Trading In Your Old Life: Post 2 for Invisible lllness Awareness Week

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Day Two post in support of Chronic Invisible Illness Awareness Week. How I was diagnosed and ways to adapt to your “new normal.”

Musings from a Mid-Century Modern Girl

In yesterday’s post, I mentioned I had been battling my invisible illnesses of Fibromyalgia and Chronic Fatigue Syndrome for more than two decades now.

And I have to tell you it has been a life-changing experience, one that has required a lot of adjustment.

From Elation to Concern
I was first diagnosed by a physician’s assistant at the medical center at Maxwell Air Force Base. As it happened, he had been trained by a civilian physician who regularly treated FMS patients. After listening to me explain the types of symptoms I’d been dealing with for months, he nodded thoughtfully, then started pressing certain spots on my shoulders, my back, my hips . . . I almost jumped off the examination table.

Every spot he pressed stung and burned. You see, I was in a full-blown FMS flare, and the potential trigger points were all “fired up.”

big Trigger points for FMS front and…

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About fedoralady

I'm an LA native--Lower Alabama, that is. My husband of more than 30 years and I live here on a portion of my family's former farm with two gorgeous calicos and a handsome GSD mix. My background is art education, and over the years I've been a teacher, department store photographer, sales associate and a journalist. My husband, his business partner and I have Pecan Ridge Productions, a video production company, for which I shoot & edit video and stills and manage marketing. I also still write part-time for the local paper. I love movies, music, art, photography and books, and my tastes in all of them are eclectic.

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