cerebral palsy, Limits, Powerlifting

I Need A Hand.

Goose says this looks like a chicken’s leg. She’s supportive like that.

Rejoice in hope, be patient in tribulation, be constant in prayer ~Romans 12:22

As many of you know, this year has proven to be an explosion of unforeseen events. Well, to rock my world again, I had to have surgery on my hand on February 6th.

In January I broke my left hand walking upstairs. The otherwise routine break was complicated when my hand muscles spasmed while in the cast and pulled my pinky bone out of place.  As a result, the break didn’t  heal correctly. When the cast was removed,  my eyes bugged out of my head! My pinky had rotated outward and was laying on my ring finger. My doctor, a hand  specialist  from Munich, Germany, said,  “Well that s not good!”  It’s a good thing he is cute and has an accent because at that moment  I was in no mood.

He preceded to tell me I needed surgery to re-break my hand and put on a plate with four screws. I looked at him like a deer in headlights and preceded to ball my eyes out.  The first thing I questioned after I processed the information was, will I be able to lift again?  I was  assured  that I will be able to, but it would be a long, hard road.

And let us not grow weary of doing good, for in due season we will reap, if we do not give up. ~Galatians 6:9

I will be in a splint for four months, but  I can take it off to shower and do my physical therapy. I began physical therapy about a week ago. I endure an hour of excruciating exercises twice a day that makes my wrist and hand throb for hours after. A few days ago I made a loose fist for the first time.  The swelling won’t be down until months from now.  I worked so hard to get to where I was strength-wise, not only on my left side but my entire body, and now it’s gone. I’m way worse than before  I broke my hand.   I know that sounds pitiful,  but although  I am depressed and angry, I am not a quitter and won’t stop until I get back to competition shape. It’s going to be a long time though.

My arm from elbow to finger is stiff and weak, but there is nothing I can do about it beyond having patience and applying myself to my physical therapy.  Maybe that’s the lesson in all of this. Be patient—which I definitely am not—and don’t quit. I will never give up, and give all the glory to my Lord and Savior.

Advertisements
cerebral palsy, Powerlifting

Local New York Paper Picks Up Powerlifter’s Story

Thrilled to step in here to say that Linda’s story and blog has been picked up and shared by a local New York newspaper. Such a great article to help spread the word about what determination and belief in God can do to transform a life. ~Jennifer Deschanel

http://www.wvdispatch.com/news/powerlifter-with-cerebral-palsy-is-an-inspiration-to-others/

 …My food is to do the will of him who sent me and to accomplish his work.~John 4:34

cerebral palsy

One Angry Goose.

Jennifer stepping in here. Linda knows me as Jenny or more commonly by my nickname, Goose, but that’s a story for another post. I’m the silent partner here, the behind the scenes “quiet” one, the “bad influence” (if you ask her mother ) and right now…. I am peeved.

angry-goose-wallpaper-1
This is an angry goose.  My face looks very similar when I get ticked off. Do not make pull out the Angry Goose.

When I spoke to Linda this morning and told her I was taking over the blog for this topic, her reply was, “Oh no. You have a tongue like a whip!”

Well when it comes to stigma, yes I do! I promised her I’d behave. If I was over on my website… not so much.

Newsflash folks: Linda. Is. Not. Retarded.

I stumbled on a blog on Birth Injury News while spreading the word about The Power Project (that’s the name of our little blog here, we’d appreciate you spreading the word too). It was  about a young lady who is being discriminated against because of her cerebral palsy. She is being labeled retarded by Child Protective Services, and CPS is threatening to remove her children from her and her husband due to their assumptions of her mental capability. Frankly, that pisses me off. She has cerebral palsy–she is not mentally retarded!

That post…. was personal for me.

I have witnessed people look at Linda like she is stupid. I have heard people slow down their speech when they talk to her as if she is a two year old. She has a speech impediment due to her CP–that does not make her slow or stupid!

A fool takes no pleasure in understanding, but only in expressing his opinion.~Proverbs 18:2

When I first met Linda in 1989 I had no formal introduction. I had no idea she had cerebral palsy. She  looked at me and said whatever it was she said and my first thought was, “Make direct eye-contact, she could be deaf.”  That was an innocent and natural first reaction for that is how she sounded to me, like she’d been deaf since birth. I have no clue when I learned about her CP but never assumed she was retarded.

Linda once told me a story about a man in a grocery store who looked at her and said “are you stupid or something?”  In true Linda style she looked him right in the eye and said “No, are you?” If only everyone had the self-confidence to do that.

stigma-4Stigmas like this have GOT to end. Ignorance and fear are  what causes them to perpetuate. I see it all the time with my Pure-O, that’s a form of Obsessive Compulsive Disorder that manifests in pure mental obsessions.  I believe that it is the fear of asking questions that causes assumptions towards those who are different. I have yet to meet someone with a disability unwilling to explain, if asked, what afflicts them. When did we stop teaching children, or ourselves, how to interact with others with compassion?

Due to things I have experienced in my life I am an advocate for empathy and empathy is not easy to be willing to share. You have to reach into yourself and find a similar hurt or hang-up and be willing to be vulnerable.

Help us stop stigma wherever you can. Speak up and out when you see it being spread and help me keep from having to pull out the Angry Goose posts.