Saturday, April 19, 2014

4/19/14 Important Thoughts



Just watched an interview with Robyn Lawley, a "plus" sized model (she's a fantastic blogger too, absolutely adore her!), who has graced the covers of many magazines but is most known for being the covergirl of Vogue Italia's 2011 June issue. Now as I'm watching this interview and she is talking about how she loves her body and the audience is cheering I'm just shocked and disgusted with how "inspirational" this is.
Now that isn't to say that Robyn Lawley herself can't be your inspiration, because she is one of mine. 
It shouldn't be inspirational since it should be something that we feel and understand and realize every day. That we can be more then a size 7 and be beautiful.
 

Our society has made it so when a women is of normal height and weight and LOVES herself that is SHOCKING. It shouldn't have to come as a surprise that someone is comfortable with who they are and we shouldn't be in awe that a "plus" sized model loves to eat and loves herself and loves to model and is still on the covers of Vogue. It shouldn because we should all respect and love who are we. Society puts too much pressure on everyone to be skinny that when a healthy women isn't a twig but is still beautiful we find that crazy and almost unbelievable. And THAT isn't healthy.
 
  Robyn Lawley shouldn't be considered a plus sized model when she is 6'2 and is a size 12! That is so sick and so wrong. She is lovely and so strong and so beautiful. She's fierce and no one should have to feel that they need to be "skinny" to be beautiful. I agree what she said in an interview with 'Clique'"I don't think anyone should be called plus-sized,' she adds. "I think it's derogatory to anyone-it's a label.' "I'm a model; I don't think I need 'plus-sized' in front of it."  
    We need more Robyn Lawley's to be covergirls. Not because she is inspirational, but because we are not all sticks. She a healthy women. A strong activist in not being 'plus sized', but being the right weight for your own body.
 
   And it almost seems hypocritical coming from me; someone who struggles so much with the loving herself in her own skin no matter how many times she is told that she is beautiful, because our minds are filled with the ideals that we are suppose to be perfect and smart and beautiful and be able to juggle so many things at once. I'm probably not the best example of loving myself. And I wonder if I ever will be. But I can try. I'll say it, even though I have a hard time believing myself sometimes, WE DO NOT NEED TO FEEL LIKE TRASH BECAUSE WE DO NOT THE BODY THAT IS DEEMED 'BEAUTIFUL'.
 
Anyway....those are just my thoughts on this matter.

 
XOXO,
Dana
 
 
The lovely Robyn Lawley!
 


PS: Check out her food blog for some great recipe ideas

Thursday, March 20, 2014

What Happened to You?!

   Oh boy..how many times do I get this question? I really don't have a problem when people ask me why I'm in a wheelchair, why I'm wearing leg braces, or if I'm using my walker, but once I've answered the question more then five times it begins to get old. I have two main problems with people asking questions: 1) The way they phrase the question 2) The assumptions that people make about me.

   People tend to be curious. That's human nature. But people can be rude as all get out. The way they ask and the timing is often not ideal. I mean you really wouldn't believe how appalling this questions can be.

Examples:
  • Dude....what's wrong with your legs?
  • Are those shin guards (my leg braces)?
  • So when did you get in a car accident?
  • What did you break/tear/injure?
   Crazy right? Like I said, I am open to people asking questions as long as they're phrased in a way that is respectful and the time is appropriate. I mean obviously while I'm about to go to lunch and I'm trying to beat the crowd of kids to the cafĂ© it's probably not the best time to sit down and talk to you about my CMT. I've had an experience in 7th grade with something along the lines of the previous statement. A boy stopped me in the hall and asked why I was in a wheelchair and when I told him my reasons for wanting to get to the cafeteria he gave me an irritated expression and said "So are you just too lazy to get up and walk?"

   Yeah...I had the same jaw dropping reaction. But just as I've had people who are rude I've met people who phrased the question in a great way. I remember at my junior high school there was a girl (who is now a good friend) who said "May I ask what your disability is?" And at that moment I had my service dog with me and had been talking about my CMT with a couple other students. See perfect time and place!

