...it's not easy, living with a disability people can't see--and as we can see with that MP from Manchester trying to tell we that have them, that our learning disabilities don't exist, and, in the wake of the tragic death of Jett Travolta, the revelation that scientologists don't believe that mental illness is real, either ...it really is hard living with an "invisible" disability.
I imagine its much like a homosexual, being told by some fearful and ignorant homophobe that they're not really gay, I suppose. Sometimes human beings are just plain thick beyond words. Deliberately thick, I mean. Normally intelligent people, showing ignorance and/or verbal cruelty, for no other reason than these people are either too cowardly to face life's facts, or too lazy to take the time to fully grasp the truth...or possibly both.
So, yes, it's quite hard to live with a learning disability or mental illness--but living with three...it's a bit of a challenge, at times...but like most everything else, you get used to it over time.
I first learned that I had bi-polar disorder around 1990. I learned that I had dyscalculia around 2002. I only found out about the mild DCD (dyspraxia) a couple of years ago, because while my dad was alive, it was forbidden of my mum to tell me about it...well, that "clumsy child" diagnosis came when I began cursive writing in my second year class, around 1968, and it apparently--because if its association with mild retardation (even tho' it doesn't mean a child is actually retarded)--embarrassed the hell out of my easily embarrassed dad, and it became a taboo subject and so I was never told about until after the death of my dad, in 2004.
Pretty much I went through my whole life, thinking I was genuinely stupid, or at least mildly retarded...I was slower to develop, both physcially and emotionally, than my sister and my peers...never knew why, and having teachers and family treat me like an imbecile who couldn't tie her own shoelaces properly (well, actually...that bit's true)...it didn't do a whole heck of a lot for my personal self-esteem (as in, 'what self-esteem?').
I've learned coping strategies for all my invisible disabilites over the last few years, and they do help. Still, I have to say there are times when I wish I had some personal guidence, or at least someone around to give me a kick in the ol' bum from time to time, when I "slip up."
Yet, it's still so painful sometimes....and isolating, very isolating. It's hard to put it all into words. I tell myself that someday I will write a short story or play or something, about it...but, can't bring myself to do it. Too depressing I suppose...who the hell would want to read about something so hard to understand?



Now you can see why I'm an old maid, ha-ha...but hey, at least my hair is neat. 

