Having a child who has Spina Bifida hasn't turned me into some superhero mom. Most days I am living my life like any other mom raising two boys, my feet hurt probably because I stepped on another Lego, I have ketchup stains on a brand new shirt and I probably ate a cold dinner. There are some nights I get to my pillow and I think somewhere in the ceiling there should be confetti cannons going off and a cheering squad chanting “you did it, you did it! You made it through this DAY!!!”

Henry is almost 4 now and the learning curve has been steep for Nathan and me for sure. The day Henry was born I didn’t just gain the title of Henry’s mom, I became Henry’s nurse, his advocate, and got a crash course in medical school. But, please don’t miss what I said -- I said we are living our lives. We are laughing, we are finding joy in watching our boys become brothers, we watch Oliver make Henry laugh so hard we have to take Henry into the next room so he can catch his breath, and we celebrate milestones like you wouldn't believe.

Spina Bifida is never going to be the coolest thing about Henry Hinson and that's why I Walk-N-Roll. I want the world to look beyond the way Henry gets from point A to point B. See him through my eyes. Henry is a little boy who loves to read, especially if it's Pete the Cat; he is a little boy who gets excited to see the UPS man, he's a little boy who has dreams of becoming a doctor, he's a little boy who gives the very best hugs and has a laugh that will make your day brighter. Join our team, donate a dollar, share our story whatever you can do we appreciate the love and support!