Spina Bifida Association of America

Our Group organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Spina Bifida Association of America

American people who lives with Spina Bifida, which is permanently disabling birth defect in the new born baby’s. The goals are to develop better treatment, better understanding of causes, and new ways to prevent Spina Bifida. Despite the impact of Spina Bifida on individuals, families, society, Organizations, and the nation, sadly, some research has been conducted on the many components of this complex birth defect in the early stage of the baby. For few of the conditions and complications associated with Spina Bifida, treatment options are limited in Spina Bifida. For others, Spina Bifida is practically nonexistent. Because Spina Bifida manifests itself as a number of conditions, it is unlike any other disability and complications in the body structure in the fetes while in the womb. While some conditions are primarily associated with Spina Bifida, others are common to other kinds of disabilities. In these areas, research conducted by the Spina Bifida Community will reach beyond those who live with Spina Bifida and will benefit Millions and perhaps thousands of people. In the United States of America Spina Bifida is the most common permanently disabling birth defect. Every day, about 8 babies born in the United States have Spina Bifida or a similar birth defect of the brain and spine. Spina Bifida literally means “split spine.” Spina Bifida happens when a baby is in the womb and the spinal column does not close all of the way. The key to a better life for the 166,100

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