Introducing Team Lempa!

As some of you know my Dad has been diagnosed with ALS. On May 18th my family will be participating in the Greater Chicago Walk to Defeat ALS. I am hoping to raise $1,000 to support the ALS Association and the work they do for individuals and their families that are living with ALS. Please click on this link to make a donation.

My Mom and I also invite you to join Team Lempa. If you are interested, please contact one of us.

More details will be posted on the attached link and as well as on this website. If you are on Facebook, please consider joining Team Lempa on Facebook.

About the ALS Association:

Established in 1985, The ALS Association is the only national non-profit organization fighting Lou Gehrig’s Disease on every front.  By leading the way in global research, providing assistance for people with ALS through a nationwide network of chapters, coordinating multidisciplinary care through certified clinical care centers, and fostering government partnerships, The Association builds hope and enhances quality of life while aggressively searching for new treatments and a cure.

As the preeminent ALS organization, The Association leads the way in research, care services, public education, and public policy — giving help and hope to those facing the disease.  The Association’s nationwide network of chapters provides comprehensive patient services and support to the ALS community. The mission of The ALS Association is to lead the fight to treat and cure ALS through global research and nationwide advocacy, while also empowering people with Lou Gehrig’s Disease and their families to live fuller lives by providing them with compassionate care and support.

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