Join me and Limitless Lisa in a month-long solo road trip from July 16 to August 16, 2025, to raise $10,000 for ALS United Greater New York. As I drive across the country, I’ll share on-camera stories from people living with ALS, shining a light on their resilience and the challenges they face. Every dollar you give will go directly to patient services, resources, and critical research.

Why I’m Doing This

ALS (amyotrophic lateral sclerosis) slowly takes away a person’s ability to walk, speak, swallow, and breathe. There is no cure, and most people live only two to five years after their diagnosis. My mother fought ALS until she passed away in August 2021, and I know firsthand how isolating and overwhelming this disease can feel. Through Limitless Lisa, I want to honor her memory by humanizing ALS, building understanding, and rallying support for families who need it most.

What to Expect on the Road

From the East Coast to the West, I’ll conduct interviews within or near ten cities-Columbus, Chicago, Douglas, Portland, Reno, San Diego, Phoenix, Atlanta, State College—where ALS United chapters are making a difference. At each stop, I’ll spend time interviewing those affected with ALS and, their support system. You’ll meet a truly diverse group of individuals each uniquely impacted by ALS yet united by an unshakable willingness to fight. I’ll post full interviews on YouTube and share highlights on Instagram (@LimitlessLisa) so you can join the journey in real time and witness their courage.

How Your Support Helps

ALS United Greater New York provides in-home equipment, medical supplies, emotional support, and funds research into new treatments. Your gift—whether $5 or $500—will help:

* Fund adaptive devices and home-modification projects that improve quality of life

* Support innovative research that brings hope for better treatments—and ultimately, a cure

 

 

 

Your donation means more than money; it means community, compassion, and hope. If you’re unable to give right now, please consider sharing our story, following the trip on YouTube and Instagram, or encouraging friends and family to get involved. Together, we can make sure no one faces ALS alone. Thank you for being part of this journey.