For as long as I can remember, people have asked me what it’s like. What’s it like to limp around on crooked legs? Does it hurt? Don’t I wish I was normal?

I was born with Cerebral Palsy. I’ll spare you all of the scientific medical details and tell you that while my mind is fine, I have a lack of control in my muscles, mostly on the left side of my body. I have an obvious limp, which is what attracts most of the stares and questions.

I’ve gotten used to the staring. Friends and family (namely my husband) notice it a lot more than I do. When I do notice it I admit I do tense up a bit… which ironically makes the limping worse, but I usually just smile and keep walking. I prefer to use my disability as a good example of sorts, as opposed to turning in to that stereo typical bitter, angry-at-the-world, disabled girl. Don’t get me wrong, I have my bad days. But for the most part I try to inspire; not punish.

Let me introduce myself a little better. My name is Ali, I’m 27, and I’m married with two kids, ages 8 years and 5 months. Music is my passion, I’m a little OCD about fitness, and I’m addicted to chocolate. I try (but sometimes fail) to see the bright side of everything, and in spite of my relationship with a loving God Who’s mercies are new every morning, I’m way too hard on myself. That’s just because I’m constantly trying to improve. Some of you are gagging by now I realize, but I’m just trying to give you an honest portrayal.

And now for my intentions of this blog. I’m writing this blog to answer the question “What’s it like?”. To hopefully be an inspiration. Even to help myself realize that sometimes it’s okay if when I did such-and-such it didn’t turn out as well as So-and-So’s.

I’m not writing this blog to complain, or to throw myself a pity party (though I reserve the right to be upset and vent anonymously on occasion). I honestly believe that my handicap can be a blessing in disguise. I’ve lived it. I also believe there is a reason for everything. There is a purpose for this, even if I can’t see it. And if I’m being completely honest, I’m also writing this blog to try to put an end to some stereotypes and judgements about me and other disabled people. Before you can judge and say what I should do or you would do, you have to go a mile in my wheelchair.


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