Oh I hear ya, Donnaeil!!
I'm sure the commentary was well indended but people just don't "get it" do they? If they did they'd react a lot differently, at least I should hope that they would. The pain aspect of our problems seems to be the thing that the people in my life don't understand.
I keep looking around websites to see if anything is going to be going on in my area regarding FMS Awareness Day (May 15th). But so far nothing. I think I'm going to have to be the one around here to get something going.
As I've said many times.. these people are most likely uneducated in the matters of fibro. And for them, ignorence is bliss. Sad but true. Hugs,
Fibormyalgia, 4x Lyme Disease Survivor, Depression, Anxiety Disorder, Dyslexia, 2 Lumbar Disk Herniations, Allergies, Bi-lateral Carpal Tunnel, Psoriasis.
Meds = Elavil, Tramadol, Xanax, Lipitor
"Shoot for the moon, even if you miss, you'll land among the stars" - author unknown