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
  • ALS Education
    • ALS Learning Series
    • My ALS Decision ToolTM
    • ALS & Health Insurance
    • ALS & Money
    • 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
    • Hope Through Caring Gala
    • Lou Gehrig Day
    • ALS Walk for Life
    • Team Race for ALS
    • All in for ALS Casino Night
  • Get Involved
    • Ways to Donate
    • Advocacy
    • Volunteer
    • Young ProfessionALS Group
    • Gratitude Group
    • Fundraise Your Way
    • Become a Corporate Partner
    • March of Faces
    • Celebration of Life
  • About Us
    • About Us
    • Board of Directors
    • Support Services Committee
    • Staff
    • Financial Statements and Reports
    • Employment Opportunities
    • 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
  • ALS Education
    • ALS Learning Series
    • My ALS Decision ToolTM
    • ALS & Health Insurance
    • ALS & Money
    • 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
    • Hope Through Caring Gala
    • Lou Gehrig Day
    • ALS Walk for Life
    • Team Race for ALS
    • All in for ALS Casino Night
  • Get Involved
    • Ways to Donate
    • Advocacy
    • Volunteer
    • Young ProfessionALS Group
    • Gratitude Group
    • Fundraise Your Way
    • Become a Corporate Partner
    • March of Faces
    • Celebration of Life
  • About Us
    • About Us
    • Board of Directors
    • Support Services Committee
    • Staff
    • Financial Statements and Reports
    • Employment Opportunities
    • Contact Us
  • ALS News
  • Donate
  • Search

Tag Archive

Below you'll find a list of all posts that have been tagged as “als”

Faces of ALS: Channeling Mom’s Positivity in the Face of Familial ALS

lesturner September 27, 2022Faces of ALS, Home Page

As a healthcare worker, Tina cared for people diagnosed with ALS, including her mother. Prior to her mom’s passing in 2018, Tina started to experience symptoms that were eerily familiar. “Towards the end of my mother’s battle with ALS, I began …

Read More
alsfamilial alslou gehrig dayois Insolia Clinic at Northwestern Medicine

September 2022 Foundation eNews: ALS Walk for Life!

lesturner September 20, 2022Foundation eNews, Home Page

  Foundation News These people are unstoppable. The ALS Walk for Life brings together thousands of walkers who have dedicated their time to helping people living with ALS. We’re excited to gather with the ALS community and raise much needed …

Read More
alsals walk for life

September 2022 Foundation eNews

lesturner September 13, 2022Foundation eNews, Home Page

  Foundation News ALS Walk for Life, Saturday, September 24! If this is your first ALS Walk for Life, you’re not alone. Suzanne will be participating in the Walk for the first time – and walking in memory of her …

Read More
alsals learning seriesals walk for lifeAMX0035Amylyx PharmaceuticalsFDAhome automationles turner symposiumNorthwestern Medicine

Donor Spotlight: Robert P. Ives

lesturner August 30, 2022Donor Spotlights, Home Page

Robert “Bob” P. Ives is a familiar face at the Foundation. He has presented at our ALS Learning Series webinars, provided feedback on the My ALS Decision Tool™, and participates in our support groups. Bob and his wife Mary are …

Read More
alsals learning seriesdonordonor spotlightveteran

August 2022 Foundation eNews

lesturner August 30, 2022Foundation eNews, Home Page

  Foundation News We’re in it Together at the ALS Walk for Life! The ALS Walk for Life, which will take place on Saturday, September 24 at Soldier Field, brings together thousands of walkers to create ALS awareness and raise …

Read More
alsals learning seriesals walk for lifeles turner symposiumMy ALS Decision ToolNIHNINDSU.S. National Institute of Neurological Disorders and Stroke (NINDS)

Faces of ALS: Tackling Those Miles for Mitch

lesturner August 16, 2022Faces of ALS, Home Page

Marathon runners choose to run for a variety of reasons. Some love to run, enjoy the challenge, or want to cross off an item on their bucket list. Others are running for something – or someone – beyond themselves. Nathan …

Read More
alsteam race for als

August 2022 Foundation eNews

lesturner August 9, 2022Foundation eNews, Home Page

  Foundation News Show Your Support at the ALS Walk for Life on September 24!  The ALS Walk for Life brings together thousands of people…and among them are thousands of incredible stories. Lori couldn’t wait to return to the Walk …

Read More
alsals learning seriesals march of facesals walk for lifeInternational Symposium on ALS/MNDPatient Fellows Program

Faces of ALS: Michelle Gutierrez — Batting Against ALS

lesturner August 2, 2022Faces of ALS, Home Page

Michelle has been a lifelong Chicago White Sox fan. But when she went to a Sox game in June, she saw something that left her in disbelief. Prior to her ALS diagnosis, Michelle and her longtime partner Sue led an …

Read More
alsLes Turner Centerlois insolia als clinicNorthwestern Medicine

July 2022 Foundation eNews

lesturner July 26, 2022Foundation eNews, Home Page

  Foundation News Gather up your teams – it’s time to walk! Registration for this year’s ALS Walk for Life is open! Join the Les Turner ALS family on Saturday, Sept. 24 at Soldier Field for our largest gathering of …

Read More
alsals walk for lifeInformation GuidesInternational Symposium on ALS/MNDstrike out als

July 2022 Foundation eNews

lesturner July 12, 2022Foundation eNews, Home Page

  Foundation News The Foundation represents the European Network to Cure ALS (ENCALS) In June, our CEO, Andrea Pauls Backman, attended the European Network to Cure ALS (ENCALS) conference in Edinburgh, Scotland, along with 650 ALS/MND researchers, patients, and advocates. …

Read More
alsals walk for lifeAMX0035Amylyx Pharmaceuticalsles turner symposium
  • Page 14 of 22
  • ←
  • 1
  • ...
  • 13
  • 14
  • 15
  • ...
  • 22
  • →

Recent Posts

  • April 2026 Foundation eNews
  • Leading ALS Organizations Celebrate Introduction of ACT for ALS Reauthorization Act: Call for Swift Congressional Passage
  • April 2026 Foundation eNews
  • Searching for the cause of ALS, researchers look to metabolism within cells
  • March 2026 Foundation eNews

Archives

  • April 2026
  • March 2026
  • February 2026
  • January 2026
  • December 2025
  • November 2025
  • October 2025
  • September 2025
  • August 2025
  • July 2025
  • 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

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

    May 26, 2025
  • ALS Awareness Month: Frank Granata on the Financial Toll of this Disease

    May 21, 2025
  • ALS Awareness Month: “My mom’s diagnosis broke my heart.”

    May 14, 2025
  • ALS Awareness Month: “I Knew Something Was Wrong”— Stories of Delayed ALS Diagnosis

    May 12, 2025
  • ALS Awareness Month: A Mother’s Day Reflection Balancing ALS and Motherhood

    May 11, 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