(continued from “Rude Awakenings”)
"Humpty Dumpty sat on a wall,
Humpty Dumpty had a great fall..."
My lung collapsed. And while I can explain to you the physical repercussions, which were life-threatening, there was something scarier about it to me.
My doctors; the professionals with the answers and the plans; the ones I trusted to the point of allowing them to cut my entire body open like a fish; the ones I allowed to fuse metal rods to my spine, a procedure that could have led to paralysis or death. These great men that I loved and trusted – how could it be that they of all people would now have no definite answers for me?
Aren’t doctors supposed to know everything? Isn’t that their job?
And aren’t parents supposed to be able to tell you that everything is going to be okay?
Wasn’t I supposed to only be here for 4 to 6 weeks? I remember them saying I was going to have a surgery. I remember them saying how long I’d be in the hospital. But when were they going to tell me what happens afterwards? When was I going to wake up from this nightmare? When was everything going to go back to how it was before I ever came to this crazy hospital? When was I going to be normal again?
I was so naive. “When was I going to be normal again?” What a stupid question. It just shows how little I understood about what was going on.
And you know what’s really pathetic? I’m crying right now as I write this, because I haven’t learned a thing in all these years. I’m still waiting to “return to normal”. Every year that goes by I have to face a new reality – a new machine to sleep with, oxygen 24/7, and now for the second time in my life, a tracheotomy. That means suctioning, new machines, new procedures, new employment goals, new fears about what “attractive” means – it affects everything.
And even though I know, I KNOW, that these are the realities of the deterioration of my condition, I still keep waiting for that day when it all just goes away. I even asked my new lung doctor last week, “Do you think I’ll have a tracheotomy forever?” He laughed and said “No, just until you die.” I was crushed. But why? Why can’t I accept what has happened and is continuing to happen to me?
I think it goes back to that blog I wrote a while back… "It Shouldn't Be Like This..."
But it is. That’s where I am and that’s where I was at all those years ago. It all happened so fast and there I was, facing a new dilemma, and all I wanted to do was go home and go back to school. It felt so far away – like I hadn’t been there in years.
And, to my horror, “All the King’s Horses and All the King’s Men…” didn’t have any idea how to re-inflate my lung again.
(to be continued)
4 comments:
Since you have been sharing your story about all that has happened to you and how you feel about it, I have begun to understand in a small way about who you are and I feel like I am getting to know you through your blogs. I have heard it said that we are a composite of all that we have experienced in our lives. Your sharing has helped me see you in a way I didn't know before. I am amazed at your sweet spirit in light of all that you have endured. You are inspiring. Love, (other) Mom
I don't really know what to say except thank you. That means the world to me.
Sweetheart you are normal. Normal is an unattainable goal, therefore we all are. I am ashamed when I read that your doctor laughed at your question.
That was wrong. Please remember you are beautiful, and to love yourself.
Kateryna Fury
Thank you textualfury, that was very sweet of you to say. I think I have good days and bad days in terms of accepting my disability.
And while he did have a harsh way of putting it, I know my doctor is right... I pray that there is a heaven, and I will someday live without any of these issues.
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