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.
Last year, my dad, my biggest fan, was diagnosed with ALS. If you know anything about Mark Stolz, you know he is a generous and compassionate human who faces everything with a sense of humor and a “get ‘er done” attitude. You also know that, while he is the first to volunteer to help anyone else, he is not one to ask for help for himself . As his daughter, it’s hard to put into words the absolutely crushing reality of watching the disease progress and steal his physical strength and endurance. However, his stubbornness and humor in the face of this daunting diagnosis remind us of the importance of supporting the ALS Association.
By walking or donating, you can help fund critical research and support services that make a real difference for patients and families affected by ALS. Your involvement not only honors dad’s fight, but also contributes to a future where others may find hope and healing.
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!
