FacebookLinkedInFoursquareYouTubeInstagramFlickr
Les Turner ALS Foundation Navigation
  • What is ALS?
  • ALS Support
    • Support Services Team
    • ALS Support Groups
    • Grant Programs & Equipment Loans
    • ALS Communication Passport
    • National ALS Registry
  • ALS Care and Research
    • Les Turner ALS Center at Northwestern Medicine
    • Lois Insolia ALS Clinic
    • Making the Most of Your ALS Clinic Visit
    • ALS Clinical Trials and Studies
    • Les Turner Symposium on ALS
    • Physician Education for CME/CE
  • ALS Education
    • ALS Learning Series
    • My ALS Decision ToolTM
    • ALS & Participation in Clinical Research
    • ALS & Activities of Daily Living
    • ALS & Breathing
    • ALS & Communication
    • ALS & Genetics
    • ALS & Genetic Counseling and Testing for Family Members
    • ALS & Home Modifications
    • ALS & Mobility
    • ALS & Nutrition
    • ALS & Children
    • ALS & Caregiving
    • ALS & Caregiver Self-Care
    • ALS & Relationships, Sex and Intimacy
    • Trusted Resources to Learn About ALS
  • Events
    • Calendar of Events
    • Lou Gehrig Day
    • Cruisin’ for a Cure
    • ALS Walk for Life
    • Team Race for ALS
    • All in for ALS Casino Night
    • Hope Through Caring Gala
  • Get Involved
    • Ways to Donate
    • Advocacy
    • Volunteer
    • Young ProfessionALS Group
    • Gratitude Group
    • Fundraise Your Way
    • Sustainers for Hope
    • Become a Corporate Partner
    • March of Faces
    • Celebration of Life
  • About Us
    • About Us
    • Board of Directors
    • Support Services Committee
    • Staff
    • Financial Statements
    • Careers
    • Contact Us
  • ALS News
  • Donate
  • Search
  • What is ALS?
  • ALS Support
    • Support Services Team
    • ALS Support Groups
    • Grant Programs & Equipment Loans
    • ALS Communication Passport
    • National ALS Registry
  • ALS Care and Research
    • Les Turner ALS Center at Northwestern Medicine
    • Lois Insolia ALS Clinic
    • Making the Most of Your ALS Clinic Visit
    • ALS Clinical Trials and Studies
    • Les Turner Symposium on ALS
    • Physician Education for CME/CE
  • ALS Education
    • ALS Learning Series
    • My ALS Decision ToolTM
    • ALS & Participation in Clinical Research
    • ALS & Activities of Daily Living
    • ALS & Breathing
    • ALS & Communication
    • ALS & Genetics
    • ALS & Genetic Counseling and Testing for Family Members
    • ALS & Home Modifications
    • ALS & Mobility
    • ALS & Nutrition
    • ALS & Children
    • ALS & Caregiving
    • ALS & Caregiver Self-Care
    • ALS & Relationships, Sex and Intimacy
    • Trusted Resources to Learn About ALS
  • Events
    • Calendar of Events
    • Lou Gehrig Day
    • Cruisin’ for a Cure
    • ALS Walk for Life
    • Team Race for ALS
    • All in for ALS Casino Night
    • Hope Through Caring Gala
  • Get Involved
    • Ways to Donate
    • Advocacy
    • Volunteer
    • Young ProfessionALS Group
    • Gratitude Group
    • Fundraise Your Way
    • Sustainers for Hope
    • Become a Corporate Partner
    • March of Faces
    • Celebration of Life
  • About Us
    • About Us
    • Board of Directors
    • Support Services Committee
    • Staff
    • Financial Statements
    • Careers
    • Contact Us
  • ALS News
  • Donate
  • Search

2020 Fall Newsletter

lesturner November 30, 2020Foundation eNews, Home Page, Support Services

2020-Fall-Newsletter-Issue2_Digital
als learning seriesals walk for lifehope through caring gala

