Well, today I woke up with an “F” word flair up.
“F” = Fibromyalgia
I seldom have a Fibro flair, but when I do….oh boy.
I think if I don’t say the “F” word than it won’t be real…
The medication (steroids) I take to manage my Addison’s is similar to prednisone (cortef), and I believe that it helps with any inflammation on a day-to-day basis. I’ve taken some NSAIDS and it has barely touched it, so I am considering taking a tiny bit of Cortef to see if it helps.
How you Babes handle this pain on a day-to-day basis is beyond me. I don’t know how you function. I empathize with all of you.
I think I will go to my Mom’s and soak in her big bathtub. Maybe that will help with this pain.
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