Grab limited-release Live Like Lou gear inspired by Lou’s jersey in all your favorite teams’ colors. https://t.co/T5QWaxqIye
With shirts, sweatshirts, water bottles, and hats, you’ll be ready to represent Lou at our Lou Gehrig Day games and help create awareness for #ALS.
.@Cigna, your flawed decision to deny people on your insurance coverage for Relyvrio is inhumane. Your decision impacts real people who are trying to fight a 100% fatal disease. They don’t have time to wait. Reverse your decision now.
In collaboration with Brian Fraser's parents, Phi Delta Theta will memorialize him through the Brian Fraser Presidential Memorial Scholarship.
Funds raised in Brian's memory will support future Michigan Beta presidents in funding their education. https://t.co/SUNK9tE4kq
Leading off for Live Like Lou in 2023... a new look! https://t.co/6AuwsKwtF3
After months of research, strategy, and countless conversations with our team of supporters, Live Like Lou is beginning the new year with a new brand. #ONWARD
We are thrilled to debut a new look and website. Inspired by the Alexander family’s vision in founding https://t.co/FqLcbVwzRX in 2012 and its visual identity reflecting Lou Gehrig’s autograph, our new logo honors that inspiration and includes his signature as its focus. #ONWARD
Congrats to Wes Faust of Indiana Gamma (@BUPhiDelt) for becoming Iron Phi #1476. He has raised $1,128 and played four days of disc golf with a certain number of holes each day representing various Gehrig-related statistics and dates.
Wes is the 253rd Iron Phi of 2022.
Happy #InternationalDogDay! Here's a picture of Lou with his beloved German Shepherd, Afra of Cosalta, who fared very well at Westminster in 1934.
Dogs also serve as a great companion to many of our #LiveLikeLou staff, supporters, and #ALS families💙
Our board & staff met to finalize our strategic initiatives through 2025, hear stories of impact from ALS family scholarship recipients and volunteers, & spend time connecting and developing as a team. We are thankful to our board for their support and dedication. #livelikelou
People living with aggressive, fatal neurodegenerative disorders like ALS need access to safe therapies. I'm proud to work with my colleagues on both sides of aisle to urge the FDA to work more quickly to approve life saving treatments.
Read our letter below:
Congrats to @wendyfaust, Executive Director of the LiveLikeLou Foundation (@LiveLikeLou4) for surpassing $1,000 raised. She has raised $1,005 and will become an Iron Phi after completing the @orangetheory Fitness “Dri-Tri” – an indoor triathlon on March 19.
Love seeing #LiveLikeLou activity at one of my favorite universities. Thanks to the incredible men of Phi Delta Theta at @ChapmanU for supporting @LiveLikeLou4!
The @phidelt chapter at Chapman University has been raising money for ALS for years, with their most recent fundraiser bringing in more than $20,000 🎉
Thank you, California Phi, for working to ensure the #LiveLikeLou Foundation leaves #ALS better than we found it. #ONWARD
I'm raising $1,000 to become an Iron Phi and benefit @LiveLikeLou4 to continue our work to leave #ALS better than we found it! Visit my page to learn about my Iron Phi athletic goal and support my efforts! https://t.co/B6EZEBpCZx