Madrid’s Association of Spina Bifida (AMEB) gives us their testimony: When we talk about Spina Bifida, we are talking about real people, with names and surnames. For us, it is essential that everybody knows what Spina Bifida is. We want that the disability world is well known by everyone, to finish with current prejudices and fears. We need more research and resources. Because we want a better future and a present full of quality of life. March 3, World Birth Defects Day