There is no awareness day for LS. None. There's a Vulvar Health Month-March-but no LS Day. No support for those who itch, burn, and scratch miserably all day, every day (like me this week.)
But I want to change all that. Fibro and Lyme's have their day (or month in the case of Lyme's), so why can't my other, infinitely more annoying condition?
I chose March, obviously, and in picking a day, I chose March 7 because apparently that's "Be Heard" day. I already wrote my Congressman and started a fight on the LS page (my ribbon apparently is superseded by someone else's...and hers suck.) Mine is nice and simple and is open to improvements. Never mind that I have no artistic ability at all.
Hers is...green and purple? Apparently it's for gyn awareness (teal) and chronic pain (purple). And she did pinkish for rare diseases on one of the curves and zebra stripes for scarring.
No one seems to be listening to my ideas and it's ticking me off. I think I should get off Facebook and get some actual work done before I start Hulk-smashing the computer screen.
Why does no one ever listen to me?
On top of that, my neck and shoulder on the right side seized up this morning. No reason why. Just because. I could barely turn my head before I had painkillers in my system.
I should get back to work. Let you know if Duffy the Doofus gets back to me or shuts me down.
Ta,
Bec
No comments:
Post a Comment