I was diagnosed with ALS on May 21, 2009. So far, the only effect has been on my speech and voice.  Hope is an important part of dealing with such a diagnosis.  ALS patients typically live between two and five years. The disease progressively destroys all voluntary muscular movement. 

At present there is only one drug to treat ALS; its effects are very modest.  It extends the lifespan of an ALS patient by an average of 3 months. Research may lead to better treatments that provide real hope. But, research takes money, and that's why I'm asking for your help. 

In addition to research, the ALS Association supports patients by offering free loaner tools such as walkers, wheelchairs and speech assistant devices.  For these reasons I'm asking you to join us at the annual 'Walk to Defeat ALS' at Principal Park on Saturday, Oct 10th.  Funds raised for this walk are used to further research to stop ALS and to provide loaner equipment to ALS patients.  This is an exciting opportunity for us to work together to support those affected by Lou Gehrig's Disease and to spread awareness of the urgency to find treatments and a cure.

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. I encourage you get your friends, family, neighbors and coworkers involved!

Hope to see you on the 10th!

Registration starts at 8:30 a.m. at Principal Park in Des Moines and we will start walking at 10:00 a.m.