Disability News Service, Resources, Diversity, Americans with Disabilities Act; Local and National.

Friday, April 24, 2015

Reinstate Respite Care program funding for Developmentally Disabled in Illinois - ONLINE PETITION

Recieved this Change.org petition. Another avenue to support, as are so many efforts in Illinois and the drastic budget cuts the disability community in Illinois are facing.

Through this program agencies provide cost-effective, short-term, intermittent care for persons with a diagnosis of Autism, Cerebral Palsy, Epilepsy or Intellectual / Developmental Disabilities. This program provides the primary caregivers the opportunity to handle the daily struggles in their lives with the comforting knowledge that their children are being well cared for in their absence. One of the primary benefits of the Respite Care program is to defer or deter costly residential placement of individuals who have a developmental disability, which is roughly$60,000.00 a year in a CILA setting or $240,000.00 in a state-operated facility.  
Respite Care is essential to maintaining family’s lives! Please do not allow so many children and families to go without service as the few dollars saved will certainly be realized in the quality of lives for far too many!

To Sign this Change.org Petition, go to:





To Sign the Petition at Change.org, visit:

Illinois Senate votes to restore human service cuts; bill moves to House for consideration - Disability Service cuts by Gov Rauner

hopefully some good news, will update as this proceeds through Illinois Legislator

Illinois News Network, article by MARK FITTON | April 23, 2015

SPRINGFIELD — By a vote of 57-1, the Illinois Senate on Wednesday authorized additional fund transfers to restore $26 million in cuts made to human service programs on Good Friday.
The bill now moves to the House, where it’s fate Wednesday appeared less certain.
Sen. Dan Kotowski, D-Park Ridge, sponsored the measure, which he said would authorize transfers from funds that still have surpluses for fiscal year 2015, including a supplemental energy assistance fund that has an available balance of $75 million.
The proposal, Senate Bill 274, does not include transfers from road fund, the state construction fund or the motor fuel tax funds, the senator said.
Speaking on the Senate floor Wednesday, Kotowski said the emergency funding measure was drafted with the cooperation of the Democratic and Republican caucuses in the Senate and with Gov. Bruce Rauner’s office.
Sen. Matt Murphy, R-Palatine, thanked Kotowski for his tenacity in attacking the problem, but the deputy Republican leader added all legislators must be mindful of tough decisions ahead, as the 2016 budget remains to be negotiated.
While senators could take momentary satisfaction in being able to help, legislators must realize Illinois has been “been spending more than we can afford and difficult decisions are coming down the pike,” Murphy said. “We need to brace ourselves.”
Sen. Donne Trotter, D-Chicago, also thanked the negotiators and his colleagues.
“We do have to organize and come up with a better way to spend the limited dollars we have, but we should not lose focus,” Trotter said.
“Some of these program that we call social services are actually life-giving services to the people who receive them,” he said.  “This is not just math; this is about people.”
Sen. Mike Noland, D-Elgin, cast the lone dissenting vote. He said he opposes the practice of last-minute fund transfers.
The April 3 spending cuts by the Rauner administration caused some friction between the Republican governor’s office and leading Democrats.
The General Assembly in late March approved a bill authorizing $1.36 billion in fund transfers and imposing a nearly across-the-board 2.25 percent budget cut to get the state through fiscal year 2015, which ends June 30. The goal was to close a $1.6 billion gap.
For a short while after the votes, work on the bills was hailed as outstanding bipartisan governance.
But Democrats said they were stunned when the Rauner administration then cut $26 million to programs including help for the autistic, burials for the poor and addiction prevention and treatment programs, among others.
Those legislators said they thought the programs — especially those having to do with mental and developmental health —had been funded and were safe for the remainder of the fiscal year.
Sen. Heather Steans, D-Chicago, who sponsored the March compromise bills in the Senate, said, “I felt like I had a kick in the stomach on April 3rd, ” when phone calls about the cuts began coming in.
Late Wednesday afternoon, a spokesman for House Speaker Michael Madigan, D-Chicago, said Kotowski’s bill was under review.
But Steve Brown of the speaker’s staff added House Democratic leadership felt the March bills gave the Rauner administration adequate funding and authority to complete the fiscal year without the cuts, especially those to mental health programs.
The bills did not decrease funding for those programs while it cut other state programs, he noted.
The compromise package was sponsored in the House by Majority Leader Barbara Flynn Currie, D-Chicago, and supported by Madigan, both of whom spoke on the floor and told members that services for the mentally ill, people with developmental disabilities and autistic children would be spared from further cuts.
http://ilnews.org/4562/senate-votes-to-restore-human-service-cuts-bill-moves-to-house-for-consideration/

