In August 2014, a viral phenomenon took over social media feeds across the globe with people accepting the ALS Ice Bucket Challenge. Friends challenging friends, patients challenging celebrities and teenagers challenging grandparents to douse themselves with ice cold water while …
Guidelines for Clinical Trials in ALS/MND – 2016 update
This past March, 140 international thought leaders in the field of ALS met at the ALS Clinical Trials Guidelines 2016 Workshop. Among those in attendance included Dr. Teepu Siddique and Dr. Senda Ajroud-Driss on behalf of the Les Turner Research …
A summer of groundbreaking genetic discoveries in ALS
It has been a summer of groundbreaking genetic discoveries in ALS! In July, the Les Turner ALS Research and Patient Center at Northwestern Medicine shared the news from the lab of Dr. Teepu Siddique of the discovery of a third …
Racing for Awareness
Since Derek Hogg was diagnosed with ALS in 2013, he has become a staple at the Les Turner ALS Foundation’s Strike Out ALS 5k. Whether running, using his son’s stroller for support or peddling a special recumbent bike, Derek defines …
Community: The Newsletter of the Les Turner ALS Foundation
Each year, the Les Turner ALS Foundation creates a print newsletter in July and November to highlight the various ways Hope and Help for people living with ALS is displayed in Chicagoland, and across the country. Issue I of Community …
From Generation to Generation: Embodying the True Spirit of “Paying it Forward”
While out on a bike ride, Barrington community member Bob Lee came up with an idea called the Ride for 3 Reasons after being inspired by Mitch Albom’s Tuesdays with Morrie. During 12,000 mile journey across the country, Bob had …
March of Faces Banner
Honor a loved one by including them on a March of Faces banner. The banners travel with the Foundation and are displayed at various events throughout the year as a way to recognize those we have lost to ALS despite …
Personalize Your Care Act
Take action and urge your Representative to support the Personalize Your Care Act (PYCA)! This act was introduced by Earl Blumenauer (D-OR) and Rep. Phil Roe (R-TN) in the US House of Representatives to increase accessibility to and public awareness …
Senate votes to pass amendment to the National Defense Authorization Act
The Les Turner ALS Foundation is pleased to announce that, this week, the Senate voted to pass Senator Dick Durbin’s (D-IL) amendment to the National Defense Authorization Act to protect crucial medical research programs for ALS funded by the Department …
Today’s Caregiver: 5 Lessons I Have Learned From Being A Young Caregiver For My Husband With ALS
Wife of PALS, Sherlyn Brubeck recently shared the five lessons she has learned from being a caregiver to her husband with Today’s Caregiver. Since being diagnosed with ALS in 2014, Sherlyn has become her husband’s primary caregiver. To read the …
