OLYMPIA, Wash. - Esta mañana (miércoles), personas con discapacidades que requieren atención en el hogar se reúnen en la capital del estado para manifestar su apoyo a dos proyectos de ley (HB 1273 y SB 5346) que restablecen las horas de servicio de atención domiciliaria, que se han reducido en los últimos años a consecuencia del déficit en el presupuesto estatal. Comenta Corinna Fale de Everett, defensora de la organización The Arc of Washington. Imagen disponible:

Las horas de atención que reciben las personas discapacitadas en su domicilio están entre las víctimas del déficit del presupuesto estatal, pues ese tiempo se recortó un promedio de diez por ciento en 2010. La manifestación que se lleva a cabo hoy en la Legislatura es para apoyar dos proyectos de ley que restablecen las horas de servicios a los niveles pre-crisis. Corinna Fale, defensora en la organización The Arc of Washington, dice que a causa de su parálisis cerebral a ella se le dificulta levantarse y ponerse a trabajar. La vida se le ha complicado más por los recortes en las horas de servicio de atención domiciliaria, y quiere hacérselo saber a los legisladores.

"Se me hace muy dificil, porque siempre estoy haciendo malabares con proveedores de atencion medica, y tratando de averiguar cuando pueden venir y cuando no; asi que participo en la manifestacion con la fe de que me van a escuchar y que estaran de nuestro lado."

Olympia, WA - Este miércoles, personas con discapacidades que requieren atención en el hogar se reúnen en la capital del estado para manifestar su apoyo a dos proyectos de ley (HB 1273 y SB 5346) que restablecen las horas de servicio de atención domiciliaria, reducidas en los últimos años a consecuencia del déficit en el presupuesto estatal. Esas horas de atención a las personas discapacitadas están entre las víctimas de dicho déficit, pues ese tiempo fue recortado un promedio de diez por ciento en 2010.

La manifestación se lleva a cabo en la Legislatura para apoyar que se restablezcan las horas de servicios a los niveles pre-crisis. Corinna Fale, defensora en la organización The Arc of Washington, dice que a causa de su parálisis cerebral a ella se le dificulta levantarse y ponerse a trabajar. La vida se le ha complicado más por los recortes en las horas de servicio de atención domiciliaria, y quiere hacérselo saber a los legisladores.

“Se me hace muy difícil, porque siempre estoy haciendo malabares con proveedores de atención médica, y tratando de averiguar cuándo pueden venir y cuándo no; así que participo en la manifestación con la fe de que me van a escuchar y que estarán de nuestro lado.”

Para recaudar el dinero necesario para restablecer las horas de cuidados a domicilio, ambas iniciativas proponen terminar con la exención del pago de impuesto sobre la venta a las personas que no son residentes del estado. El proyecto de ley del Senado propone también cobrar el impuesto de venta en todo tipo de servicios de cobro de deudas. Ambos proyectos están todavía en su Comité y sus partidarios son demócratas.

Fale, junto con otros defensores de las personas discapacitadas, dicen que el estado también ahorra millones de dólares cuando son atendidas en casa en vez de asilos. Añade que los clientes de atención en el hogar también ayudan a promover mayor independencia y dignidad.

"Creo que la gente tiene el derecho a vivir en sus comunidades y ser parte de su comunidad local, como cada quién pueda.”


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After more than 50 years of use, some Michigan lawmakers say naloxone may not be the best choice in an overdose situation.

Naloxone is sometimes called the "Lazarus drug" because of its powerful ability to seemingly resurrect people after a drug overdose.

Sen. Kevin Hertel, D-St. Clair Shores, and some of his colleagues have introduced a bill which would open the door for what they say are more costly, but more powerful, antidotes.

"Given the prevalence of fentanyl in our communities, and how much stronger some of these drugs that we're now seeing are, we believe -- and in talking with others -- that there should be other tools to respond to an overdose," Hertel explained. "To make sure we're doing everything we can to save somebody's life."

Not everyone is on board with the proposed legislation, Senate Bill 542. Opponents argued the more expensive naloxone alternatives are not necessary, and using them would only increase profits for the pharmaceutical industry.

Jonathan Stoltman, director of the Opioid Policy Institute in Grand Rapids, said while the naloxone alternatives do help in overdose situations, they can also cause nasty side effects.

"The newer approaches, they put people into more severe withdrawal," Stoltman pointed out. "That's a pretty profound negative side effect. The one approach is very inexpensive and works great; the other approach is far more expensive and has this strong negative side effect."

Sponsors of the bill say they're hoping to give Michigan residents a chance to chime in on the issue in a public hearing sometime in June. Michigan saw more than 3,000 opioid overdose deaths in 2021.


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New Mexico saw record enrollment numbers for the Affordable Care Act this year and is now setting its sights on lowering out-of-pocket costs - those not reimbursed by insurance. More than 56,000 New Mexicans are enrolled in a medical health insurance plan on the state exchange - an increase of 12,000 people overall.

Colin Baillio, deputy superintendent with the state's Office of Insurance, said the state has boosted its outreach and made efforts to improve the overall consumer experience.

"We saw a 40% year-over-year increase, and New Mexico saw the biggest percentage increase during the open-enrollment period among all of the state-based marketplaces," he explained

Part of the enrollment increase is due to what's called the "unwinding" - a federal directive that required all states to redetermine Medicaid eligibility following a three-year pause on checks during the COVID pandemic. He said by using expanded tools made available by the federal and state government, 8% of New Mexico's population is now uninsured - down from 23% in 2010.

Following approval by lawmakers in the 2024 legislative session, the New Mexico governor signed seven health care-related bills into law - one of which requires annual reporting of prescription drug pricing. Baililo said the Affordable Care Act built the foundation that has allowed the state to pursue additional affordability initiatives.

"I'm really glad to see that there's so much interest in the next step of health reform, really leaning into these out-of-pocket cost issues and making it easier for people to afford to stay covered and see their doctors," he continued.

Two years ago, the state also passed a one-of-a-kind law that did away with behavioral health co-pays for people in certain insurance plans.

New York's medical aid-in-dying bill is gaining further support. The Medical Society of the State of New York is supporting the bill. New York's bill allows terminally ill people with only six months to live to use this option, with safeguards requiring two physicians' approval.

The bill's Assembly sponsor Amy Paulin, D-Westchester, said despite the growing support, other hurdles lie ahead.

"Now we have what I believe, if it came to the floor, a majority. There's still a hesitation on the part of leadership. You know, we need members to assure leadership that they no longer have reservations," she said.

Other newly resolved concerns center on making sure insurance companies and doctors who don't support this aren't held liable. She's optimistic the bill will pass after nine years in the Legislature. New York would be the 11th state along with Washington, D.C. to have medical aid in dying legislation.

Corinne Carey, senior New York campaign director with Compassion and Choices finds the pandemic drew a vivid picture of a person's end-of-life experience. There were images of people dying on ventilators, apart from loved ones, and unable to communicate. She said people began thinking about a "good death."

"And, what is a good death is being surrounded by loved ones, having some measure of control, experiencing the touch of your loved ones, and being the one in the driver's seat," she explained.

Now people have different options for end-of-life care, each of which presents various challenges. Polls show medical aid in dying has garnered considerable support since being introduced in 2015. A 2022 Compassion and Choices poll finds 57% of nurses support medical aid in dying professionally, although fewer support it personally.