My name is Casey Kasselder; I am 25 years old and from Tri-Cities, WA. I graduated from college in June 2017 with a Criminal Justice degree, with the hopes of impacting the world one day. I have organized
numerous fundraisers including a hockey tournament in Canada. I love organizing fundraisers and the
smiles and happiness created as a result. I have this dream to organize a fundraiser in each state of the U.S., and every Providence of Canada before I am taken home. I know it sounds silly, but I want to leave
a huge impact on this world and I am sure we can all agree when I say “this world could use MORE love
and happiness.” I have a huge passion for inspirational speaking in hopes of inspiring people to follow
their dreams, live life to the fullest, and see that the negative obstacle of yesterday, is an awesome gift
for the future. I also LOVE sports like hockey, football (GO SEAHAWKS!!!), and baseball! I may not
understand every rule, but I definitely enjoy games, when on! 
I’ve always been a dreamer. From the time I was a child, I’ve imagined the kind of work I would do. Work
that made a difference in the lives of people. Work that required physical strength, stamina, and
courage. I fantasized about joining the military, becoming a police officer, a social worker, anything that
would impact the lives of people in a positive way. I dreamed of being a her

Screen Shot 2019 03 04 at 4.27.39 PM

Growing up life was hard. My mother had been injured in an accident and become dependent on drugs
to survive. Eventually, her dependency turned to addiction and the mother I knew and loved became a
stranger, more interested in her next fix than in mothering her children. The police were constantly
called to our home until one day my father forced her to make a choice. The drugs, or her family. She
chose drugs and disappeared from our lives. I guess one could use that as an excuse, sink into
depression, but I chose to continue to dream of making a difference. Then one day, eleven years ago, I
was forced to face an ugly, painful reality. I was sick. I had started falling, a lot. My gait was unstable, my hands were uncontrollable, until one miserable day when I fell on my face, breaking my nose and causing considerable facial breaking.


The good thing was, there was finally an explanation for my physical problems. The bad thing was that the explanation was a diagnosis of Friedreich’s Ataxia (FA).  Incurable, life-altering, likely terminal. I was in the seventh grade, all life was ahead of me, dreams to fulfill, and now it was supposed to stop, to take a backseat to manage my illness. I was expected to stop dreaming. To sit at home and wait for the inevitable loss of movement, and independence. I was angry, in denial about what this diagnosis would mean to my future. My Dad wanted me to quit school. He couldn’t see any reason for me to “waste” any of my time on education I would never be able to use. I fought back. School was my salvation. A place where I could prove that there was more to me than this illness. A place where I could be known for something, something that mattered. 
Before FA, I had this perfect image of what my life was supposed to be, and after FA finding the pieces of that image torn and scattered throughout the rubble of a destructive tornado. As much as I have hated this diagnosis and what it did to my fantasy of a healthy, productive life, I have come to find value and purpose through the experiences that have come my way as a byproduct of my illness. I always wanted my life to be one of purpose, wanting to make a difference for others. That goal wasn’t going to be reached in the way I had dreamed, but I determined that it was going to happen. 
My disease has opened so many doors and given me numerous opportunities to influence others that might not have happened in my fairy tale life. I have learned that I have a purpose for living and that purpose wouldn’t come if I just threw in the towel and give up. I have a voice that can stand up for
others facing trying circumstances and point them to a better outcome. I am not going to lie or sugarcoat my life with FA. It’s hard. On some days the pain and uncertainty are overwhelming. It has robbed me of so many precious things, and precious time I will never get back. I can live in regret, and anger about my circumstances or I can take life by the horns and fight back. I can shut myself in my room and wait for the outcome, or I can step up to the plate and hit the ball. Maybe I can hit a home run. Maybe I can see another person struggling with a devastating diagnosis look at my life, and say “if she can do it, so can I.”  Maybe I can be the voice of those who society chooses not to see and value. Maybe I can prove our value and worth, through dignity, determination, and hard work. I can fight back and fight through whatever comes my way. Because the alternative is to waste this most precious gift of life. FA is my biggest challenge in life, but it’s also the biggest blessing in my life!
"Creating smiles for people, even through their storms, trials, and tribulations, is the best thing in the world."