Hello, my name is Kaelyn, but please call me Kittie.
I'm 16 and have chronic lyme disease, ehrlichia/anaplasmosis, babesia, and bartonella. My mother is samjones1122, I'm sure many of you have heard of her or seen her before. I'm in high school, which isn't easy without being sick, so having lyme creates a whole other layer. My mother told me that there are a lot of people on here who have kids with lyme, and aren't sure how to go about
it. It's understandable, considering we do think a lot differently in many situations, and we go through school, teenage social lives, and hormones that adults don't understand very well. (Things have changed since you were this age, you know! lol) I'm here to tell you that I know how to deal with these things, and I know what it's like to go through them. If you have any questions, or need help, I absolutely love to help people.
A quick look at my history: I was born with lyme and went 14 years undiagnosed. I was given hundreds of misdiagnosed ailments and diseases, and even told that I was lying. Began treatment January 2011, and went through severe pain, cognitive impairment, paralysis, muscle/joint problems, scoliosis, hormonal imbalances, thyroid issues, severe acne and skin disorders, tooth and gum problems, stunted growth (Finally growing!), and numerous others.
Treatment: Both herbal and abx
~With Love, Kittie.
Post Edited (Kittie483) : 1/10/2013 11:51:33 AM (GMT-7)