Kim Owens

Inclusion Resource: Taking the Alternate Assessment Does Not Mean an Education in a Separate Setting

If you have been told, or have concerns, that your child cannot be educated in the general education classroom because he or she takes an alternate assessment a brief published by the TIES Center, which is co-authored by Ricki Sabia, NDSC Senior Education Policy Advisor and TIES Center parent liaison, and Dr. Martha Thurlow, Director of the National Center on Educational Outcomes (NCEO) and Ties Center Advisor, may be a useful resource to you.  The brief can be downloaded by clicking on the link on the bottom right side of the TIES Center home page https://tiescenter.org/.

Read More

Mi Hijo Con Síndrome de Down Quiere Ser Independiente

Via The Mighty

Nota del editor: ¡Gracias por leer The Mighty! Por ahora, como te darás cuenta, la mayoría de nuestro contenido está en inglés. Estamos empezando a cambiar esto porque, aunque estamos ubicados en los Estados Unidos, nuestra comunidad es global. De cualquier manera, ahora mismo puedes publicar en nuestro sitio o hacer preguntas en español — o en cualquier idioma que desees — para conectarte con otras personas en nuestra comunidad. Y no olvides seguir nuestra página en español!

Elías está creciendo.

Esto no debería ser una sorpresa, todos los seres vivos crecemos, pero cuando hablas de que es un niño que tiene síndrome de Down, de pronto se vuelve “sorpresa.”

Ajá, porque aparentemente las personas con síndrome de Down son niños eternamente, digo no lo son ni en estatura, ni en físico, pero en mente sí, no? Pues ese es un mito de los que queremos borrar.

Vaya que nos está pegando la “juventud” por aquí.

Jamás creí que ser mamá de un pre-adolescente sería tan difícil.

Y ha sido muy notorio, porque ahora discutimos, y discutimos mucho, desde que iniciamos con medicamento, hemos visto un incremento considerable en su comunicación, aun sigue en un nivel bajo, pero ahora expresa muchísimo más de lo que piensa, siente, te hace cuestionamientos de esos que terminas diciendo, “Porque sí, soy tu mamá y ya.” Pero sobretodo empezó a reclamar más su independencia y no me refiero a actividades en el hogar, eso ya lo hace desde hace mucho, me refiero a que quiere salir sólo.

Despertamos una mañana y no estaba.

En mayo pasado fuimos a Cancún, alejado de toda civilización, super tranquilo, todos muy amables, el hotel grandísimo, así que desde el día uno, como todo parecía un laberinto, le enseñé a Elías a que prestara atención el camino para llegar al cuarto, por cual entrada, por cual elevador, el pasillo, el piso, hacia donde caminar saliendo del elevador, etc.

Los niños dormían en una habitación, nosotros en otra, sinceramente no pensé ni siquiera en Eva que se fuera a salir, un día despertamos y Elías no estaba, bueno, más bien mi esposo despertó y yo desperté cuando me dijo “Elías no está!” Ya se imaginarán, ¿cómo? ¿cuándo? el estrés a todo lo que da, mi esposo sale del cuarto y yo me quede esperando por si acaso.

De rato llegan, Elías “regañado” y me dice mi esposo que lo encontró en el Lobby; un empleado lo llevo ahí.

Hablando con Elías nos dice que él sólo quería ir a ver a la gente en la fiesta, porque una noche antes había sido la boda, entonces, no sé, tal vez pensó que el baile seguía, realmente no nos apuraba que se hubiera metido al mar o a la alberca, el es demasiado precavido para eso, pero si el hecho de que se hubiera perdido entre tanto pasillo, elevador, etc. Pero no, él sabía el camino exacto.

Más tarde diferentes personas que habían ido a la boda nos dijeron que lo habían visto caminando sólo, y como lo conocen, y como nos conocen, y lo vieron tan seguro, que no pensaron que se hubiera escapado.

Y desde ese día todo cambió.

En diferentes ocasiones nos dimos cuenta que se quiso salir de la casa.

Nosotros: Elías! es que no te puedes salir así como así.

Elías: Porqué no?

Nosotros: Porque tienes que pedir permiso, y si alguien te roba, y si creemos que algún villano te hizo algo malo?

Elías: Pero no pasa nada, estoy bien! Soy joven!

Puffff…. así de pronto, dejó de ser nuestro niño, a ser un joven.

Le insistimos muchísimo que tenía que pedir permiso, así que obvio empezó a decirnos cada rato en que quería ir a la tienda sólo.

Estábamos en un proceso.

Íbamos a la tienda, lo esperábamos afuera mientras el compraba, el era feliz, pero ya no era suficiente, quería más.

