Spina Bifida affects half a million people worldwide.

The Laurita Spina Bifida Project

Hi, I'm Laurita!

It's time to talk spina bifida

The Laurita Spina Bifida Project, Inc. (The LSB Project) is a 501(c)3 tax-exempt, non-profit organization founded in 2014 by Laurita Tellado. Our mission is to start a global conversation about spina bifida, while connecting individuals and families living with it around the world, and to educate health professionals from all fields on the issues affecting this community, including mental health and adult-centered care as part of the action plan.

Children with spina bifida continue to be discriminated against, especially in the developing world. They are denied a chance to participate in activities that promote inclusive development in societies. This makes them more vulnerable to secondary disabilities, all forms of abuse, and always at risk of early mortality.

However, working together, with your support, we can make a difference in their lives. Thanks to The Laurita Spina Bifida Project for all the efforts to reach millions of such children.

Ambrose Ganshanga
Founder & Director, Hope Inclusive School, Uganda

Buffalo Family Scores Nothing But Net with Inclusive Wheelchair Basketball League

By Laurita | October 25, 2019

Posted in Activism, Disability, Spina Bifida, Your Stories

Emily is 10 years old and has spina bifida, and this is her family’s story about building something yourself when […]

Why the ‘Heartwarming’ Story of a Little Girl Carried by Her Teacher is Problematic

By Laurita | October 15, 2019

Posted in Activism, Disability, Spina Bifida

Many of us have seen it– the “inspiring” and “uplifting” feel-good story about a teacher in Kentucky who carried a […]

5 Ways You Can Be There for Someone During Recovery

By Laurita | February 14, 2019

Posted in Disability, Spina Bifida

When a friend or loved one is recovering from surgery, illness or injury it can often be challenging to figure out the best way to approach them. Here are a few tips.