related post: Illinois Governor Rauner ordered the suspension of $26 million worth of state grants through June 30, 2015, effective immediately

U.S. Access Board Webinar: Application of the ADA and ABA Accessibility Standards (May 7)

laptop with Access Board sealThe next webinar in the U.S. Access Board's free monthly series will take place May 7 from 2:30 – 4:00 (ET) and will cover application of the ADA and ABA Accessibility Standards in new construction, alterations, and additions. The session will address the scope of the standards, which encompass a wide range of facilities in the public and private sectors, and review scoping provisions for spaces and elements, general exceptions, and other provisions relevant to application. Questions can be submitted in advance of the session (total limited to 25) or can be posed during the webinar.

For more information, including registration instructions, visit www.accessibilityonline.org.

*as shared by the U.S Access Board



Wednesday, April 22, 2015

National ADAPT in Washington, DC, in 2015 Advocating for Disability Home and Community Services at the Federal Level

as posted at National ADAPT on April 22

ADAPT strikes at Four Spots in Washington DC

ADAPT Activists at the Department of Justice, Health and Human Services, the Republican National Headquarters and the Democratic Party.

By Mike Ervin,
Photos by Kevin McBride and Dave Fulton
ADAPT Activists at the Department of Justice. Photo by Dave Fulton
It sure was ironic. The headquarters of the U.S Department of Justice was surrounded by barricades, those metal riot fences that hook together. DoJ apparently knew ADAPT was in town and they must’ve had a guilty conscious.
Sure enough, the ADAPT march line approached and instead of storming the fortress we swirled around and took over street. D.C police blocked traffic. We faced the cement block with windows that is DoJ and unfurled our orange banner.
ADAPT was fed up with DoJ’s inertia when it comes to enforcing the community integration mandate of the Americans with Disability Act (ADA), the subsequent Supreme Court Olmstead decision and the Civil Rights of Institutionalized Persons Act.
ADAPT demanded that the DOJ:
1) Pursue high-profile Olmstead/ADA or CRIPA enforcement actions in every state to address the institutionalization of thousands of people with disabilities of all ages.
2) Address the decades-long waiting lists that should be moving at a reasonable pace.
3) Accept and take immediate action on the ADAPT of Texas ADA complaint that Texas’ failure to establish adequate rates for home and community based services has significantly restricted the opportunity of people with disabilities to live safely in their own homes and community.
4) Initiate action in at least other four other states to address inadequate Medicaid rates which impact attendant wages, the attendant workforce and the opportunity for community living; and
5) Meet with ADAPT and other disability rights advocates in every state to develop a list of violations that exist in public nursing facilities and other institutions covered under CRIPA that need to be addressed.
So for about 30 minutes ADAPTers testified in the streets. We heard how attendants in Texas make $7.86 per hour. Beyond ridiculous, right? And we head how of course it makes it damn near impossible to find and keep good workers.
Finally, Bruce and others were escorted inside to talk to the suits. Down on the street—more chanting, more testifying until Bruce and team emerged with Eve Hill, Senior Counselor to the Assistant Attorney General for the Civil Rights Division at DoJ. Addressing us on the bullhorn she said DoJ was anxious to move forward on an Olmstead case involving someone in an institution but it needed to be a strong case with an excellent chance of winning. She agreed to work with ADAPT to try to locate the ideal plaintiff.
After our McDonald’s break we proceeded to HQ of the Department of Health and Human Services. The barricades were up at HHS, too, but that’s always the case when ADAPT comes to town. Guilty conscious again? Well anyway, again instead of charging we lined up and stared them down. We chanted for HHS Secretary Sylvia Burwell to come out.
ADAPT was at HHS because the Department of Labor recently promulgated new rules that mandate overtime for in-home attendant care. Without adequate Medicaid reimbursement critical service hours are being cut and persons with disabilities who live in the community are at risk of being forced into nursing homes. In addition, low wages for attendants are making it increasingly difficult for persons with disabilities to recruit and retain quality attendants. ADAPT demanded that Burwell:
