ABOUT US
Through fundraising events, advocacy, and community building, we are committed to a future where individuals with SMA have access to life-changing treatments, greater independence, and the opportunity to fully participate in the world around them.
We are committed to fueling groundbreaking research, expanding access to care, and accelerating treatment development. Every dollar raised brings us closer to our mission.
RAISE FUNDS.
GENERATE AWARENESS.
We aim to amplify the experiences of those living with SMA and educate the public with an informed perspective. Through our awareness efforts, we hope to build better support and advocacy.
Hope is what keeps us going. With promising treatments on the horizon and a growing network of advocates, we believe in the power of hope to remind us that progress is always within reach.
PROVIDE HOPE.
FUELING SMA RESEARCH AND BUILDING A FUTURE WHERE STRONGER OUTCOMES ARE POSSIBLE FOR SMA.
2010
Our first fundraiser for SMA.
2014
Became an official nonprofit organization.
People and businesses supported our mission.
1000+
Dollars raised for SMA.
500,000+
At just eight years old, our founder, who was diagnosed with SMA 1, sparked the inception of WOW with a simple dream: to raise $100 for spinal muscular atrophy with a lemonade stand. Though she didn't realize it then, those humble beginnings were the catalyst that catapulted her into this remarkable journey.
WHERE IT ALL BEGAN