Fighting Lou Gehrig's Disease on Every Front!

Our Mission: To lead the fight to cure and treat ALS through global, cutting-edge research, and to empower people with Lou Gehrig’s disease and their families to live fuller lives by providing them with compassionate care and support.

Wednesday, April 27, 2011

Jeff's "Road to Graduation"


This Saturday, Jeff Lester will join his fellow students in Dearborn as he graduates from the University of Michigan with his Masters in Business Administration and his Masters in Finance. While this may sound impressive on its own, Jeff’s story is made more incredible by that fact that when he began his studies in 2007, he was quadriplegic and on a ventilator and had already been fighting ALS, Lou Gehrig’s disease, for more than 10 years.

Due to his physical limitations, getting from his Missouri home to graduation here in Michigan has been a unique challenge. Jeff’s determination to get to graduation has been the subject of national attention. Jeff has been featured on USA Today and has a website dedicated to his effort, www.getjefflestertograduation.com. Jeff has also had a major presence on facebook.

Jeff’s journey has inspired many organizations, including some here in Michigan, to get involved. When The ALS, Association, Michigan Chapter heard of Jeff’s travel plans, we got busy arranging for the equipment that he needed to be taken to his hotel. Using items from the Chapter’s Durable Medical Equipment Loan Closet, a free service that allows ALS patients to use medical equipment at no cost, the Chapter’s Patient Services staff worked closely with the New Hudson branch of United Seating and Mobility, to prepare equipment and have it ready and waiting for Jeff. Michael Mills, one of our Chapter's most active volunteers, met Jeff Gonzalez from United Seating and Mobility this morning in New Hudson and dropped everything off at the hotel. A HUGE thanks to both Mike and Jeff (and the entire United Seating and Mobility team) for their hard work.

An organization truly dedicated to helping ALS patients, United Seating and Mobility plans to be on call all weekend should Jeff need anything. Joe Newhouse from Permobil, a major power wheelchair manufacturer, offered to provide their services as well. Also joining in the effort was ALS Guardian Angels, a non-profit organization dedicated to helping ALS patients and families live a full life. They initially contacted The Michigan Chapter for help.

Jeff’s journey to graduation is a remarkable example of the good that can be accomplished through collaboration. He hopes that his graduation will create awareness for Lou Gehrig’s disease, and it is well timed, with May being ALS Awareness Month. Jeff’s story is an inspiration to all involved, and his congratulations are certainly deserved.

Congraultions Jeff Lester from all of us here at The ALS Association, Michigan Chapter!


On May 8th, staff from The ALS Association, Michigan Chapter, volunteers and families will join others from around the country in Washington D.C. for National ALS Advocacy Day. They will spend three days in Washington, learning more about legislative needs for ALS, being updated on the latest happenings in ALS research, and meeting other ALS advocates working towards a cure.

On Tuesday, May 10th, they will "head to the Hill", sharing the stories of constituents at home with their Senators and Congressmen and asking them to support ALS research and the National ALS Registry. The most effective tool these dedicated advocates can take with them is YOUR STORY! It is so important that our legislators see that ALS has a face and is effecting the people they represent.

We need your help to advocate for ALS. Please, share your story with our Chapter, and ask your family and friends to do the same. You can email your story to us at kristen@alsa-michigan.org. Thank you!