Y pues el estaba pidiendo permiso, así que se lo dí.

Cuando vi que dio la vuelta lo seguí, cruce la calle y desde enfrente, escondida lo vi, emocionada, nerviosa, quería gritar, seguramente me veía sospechosa, pero no me importó.

Elías fue y regresó sin problema.

Estoy aprendiendo a soltarlo.

Quisiera que el doctor que me dijo que tendría un ángel conmigo para toda la vida lo viera.

Confieso que no es fácil, estoy aprendiendo a confiar en él, en sus habilidades, en todo el trabajo que hemos realizado durante todos estos años, en la gente que vive a nuestro alrededor, pero sobretodo aprendiendo a confiar en la promesa de Dios de que haría lo inimaginable en la vida de Elías.

Hace unas semanas, antes de salir a Panamá lo envié a la tienda, sin ir detrás de él, me conecté al Facebook live, y pude compartir los nervios con otros tantos que me acompañaron.

Hoy recién acaba de llegar, lo mande por unas galletas y me dice, “Lo siento no había, te traje cacahuates.”

Ahora cada vez lo hace más rápido, más seguro, y sobre todo, supongo, se siente feliz de que le estemos dando la oportunidad de ir a la tienda sólo. Y yo cada vez me siento más tranquila también.

Estamos creciendo juntos.

Action Alert – EMPOWER CARE ACT

ASK YOUR SENATORS TO FUND THE MONEY FOLLOWS THE PERSON PROGRAM BY PASSING THE EMPOWER CARE ACT!

On June 18, the House passed a bill that included 4.5 years of funding for the Money Follows the Person (MFP) program. This is great news, but it is time for the Senate to act! Please call your Senators and urge them to pass the EMPOWER Care Act (S. 548) to reauthorize MFP.
Background
The Money Follows the Person (MFP) program is a Medicaid program that has helped more than 75,000 people with disabilities and seniors move from nursing homes and other institutions into the community. First authorized in the Deficit Reduction Act of 2005 with strong bipartisan support, the MFP Demonstration program was designed to assist states with (1) supporting Medicaid enrollees who want to transition from institutional settings to community-based settings; and (2) developing infrastructure to promote and enhance access to Home and Community Based Services (HCBS). HCBS provides critical supports to people with disabilities to enhance their ability to be included and integrated into their communities instead of receiving care in restrictive, institutional settings. Each state can decide how to use the MFP funds, which they have used to expand or enhance HCBS programs, reduce waiting lists and fund housing supports.

The MFP program has been widely adopted – with 47 states participating since its inception – and has helped states to make significant progress on “balancing” their long-term services and supports systems to improve access for HCBS. The success of the MFP program has been widely recognized and documented, both in terms of effectively moving individuals from institutional to community-based care settings, reducing waiting lists for HCBS services, and savings states money (See Empower Care Act for more details).

Congress had passed stop gap funding for the MFP program in January 2019, but those funds will run out in September.

How to Help

You can help support the passage of the EMPOWER Care Act by calling the main Capitol line at: (202) 224-3121 (voice) or (202) 224-3091 (TTY) and click HERE to send an email to your Senators. They must hear that their constituents strongly support the Money Follows the Person Program and need them to vote YES on the EMPOWER Care Act to #FundMFP!

Thank you for your advocacy efforts!
The NDSC Policy & Advocacy Team

TALKING POINTS

• I am a resident of [Town, State] and your constituent. [I/my child/sibling/friend/co-worker, etc] is a person with a disability.
• I am calling to express my concern about the expiration of the Money Follows the Person (MFP) Medicaid program, and I am asking you to pass the EMPOWER Care Act and reauthorize Money Follows the Person through 2022
• MFP has enabled over 75,000 seniors and people with disabilities living in institutions to transition back to their communities.
• MFP is fiscally responsible – it has improved the quality of life for thousands of individuals while saving states money.
• The MFP program expired over a year ago, and states are running out of money for these services and already having to scale back. Congress had passed stop-gap funding in January 2019, but that funding will run out by September 2019. Without new funding, states will have to completely eliminate this program.
• Please help keep people with disabilities and the elderly in their homes and in their communities and reauthorize the Money Follows the Person program!

