Yeah for Soy!

We went to the Cincinnati Children’s Hospital on the 26^th through the 28^th. We were trialing soy since our last visit. It continues to be difficult to assess his progress with the addition in his diet. However, the results came back with no eosinophils. Which means, he can move on to wheat trials, which last four months, while eating soy.

They also did a dexa scan, which looks at his bone density. Last year when it was done he was at a -2%. For those of you who don’t know what that means, he is in the negative percentile from other children around his age. They like him to be in the range of 40% to 60%. When tested again he was in the same percentile. He will need to ingest more vitamin D in order to combat the problem with the bone density.

Other than that, Austin has had an exciting summer break already. We went to Disney 4 weekends ago and he started at the Palm Beach Recreation Center. Yesterday they went canoeing, tomorrow they are off to Rapids Water Park and then they cap the week off with a movie. I think I might consider summer camp myself.

Please review the list of allowed food items on the right as well as his medication list.

Back to Ohio

Austin and I will be traveling out for another appointment at the Cincinnati Children’s Hospital on February 1st and 2nd. We will be traveling to the Dayton facility instead of the hospital in Cincinnati. The flights are much less expensive.

His procedure will be on the 1st at one o’clock. It will be performed by the same doctor that performed his other procedures. His name is James P. Franciosi.

There are two things that they will be looking for with this endoscope. First is to make sure that he has maintained with the increase of steroids and prevacid. If so then they will consider giving him another food that was eliminated from his diet. He was given back milk back after our last visit. Our options for this trip are Nuts, Soy and Wheat. John and I are leaning towards soy.

On the last visit they did a biopsy of his upper intestines and found white blood cells. Apparently those are not supposed to be there. This is called Eosinophilic Gastroenteritis. They will be gathering more biopsies to see if he does in fact have Eosinophilic gastroenteritis.

Stay tuned.

Happy Days

Some parents find that a report card with A’s and B’s on it bring smiles to their faces. For a mom who has a son with eosinophilic esophagitis a picture of his esophagus that is all shiney and happy looking makes me grin ear to ear.

Austin as usual charmed the nurses and pleased the doctors. We traveled on Monday morning for his scope later that day. He was so good during the flight. He impressed me with his patience. When he has a scope he may not eat for a majority of the day. In this case he was allowed cereal in the morning and clear liquids until noon. Then he was unable to eat again until after his procedure. His procedure was scheduled for 4:30. That is a very long time for a 7 year old to go without food. I know that I would be cranky for that amount of time on top of traveling for the day.

However, after the scope I met with the doctor, who also had a smile on his face. He said that everything looked good and he appeared to ready to take on a new food. Because of the osteopenia the doctor and I decided that milk was a good place to start. However, we need to wait until after the biopsies come back from the lab.

So keep those finger crossed that Austin is able to start eating icecream.

Fingers Crossed

Austin and I are off to the Cincinnati Children's Hospital once again. Hard to believe that it has been 3 months since our first visit. Austin has been on the new medicine routine since then. Which was an increased dosage of steroids in the evening and at night, previcid and the elimination of eggs, soy, wheat, dairy, fish, wheat and nuts.

Today at 4:30 he gets a scope. With any luck, if things look good the team that oversees him will give him back some foods. Of course he won't have the opportunity to get back eggs, nuts or fish but maybe milk or wheat. The results won't be back in for a few days. Maybe we will have a ice-cream social to celebrate.

Austin was an army man for Halloween. Obviously he ate something that disagreed with him because while running late for the airport Austin decided to lose his stomach contents in my car. He is a trooper! He ran inside, tears in his eyes, brushed his teeth, changed his clothes and we were off to the airport.

New Treatment

I know that it is a little late but I promised to share what John and I decided to do for Austin’s treatment for EE. His dosage of steroids has been increased from 440 micrograms to 880 micrograms a day. He is getting calcium supplements for the osteopenia. His diet will still exclude milk, eggs, nuts, fish, soy and wheat.

In 3 months (November) we will travel back to Cincinnati for a one day trip for and endoscope. If everything looks okay we will introduce back Milk in to his diet. We will give him Milk for a set period time and repeat the process of going back to Cincinnati for another scope and introducing back another food.

As far as the osteopenia he will continue on calcium supplements for a year and then we will go to Cincinnati for another DXA scan to see if his bone density has improved.

A Place for Austin

There was a NEWS broadcast this morning on FOX about a boy with eosinophilic esophagitis. His mother created a blog to keep her family members abreast of Sy and his disease. (http://www.wflx.com/Global/story.asp?S=13067614) What a great idea! I have created a site for Austin and I will post new information about his treatments. I have also put a list of the foods Austin is not allowed to have on the left hand side of the page. If you forget, you can come back and review the list again.

The url for Austin’s site is sabosee.blogspot.com. Sabosee stands for Sabo’s eosinophilic esophagitis. Please bookmark this page so that you can reference back to it as I post new information.

Austin's Vacation - Email sent on 8/12/2010

So this week has been very informative. The Cincinnati Children’s Hospital does a really good job at making sure that the families that come here are taken care of. There are nurses, doctors, social workers, teachers, dieticians and a slew of other people waiting to talk to you about your son and your medical history.

Most of you know what Austin has but for those of you don’t or aren’t sure, he has a disease called eosinophilic esophagitis (EE). Eosinophils are a type of white blood cells. They are common in things like parasitic infections, allergy, connective tissue disease and tumors. They are not typically present in the esophagus. Well of course that is where my son happens to have them, in the spot that they aren’t typically found. These eosinophils will cause a hardening and constricting of the esophagitis.

Endoscopes are used to diagnosis EE. During the endoscopes they collect tissue and biopsy them to count the amount of eosinophils. Generally anything over or between a range of 15 to 25 eosinophils will constitute a diagnosis of EE. Austin has had 5 biopsies since he was originally diagnosed in 2008. They bounced between 10 to 40 to none eosinophils in his esophagitis.

We have used a plethora of things to try to reduce the amounts of eosinophils. Elimination of foods that he is allergic to, removal of foods that he isn’t allergic to but have proven to be effective in reducing EE, acid reducers and steroids.

On Monday we started our little ride here at the Cincinnati Children’s Hospital. We meet with a gastro doctor. He explained what would happen for the rest of the week. Austin had:

Upper GI to get the biopsies
DXA scan to look at bone density
Allergy testing (scratch and patch)

So far we have received the results of the DXA scan and the upper GI.

The biopsies didn’t come back with the numbers that we thought that we would see. His eosinophils were 229 in the middle of his esophagus and 104 in his lower esophagus (if you haven’t figured it out, those aren’t good numbers). His DXA scan showed that he was in the -2% for bone mass density for his age. The chart looks much like growth charts.

Eosinophilic esophagitis is a chronic disorder. He won’t grow out of it. It won’t spread. He has EE and that is all it is. It runs in families and it affects men 3 to 1. That is all I know and that is all I know about what has happened this week. We have spoken to doctors and they have given us some options for treatment. We need to talk to the allergist and the dietician tomorrow before we have a full enough picture to make a decision.

We will let everyone know when we know. In order for the treatment that we pick to be effective everyone will need to be aware and actively participating.