Anyhow, the pump is about the size of a hockey puck and will be placed inside his tummy and it will have a tube that will run up to his spine, in the neck area because his spine has been fused below that.
Front View to Spine. The x-ray shows rods, screws and wires that were used in Andrew's Spinal Fusion.Side View of Spinal Fusion and rods.
The pump will give him doses of medication throughout the day. About once every six months, maybe less, we have to go in so more medication can be inserted into the pump. This is done through the skin and into the 'hockey puck'.
Currently, Andrew is taking the pill form of Baclofen but through the pill he only recieves about 10% of the medications effect, where through the pump, he will benefit from 97%.... a huge difference. A couple or so weeks ago we underwent a trial form of the medication and you would not believe the difference it made and how happy he was. The little guy was smiling and laughing and jabbering on and on like you wouldn't believe, a totally different kid.
My only concerns, besides the fact that he has to undergo yet another surgery, is that there are risks to this. With the trial proceedure, his heart rate had fallen really low but they eventually got it to stabilize, especially after I came back to the recovery and worked with Andrew some. A mother's voice and touch can do wonders ^_^. Also, because of how they will have to do this particular surgery (normally the tube goes in the lower spine vs. the neck) it will be much more invasive. I know that everything is in God's hands and it will all work out according to his Will but I still feel anxious about the amount of hardships that we will face in the next coming weeks because of it.
Well, for now that is all I have to write on this. I will keep you posted when I learn more or if there are any changes.



