Welcome to the fight for my wife's life!

As many of you know, my wife, Michelle, was diagnosed with amyotrophic lateral sclerosis (ALS) in October of 2008. I am incredibly thankful to the ALS Association, their endorsed clinics, their social workers, and their doctors for the love, support, and dedication that they have shown to Michelle and our family since Michelle's diagnosis.

ALS is a progressive, fatal disease. There is no known cure for ALS at this time. There are also few treatment options. Most people with ALS *die* within 2-5 years after diagnosis. I feel incredibly blessed that Michelle's progression has been slower than "the norm" so far. The reality is, however, is that each day we have is a day that we must cherish.

We are asking our friends and family to join us in the FIGHT against ALS. As Michelle and I prepare for the birth of our first child, we are asking for everyone's help to fight ALS. Our family's future and the future of so many individuals count on the research at the forefront of this battle. By supporting our walk team, $0.91 cents of every dollar you donate goes directly towards ALS research and to support patients living with ALS.

Please consider supporting us by making a contribution to our walk or joining our walk team. Please consider sending this link to your friends and family and spread the word about our story.

Why We Need Your Help

Often referred to as Lou Gehrig's Disease, 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 an ALS patient 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.

This crippling disease can strike anyone. Presently there is no known cause of the disease though support is bringing researchers closer to an answer. In the mean time it costs an average of $200,000 a year to provide the care ALS patients need. Help make a difference and donate or join a Walk today.

If you think this page contains objectionable content, please inform the system administrator.