Amyotrophic lateral sclerosis (ALS) is a progressive and fatal neuromuscular disease with no cure or treatment. Once diagnosed, the average life expectancy is 2–5 years.  The physical, financial, and emotional toll on ALS patients and caregivers can be overwhelming. Many people are living with this devastating disease in our community as Michigan is rated a top state in the country for ALS diagnosis. The mission of the Susan Mast ALS Foundation (SMAF) is to provide excellent support to ALS patients, families, and caregivers living in West Michigan. Our services focus on all areas of need for the regional ALS community with special emphasis on respite care. The vision of SMAF is to build a strong foundation to ensure all ALS patients and families have the much-needed support, guidance, and resources available to them today and for years to come.  We strive to strengthen and to build our relationships with community partners so we can continue our mission.