1) Recognize that inadequate Medicaid rates have driven down attendant wages and consequently undercut the ability of Americans with disabilities to live in freedom. We therefore further demand that Secretary Burwell use HHS’s authority to ensure that state Medicaid rates are sufficient to secure the workforce needed for community integration.
2) Utilize HHS’s authority regarding Medicaid rates to ensure that states have adequate Medicaid rates to cover the increased costs associated with the Companionship rule changes made by the Department of Labor.
3) Instruct the Centers for Medicare and Medicaid Services to utilize their authority to ensure that states implement managed care in a manner that promotes community living. We believe that HHS can accomplish this by including and enforcing strict terms and conditions as part of the process for approving community living waivers (also known as1115 waivers).
ADAPT Activists at the Republican National Headquarters. Photo by Dave Fulton4) Instruct the HHS Office for Civil Rights to take a stronger role in enforcement of the Supreme Court’s Olmstead decision by implementing a plan to promote community living that complies. The Olmstead decision established that the Americans with Disabilities Act provided persons with disabilities the civil right to live in their own homes and communities. Recognizing that some states might rely on institutional settings in violation of the ADA, the decision also provides states with a defense from lawsuits. This defense involves developing effective plans for ensuring that persons with disabilities can transition from and avoid moving into nursing facilities.
5) Meet with ADAPT and Congressional representatives to support the development of civil rights legislation clarifying and strengthening the ADA’s integration mandate. This mandate will ensure that people with disabilities have a community-based alternative to institutional placement that allows them to lead an independent life.
A woman wearing a pink jacket came out. It wasn’t Burwell. It was Kathy Greenlee, Administrator for the Administration of Community Living at HHS. Off to the side, she negotiated with Bruce, Mike Oxford, Anita Cameron and Cathy Cranston. Then it was Greenlee’s turn to address us with the bullhorn. She agreed to take our demands to the Secretary and her chieftains and to arrange a meeting with ADAPT and them to discuss it all.
All this was accomplished and it was only 3 p.m. So the color teams split off. One batch of ADAPTers marched to HQ of the Democratic National Committee and the other batch marched to the Republica National Committee. The demand at both places was for the parties to endorse the Community integration Act (CIA). More on the CIA tomorrow.
At the DNC we were greeted by Reverend Regina Thomas, Director of Community Engagement. She was cordial but nervous. She agreed to meet in the near future with ADAPT.
The DNC ADAPTers then joined the RNC batch, who had been greeted by a locked door. But enough ruckus was made to persuade RNC Communications Director Sean Spicer to come out. Spicer agreed to take ADAPT’s CIA endorsement to the RNC platform committee.
It was a trifecta plus one. What do you call that? A quadrafecta? Whatever you call it, it was a productive day.
http://www.adapt.org/freeourpeople/2015dc/report04.php

To follow National ADAPT on Twitter, use @nationaladapt or go to www.twitter.com/nationaladapt.

U.S. Senate Passes Steve Gleason Act! restore SGDs and allow People with ALS to access email, the internet, etc.

as shared  today by The ALS Association - 1275 K Street NW - Suite 250 - Washington, DC 20005

Dear James,
 
Great news in the fight to ensure access to speech generating devices (SGDs)…  less than five minutes ago, the Senate passed the Steve Gleason Act (S. 984)!   The bill would restore a person’s ability to upgrade SGDs and allow people with ALS to access email, the internet and environmental controls.  The bill also would ensure that people with ALS can keep their SGDs if they are admitted to a hospital, nursing facility or hospice.
 
The legislation now heads to the House of Representatives where we will try to pass it as soon as possible.  Keep an eye out for our Action Alerts as the process moves forward to learn how you can help.
 
