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We look to the sky to remind us that some things will never change. But in all actuality we are witnessing just the opposite. For the sun itself does not rise and fall in the same place in the course of a given year, and neither do we. Each day is new. It is brilliant with possibility rooted in a certainty only born through change.
Because it’s always filled with so many unknowns in which we cannot control.
In a life lived with cystic fibrosis, change and certainty have a complicated relationship. Our bodies are vying to destroy us - changing without our permission and we cling to any certainty we possibly can. It’s a brutal balance. One in which we know we can’t live without. Because in every new treatment to save us lies the certainty of change - it just might not be realized in the hope our hearts had set upon it. But there will be change. Sometimes that change comes like the mere rising and setting of the sun, easily seen and understood, becoming an assured certainty to the landscape of our life. Sometimes that change lies within the hidden certainty of mere minutes in the form of growing daylight - embraced by the small quieted certainties of progress.
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Feeling its Effects
- Day 6 -
The miracle that is this drug is not lost on me. I know there are changes happening within my body that I cannot even begin to fathom, nor can I readily feel or see. But, nonetheless change is happening - both positive and challenging.
Yesterday came with continued challenges in the form of joint and body pain. I seemed to be able to stay on top of the worst of it and keep the edge off for most of the day with strategic timing and dosage of nsaids. Pain is something with CF I’ve learned to live with, but this intensity is pretty brutal and exhausting. With the good comes the trying, and I’m hopeful that this is just a phase as my body continues to adjust.
Tremors and neuropathy are a frustrating combo. They’re something I’ve struggled with over the course of my years and progressive usage of antibiotics. I woke up yesterday morning with my hands tremoring and neuropathy in my left arm. I know with my own journey with tremors and neuropathy there are tougher days when they appear and other days when they seemingly non existent. I rise just ready to take on the day with whatever this body and life has given me.
There are still so many incredible things that my body is rediscovering. I’m in awe of the little things that have surrounded me that I haven’t been able to know. You know when you open a carbonated drink and take the first sip and it bubbles up into your nose? It hurts, right? I felt that for the first time in years yesterday. I forgot that even existed. I can’t help but smile.
I asked Mark last night if my hands and fingers looked different to him at all. He said, “yes, they don’t look blue”. I was shocked. Maybe because I live looking at my hands all day that I have never thought them to be discolored or blue. Clearly that is not the case.
Keep truckin' Ashley. You GOT this girl!!
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