He Found My Words
After I watched this I couldn't find the words to express how it made me feel. I was stuck-literally-until I realized that the words that I wanted became clear.
It became clear to me, dearest reader, that all I've ever wanted was not the words to use but the words to hear-exactly what he says he should have said to his friend.
I've never been able to articulate what he says. I feel so small and weak just thinking about it. It triggers me. But it's dead-on. The only thing I can think to add for me is regarding the constant pain, like now. My arms feel like wet spaghetti, fingers feel like stone. Legs are cramping like crazy, right shoulder/joint, neck shoulder blade have dull to sharp aches. My hips feel like they are on marbles. i am doing the one-handed hunt and peck cause my other hand is one my swelling headache.
One of my professors/now peers has known my history and just read my blog this week. He is one of many who ask me how I get through all the things I have, how I have survived. My answer is simple-because I must.
My daily life and personal experience with Fibromyalgia, Degenerative Disk Disease, Depression, and all their overlapping issues. What you read is how I am in that day and moment. Join me on my *almost* daily gauntlet as I traverse this invisible illness from the inside perspective and look at the events of my life. There will be heavy emotions, much cussing and definite sarcasm! I would love to hear from you!
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