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 – NEW
    • 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
    • ALS Walk for Life
    • Team Race for ALS
    • All in for ALS Casino Night
    • Hope Through Caring Gala
    • Lou Gehrig Day
  • Get Involved
    • Ways to Donate
    • Chipping Away at ALS
    • Sustainers for Hope
    • Volunteer
    • Young ProfessionALS Group
    • Gratitude Group
    • Fundraise Your Way
    • Become a Corporate Partner
    • ALS Awareness Month
    • March of Faces
  • About Us
    • About Us
    • Board of Directors
    • Support Services Committee
    • Staff
    • Financial Statements
    • 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 – NEW
    • 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
    • ALS Walk for Life
    • Team Race for ALS
    • All in for ALS Casino Night
    • Hope Through Caring Gala
    • Lou Gehrig Day
  • Get Involved
    • Ways to Donate
    • Chipping Away at ALS
    • Sustainers for Hope
    • Volunteer
    • Young ProfessionALS Group
    • Gratitude Group
    • Fundraise Your Way
    • Become a Corporate Partner
    • ALS Awareness Month
    • March of Faces
  • About Us
    • About Us
    • Board of Directors
    • Support Services Committee
    • Staff
    • Financial Statements
    • Contact Us
  • ALS News
  • Donate
  • Search

Post Archive by Month

Below you'll find a list of all posts from March, 2019

Faces of ALS: “They’re like a second family…”

lesturner March 21, 2019Faces of ALS, Home Page

On Saturday, March 9, we honored Mindy Evans-Williams with the Hope Through Caring Award at our annual Hope Through Caring Gala. Mindy has been living with ALS for over two decades, supported by the Foundation every step of the way. …

Read More

March 2019 Events eNews

lesturner March 12, 2019Advocacy, Foundation eNews, Home Page

March 2019 Foundation eNews

lesturner March 6, 2019Advocacy, Foundation eNews, Home Page, Support Services

Recent Posts

  • November 2024 Foundation eNews
  • Faces of ALS: A Veteran Nurse’s Journey of Service and Strength
  • National Institute on Aging invests an additional $7.3 million into NU-9
  • October 2024 Foundation eNews
  • October 2024 Foundation eNews

Archives

  • 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
  • Uncategorized
  • Walker Wednesday

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
Together toward a cure.
Sign up for the latest news on ALS care and research, upcoming events and resources for people living with ALS. Because nobody in our community fights ALS alone.
Join our email list
close-link
Powered by Convert Plus
DONATE