ALS Walk Oshkosh – September 12, 2026
The Walk to Defeat ALS is so much more than a fundraiser — it’s a movement that brings people together in support of those living with ALS, their families, and their caregivers. 💙
As OPALS 4 ALS continues to grow, we are so grateful for the opportunity to be present at The ALS Association’s Walk to Defeat ALS events throughout Wisconsin.
Remembering Mike
Mike passed away peacefully, surrounded by his loved ones, on August 23, 2026.
His wife, Kim, shared how grateful she and Mike were for the love, care, and support Mike received through OPALS 4 ALS. Knowing that our organization was able to bring some comfort and joy to Mike and his family means more to us than words can say.
Gordon Flesch Charitable Foundation Award
We are incredibly honored to share that OPALS 4 ALS was selected as a 2026 recipient of the Gordon Flesch Charitable Foundation Award! ❤️
The mission of the Gordon Flesch Charitable Foundation is one that means so much to us: enriching lives through local community organizations that assist people of all ages with disabilities, illness, hardship, or disasters.
Remembering Sue
We remember Sue with gratitude and honor her memory. Through OPALS 4 ALS, Sue received a haircut, massages, and nail care. It was a privilege to provide these wellness services and support her during her ALS journey.
Sue passed away on June 5 after living with ALS. In lieu of flowers, her family requested that memorial donations be made to OPALS 4 ALS. We are deeply grateful to Sue's family and friends for their generous contributions in her memory. Their support helps us continue providing comfort, care, and wellness services to others living with ALS.
We are thankful for the opportunity to have made a positive difference in Sue's life, and we will remember her with warmth and appreciation.
Amy's Story Featured by The ALS Association
We are incredibly proud to announce that our very own Amy was recently featured on The ALS Association's social media platforms to share her powerful journey. Read the full post to view her featured post and learn how sharing personal stories like hers is a vital step in generating the support needed to defeat this disease.
ALS Awareness Month Activities
This past May, the OPALS 4 ALS community turned awareness into action. From confronting the staggering statistics of the disease to shining a light on the daily realities faced by people living with ALS and their caregivers, we spent ALS Awareness Month educating and rallying our supporters.
A Sea of Blue: The Meaning and Making of the I AM ALS Flag Display
In May 2026, the National Mall in Washington, D.C., transformed into a powerful sea of blue. Hosted by the advocacy group I AM ALS, the 5th Annual Community Gathering featured over 6,000 blue flags stretching toward the Washington Monument—each bearing the name of someone impacted by ALS. This striking display represents the 6,000 Americans diagnosed with the disease every year. Read on to learn about the profound meaning behind this installation, the incredible volunteer effort required to plant every single flag in the hard-packed earth, and how this visual demand for action is fueling the fight for a cure.
Heidi’s Testimonial
Heidi's message after receiving services highlights the positive impact that OPALS 4 ALS can have on a person's well-being. Her words reflect the comfort, relaxation, and support she experienced, while expressing heartfelt appreciation for the care provided and the meaningful difference made.
Peggy’s Testimonial
Peggy shares her heartfelt gratitude for OPALS 4 ALS, describing how receiving permanent makeup transformed her daily experience living with ALS. What was once a source of frustration and loss has become a moment of confidence and joy, helping her feel like herself again. Through the compassion and skill of the OPALS 4 ALS team and volunteers, Peggy found not just a service—but a renewed sense of identity and comfort.
OPALS 4 ALS Honored in CBS 58 “Natalie’s Everyday Heroes”
OPALS 4 ALS was recently featured in a CBS 58 “Natalie’s Everyday Heroes” segment, highlighting our mission to provide pampering and personal care services to people living with ALS. Through the generosity of volunteer beauty professionals, we help restore confidence, dignity, and a sense of normalcy for those facing the challenges of the disease. This recognition underscores the meaningful impact small acts of care can have on quality of life.
Birthday Fundraiser
Amy is turning 50 — and instead of gifts, we’re turning this milestone into something bigger… hope for families facing ALS.
Sue’s Testimonial
A daughter reflects on the impact of seeing her mother with ALS experience moments of joy again through OPALS 4 ALS services. Simple acts of care—like a haircut or manicure—restored comfort, dignity, and happiness, offering both mother and daughter meaningful moments amid the challenges of the disease.