Lupus Groups and Lupus Buddies
So, I recently joined a couple of groups on facebook. All of them Lupus support groups. And I'm undecided about how much good they're doing me. I like that I can read about people suffering some of the same symptoms that I do. But then I get online and see people that have it so much worse than me or know so much less than I do and my heart hurts for them. When you're living in the clutches of this disease and your life seems like it's one flare after another, it's hard to find which way is up. And for a lot of us, even a few years after diagnosis, it's hard to remember all of the crazy ways this disease can churn us up. I've learned a few things that have been awesomely helpful. The rashes that I get on my arms and chest instead of the butterfly rash is not uncommon at all. Apparently, kidney involvement is NOT AT ALL rare. Me getting shingles in a place that was mistaken as genital herpes has actually happened to others (HOLY SHIT! FOR REAL?!?! I'...