Spina Bifida of Jacksonville

Our Story

Founded in 1973, the Spina Bifida Association of Jacksonville is dedicated to advocating for and supporting families impacted by Spina Bifida, the most common permanently disabling birth defect in the United States.

Impact

With over 166,000 Americans living with Spina Bifida, this organization provides vital resources, including medical reimbursement and adaptive equipment, to enhance the quality of life for these individuals.

Why Donate?

Your contributions empower families affected by Spina Bifida, providing them with greater mobility and access to essential resources and medical care through initiatives like the 'Love What Drives You' campaign.

Get Involved

Join the mission to support families in need. Donate cryptocurrency or cash today to help transform lives and provide critical resources for those living with Spina Bifida.