Brianna Gives Hope: Waiting for a G-Tube

Monday, September 10, 2007

Waiting for a G-Tube

TUESDAY, SEPTEMBER 11, 2007 11:29 AM, EDT
Brianna is looking better and better each day. Turning into a little butterball! Heck, by the time we go home the incision on her chest will probably be healed The earliest the g-tube can be inserted is Wednesday morning. The procedure can be done in the unit she is in (PICU) now. The gastrointestinal doctor and his staff bring their equipment with and perform the procedure in her room. The doctor told us this morning that if everything goes as planned, we should get home during the weekend....glad they told me that now, I've been hoping to go home on Friday. Oh well, what's a couple more days now that we have been here 2 1/2 weeks.
This morning the third negative came back regarding the infection. Good news. Although I don't mind that she has been on isolation, to me that means no extra germs have been coming in either.

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Definition of Trisomy 18

Edwards Syndrome : Edwards Syndrome (Trisomy 18) is a chromosomal abnormality where there is an extra chromosome present in every cell of the body. This is an example of where “the more the merrier” is not true. This extra chromosome means that every cell has extra information encoded into it. The extra information causes confusion in the way that the cells are formed and results in the potential malformation of all of the body systems. Sadly, this condition is considered "not compatible with life". Just like with Down's Syndrome (Trisomy 21), there is a wide range of how this condition will play out (what the doctor's will refer to as your child's phenotype). Unfortunately because there is more information encoded on the 18th chromosome, the severity of this condition is greater than that of Down's Syndrome. Current studies show that while 1:1500 children will be diagnosed prenatally with trisomy 18, only half that number (or 1:3000) will be born alive at full term. Of those who survive to birth, only half will make it to two months of age, and only 10% will survive to their first birthday. Children who live can be an important part of their family and community, but are profoundly developmentally delayed.

But oh, how we love these special little babies. When Brianna was born we were told she would probably leave this earth within 24 hours...but look at her now. 24 months old, healthy, adorable and amazing. God has been so good. Brenda

Bri's Medical Condition

Brianna was full-term born on April 12, 2007, weighing 5 lb 18 oz and 18" long. Her Apgar scores at birth were 8 and 9. Approximately 15 hours after her birth we were advised of the tentative Trisomy 18 diagnosis.

Immediate health issues had to do with her heart: Mainly, a VSD (Ventricular Septal Defect); PDA (Patent Ductus Arteriosus) ; and a PFO.

Open Heart Surgery at 4 months and

G-tube placement before we came home.

Eye surgery in Spring of '08 to correct cross-eyes.

Tubes placed in ears in Fall of '08 hoping to quash the numerous ear infections.

Scan of abdominal section in Dec. '08. Everthing appears normal.

Brianna takes formula by g-tube but eats baby food by mouth. She can hear, see, is rolling over, sitting up, trying to crawl, playing with toys, says "da da"; "do it, do it, do it" and various other sounds. She is the happiest child we have ever known.

We are so very blessed.

Brianna Gives Hope

Monday, September 10, 2007

Waiting for a G-Tube

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Our Family, Nov 2007

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