"Hearing Directly From the ALS Community Through ALS Focus…"

Welcome to Connecting ALS. This week we turn our focus to ALS Focus, a survey platform that brings the needs and perspectives of people living with ALS to the center of our fight.

This week, Mike and Jeremy turn their focus to ALS Focus, a survey platform that brings the needs and perspectives of people living with ALS to the center of our fight. They are joined by Dr. Sarah Parvanta, director of ALS Focus, and John Robinson and Lora Pollari-Welbes, two members of the ALS Focus advisory committee, to walk us through what we learned from the first survey and how listeners can get involved.

To learn more about ALS Focus, go to https://www.neuroserver.org/als-focus/Home/wiaf

To participate in future ALS Focus surveys, check out https://www.neuroserver.org/als-focus/Home/login

Read more about the results of the first ALS Focus survey here https://www.als.org/stories-news/als-focus-survey-1-key-findings-show-high-financial-burden-als-community

Check out bios for the ALS Focus Patient and Caregiver Advisory Committee here https://www.als.org/als-focus/als-focus-structure

Find a transcript of this episode soon on Tumblr.

This episode was produced by Garrett Tiedemann and is brought to you by The ALS Association’s national office and the Association’s Minnesota/North Dakota/South Dakota Chapter
Brought to you by The ALS Association. © 2020 The ALS Association