Que pueda por sí misma andar por la vida: Mis días con Violeta
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Que pueda por sí misma andar por la vida: Mis días con Violeta

Hace tres años me enteré que la bebé que esperaba tenía Síndrome de Down. Al principio fue difícil para mi entenderlo y aceptar. Nunca había tenido contacto con alguien con Síndrome de Down y tenía muy poca información. Pero felizmente tuve mucho apoyo de mi familia, que me animaban diciendo que todo iba a estar bien.

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So she can walk through life on her own: My days with Violeta
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So she can walk through life on her own: My days with Violeta

A little over three years ago, I found out that the baby I was expecting had Down Syndrome. At first it was hard for me to understand and accept this. I’d never had any contact with someone who had Down Syndrome, and I had very little information. But, happily, I got a lot of support from my family who encouraged me, saying that everything was going to be fine.

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Vaccines with care
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Vaccines with care

Our team understands disability and how to get creative to meet diverse needs. Here’s a great example.

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From COVID through college, separate is not equal

The pandemic has revealed how important it is that disability is included in every equity conversation, including transition and higher education conversations about students with intellectual developmental disabilities accessing college.

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Know the facts about public charge

As of March 9, 2021, the discriminatory, expanded Public Charge rule is permanently BLOCKED, and is no longer in effect anywhere in the United States. Now, immigrants can safely get public benefits that support their health, nutrition, and housing without fear of impact on their immigration status.

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Will's college reflection (video)

Will, one of the first students to complete the College and Community Studies program at PSU, and staff member at NWDSA/ABI reflects on his transition and college experience.

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Working side by side
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Working side by side

Hunter is our oldest, so when his little sister came around it was shocking to me that I didn’t have to fight for her in the same way I do for Hunter, who has Down syndrome

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