   My second problem is the assumptions that people come up with either about me or my life. It's one thing if you're a child (under the age of lets say 9 or 10) and you ask me if I was in a car accident, but if you're fifty five don't ask me that. There are many reasons that people are in wheelchairs and people who have a chronic illness or disability often take offense when people make assumptions.
 
   There have also been times if someone is rude to me asks what's wrong with me and I've said "OH! A shark bit my spinal cord" (I live in Texas so it's safe that I won't get attacked by a shark) or something crazy. Most of the time I tell the truth, but I like to play with people who are already so rude or so ready to believe something before getting the truth.  This "Oh I know what happened to her" type of thinking sometimes leads to people who believe that they know more about the disability then I do or I'm lying, my disability doesn't exist, and/or that it isn't possible.

   Another one is that because my legs are messed up it must mean that there's something wrong with my brain. Aha that's where you're wrong. I'm actually pretty darn smart. I'm a freshmen in highschool and manage to finish my homeschooling by 2:00 each day (starting at 10 and factoring in lunch). I love to read and I love to learn. I don't need you to yell at me while you talk or slow down and be all sugar sweet to me. I hate that. That lack of sincerity in conversations or the pity talk (you guys who have disabilities or know someone with a disability know what I'm talking about).

   People also assume that just because I'm 'handicapped' that I'm not happy or that I'm living some incredible, inspirational life...which (I hate to crush your dreams) I'm not. I'm living a life that has ups and downs, a lot of downs, but those bad things are balanced out by the people I choose to be surrounded by. When I go to the mall in my wheelchair I'm not doing anything "exceptional" it's just what I do. I have always done this. I'm not being rude, I'm just trying to be truthful. Don't assume that everyone in a wheelchair/have a disability always mope around at home (which sometimes I do) because they don't have a "normal life" or that they are always happy and love getting people inspired (which we don't always like or are).

   We are people. We have feelings. So please when you ask a question about me or my disability be kind and be ready to keep an open mind.

XOXO,
Dana
                                                                                                                                                

Friday, February 21, 2014

P&G Tough Love

P&G released a commercial called "Tough Love", another tribute of their Thank You Mom campaign. First I'd like to start off by saying thank you to P&G for making such a touching and appropriate video. Second I'd like to thank my Momma who made me tougher and stronger.

    This commercial starts off by showing a mother pulling out a wheelchair for her young son and the first words are "You could have protected me." At first I was confused and automatically put my guard up. I'm not sure how familiar y'all are with how people with disabilities are usually shown in America, but it is more often then not it is very disrespectful; portraying us as weak or 'Inspirational (I've previously written about this).
    But as I watched my heart beat faster, I got goosebumps, and I started to tear up. This is the first commercial that I've ever seen that is dedicated solely to the Paralympic games that was made in the US (Coke's commercial included Paralympics but focused more on the regular Olympics). If you take a look at how the Paralympic athletes were shown in the 2012 Paralympic Games in London you would've noticed that there were banners, signs, and tons of press following those athletes around...just like the Olympic athletes. But then you look at America...whose (at least from what I've seen) never made an effort to show us any support. It sickens me when I have to explain what the Paralympics are. I shouldn't have to. Just as the announcer in the opening ceremony in 2012 said "Paralympics mean parallel to the Olympics."
   
    This commercial  shows people with "disabilities" (still hate saying that word...but OK...) in a light that isn't very popular. It showed us as people with strength and confidence. It showed the reason we've grown into the people that we are today; our mothers and fathers..

Thank you P&G. Thank you for giving us a voice. A stronger voice. A voice that is louder then anything. A voice that wants nothing more then to be heard. Thank you.

