Bradly at CHOC the night we got there. |
Pediatric Gastro Specialist would be in the following morning to go over everything with us.
looking up at the mobile |
My mom made a joke to Dr. Grant about me needing meds to handle him so I don't toss Bradley over the balcony and since she said that Dr. Grant looked at me a little differently as if she was serious. He told me to go on vacation if I get to stressed and that I need to get a break since I am having a hard time with this. I told him that I was having a hard time since he cries most the day, but not because he is crying, its because I can't do anything to help him feel better. Its painful as a mother to know your baby hurts and not be able to do anything about it. He didn't seem to believe me.
So his diagnosis was he was constipated and that was it. His treatment was complicated and I am still not 100% on board with that one...
1tsp Milk of Magnesia once a day - if that doesn't work to continue upping the dosage every 3 days until he goes daily and on his own
1 pill of Lactalose (probiotics) daily
1tsp Maalox twice a day with the same thing as the M.O.M, up dosage as needed
Tylenol for pain as needed
1/8 of a cup of Miralax once a day and up dosage as needed
Change formula from Soy to Enfamil Gentlease.
He didn't feel that Bradley is lactose intolerant and that it's just that his stomach was not mature enough for the milk proteins. He also said that he thinks Bradley's tummy just ins't mature enough to poo normally. That he may just have slow bowels, or possibly that he had too many solid poos that hurt him so badly (always made him bleed) that he is now afraid to go since it will hurt. So with all the meds it will soften it up so much that he wont have a choice but to let it out and it will "re-train" him that its OK to go. He said that his plan is to start with the meds I listed at those dosages and to continue upping everything until he was going on a normal schedule and then stay at that dosage for up to 2 years, but potentially longer.
He made it all seem like it was no big deal and he didn't seem concerned at all with the fact that my boy is uncomfortable at all. When I asked to make him feel better he said Tylenol, but only getting his pooper working is going to work 100%. I mentioned to him that this all seems like a lot of medication for my 3 month old baby and he seemed like it was nothing and kept referring to that girl who goes 20 days. He kept making references to Bradley's future of needing MOM to go and how he may have poo issues for his entire life. I don't understand how this can be life long with out tknowing how it happened.
Before he left he said that he wanted to run one more test to rule out a more serious issue, the test is called Barium Enema, which basically is like colon hydrotherapy they put a tube in his bum, tape it closed and allow 500cc's of colored water (with barium) so it will go into his bowels and intestines and then take several x-rays. They contrast of the color will black out on the x-rays so they can see if there were any leaks or crinkles that would cause poo to get backed up. They were also looking for something more serious called Hirschsprung's Disease and basically ment that part of his intestines had nerve damage and didn't work and would need surgery. The test was negative thank goodness!
My issue with all this is we still don't know why this is going on, which I asked several times. I don't understand how we can treat something when we don't know whats causing it. How can we change whats going on with out knowing what to change.
I do have to admit he has gone to the restroom by himself 3 times now since we were discharged and is in much better spirits. I just don't want to over medicate my baby. I went to my pediatrician and she was shocked at how much Dr. Grant wants Bradley taking... that makes this even more difficult. UGH.
My troubling question... How do you know whats the best thing to do? Who do you listen to?
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