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
RECENT POSTS
Laurita to airlines: don’t subject travelers with disabilities to “junk fees”
Laurita took to Medium.com to address the airline “junk fee controversy” that has played out in the news in the …
Laurita to airlines: don’t subject travelers with disabilities to “junk fees” Read More »
Dear Grey’s Anatomy Writers: Give Us An Honest Portrayal of Spina Bifida
Dear Shondaland Team, My name is Laurita Tellado, and I am the Founder and President of a small, family-run non-profit …
Dear Grey’s Anatomy Writers: Give Us An Honest Portrayal of Spina Bifida Read More »
How We Use Your Donations | #GivingTuesday
Happy Giving Tuesday! The Laurita Spina Bifida Project is the sole funder of the Hope Inclusive Center in Mbarara, Uganda. …
Laurita Writes about Accessible Travel for Wanderful
We are grateful to Wanderful, a global lifestyle brand and platform that connects women in travel, for publishing Laurita’s article …
Laurita Writes about Accessible Travel for Wanderful Read More »
An Update on Jackline, a Young Girl in Uganda
In October 2019, we shared this story on Facebook of a nine-year-old girl living with spina bifida whose mother has …