Thank you to Senator David Vitter (R-LA) for all of his leadership to champion the Steve Gleason Act in the Senate.  Thanks also to the bill’s other champions:  Senators Susan Collins (R-ME), Charles Grassley (R-IA), Angus King (I-ME), Mark Kirk (R-IL), Amy Klobuchar (D-MN), and Lisa Murkowski (R-AK).  Their collective efforts made the bill a priority in the Senate, but it was your efforts to reach out and tell the ALS story that led to its passage.
 
Thank you to everyone!  You clearly have made a difference!

U.S. DOT public meeting April 20 in D.C.,on user needs for Accessible Transportation Technologies Research Initiative (ATTRI)

Federal Transit Administration

ATTRI is a USDOT initiative to develop transformative technology solutions to enable people with disabilities, older adults, and veterans and wounded warriors to reliably, safely, and independently plan and execute their travel. This event seeks input from stakeholders to complete the ATTRI user needs assessment.  The workshop will be interactive with breakout sessions to gather participants’ thoughts and input.  The information from participants will be used to better understand the challenges and faced by the travelers with disabilities and to design technological solutions to address those needs. 

  • Event: U.S. DOT Public Meeting:  Accessible Transportation Technologies Stakeholder Research Initiative (ATTRI) Stakeholder Engagement: User Needs Assessment Workshop
  • Date: April 30, 2015
  • Time: 8:30 am to 4:30 pm Eastern Time
  • Location: The Mayflower Renaissance Hotel , 1127 Connecticut Ave NW, Washington, DC  20036
  • RSVP to: Ms. Jodi Rizek at rizekjm@battelle.org or (614) 424-7976 or Ms. Charlene Wilder at Charlene.wilder@dot.gov (202-366-1077)
  • RSVP by: April 27, 2015
All travel and per diem expenses, including meals, for persons attending the workshop must be paid by their agencies.

Background on ATTRI: 

http://nationalonlinedialoguetadt.ideascale.com/a/pages/backgroundonattri

Tuesday, April 21, 2015

Rules Proposed for 2015 Workforce Innovation & Opportunity Act (WIOA) - effects Veterans, People with Disabilities


The U.S. Departments of Labor and Education want to have input from you about proposed rules for the WIOA. This law will improve employment and training services for America's workers and help federal, state and local agencies better coordinate how they offer these services. The five proposed rules to implement the WIOA address ways to improve education and employment services for Veterans, people with disabilities, youth and many other jobseekers. 
Comments must be sent in by June 15, 2015.
###

News Release: [04/16/2015]
U.S. Department of Labor Department

Release Number: 15-0691-NAT

Obama administration seeks public comment on proposed rules to implement the Workforce Innovation and Opportunity Act

