Diagnoses

Children w/ CHD(s), My Story

The other day, I once again, felt that kick in the gut.

In the military, there is a program called the exceptional family member program, or the EFMP. The purpose of the program is to make sure that the base you are stationed at has sufficient medical facilities, or educational programs, for every member of your family.

So, for example, Zachy and Natalie are enrolled in the program. When we go to move, a red flag will go up in Matt’s file saying we have special needs. The base we go to will have to be able to accommodate their needs, or we can’t go to that base.

Since we are getting ready to move (PCS, permanently change stations), we have to update all their EFMP paperwork.

The paperwork requires letters from their doctor, stating what exactly, they need. Since we are PCSing, the doctor also gave us a copy of their records.

Since I always feel the need to read every report I’m ever given, I decided to read this one too.

I read through Zachy’s. His diagnoses were, TAPVR, Sick Sinus Syndrome, and pacemaker present. Yep, all pretty straight forward.

I then went to Natalie’s. Her diagnoses read TAPVR, <i> and </i>Pulmonary Vein Stenosis.
It also goes on to state that there is a chance, although slight, that she will need another surgery to correct the stenosis.

So here’s where I felt the kick in the gut….we have always said, in passing, that one of her veins might be slightly narrow, but I never thought it was something that would be a diagnosis. I never really thought she would need another surgery. And, she probably won’t. But the fact that it was written in her records, it just makes it that much more real.

I’m sure her nurse from the NICU, Jeremy, would be telling me she is doing everything that is expected. He was always good at telling me that. Still, even if it is to be expected, I just never expected to see it in print.

Stenosis is not something we ever dealt with with Zachy. And we know it is the main complication of TAPVR after repair. It’s just not supposed to happen to us. She is supposed to have one diagnosis..not two diagnoses.

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1 Comment

  1. Dana  •  Jul 29, 2010 @4:47 am

    Would the author of this post PLEASE contact me. I am the mother of 2 children with Pulmonary Atresia with Intact Ventricular Septum. I have been told that having 2 children with a CHD was uncommon – but I am finding that it is far more common than was impressed upon me. I was told that my having 2 with the same condition was something they “could not even calculate the odds for”. Yet, here you are, posting with 2 children with TAPVR. I'm searching far and wide for families with stories like this.
    Also – my youngest also suffers from p/o Pulmonary Vein Stenosis, and yes, it's noted that he will almost certainly require future interventions to repair this. I hope you do not mind me contacting you this way, and please, please contact me. Dana (at) HotSpringsAR (dot) com (I write it that way in the hopes to avoid some of the spam mail auto bots) Please make sure you put “Responding to your CHD Post” in the subject line, so that I won't miss it!

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