
Wednesday, November 18, 2009
I'm Sick and it's My Fault

Everything kind of slowly goes downhill when I start missing my runs and workouts. With all of the traveling I've been doing lately, my schedule has been all over the place. I mean, I brought my running shoes to Dallas with me, but did I use them? NOPE. And that's completely on me. I can't blame lack of time. I can't blame weather. I can't blame how I feel. There's nothing to blame but the guy I see in the mirror everyday. Cause here's the deal: I've managed to run when I had even less time, there was worse weather AND I felt even crappier. So there is only one thing left to blame: Ronnie. I've made choices over this last month that have allowed my lung function to slip. I could have pushed harder. I could have scaled back on work. I could have went to bed earlier. There's a million things I could have done differently, but I chose a different way.
Now I have another choice to make: I can sit here and sulk and wonder how things would be different without CF or I can learn from how I'm feeling right now and realize that I don't like it and I CAN control the outcome next time. I'll pick option number two. If I sit around and wonder why, I'll be wondering the same things on my death bed. I don't see the point in asking a question that really doesn't have an answer...and to be frank, if it did have an answer, I wouldn't care what it is. All of this "feeling sick" crap is what actually makes life even more interesting for me. With everyday that passes, I'm learning a little more about myself and my opponent. The fact that I get to face a "challenge" everyday is something that I thrive on. It drives me like you would never believe to prove all of the statistics, numbers and nay sayers wrong. If I lose this challenge, I can guarantee you it won't be Cystic Fibrosis' fault...it will be mine.
Labels:
Attitude,
CF,
Challenge,
Competition,
Cystic Fibrosis,
Hemoptysis,
PFT
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I'm Sick and it's My Fault
2009-11-18T01:00:00-07:00
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Attitude|CF|Challenge|Competition|Cystic Fibrosis|Hemoptysis|PFT|
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Katelyn · 802 weeks ago
I hope you feel better soon. I think it is very wise of you to do be doing what you're doing.
RunSickboyRun 96p · 802 weeks ago
Misha · 802 weeks ago
Hope you get to feeling better soon
@CysticMom · 802 weeks ago
cara · 802 weeks ago
Cystic Gal · 802 weeks ago
The good thing is that now you're taking the time to fight the beast of CF. But, I don't think you should ever blame yourself for your illness flaring up. You don't need to spend your emotional energy feeling guilty that you need some extra care right now. I think a lot of CFers actually end up resisting the care they need just BECAUSE they always feel this guilt when they are actually hospitalized. They feel like, "look at me here, I'm a failure, I got myself sick again." - so the next time they are sick, they avoid the hospital because some part of them remembers that guilty feeling.
So you went to Dallas, so you stayed up late smooching your new fiance instead of sleeping, so you skipped a workout. Next time you might not. But you also might. You might travel and stay up late and be busy livin' your life for a couple weeks. Damn right! You're keeping that body well so you can live that life- and there will be setbacks but don't blame yourself. Just get back on the horse and move forward!!!!
LOVE LOVE LOVE, CG Beth Peters
RunSickboyRun 96p · 802 weeks ago
Ronnie
Colleen · 802 weeks ago
Emily · 802 weeks ago
Somer Love · 802 weeks ago
Piper · 802 weeks ago
Wallowing in self pity isn't productive, but neither are guilt and blame. Move forward, enjoy your turkey in the hole (sounds like a gourmet dish!), and keep doing exactly what you do every day. In other words, keep making us all smile.
Love and good vibes for a speedy recovery!
Piper
PS: LOVE the engagement video! Congrats to you and Mandi on making such a beautiful, fun, and spirited couple!
Jada · 802 weeks ago
Take care,
Jada
Sara · 802 weeks ago
Congratulations on your engagement!!!! :)
Katey Ballard · 802 weeks ago
Ophelia Hart · 802 weeks ago
Anyhow, get better soon. Your blog is fantastic and reaching the lives of so many people, with and without CF.
Ophelia