Matthew 6:25-33

"Do not be worried about the food and drink you need in order to stay alive... After all, isn't life worth more than food?"

What is CSID?

Sucrase is an enzyme produced in the brush border lining of the small intestine and is responsible for the metabolism of sucrose, a disaccharide commonly known as table sugar, into two component monosaccharides, glucose and fructose, which are then absorbed into the circulation

In the absence of the sucrase enzyme, sucrose cannot be absorbed and passes unchanged into the large intestine

Currently, treatment of CSID consists of lifelong adherence to a sucrose-free diet. As expected, compliance is difficult, especially for a child. Data suggest that even after diagnosis and dietary treatment, major gastrointestinal symptoms persist, and there appears to be a high frequency of decreased weight for height and age in these patients

What is EE?

Eosinophilic (ee oh sin oh fill ick) disorders occur when the body reacts to trigger(s) by creating too many white blood cells (eosinophils) which hang out in inappropriate places creating trouble. White blood cells target germs and other invaders; in eos kids, they recognize normally harmless things as *enemies*.


This has been referred to as "The Mother of All Food Allergies". Kids with eos disorders may or may not also have IgE allergies, but the reality is that their bodies react inappropriately to triggers, which frequently include food(s).
Common symptoms include:


Reflux that does not respond to usual therapy (medicines which stop acid production in the stomach)
Dysphagia (difficulty swallowing)
Food impactions (food gets stuck in the esophagus)
Nausea and Vomiting
Failure to thrive (poor growth, malnutrition, or weight loss) and poor appetite
Abdominal or chest pain
Feeding refusal/intolerance or poor appetite
Difficulty sleeping

EE is a relatively uncommon disorder that doctors may not encounter often. The diagnosis of EE is often delayed, sometimes for years, because of lack of awareness of these disorders.

APFED

G Tube surgery

Zach had surgery Thursday, he did great. The surgery took about 2 hours which was forever in my book. He woke up fine, no screaming or kicking. He got a little grumpy in recovery right before we went to his room so he got some morphine and was happy. He was pretty sleepy all day and did really well with the pain. He could have the morphine as often as needed but he only needed it maybe 5 times all day and night. Today, Friday he is on tylenol and almost back to normal. His tummy looks good, no bleeding around the button and so far he is not messing with it. The surgeon put in a mic key button, which looks like a beach ball valve.
Hopefully we get to go home tomorrow, he is tolerating his feeds good so as long as he does good all day we can leave in the morning. I know he will be happy, he doesn't like not being able to run around.

Meeting with surgeon

So this week has been very difficult. Zach has had his NG tube for aobut 7 weeks now and for the first 5 weeks did so well on it, he never tried to mess with it. As of today we have had to replace it 4 times in the past 10 days. He figured out how to take it out, so at night he pulls it out and I get to wake up to it hanging from his face and formula all over his bed.
We spoke to Dr Young a couple of times this week and he thinks it is time to go ahead with getting a G tube. He set up for us to meet with Pediatric Surgeon, Dr. Petty at Baptist on Tuesday at 11am to discuss when to schedule his surgery. We know it will be easier and better on him but it is still scary because this is major surgery. Dr Young feels that since his disorder is complex and we can't find any food yet he can eat (he failed eggs) that the tube feedings will be long term, how long term we don't yet but probably at least a year.
Thats all I know for now, hopefully we can keep the NG tube in over the weekend and get some answers and dates next week.