Skip to main content

What Does It Mean to Have CP?

You know this month is CP awareness month so I thought it would be fitting to write about what I feel everyday..So here we go

When you wake up and get out of bed and think man my leg muscles are tight. When you walk into a store and you get the looks. The looks of curiosity, looks of wow that girl sure walks different, looks that make you feel like you just don't fit in. When you go to pay and you are struggling getting that money or credit card out and you start to blush because you know that cashier or the person behind you is thinking "that poor girl". When you are asked to repeat yourself 2-3 times because that person can't understand you and you just want to say never mind. When you have to buy new shoes more often than normal because you ruined the toe part of your shoe or you have a hole on the bottom due to walking toe-heel instead of heel-toe. When you have to use adaptive tools like a button hook. When you can't open a water bottle or you spill your drink because your so stinking shaky. Or how about when you look at your fingers and they are all weird looking.. You know I can go on and on but I also want to bring you the beautiful side of CP

I get to use my disability for good and be an advocate for my different population. I get to look my students in the eyes and say you are worthy and you are capable. I get to show them and their parents that they can be successful and live an independent life if you push them to strive for more than what society tells them. I get to show people everyday that a person with a disability can be independent and be positive and love the life the Lord has given. I get to prove others that the impossible can be  possible. Most importantly, through this blog and through my everyday life I get to let people know that different is beautiful and we all deserve a chance to be loved and to be known for the beautiful people who have CP are. I get to be apart of a population that sees the world through hardships but choose to keep pushing on and to tackle whatever life throws at us.

So go and get to know a person with CP this month or go and love and cherish someone with CP because we are people that deserve to be loved and not to be known for just our disability. I have CP and CP does not have me.

Comments

Post a Comment

Popular posts from this blog

Struggle is Real with Adult CP

 Here is something that frustrates me about the state of California. Basically since I was diagnosed with CP I went to CCS (California Children Services). They provide free occupational and physical therapy until your 21. This is so awesome and I would go twice a week until high school where I would do more check ins because I was becoming more independent and doing so well I did not need it as much. Now I know what your thinking...um Nicole why are you frustrated with this? Well did you noticed I bolded until your 21? This is the issue. Once you turn 21 they are like bye bye good luck with the rest of your life. It has been difficult because you get dropped off and on your own without any recommendations of where to go next in life.  Most of you know that hot yoga has been a life saver for me and has basically become my physical therapy and it has been great until...covid. Due to the shutdown it also caused a shut down of my body because my physical therapy (aka yoga) was taken away (
2 comments
Read more

Acceptance

For those of you that follow me on Instagram or Facebook you have probably seen my yoga videos that I have been putting up. On the recent one I had a friend comment about how much she loved my openness and confidence. This really got me thinking about what a road I have been on to get me to where I am at today. Back when I was a senior in high school I got nominated the most inspirational senior. Now when you are nominated for this award you have to write a speech and make the speech in front of the whole school at an assembly. I remember when I first found out I started bawling. Like what? People think I'm inspiring? At that time I was NOT comfortable speaking about my disability. In fact I couldn't even read the speech my principal had to because I was a wreck and was far from confident in myself. Even halfway through college I was not comfortable mentioning my disability. It was like the BIG elephant in the room. It made me nervous and I thought people already see that I
3 comments
Read more

A Whole New Decade

 It has been over a year since I have been on here but I thought that my upcoming birthday of turning 30 was fitting to write a post about this last decade of my life. Especially since this blog has been a part of my 20s. So I thought I would write a letter to my 20 year old self.. Hey girl, It is me, the older, stronger, more independent version of yourself. I know right now you are so excited because you just got your driver's license which is the first step to independence and knocking down a boundary that people said you could not break through. But girl that is just the start. You truly have no idea how God is going to move you to become such a successful independent woman. I know right now you are worried that no one is going to want to hire you for being a special education teacher. I can tell you it is not going to be easy. You are going to have to fight for your abilities but the right principal is going to see you and believe in you and give you that chance because here w
Post a Comment
Read more