We encourage you to stay engaged in our advocacy efforts by:

(1) Registering for NDSC Action Alerts- click “Quick Sign Up
(2) Subscribing to the NDSC Policy & Advocacy Newsline
(3) Joining our national grassroots advocacy program, the National Down Syndrome Advocacy Coalition
(4) “Liking” NDSC Policy & Advocacy on social media Facebook and Twitter

NDSC E-News ~ June 2019

NDSC’s Mission Moment

with Executive Director David Tolleson 

 

It’s a busy time at the NDSC Center as we put the final touches on this year’s NDSC Annual Convention!  We’re all very excited to see you – old friends and new – when the world’s Down syndrome community comes together in Pittsburgh.  If this is your first time attending an NDSC Convention, I strongly encourage you to attend the First Timer Orientation session Thursday night – it will help you get the most out of your conference experience.  No matter how many times you’ve joined us, it will help to get familiar with the Convention App well before you arrive.  You’ll find instructions on how to download this handy tool below.

Read More

Convention Insider ~ June 3, 2019

 LAST CALL Banner

Tuesday, June 4th is the last day to pre-register for the 2019 NDSC Convention. Registration will re-open onsite at the David L. Lawrence Convention Center in Pittsburgh Thursday, June 27th at 4:00 PM. Register now and skip the lines on-site. If you have already registered, please review your email confirmation to ensure you have a conference listed for each person in your family attending and have registered or purchased all optional add-ons, such as the Evening of Champions tickets, t-shirts, flash drives, etc. Changes or additions to existing registrations can be done by calling the NDSC Center at 770-604-9500 but must be done by 5:00 PM, June 4th.

Read More

Action Alert – Equal Pay for People with Disabilities

ACTION ALERT:
Comment Today to Support Equal Pay for People with Disabilities!

This week the Department of Labor announced its new website, “the Section 14(c) National Online Dialogue.” The purpose of the website is to collect comments from the public about the impact of paying subminimum wages to people with disabilities under section 14(c) of the Fair Labor Standards Act. Employers with 14(c) certificates can legally pay people with disabilities less than the federal minimum wage, often times pennies on the dollar. Section 14(c) certificates are typically used in “sheltered workshops,” where people with disabilities are segregated from the broader community. The vast majority of disability advocates view Section 14(c) (created in 1938) as outdated, discriminatory, and reinforcing a life of poverty, segregation, and dependency on public support for people with disabilities. It is critical that you make your voice heard!

Input from people with disabilities, families, employment providers and employers is important. Share your perspective online here. COMMENT DEADLINE HAS BEEN EXTENDED TO FRIDAY JUNE 21,

Read More

Policy & Advocacy Newsline ~ May 21, 2019

Transformation to Competitive Employment Act

Great news – the Transformation to Competitive Employment Act (H.R. 873/S.260) was featured at a hearing entitled “Eliminating Barriers to Employment: Opening Doors to Opportunity” in the House of Representatives on Tuesday, May 21 before the full Education & Labor Committee. This is a very positive step towards promoting awareness of this bill and generating support for it, but we need YOUR help to get more cosponsors onto this bill so that it can continue to advance! Please contact your Members of Congress through this NDSC Action Alert and let’s build support for this bill.

Introduced in the Senate by Senators Bob Casey (D-PA) and Chris Van Hollen (D-MD) and in the House by Chairman Bobby Scott (D-VA) and Representative Cathy McMorris Rodgers (R-WA), this bipartisan legislation will address barriers to employment and expand opportunities for competitive integrated employment for people with disabilities while phasing out subminimum wage certificates under Section 14(c) of the Fair Labor Standards Act over a six-year period. In addition, for those who choose not to work, work part-time, or for whom their disabilities make it too difficult to maintain work in a competitive integrated setting, this bill includes individualized wraparound services that provide them with opportunities for meaningful training and social activities in the community.

You can find a two-pager about this bill and additional resources on the Collaboration to Promote Self-Determination website. For information about Competitive Integrated Employment, please see this new website developed with our partners in the newly formed Coalition to Advance Competitive Integrated Employment. Please #WorkWithUs and build more opportunities for competitive integrated employment!

Read More

Convention Insider ~ May 15, 2019

Best Value Prices End This Friday, May 17th

Are you planning to attend NDSC’s giant family reunion in Pittsburgh, June 27 – 30?

Register now and take advantage of best value prices before they end this Friday, May 17th.

This is also the last day to register for the Youth & Adults and Brothers & Sisters Conferences.

Best Value Pricing w right border

There are a few remaining spots in Kids’ Camp Friday, June 28th! If you were hoping to attend a pre-conference session this is a great chance to spend 4 hours diving deep into a topic while we provide a safe, structured, and fun environment for your child. Kids’ Camp is available for children with Down syndrome – ages six months to 14 years old, and their siblings – ages six months to rising 3rd graders. (Rising 4th graders and older may register for the Brothers & Sisters Conference.)

For a complete list of convention fees and pricing deadlines visit our website.

Read More