Showing posts with label Lyme Disease. Show all posts
Showing posts with label Lyme Disease. Show all posts

Tuesday, August 16, 2011

Coming to Terms

I ran today. Not very far. Alka was kind enough to allow me to join her on her run around the Highland Park reservoir and even though I ran about 13% of the distance she did, it was still among the most triumphant moments I've experienced post-illness.

I am not completely well. I still ache each morning, pop 12 pills each and every day, and require significantly more rest than I ever had before. But I am steadily improving, and for all intensive purposes, I have my life back.

There are certain things that come with this knowledge that have become challenging to accept, however. It is, for example, a sharp reality that things will never "go back" to how they were before. I am a different person. There is nothing that can ever restore that easy-going, carefree, lucky spirit I possessed only 2 1/2 short years ago.

I am angry now. I mock those who complain of life's simple difficulties and frankly detest any suggestion of being "too sick" to do anything at all. You have no idea what sick is. You have never--ever--not been able to tie your shoes at the age of 23, have your mother bathe you in what should be the prime of you life. You do not know what it feels like to experience such physical anguish that you would sincerely give it to the person you loved the most just to be relieved of the burden. Chronic pain, and the hopelessness that accompanies it, is perhaps the absolute worst ailment one can endure because it--without reservation or care for your spirit--brings out the absolute worst there is in you, and leaves you, alone.

Do not, however, believe for a second that my cynicism and bitterness negate appreciation for every day I wake up alive. But those things are still very much a part of me. They are a reality of my being just as much as the color of my hair. My experience has changed me; there is no going back. And the simple suggestion that I am young or inexperienced, or "do not understand" is nothing short of infuriating to me. So, tread lightly with these topics, because I will not hesitate to introduce you to your ignorance.

There is no question, and I say without a hint of hesitation, that I am stronger than I was before. But I cannot even entertain the idea that I am somehow "better" for my trials, perhaps enlightened or even fortunate to have experience what I did. I cannot bring myself to say it eloquently. Fuck that nonsense. What I wouldn't give to have never known what it feels like to come to a resolve with yourself that, if the future looks as grim as the present, you absolutely will take your own life. No, I could do without that lovely notion, wisdom and all.

I could go back to being carefree.

Thursday, January 21, 2010

Milestone

Busy little beaver me has allowed a major even in my life to breeze by without so much as a word on the blog.

Last Monday, January 11th, after over a year of wondering, I was diagnosed with Lyme disease. Finally I know what is wrong with me. Finally, a little clarity.

Perhaps it's fitting and even a little kind of fate to have the onset of this disease and its diagnosis happen in two Januaries a year apart. It allows me to reflect on my struggles with it in a somewhat easier manner, compartmentalizing 2009 as a year of ups and downs.

Think about it. The Steelers win their 6th Super Bowl, the Penguins return for a Stanley Cup rematch and walk away the victors in a season I began with them across an ocean. I finished my Master's degree despite turmoil and near depression. My mom got a job, a good job, and I moved home to Pittsburgh--much desired and deserved! I traveled to Denmark and Las Vegas (several times) and met the man of my dreams who also landed me in London and all new territories when it comes to partners and companionship.

But, the counter to these great things was heavy and at times nearly unbearable. They say you aren't handed more than you can handle. I say, define handle.

I suffered pain I'd never know with little rest or reprieve. I couldn't sleep through the night and was terrified for an entire semester that there was no possible way I could pass my comprehensive exams in that condition. I had my palms injected so that my fingers would work so I could type my answers for my comps questions and my final papers. I did not miss a single day of teaching, and only one class, and that was not because of pain, but due to the effects of taking vicodin for the first time, which did not ease my aching in the least. Many days I could not tie my shoes, turn the ignition in my car, or get myself ready in the morning. I had good days, but all these seemed to do was undermine my position as those people who saw me said, she's not really sick.

Through all of this, the most painful thing has been knowing that there are people--even people close to me--who simply do not understand. They think I am weak, the pain's not really that bad. They think I am pity seeking, who wouldn't take advantage? They think I'm a liar, what could be that bad? It hurt so much and really, always will.

But I am grateful. Very grateful. Because I know what it's like now. And you cannot unless you've been there. You can't know what it feels like to miss your friend's goodbye party or go to bed at 10 when you're on vacation, or be embarrassed to try and open a water bottle in front of people you don't know very well until you've been there. I always thought I understood. Watching my dad with rheumatoid all my life. Seeing his struggle. I thought I was pretty empathetic, that I got it more than most.

No, no I didn't. But I do now. And I will forever have that perspective that is, to me, invaluable. I'll take all the good I can get.