We are a group of ALS patients, family members of patients, and volunteers whose lives have been impacted by Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig’s Disease. We have formed a non-profit organization to serve the ALS community in the Inland Northwest and to offer assistance to other non-profit organizations that help patients and families with ALS. We have joined together in the belief that together we can make a difference in the quality of the lives of those currently living with ALS. Due to our experience with the disease, we are able to offer support in many forms. We can provide meals, rides, shopping, chores, social calls, fun activities, home modification projects, and installation of adaptive equipment. If requested by patients and families, we can share our experiences of what worked for us and provide other needed assistance that is within our capabilities.

Provide equipment/adaptive items to patients

Support patients and families with meals on our Cooking Saturdays and also with a weekly ALSSO Meals on Wheels when it appears the family could use more food support

Social visits!

Happy, fun, nice things for PALS/CALS on any day and on birthdays

Establishing a Helping Hands for ALS teen program in our community

Attend support group meetings of ALSA, MDA, TDI, any that support PALS/CALS