Hey there --
Some of the stuff I post may sound a little scary/gross, but know that when I talk about it, it's not as bad as it sounds. Well, my nervous system may think so, but my brain knows better. That's the nature of Fibro -- well, part of it. The disorder affects people differently. In a way, I am lucky. Most people with it are more hindered by it. Many have pain to the degree that they cannot function. I get like that on occasion, but not frequently. With me, it's mostly bizarre neural miscommunications. My brain will, say, get the message that my foot is on backwards. I can look down and see that it is facing forward, but it still feels backward. Or upside down. Or missing. You get the idea.
So, if you want to come along for the ride, I'll post some of the more interesting ones as they come up. If I don't post for a while, maybe I'm feeling normal -- whatever that is...
I'm gonna forward this to my daughter, if that's okay. She's a FibroGal. Sometimes I think the battle is about not feeling like you're the only one! It is a difficult road you travel - thank you for you willingness to share!
ReplyDeletePlease do share it -- that is part of the goal! I'm just sorry to hear that she is a part of my 'extended family'...
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