
Run, Lacy Run for CJD
By: Lacy Hladky
Just about one year ago, my father was a
healthy, active and happy 57 year old man
making the most of his retired life. However,
CJD crept out of nowhere and in less
than three months, brutally robbed him of
his life.
Lawrence “Larry” Hladky was truly an
amazing man. There are no words to describe
just how special he was to me and
many others. He was easy going and always
aimed to have fun with each and
every day. He was young at heart and
loved to bring joy to everyone around him.
My dad is my inspiration and I thank God
every day for the honor of being his daughter.
Throughout his suffering, he was so
patient, so humble, so strong and so full of
love for God. He made the most of the
situation, brought smiles to our faces either
by making weird looks or saying something funny out of the blue. He was such a light of the comfort
that God's love brings because even as he cried and we quickly rushed to be by his side and hold him,
he instead comforted us by saying, 'I'm happy.'
Even though it still haunts me every day to have witnessed CJD quickly take my father’s every ability
down to his last breath, the memories of his humility and love calm my heart. I will never completely
jump over this hurdle of missing my dad, but I'm slowly coming out of the stage of unconsciousness.
Before it was all just a bad dream, but now the dark clouds are starting to clear and I feel this tug at my
heart to take action by educating myself and others about CJD. I am a first-hand witness of this disease
and all its horrors, but I couldn't seem to find words to explain it to people when they asked. I often
feel that I'm alone and trapped behind all of the unknown and conflicting information out there about
CJD. Our family has been given the run around with this disease and the more I talk to others affected
by CJD, the more they recount the same experience.
Because I don’t want my dad to be lost between the cracks, I have decided to run a marathon in his
honor and all the while raise awareness and funds for CJD. I started a blog where I post messages
about my running adventures and information about CJD. It can’t be denied that CJD is increasing in
force and even more so, it is hiding from us the root of its indestructible power. We are walking around
blind to CJD and this puts us all at risk. We need to know more to protect ourselves and others from
being attacked by this horrible disease. It is time to take action. Please help me to spread the word
about CJD. I need your help because I definitely can’t fight this battle by myself. I greatly appreciate
your support!
Donations received will be split in half between the CJD Foundation to help spread more awareness
and to the National Prion Disease Pathology Surveillance Center to help with more research to find a
cure.
www.runlacyrunforcjd.blogspot.com
A special thanks to Iren Hunter and Jodi Hanson for contacting me to share your stories. Even though we have never met, we are joined as sisters through tragedy. We've lived through something that not many have or will ever experienced. It is a trial, but together we will remain pillars of strength for others who will be strickened by CJD. It is a lot closer than you may think. This is proven to me every day. Thanks for your support and love!