When you live with pain, you learn to run on pure adrenaline to get you through the day... or at least that is how my body is coping. I don't do a whole lot, most days. I wake up, have breakfast with my family, take a nap, then get the few things I need to to get done for the day, whether it is running a couple errands, or just checking some messages on the computer. I also have my son to take care of, and as any parent knows, every toddler has there moment. But I get through the day, and I'm sore, but still unable to sleep.
Today, I experienced something I very rarely feel these days. Pure out of breath, barely able to move exhaustion. Even after napping. What changed? I had company, and we ran an errand, and I also pushed myself a little but harder to keep up to her pace- taking her dogs out to play with them, chasing my son around. I sat down half as much I am used too.
Then it hit me like a ton of bricks. The adrenaline was gone, and I was scared and sore... this wasn't a panic attack (I have had those). This felt like I had run 20 miles while carrying 100lbs on my back. The moment I sat down, I was done for.
It has taken my 4 hours and some to start to feel some what normal. I'm still exhausted. I'm not tired, just fatigued. It's days like this I wish I could show the doctor what was going on.... It's days like today that I can't stand the uncertainty. Is this the RSD... no. Is it a result of chronic pain... I highly doubt it. But for now, that is all I have.
My journey and experiences as a young woman just diagnosed with Reflex Sympethetic Dystrophy, or RSD. A mother, daughter, sister, and ones partner. How it not only effects me, but how it effects the people I love, and how the medical world and public treat me.
Showing posts with label fatigue exhaustion health uncertain. Show all posts
Showing posts with label fatigue exhaustion health uncertain. Show all posts
Sunday, October 24, 2010
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