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You’ve inspired us. This community is for you.

Our commitment to special needs families goes beyond our products. That’s why we created the #LiveInspired online community. Explore resources, connect with other families, and even share your story here.

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Our commitment to special needs families goes beyond our products. That’s why we created the #LiveInspired online community. Explore resources, connect with other families, and even share your story here.

It Begins with Real Families Like You

We're Here To Help You Find Resources

Meet Our Bloggers

ELLEN SEIDMAN

Ellen Seidman writes Love That Max, an award-winning blog for parents of kids with special needs who kick butt. Its namesake: Max, a teen with cerebral palsy who…kicks butt. A mom of three, Ellen’s also a web content consultant, magazine editor and writer, and professional snacker. Find her on Twitter, Facebook and her website.

TARA THOMPSON

Tara Thompson is the Aussie mum of two behind @willows-cpjourney, where she documents the journey of her youngest daughter living with Cerebral Palsy. Co-author of the e-book Therapeutic Play Ideas for Children, Tara uses her creative flair and teaching background to do everything she can to assist not only her daughter, but all children in their fight against living with Cerebral Palsy.

ILEANA SOSA

Ileana is the voice behind The Special Life of Us, a personal blog where she shares her perspective on motherhood and learning how to navigate through the world of cerebral palsy and microcephaly with her youngest daughter. Ileana is a wife, mother of two girls, and resides in Corona, California. You can follow their adventures on the blog, and on Instagram + Facebook.

TAMARA SIMMONS

Tamara Simmons is the author of The Funding Guide for Children with Disabilities, a free downloadable eBook with proven fundraising techniques. Through working with her family’s nonprofit, Project Mobility, Tammy has become an expert in fundraising, helping families obtain the life-changing technology they need but can’t afford.

JOSH ARGALL

Josh is a passionate advocate for patients and families affected by muscular dystrophy. His son Devin, who lives with Duchenne muscular dystrophy, is the Wisconsin State Ambassador for the Muscular Dystrophy Association. They’d love for you to follow their journey on Facebook, Instagram , or the Devin Strong Website.

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