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.

laurita tellado
hope
Ambrose Ganshanga

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

RECENT POSTS

To the Woman Who Aborted Her Baby with Spina Bifida

By Laurita | February 7, 2015
Posted in ,

Dear Woman, First off, let me say that I am not writing this on an impulse. In fact, I have …

To the Woman Who Aborted Her Baby with Spina Bifida Read More »

I Don’t Always Have Spina Bifida

By Laurita | July 9, 2014
Posted in ,

Yes, I know. That’s quite the inflammatory title. This is a topic I’ve been reflecting on for a long time. …

I Don’t Always Have Spina Bifida Read More »

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