Welcome to our ALS Team Julie Fundraising Page, a dedication to the memory of our mom who bravely battled Amyotrophic Lateral Sclerosis (ALS) following an unexpected diagnosis at the age of 46. Julie was a kind soul who loved to cook, sing, and play both the guitar and piano. She also held a special affection for lighthouses, symbols of guidance and strength in the face of adversity. In honor of her enduring spirit, we are raising funds for ALS research and care, aspiring to make a meaningful impact on the lives of those affected by this relentless disease. Every contribution, big or small, brings us one step closer to advancements in research and improved care for individuals and families confronting ALS. Thank you for being a part of our team and for contributing to a cause that holds a special place in our hearts.
With heartfelt thanks,
Kim and Kristy
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!