On June 13, 2017, my diagnosis of PLS changed to ALS. Our local organization, now known as ALS Northwest, has supported us every step of the way! Whether it is borrowing from the loan closet, help with setting up assistive devices, home visits, grants, or our wonderful support group, we know they are there when we need them! But all of this takes money.

For the 8th year in a row, my family and I will be participating in the Walk ALS Event. This year we are joing the SW Washington Walk on May 19, 2024.  We would be honored to have you join Robin's Caped Crusaders!! 

Are you unable to join us? We could still use your help. Help us reach our team goal of $1,000. Every dollar gets us one step closer to ending ALS.