CARL'S STORY
In life, you can count on one thing; everything can turn around in one day or even in one minute. For us, this minute was on May 19th 2021. Our amazing, loving, generous, funny, strong father was diagnosed with ALS/Lou Gehrig’s Disease.
This has shaken our hearts and our worlds to the absolute core. He is a brother, a father, a husband, a son, a friend, a grandpa, a confidant, a man of God, and a pillar of strength to so many. Love, prayer, and strength come in many forms and through many people. We need as much as possible right now and in the coming days. The outpouring of love and support has truly been unbelievable; and for that, we are ever so grateful.
This is going to be a journey we could never be prepared for, but we do know the power of prayer and the miracles God is capable of. We vow to remain hopeful and committed to making sure Dad has the very best care.
Our father has lived a happy life, bright and full of memories, and we will continue that with him. He is the strongest man we know- he will not give up this fight and we will be there by his side, every single step of the way. Let this serve as a constant reminder to hold close your loved ones, to live your fullest, and to never take anything for granted.
Thank you for helping us reach our fundraising goal! Together we can make a difference in the lives of those affected by ALS. Our team is committed to raising money to support people in our community with ALS and spread awareness of the urgency to find treatments and a cure. Please consider joining our team in the Walk to Defeat ALS® or choose a team member from the list and donate to our cause.
WHY WE NEED YOUR HELP
Every 90 minutes a person in this country is diagnosed with ALS and every 90 minutes another person will lose their battle against this disease. ALS occurs throughout the world with no racial, ethnic, or socioeconomic boundaries.
That’s why we’re participating in the Walk to Defeat ALS. To bring hope. To raise awareness. To provide resources and services to families free of charge. To help unlock the mystery of ALS and find the key to treatments a cure. Will you join us?
ABOUT ALS
Amyotrophic lateral sclerosis (ALS) is a progressive, fatal neuromuscular disease that slowly robs the body of its ability to walk, speak, swallow and breathe. The life expectancy of a person with ALS averages 2 to 5 years from the time of diagnosis.
ALS can strike anyone. Presently there is no known cause of the disease, yet it still costs loved ones an average of $250,000 a year to provide the care people living with ALS and their families need. Join the movement to provide help and hope today!
