You can make a difference. 

"Our journey to fight MS began in 2011, when I woke up with numbness in my arm. After 6 months of unexplained symptoms and misdiagnosis, I received the diagnosis I couldn't imagine. With a 2-year-old son and my second child on the way, I was diagnosed with MS. As my mobility and disease has progressed and treatment options have been unsuccessful, I knew I had to do something to help others fighting with MS. Our goal is to provide funding toward cutting-edge research and create a world free from MS." —Richard



We are a non-profit foundation that pledges 100% of the proceeds go toward:
funding MS research
providing assistance to people with MS who are in need
of MS-related items (wheelchairs, walkers, ramps, and more) to improve their quality of life

board of directorS

Christine and Rich Giacopelli

Advisory Board
Lorien Gallo
Greg Giacopelli
Matt Giacopelli
Carri Gregersen
Kathleen Harris
Liz Henky
Nicole Milanesi
Mandy Roth
Carla Sullivan
Lauren Weir
Beth Williams
Michael Wood

Medical Advisory Board
Matthew Schiebel, RN
Holy Name MS Center
Mary Ann Picone, MD
Director of Holy Name MS Center