WASHINGTON — The Workforce Innovation and Opportunity Act (WIOA), signed by President Obama on July 22, 2014, is the first major reform to federal job training programs in more than 15 years. WIOA is designed to improve the coordination of employment and training services across federal agencies, strengthen collaboration with state and local partners, and provide Americans with increased access to training, education and other support to succeed in the job market and in their careers. Today, the departments of Labor and Education announced five Notices of Proposed Rulemaking to implement WIOA and seek public comment.
"We are embarking on a fundamental transformation in the way we prepare people for the careers of today and tomorrow," said U.S. Secretary of Labor Thomas E. Perez. "More than ever before, we're taking a job-driven approach and making sure training programs connect businesses that want to grow with workers who want to punch their ticket to the middle class."
"WIOA will provide the opportunities for workers and learners to obtain the foundation skills necessary for 21st century jobs and foster a modern workforce that can compete in a global economy," said U.S. Secretary of Education Arne Duncan. "It makes key improvements in the nation's workforce development and education system, by emphasizing the creation of career pathway programs, improved training, and streamlined service delivery to individuals — especially for underserved youth and adults."
The proposed regulations are designed to: update and improve federal workforce programs that serve workers, job seekers, and employers; strengthen accountability and transparency; increase access to work-based learning tools, such as apprenticeships; improve relationships with employers, including through sector partnerships, and foster more cohesive planning within economic regions. The proposed rules would also improve access to education and workforce services for individuals with significant barriers to employment — veterans, individuals with disabilities, disconnected youth, and other vulnerable populations — to help them find good work.
The proposed regulations align closely with principles outlined in Vice President Joseph R. Biden's Ready to Work report on developing a more evidence-based, job-driven workforce system. The vice president's report included a call for greater coordination and more strategic use of federal resources to yield better results; transparent and relevant information so job-seekers and the public know what works, and putting business front and center so our investments are directly responsive to hiring needs. 
WIOA supersedes the Workforce Investment Act of 1998, reauthorizes the Adult Education and Family Literacy Act, and amends the Wagner-Peyser Act and the Rehabilitation Act of 1973.
The five NPRMs announced today include: a joint rule, issued by the departments of Labor and Education, in collaboration with the Department of Health and Human Services, proposing to implement jointly-administered activities related to unified planning, performance accountability, and the one-stop system; a Department of Labor rule proposing to implement DOL-specific activities under Title I; and three Department of Education rules proposing to implement the requirements of Titles II and IV.
Please visit www.regulations.gov to share your comments on the specific proposed rules, in accordance with the process outlined in the NPRMs. Any comments not received through the processes outlined in the NPRMs will not be considered by the departments.
A webinar on how to provide comments on the NPRMs will be available the week of April 27. For more information, visitwww.doleta.gov/WIOA.
Here are summaries of each proposed rule and a link for additional information:
  • Workforce Innovation and Opportunity ActThis rule, proposed by Labor, would implement changes to the adult, dislocated worker and youth formula programs; the state and local workforce development boards; the designation of regions and local areas; local plans; the one-stop system; national programs, including Job Corps, YouthBuild, Indian and Native American programs; and Migrant and Seasonal Farmworker programs. The proposed rules also would implement changes related to employment services and workforce and labor market information systems and requires the Secretary of Labor to establish a Workforce Information Advisory Council.

    https://www.federalregister.gov/articles/2015/04/16/2015-05530/workforce-innovation-and-opportunity-act-notice-of-proposed-rulemaking#addresses 
  • Workforce Innovation and Opportunity Act, Miscellaneous Program ChangesThis rule, proposed by Education's Office of Special Education and Rehabilitative Services, would implement changes to other Rehabilitation Act programs administered by the Department of Education, including Client Assistance, American Indian Vocational Rehabilitation Services, Protection and Advocacy of Individual Rights, Independent Living Services for Older Individuals Who Are Blind programs, and the discretionary grant programs authorized under Title III of the Rehabilitation Act.

    https://www.federalregister.gov/articles/2015/04/16/2015-05535/workforce-innovation-and-opportunity-act-miscellaneous-program-changes

http://www.dol.gov/opa/media/press/eta/ETA20150691.htm

2015 Study finds Doctors Often Ignore Parents' Concerns About Autism in Young Kids



A 2015 study suggests that delays in diagnosing and treating autism often occur when doctors ignore parents' concerns about their child's early development. The medical records of more than 1,400 children with autism were compared with those of 2,100 children with other types of developmental delays. Doctors were 14 percent less likely to conduct developmental tests or refer the children with suspected autism to a specialist, compared to the children with other types of delays.

as posted by healthfinder.gov 

Research suggests that needless delays in diagnosis, treatment, occur as a result.

