Thank you for helping me reach my Walk to Defeat ALS® fundraising goal! This is an exciting opportunity for us to work together to support those affected by ALS and to spread awareness of the urgency to find treatments and a cure.

Just over two years ago, my husband Mike was diagnosed with this horrible disease.  While we are so thankful he is still able to walk and care for his own personal needs, his physical struggle continues to be an uphill battle. 

We have participated in the Walk to Defeat ALS for two years in Chicago and now that we live in AZ, we look forward to having our team - the ALS Mud Warriors - walk to raise funds in Scottsdale in October. 

The past two years have brought incredible advancements in ALS research, expanded access to care for people living with ALS, and enabled legislation that impacts the quality of life of people with ALS and their families. WE CAN'T STOP NOW!

Please consider walking with me or sponsoring me. With your help, we will be able to make a difference in the lives of people affected by this disease.  Arizona is beautiful in October - come for a visit!!!

Why We Need Your Help

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.

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.

ALS can strike anyone. Presently there is no known cause of the disease, though support is bringing researchers closer to an answer. In the meantime it costs an average of $250,000 a year to provide the care people living with ALS and their families need. Join the movement to bring help and hope today!

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