings of a PDD child please let me know how to

proceed or any general info. Thanks a lot,