Hi! How is everyone?
I’m Sunshine4tullip. I’m 37. I’ve had KLS for, maybe 26 years. Since I was 11 or 12. I was diagnosed in 2005. Before that, we just assumed it was some Mystery Illness.
DURING EPISODES: It impairs my thinking greatly. It also effects my speech, balance, motor skills. Sometimes I sleep A LOT. It’s VERY hard to wake up. Sometimes I’ll walk through days in a sleepy state, where I’m awake,but it FEELS like I’m asleep. Other times I can not get to sleep. There are times when I am ravenously hungry. My stomache hurts badly because I ate so much,.... but, funny, I am still hungry.
During episodes of KLS, strangers have assumed I was either very drunk, on drugs, severely mentally disabled, or all three. (i know this because sometimes the occaisonal rude person will comment or stare. Mercifully, most of the time I don’t percieve it...but, if people are mean-spirited, that’s THIER problem.
You have to feel sorry for people with no sense of humor, right? How FUN can thier life be, with no compassion or humor?!
They must be bored out of thier minds!
NOT during episodes of KLS: I am...’normal’, for lack of a better word.
When I am well, I enjoy painting, working out, good movies and books, spending time with friends & family. I sell the occaisional painting. Once in a blue moon, since KLS has gotten so much worse. I am on dissability. My mom and I are best friends. She takes care of me when I need help. I’m Christian, and I find great comfort and friendship in God. I LOVE BIRDWATCHING and nature !
THIS PHOTO is ME and MY MOM, BFF (best friends forever!!!!)
Nothing else to say about me I guess. Nice to meet you all !
Love,
Sunshine4tullip
