“The ALS Association, what a wonderful resource. The Michigan Chapter has been a great support for my wife and I. Meeting and sharing with people who are going thru similar experiences is encouraging for all.”

– Gil Maldonado, PALS

“The ALS Association, Michigan Chapter support patients and families whose lives have been affected by Lou Gehrig’s Disease. We support vital research to find a cure for this deadly disease, advocate for those who cannot speak for themselves and work tirelessly to help patients here in Michigan lead as full a life as possible. From support groups to medical equipment loans, helping our families connect to community resources or having our Care Services Team visit them at home, our more than 400 patients and their families are first in everything we do.”

– Kristen Munyan, Care Services Director – ALS Association Michigan Chapter

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