XOXO
Dana

The video link- http://www.youtube.com/watch?feature=trueview-instream&v=7RR-r2n5DLw#aid=P6pV0Bq4-_A

Monday, February 3, 2014

Struggle

   Many people struggle through many different situations. One of mine (trust me there are a ton) is my undying, unfading want and need to get stronger and feel healthier. But with CMT that can be hard. It is a neuropathy that weakens my nerves and effects my muscles as well. This adds to the fatigue that one would normally feel when they work out.

   I swim competitively. At least I did until November of 2013 when I decided to start homeschooling. I still train to keep in shape and to get rid of stress. The pool and the gym are two places where I can actually think. But as I exercise and I get stronger, I run into a problematic cycle: For about one or two weeks I can feel my body get stronger, but then a drastic change in weather screws with my legs making them so tired that I can't walk or I get a bout of my leg pains for maybe a couple days or weeks. After the pain is gone however I am back at square one or even farther behind then I started.

   I often come across as a strong, brave person. Someone who has grown up facing obstacles and so people sometimes forget that I am human. I am weak. I bleed. I cry. I want to give up.

   I have days where I wonder "Why the heck am I even trying to walk a mile on this treadmill? What's the point? I'm just going to break again and all this work and sweat, and tears will be for nothing." I am told "take it slow" and "you'll get the hang of it" and "Dana, you are so strong". But those are just words. Just phrases that people can easily say and think of. It's harder for me to believe no matter how much you mean it. It's hard for me to believe it because for 15 years my body has rejected me. It has hated me. I have been beaten down by my own body. My legs that turn on me at the worst times.

    But I can't just throw down the towel, lay down on the floor, and cry. That's why despite the struggles and the pains that I get for exercising and forcing my body to get stronger, I'm going to try. I guess I have to. I mean....I've come this far right? I'm not sure how it's going to work out; I could very well die trying (you know falling off the treadmill, legs giving out in all...that was a joke people. Laugh).

  

                        Until then

XOXO,
Dana

Sunday, November 24, 2013

I Don't Want to Be Your Hero!

"You're such an inspiration."
"You're so brave!"
"Bless your heart!"
"You are my hero, you're such a beautiful girl on the inside!"

It's not that I don't mind 'inspiring you' to go out and donate $10,0000 to a random charity or to run that 10k, it's not that I don't mind making your day better with my 'bravery'. But I don't see my life as being any more "inspiring" then yours. I'm sorry, but my life is BORING. It really is. I like laying on my bed in sweats and eating popcorn while I watch CSI New York. I mean that is the extent of my typical Friday night.

Though, what really gets under my skin is when people say "I'm sorry you have to go through that, but God is going to use that to do AMAZING things in your life! You're a hero/inspiration for so many people going through hard times! You just have to push through it! Persevere!".....gah.

I am a Christian. I believe that God has a plan for me and that my CMT is somehow involved with that plan. That part doesn't bother me. 

The part that bothers me is when they say that like that is going to make me feel any better. That it will make the MD become less painful or that is the answer to every problem I face. As if saying those words will stop the teasing or pity talk.

Personally I didn't sign up to be your 'hero' when I was diagnosed. It isn't my mission in life.

This isn't to say that I don't like to share my story, I love to, and maybe that's why I've become that for people. But understand my friends that I'm not perfect, I'm not anything special compared to other people.

Wednesday, October 9, 2013

Soooo Relatable: Pictures

 Don't let your kids grow ignorant.

 Talk to me, I'm awkward, but I love to meet people.

 Remember: CMT is progressive, sometimes I'm in my chair and other times I'm not.

 I want kids, sure they might have CMT, but they will be perfect.

 And yes....sometimes I wish I didn't have CMT.

 Mallory Weggemann is another one of my inspirations. She's a swimmer just like me!

Sunday, October 6, 2013

Bravery

This was an assignment for my ASL class: I was suppose to write an essay about a handicap in my life....and this is the finished product.

