So I know as Im writting this how very depressing it may sound, and i appologize, Aiden is truly such a blessing and has really made us dig deep and not take advantage of anything. but this is where i can get all these feelings out in the open, somewhere where i dont have to be the constant optomist. the strong person.
So since the last update, we have continued to wean Aiden from one of his seizure meds. It is going pretty well, we are not completly seizure free but he is doing okay for the most part, most seizures happening on the day we go down on the dose. It just really sucks to watch something so horrible happen to your child and not be able to help him in any way. I know most people say that people with seizures dont know they are having them, but I dont believe this he cries his upset this sucks cry after he is done having a seizure, and latley they are knocking him out for long periods of time. Sucky thats the best way to discribe...
We are now officially on count down for his 1st bday!!! This brings such excitement and fear and realization all at the same time. The older he gets the more evident all the things he wont be doing or things I feel he will be missing out on and it breaks my heart. This pain is so unlike any other pain there is ... most other tradgetiy happens then it is over and you are able to move on. This we relive every moment of every day, in everything we do from the simple every day things like going to the store and not being able to put your child in the cart. To thinking about his first bday and how he wont be able to do the "traditional' things like digging into his first birthday cake.... and it will forever be a pain we live with getting worse by the day or year.. always having in the back of your head that at any time you could loose this fight and loose something that means so much to you and that you have changed your whole life for. And then in the same moment you have such joy from the very simple of things, a movement a smile or just eye contact.
With his first birthday coming also comes some new things. we had to take him in to get fitted for what will essentially be his first wheel chair and what they call a stander (a board we will strap him to to allow him to be in an upright standing possition with support) .. and its crazy to get past the fear of this realization and go to excitement of getting these items to help him, and hopefully how it will bring joy to him to be able to somewhat interact on our level.
Watching the superbowl at the sowards, such a boy!!
LOVE His sad face!!
Squishys first teeth!!!
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