Recent Posts

  • June 2025 Foundation eNews
  • June 2025 Foundation eNews
  • Faces of ALS: Trevor Storm, Running for a Reason
  • May 2025 Foundation eNews
  • ALS Awareness Month: Crossing the Rainbow: A Son’s Reflection on Caregiving and ALS

Archives

  • June 2025
  • May 2025
  • April 2025
  • March 2025
  • February 2025
  • January 2025
  • December 2024
  • November 2024
  • October 2024
  • September 2024
  • August 2024
  • July 2024
  • June 2024
  • May 2024
  • April 2024
  • March 2024
  • February 2024
  • January 2024
  • December 2023
  • November 2023
  • October 2023
  • September 2023
  • August 2023
  • July 2023
  • June 2023
  • May 2023
  • April 2023
  • March 2023
  • February 2023
  • January 2023
  • December 2022
  • November 2022
  • October 2022
  • September 2022
  • August 2022
  • July 2022
  • June 2022
  • May 2022
  • April 2022
  • March 2022
  • February 2022
  • January 2022
  • December 2021
  • November 2021
  • October 2021
  • September 2021
  • August 2021
  • July 2021
  • June 2021
  • May 2021
  • April 2021
  • March 2021
  • February 2021
  • January 2021
  • December 2020
  • November 2020
  • October 2020
  • September 2020
  • August 2020
  • July 2020
  • June 2020
  • May 2020
  • April 2020
  • March 2020
  • February 2020
  • January 2020
  • December 2019
  • November 2019
  • October 2019
  • September 2019
  • August 2019
  • July 2019
  • June 2019
  • May 2019
  • April 2019
  • March 2019
  • February 2019
  • January 2019
  • December 2018
  • November 2018
  • October 2018
  • September 2018
  • August 2018
  • July 2018
  • June 2018
  • May 2018
  • April 2018
  • March 2018
  • February 2018
  • January 2018
  • December 2017
  • November 2017
  • October 2017
  • September 2017
  • August 2017
  • July 2017
  • June 2017
  • May 2017
  • April 2017
  • March 2017
  • February 2017
  • January 2017
  • December 2016
  • November 2016
  • October 2016
  • September 2016
  • August 2016
  • July 2016
  • June 2016
  • May 2016
  • April 2016
  • February 2016
  • September 2015
  • June 2015
  • May 2015
  • April 2015
  • January 2015
  • November 2014
  • August 2014
  • March 2014
  • February 2014
  • February 2013
  • October 2008

Categories

  • Advocacy
  • Clinical Trials
  • Donor Spotlights
  • Faces of ALS
  • Foundation Blog
  • Foundation eNews
  • Home Page
  • Research News
  • Support Services
  • Support Services Committee
  • Uncategorized
  • Walker Wednesday

Support Services Committee News

  • June 2025 Foundation eNews

    June 24, 2025

  • June 2025 Foundation eNews

    June 10, 2025

  • Faces of ALS: Trevor Storm, Running for a Reason

    May 28, 2025

  • May 2025 Foundation eNews

    May 27, 2025

  • ALS Awareness Month: Crossing the Rainbow: A Son’s Reflection on Caregiving and ALS

    May 26, 2025

Les Turner ALS Foundation

Les Turner ALS Foundation

info@lesturnerals.org
847 679 3311

5550 W Touhy Avenue,
Suite 302; Skokie, IL
60077-3254

 

© Les Turner Amyotrophic Lateral Sclerosis Foundation, Ltd.

The Les Turner ALS Foundation is a non-profit corporation under section 501(c)(3) of the U.S. Internal Revenue Code, EIN 36-2916466

Accreditation

Better Business Bureau - Accredited Charity   Member Community Health Charities   Candid  Charity Navigator

Affiliates

Northwestern Medicine Feinberg School of Medicine - Les Turner ALS Center
International Alliance of ALS/MND Associations

Site Credit

Distortion Design

  • Privacy Policy
  • Contact Us
FacebookLinkedInFoursquareYouTubeInstagramFlickr
Together toward a cure.
Sign up for the latest news on ALS research, upcoming events, resources for people living with ALS and caregivers, and much more.
Join our email list
close-link
Powered by Convert Plus
DONATE