Whether you are newly diagnosed, years into your journey, or supporting someone you love, these conversations are designed to provide clarity, connection, and practical guidance.
This summer, we’ll begin with a community discussion of Hope for the Best, Plan for the Rest.
Our first conversation will center around Hope for the Best, Plan for the Rest—a practical, compassionate guide to navigating complex medical decisions and planning for the future with clarity and confidence.
This book offers tools and perspective for individuals and families facing serious illness, helping bridge the gap between hope and preparation.
Sign up to receive details about upcoming sessions and how to participate.
Hosted by the Tanner Foundation for Neurological Diseases, enhancing the lives of individuals and families living with ALS, Parkinson’s disease, and Multiple Sclerosis in our community.