Patient & Family Services

Living a good life with ALS is something that every person with ALS can do.

We offer resources and services support so that people with ALS and their families do not have to walk alone on their journey. Whether it is direct services, like assistance with Medical Equipment, Respite Care, Assistive Technology or if you need advice and emotional support when faced with accessing healthcare, and emotional strain we are here to help.

In the following pages you will find information on managing ALS symptoms and the direct services offered by The ALS Association of Oregon & SW Washington and how to access them. The information provided on this website is only a small fraction of the resources, ideas, and support that we can offer and make available to you. For all people living with ALS in Oregon and SW Washington, we hope that you contact us directly so that we can marshal our resources to support you as an individual.

The ALS Association of Oregon and SW Washington is a voluntary non-profit organization whose mission is 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. But, on deeper level we are creating a community of people who care about ALS and want to offer help and hope.

You are not alone.

Please contact us at 503-238-5559 or toll free at 800-681-9851 or

info@alsa-or.org