NEW YORK – Gente con discapacidades ha unido fuerzas con personas que viven con VIH-SIDA y otras para hacer un día de acción sobre los recortes que pueden venir por las leyes republicanas en el Congreso.

Una coalición de organizaciones prepara un día de actividad para hoy, con el fin de protestar por los recortes al cuidado de la salud, servicios sociales y otros programas bajo las leyes republicanas de impuestos, que van abriéndose paso rumbo al Congreso.

Las leyes impositivas que hoy se encuentran en un comité de conferencia de la Cámara de Representantes y el Senado reducirían los impuestos a los ricos, a los negocios y a las corporaciones.

Susan Dooha, directora ejecutiva del Centro por la Independencia de los Discapacitados New York (“Center for Independence of the Disabled New York”), dice que el incremento resultante de uno punto cinco trillones de dólares a la deuda nacional sería como un blanco puesto en la espalda de la gente con discapacidades.

“Esto forzará recortes automáticos a la red protectora de la que dependen tanto la gente mayor como la gente con discapacidades.”

Los republicanos se defienden con el argumento de que al reducir los impuestos corporativos se estimula la inversión y se crean empleos, pero los defensores sociales dicen que el costo de esos recortes será mortal para los menos capaces de pagar.

Bajo los cambios impositivos propuestos, Medicaid enfrenta un recorte de 25 billones de dólares tan solo el próximo año, trasladando muchos costos a los estados. Dooha señala que cuando el dinero de Medicaid es recortado, los estados empiezan por reducir la elegibilidad.

“También reducen específicamente servicios de los que depende gente con discapacidades, como fisioterapia o el acceso a medicamentos recetados.”

…servicios que, nos dice, ayudan a la gente a tener una vida independiente y exitosa.

Dooha estaba entre quienes fueron arrestados por participar en una desobediencia civil en Washington la semana pasada, cuando fueron acabados los detalles de la ley impositiva del Senado.

“Yo pediría a la gente que llame a los miembros del Comité de la Conferencia del Congreso y el Senado, y les digan que no podemos mandar a la gente grande y con discapacidades a una miseria mayor.”

Los legisladores republicanos dicen que están cerca de llegar a un acuerdo sobre una ley final y confían en que estará en el escritorio del presidente antes de Navidad.

Más información en https://www.facebook.com/CIDNYInc/posts/10155956430084894


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As the country observes Autism Acceptance Month, Nebraska families raising a child with Autism Spectrum Disorder are among those learning they will be receiving financial assistance.

The Family Support Waiver is based on passage of a 2022 bill and will provide up to $10,000 annually for 850 Nebraska families with a child with a developmental or intellectual disability, and the child will also receive Medicaid coverage.

Leslie Bishop Hartung, president and CEO of the Autism Center of Nebraska, said many Nebraska families raising children with a variety of developmental disabilities struggle to afford their child's care needs.

"It's not a lot of money but it might be just enough for families to bridge those gaps when they really need support, especially over the summer break when there's no school for children," Bishop Hartung pointed out. "And also, specific services that might be a real financial burden."

Families can use the waiver funds for services such as respite care, family caregiver training, home modifications and assistive technologies. Depending on the child's limitations and level of support needed, families can face considerable costs meeting the needs of a child with a developmental or intellectual disability.

Jennifer Clark, deputy director of the Developmental Disability Division for the Nebraska Department of Health and Human Services, said they are notifying around 150 families per month between now and August they will be receiving the Family Support Waiver. The notices are prioritized according to the family's need. Clark says this was determined by their responses to a survey DHHS sent to families with a child on the developmental disabilities waiting list.

Receiving first priority are families in crisis.

"Where the child tends to self-harm or harm others, so whether they're harming their siblings or their family members," Clark outlined. "The second priority is children with disabilities who are at risk for placement in juvenile detention centers or other out-of-home placements."

Clark added families in which the grandparent is the primary caregiver are given third priority, followed by families with more than one child with a disability living at home. Remaining families are prioritized based on the date they applied to the developmental disabilities waiting list.

Jordan Squiers, board president of The Arc of Buffalo County, said they are hopeful the waiver will help fill gaps in services, especially for older youths who do not become eligible for more inclusive services until they turn 21.

"They might be able to get additional help in their home; they might be able to hire somebody to take somebody out into the community more often," Squiers explained. "Kids that age do get the benefit of the schools but obviously we know there's lots of hours in the day outside of that; weekends, summers."

The Family Support Waiver is one of three Home and Community-Based Services Medicaid Waivers available in Nebraska.

April is Autism Acceptance Month and as rates grow, support organizations in South Dakota hope more children on the spectrum get the tools they need to succeed in school.

Researchers with the Annie E Casey Foundation say nearly 9% of South Dakota students receive special education services due to an autism diagnosis, which is four percentage points higher than a decade ago.

Carla Miller, executive director of South Dakota Parent Connection, which works with families of children with disabilities, encouraged parents of children with autism to be proactive with school officials and follow up as needed. For school districts, she stressed clear communication is vital.

"We need to be careful we're not using a lot of jargon that's our related to our field, and really make sure that we ask parents, are they understanding the information we're giving?" Miller urged.

Miller also advised classroom leaders should allow students with autism to participate in as many general class activities as possible while acknowledging their needs. With staffing shortages still a concern, she called on districts to provide more training, especially for general educators.

Miller emphasized special educators cannot foster a welcoming environment on their own and in an era of more awareness, Miller hopes school districts look at students on the spectrum as individuals who bring unique qualities to their class.

"How is autism showing up in the life of that child, and how is it impacting that child?" Miller asked. "Trying to stay away from stereotypical descriptions of autism that can put kids in a box. "

Autism presents a broad range of conditions highlighted by challenges with social skills, repetitive behaviors, and communication. Advocates stressed symptoms can vary widely and the disorder looks different for everyone on the spectrum.


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As siblings in foster care, the fear of being separated is daunting. But thanks to a loving family in Jacksonville, Fla., for two brothers in Ohio, that bond remains unbroken.

Despite Dalton's cerebral palsy and numerous medical challenges, brother Dawson became his devoted caregiver. The two were adopted by Robbin and Steven Brydges through the nonprofit "Wendy's Wonderful Kids," and they've become a beacon for disability awareness.

Now, at 15, Dawson said he's grateful for his parents' support in keeping them together through it all, as he continues to care for his brother.

"He is the most amazing brother a man could ask for," he said. "He has an incredible smile that will just brighten your day instantly. And I'm just blessed to have him in my life, that's all I can say. I'm just blessed."

March is National Disability Awareness Month, and Dawson encouraged anyone considering the adoption process to consider all kids - especially those with challenges who are often overlooked, along with older kids - when it comes to finding their forever home.

Rita Soronen, president and CEO of the Dave Thomas Foundation for Adoption, said children with disabilities or special needs - regardless of race, age, or background - often face prolonged stays in foster care or institutional settings. She underscored the need to establish a support network for families considering adoption, and said the Wendy's Wonderful Kids Program was created to assist families in navigating this journey, no matter a child's unique needs.

"Making those connections of access to networks - access to medical or psychological resources that they will need before that adoption is finalized - is critical," she said, "so that families feel that they will be supported, that they will have access, and that they can successfully raise a child in their home."

According to the Dave Thomas Foundation, its Wendy's Wonderful Kids Program is responsible for more than 14,000 successful adoptions across the United States and Canada.