Sophie's Voice Foundation

"Protecting Their Life
Before It Begins"
Sophie's Voice Foundation
"Protecting Their Life
Before It Begins"
Sophie's Voice Foundation
"Protecting Their Life
Before It Begins"
Sophie's Voice Foundation
"Protecting Their Life
Before It Begins"
Sophie's Voice Foundation

FIND SOLUTIONS FOR DAY-TO- DAY LIVING

People with disabilities can discover the latest technology, products and services to improve their daily living at the Abilities Expo, which will be held in six major US cities...

SVF Newsletter

The Winter 2012 edition of the SVF newsletter, Voices, will be available online in February. Check back to read and download information about The Center for Spina Bifida Research, Prevention and Policy.

About spina bifida

Spina Bifida or "open spine" is a neural tube birth defect that affects the development of the spinal cord, its membrane (lining), the spinal nerves and the backbone.

Latest News

Welcome to Sophie's Voice Foundation!

SOPHIE'S VOICE FOUNDATION is a charitable organization supporting family outreach programs, prenatal education and surgical studies for children and adults with Spina Bifida.

SOPHIE'S VOICE FOUNDATION was founded in 2008 by actors Boris Kodjoe and Nicole Ari Parker in honor of their daughter Sophie who was diagnosed with Spina Bifida at birth. The news hit hard, but through consulting with various specialists and by educating themselves they found a way to address their daughter's needs and provide her with the best care and treatment available today.

Make a donation to SVF from your cell phone!

Donate to Sophie's Voice Foundation (SVF) by texting SVF and the amount you wish to donate to 41444. You'll hear a message from Boris Kodjoe; have your credit card handy when you text the message. Provided by MobileCause. Messaging & Data Rates may apply. All donations are billed to your credit card. Donations are collected for the benefit of Sophie's Voice Foundation by MobileCause. Text HELP for help or STOP to stop to 41444.

FIND SOLUTIONS FOR DAY-TO- DAY LIVING

SVF Newsletter

About spina bifida

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