Bravery
Despite the normal appearances of life, things aren't always what they seem. Manhattan looks clean and beautiful until you walk the streets. Poison ivy is normal and harmless until it touches your skin. That's probably the most appropriate way to describe my crazy life. My “handicap” is more obvious than others, but at the same time you might not notice it right away. I was four when I was diagnosed with a form of Muscular Dystrophy called Charcot Marie Tooth disease. A neurological disorder that wears away the coating of my nerves and weakens my muscles in my hands and legs.
Growing up I was poked and prodded, had blood taken and nerve testings. I had physical therapy and countless different types of leg braces and boots that helped keep my feet straight and helped me walk. After a while the doctor appointments stopped, but the therapy sessions kept going and the braces continued to change over time and improved. And even though those trips to the doctor ended I was still self conscious about my legs and by how much they held me back from doing what I love to do.
At first I didn't realize how much my life had to revolve around my legs, but when I was around twelve or thirteen that's when I starts to see how my life needed to be. That was when I started to get weaker and the pain came on more intense and more often. I started having to take medicine that was suppose to prevent my legs from hurting, I had to start making arrangements for my wheelchair when we went places, and I started to miss more school causing me to work twice as hard as anybody else to keep up with the work. Worst of all my disability started to take away my passion that I've had for so many years: swimming. It had started to affect the way that I am able to swim and when I'll be able to swim. If the water is too cold my nerves ache and I can't function in the water as well as the other competition next to me. If my legs are shaking I can't dive off the starting block properly and I loose speed.
But my active life wasn't the only thing that really began to change over the last couple years. The way I see myself has changed. Being in a wheelchair comes with the stigma of being “retarded” or “ugly”. Being beautiful and being in a wheelchair aren't usually thought of in the same sentence and rarely is a person in a wheelchair thought of being able to contribute to society. Despite people telling me “I'm beautiful and have a great gift” and “opportunity to share my story with people”, I struggle with accepting who I am, because I long to feel accepted by the other people around me. I'm a people pleaser. But I can't change the fact that I walk more clumsily and awkwardly, I can't change the way I have to dress to avoid my legs getting cold and clenching up, and I can't change the way my leg braces look. Add those things with the added pressure of being beautiful in society's eyes and it's really a battle I can't win.
This year I'm still struggling with how I look and I know that I'll always struggle finding confidence in my wheelchair and when I use my leg braces. I will always have my disability and as much as I wish I could be like Forrest Gump and run right out of my leg braces, that will never happen. One of my favorite quotes is from a woman in a wheelchair, “We may be confined in our wheelchairs, but we are not defined by them.” There are people in my life, my family and friends who push me to be my best and not to sit around a grieve for the things I don't have. There are people in my life, paralympic athletes like Mallory Weggemann a swimmer, who gives me inspiration and a goal to reach each day. Then there is my God who is my courage and my strength, and without whom I don't think I would still be here, because He is the one who gives me a hope. He is the reason I can sleep in peace and keep going because I know I have a future.
So everyday I get up, I get dressed, live my life to my fullest. I go to swim practice and embrace the way I feel in the water. I am weightless and free, I am not confined in my chair or by my leg braces. I go to school and do my work. I have plans for college and I know what I want to do when I leave college. I want to fall in love and get married. And I know I want a family, despite the statistics and the people who don't think I should have children.
Mallory Weggemann summed up how I feel when she spoke at a conference and this is the perfect way to say what we need to hear. “For nearly six years I have been classified as an individual with a 'physical disability'. However, I feel that everybody has a disability of some sort. Mine is evident...but we all have something that holds us back. Whether that is physical, mental, emotional, spiritual, or financial. And the list goes on. But where I believe bravery steps in is when we choose, regardless of our disability and regardless of circumstance, that we are going to rise above and we are going to push forward. We are going to chase our dreams and we are not going to let it stop us.”
We all have something that hinders us. Growing up I was surrounded with people who had mental handicaps or people who, like me, had physical handicaps. But I was and still am surrounded by people who have different types of handicaps. They aren't as obvious as mine, but they are there. Regardless of where we have been we all have something that we need to overcome in our life. These “disabilities” and these “handicaps” are what make us who we are. They make us brave.