Originally Posted by qxp
Originally Posted by deacongirl
Originally Posted by puffin
That said, it seems to be worse if he eat gluten, and if he eats too much not great food (at birthday parties), blue food colouring is odd too. I think he just has a sensitive gut which is easily overwhelmed by some foods and stress.

Has Hirschprung's disease been ruled out? I know of kids with similar symptoms who had short-segment Hirschprung's and were diagnosed very late. It is rare but might be worth considering.

My son has Hirschsprung's disease. While it is possible to be diagnosed later in life, it is really rare. The children who are diagnosed later are very sick, with lots of failure to thrive issues, multiple hospitalizations for serious conditions, etc. The top specialists in the country on Hirschsprung's disease will say that it is nearly impossible to not be diagnosed in infancy or during the first year of life given all that we know about it.

While you can certainly read about the disease and see if it fits, I would not go too far down this road unless your son shows the following symptoms: distended belly, chronic foul liquid stools alternating with constipation, failure to gain weight, stools that smell worse than any frat house, anemia.

I don't want to sound harsh or be taken the wrong way. I am just a mom who has seen too many people throw out Hirschsprung's as an explanation for constipation when in reality, kids are extremely sick if they have undiagnosed Hirschsprung's disease. I have seen too many moms worry unnecessarily.

My son has Hirschprung's disease as well. I agree that it is very unusual that a child would not be diagnosed, however, I have met, IRL, more than one child whose symptoms were not severe enough to require hospitalization, but that did interfere significantly with quality of life, and that were diagnosed at >5 yrs. If the affected segment is very short, this can happen. A dr. would certainly not do a biopsy unless it was indicated, but given the difference having a diagnosis made for the kids I know I hate to see anyone go through what they did prior to that point.

Just FYI: my son has Down syndrome as well, and while still rare it is more common in kids with Down syndrome. Perhaps in kids with Ds who do not have severe symptoms early the diagnosis is delayed because the symptoms are attributed to low muscle tone in Down syndrome rather than other possibilities.