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.
Founder & Director, Hope Inclusive School, Uganda
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.
The week of July 4th, I had the incredibly awesome and humbling opportunity to attend the 2018 Special Olympics USA Games …
Dear Laurita, I write to you with love. Halima Juma Kasim was born on 15/3/2006 (March 15, 2006) with spina bifida…
As a young girl, I enjoyed English, drama, and music in school, and was fortunate to attend a good Catholic school that taught me very good English, both written and spoken. I continued to high school, but sadly, my mum died and life changed, I rebelled, and due to peer pressure…
The Laurita Spina Bifida Project celebrates 1-year anniversary & success of ‘Project Tanzania’ with Jewel Award at Hispanicize 2017
ORLANDO, FL- April 27, 2017- (HISPANICIZE WIRE) – The Laurita Spina Bifida Project (The LSB Project), a non-profit organization whose …