Bleh!
Today has just been…well, bleh! I don’t know why either! I woke up feeling very tired and groggy, and now I have a the “eight ball” feeling in my head (vertigo) My head is killing me. No idea why either. I guess its just one of those lovely days in the life of having NCS.
Know what I would love to do? I would love to know how many kids in Monroe actually have a form of dysautonomia. I think it would be great to go around to schools or wherever and be able to talk about having it. I know in school we used to see videos of people/kids who have very serious, life threatening illnesses and of course it kinda scared us. But, what about NCS? Unlike other disorders, this one is invisible. Unless you are passed out on the floor or turning a lovely shade of bright white, no one can tell that you have it. I just think it would be neat to talk to kids about how I have conquered the trauma I have been through and proven doctors wrong. Some of them could have been told that they wouldn’t be able to drive, go to school with the other kids, drive a car, etc. That is one of the reasons I wanted to write a blog, to kinda say “Hey! Look at me!” I have been sick since birth, had a pacemaker half my life, and I am living a fairly normal life. Its kinda fun to prove those big time medical doctors wrong, if I may say so.
Alright, enough blabbing out of me. Going back to the air conditioning and nursing my headache.