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We saw this beautiful message from Jill, shared in her caregiver widow/widower group, Still Standing: For everyone who cared for a loved one with ALS and has had to keep going after loss, please know this: you are not forgotten. 💙 Once a caregiver, always a caregiver.

The strength of caregivers is powered by love that never gives up. 💙 Tag a caregiver who inspires you! ✨ 📸 @thekaregiver #NationalFamilyCaregiversMonth #ALSAwareness #ALSCaregivers #LiveLikeLou

Tomorrow’s the night! 🎉 Our All in 4 ALS Research Trivia Night kicks off in Indy, but you can bid on our amazing auction items from anywhere in the U.S. and have them shipped to you! 📦 Big Ten 🏈 tickets, Southwest flights, & more. Bid now: bit.ly/4qJLGMH

Caregiving for someone with ALS often means unseen sacrifices. These hidden costs weigh heavily on caregivers’ well-being, yet their dedication never wavers. 💙 #NationalFamilyCaregiversMonth #ALSAwareness #ALSCaregivers #LiveLikeLou

What wasn’t Lou good at? Just like Lou, Jim Hilliard loved golf & his legacy continues to drive change for ALS families. Tomorrow, we’ll be at the Team Hilliard Foundation Golf Tournament, raising funds to leave ALS better than we found it. ⛳💙

Nearly eight years ago, Live Like Lou was just getting started & look how far we’ve come together. 💙 Because of you, we’ve helped thousands of ALS families, awarded 100+ scholarships, and built a lasting impact. Let’s keep going. Give the gift of hope: livelikelou.org/donate

Many ALS caregivers won’t ask for help but they need it more than you know. 💙 Here are a few simple ways to support a caregiver in your life and remind them they’re not alone. #NationalFamilyCaregiversMonth #ALSAwareness #ALSCaregivers #LiveLikeLou

At 11, Maycee became her dad’s caregiver. Now she moves for ALS families through her “On Your Mark” campaign & Lou’s Crew. 💙 This #NationalFamilyCaregiversMonth, honor caregivers and move in gratitude 👉 louscrew.org Read Maycee’s story: livelikelou.org/news/daughters…

When her stepdad Fred, a proud veteran, faced ALS, Mandi Bailey found strength in caregiving and now in running. 💙 Learn more about Mandi's story: livelikelou.org/news Honor a caregiver today: louscrew.org.

We honor Meg Reyes, who cares for her husband, Juan, a veteran living with ALS. Ultimately, Meg hopes every caregiver can find the same peace she strives for: the freedom to spend memorable time with the person they love. Read Meg's full story 👉 livelikelou.org/news/megreyes

On this #VeteransDay, we honor those who served and recognize a difficult truth: veterans are twice as likely to develop ALS. 💙 Today, we’ll be featuring veterans living with ALS. Stay tuned for these powerful stories. 🇺🇸 #NationalFamilyCaregiversMonth #ALSAwareness

Today, on #VeteransDay, we honor all who have served, especially those living with #ALS. 🇺🇸 Meet Juan Reyes, a U.S. Air Force veteran and author whose journey with ALS has made him a storyteller and advocate. Read his full story here: livelikelou.org/news/juanreyes

Service takes many forms, in uniform and at home. 🇺🇸 Tony’s military service shaped his resilience, now guiding him through life with ALS. By his side, Karen’s unwavering strength as a caregiver shows how love is service. 💙 Read their story 👉 livelikelou.org/news/thevicks

Get ready for winter with Live Like Lou must-haves 💙 From our signature beanie to the cozy vest and ceramic mug, you’ll stay warm while fueling our mission to support ALS families. ☕️ Shop now → livelikelou.org/store 🛍️

When ALS entered their lives, Ashley and her father, Darrell, faced it the same way he faced everything, with courage and love. 💙 A Vietnam veteran and devoted single dad, Darrell never let ALS define him. Read more about their story 👉 livelikelou.org/news/ashleylee

Guy received a Permobil wheelchair from LLL, Permobil Foundation, and Phi Delta Theta at the Phillies game in Sept 2023. With the help of his wheelchair, he once again served brunch to veterans and their families in Vineland, a tradition he’s kept for 17 years. 🇺🇸💙

Lou Gehrig showed us that courage, humility, and gratitude are the foundation of kindness. 💙 This #WorldKindnessDay and #NationalFamilyCaregiversMonth, do something kind for a caregiver or an ALS family. Write a note, lend a hand, or make a meal. Every act matters. ✨

“Thank you hardly seems enough.” 💙 After her ALS diagnosis, Rachael felt her independence slipping away until a Live Like Lou Quality of Life Grant changed everything. Now she has ramps, grab bars, and most importantly, freedom to feel the sun and breeze again. ☀️

What a wonderful All in 4 ALS Research Trivia Night! 💙 We raised $114,000 in honor of Laurie Roselle to advance ALS research & support early-career scientists. Special thanks to photographer Rick Pranitis and emcee Jake Query from 1075 The Fan, as well as our sponsors.

Happy #NationalPhilanthropyDay! We’re thrilled to partner with Phi Delta Theta to honor Lou Gehrig’s legacy. Join Iowa State and Colorado State in achieving Triple Crown status by registering to serve an ALS family, raising $444 for LLL, and reaching Iron Phi Chapter status.