Doctors Often Ignore Parents' Concerns About Autism in Young Kids: Study
WEDNESDAY, April 15, 2015 (HealthDay News) -- Delays in diagnosing and treating autism often occur when doctors ignore parents' concerns about their child's early development, a new study suggests.
A team led by Dr. Katharine Zuckerman, of Oregon Health and Science University in Portland, compared the medical records of more than 1,400 children with autism against those of 2,100 children with other forms of delayed intellectual development.
For children who later turned out to have an autism spectrum disorder, doctors and other health care providers were 14 percent less likely to have taken action -- such as conducting developmental tests or referring the child to a specialist -- in response to parents' concerns about autism, compared to children from the other group.
The researchers also found that health care providers were more likely to tell parents of children with autism that the child will "grow out of it," the researchers reported April 15 in The Journal of Pediatrics.
"We know that early identification of autism spectrum disorder is beneficial to children and their families," Zuckerman said in a journal news release. "Unfortunately, many families experience long delays between when they first have concerns and when their child gets diagnosed with autism spectrum disorder."
As the researchers explained, children with autism can develop symptoms even before they're 2, and early diagnosis is associated with better long-term outcomes.
One in 68 U.S. children has an autism spectrum disorder, according to U.S. Centers for Disease Control and Prevention estimates.
In the study, parents often had concerns about autism when their children were about 2, and discussed these concerns with a health care provider when their children were an average of 2.3 years old.
However, children with autism in the study were typically not diagnosed with the disorder until about age 5 -- nearly 3 years after parents first expressed their concerns to health care providers, the study found.
"The behavior of health care providers is likely a very important factor in delayed autism identification," Zuckerman said.
Two experts said the findings are disheartening.
"For many years, autism advocacy groups and the U.S. Centers for Disease Control and Prevention have urged parents to learn the signs of autism and act early by talking to their doctor if they are concerned about their child's development," said Alison Singer, president of the Autism Science Foundation.
"It's heartbreaking to think that these families' concerns are being ignored or rebuffed by doctors when we know that early intervention -- the earlier, the better -- can make a huge difference in a child's life," she said.
Dr. Andrew Adesman is chief of developmental and behavioral pediatrics at Cohen Children' Medical Center of New York, in New Hyde Park, N.Y.
He stressed that an autism diagnosis is not a "black-and-white" affair, and pediatricians must "walk a fine line between making an accurate developmental diagnosis as early as possible on the one hand and not rushing to judgment on the other."
Still, he said, "it is unfortunate that almost three years pass from when a parent first expresses concerns to his or her pediatrician and when the child gets a diagnosis of an autism spectrum disorder."
New guidelines that urge pediatricians to repeatedly screen toddlers for autism should boost rates of early detection, Adesman said.
In the meantime, Singer believes that "health providers need more education and training so that they can respond promptly and appropriately to parental concerns."
More information
The U.S. National Institute of Neurological Disorders and Stroke has more about autism.
SOURCES: Alison Singer, president, Autism Science Foundation; Andrew Adesman, M.D., chief, developmental and behavioral pediatrics, Cohen Children's Medical Center of New York, New Hyde Park, N.Y.; The Journal of Pediatrics, news release, April 15, 2015

Copyright © 2015 HealthDay . All rights reserved.

HealthDayNews articles are derived from various sources and do not reflect federal policy. healthfinder.gov does not endorse opinions, products, or services that may appear in news stories. For more information on health topics in the news, visit Health News on healthfinder.gov.

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http://www.healthfinder.gov/News/Article.aspx?id=698386

ADAPT ACTION REPORT in Washington D.C. - 53 ADAPT Disability Rights Warriors were arrested April 20, 2015

as posted by National ADAPT

ADAPT ACTION REPORTMonday, April 20, 2015

By Janine Bertram, ADAPT
Photos by Jerry Costley



ADAPT activists from across the nation gathered in Washington, DC and began our week of non violent, civil disobedience. We demanded President Obama act NOW to support the Community Integration Act. We were 150 strong and 53 ADAPT warriors were arrested. Justin Dart used to call us all patriots.

For me, it is like coming home to be back on the line with my ADAPT sisters and brothers. A new disability kept me home for a couple years. That and the fact that I’ve reached wise crone age sent me down memory lane today. It was great interviewing old timers and youth about what the Community Integration Act means to them.

Elaine Kolb is a wheelchair riding cultural worker and artist who joined the disability rights movement way earlier than half the ADAPTERS were born. She performed We Will Ride prior to 1990, when the ADA gave us the right to accessible public transit.

“Too many of our people with disabilities have lived and died without ever experiencing the rights and responsibilities of full citizenship and recognition of our common humanity,” says Elaine about a wrong that would be righted by The Community Integration Act.”

Jasia is 24 years old and attending the action from Brighton, England. For her, The Community Integration Act is needed because “Disabled people have the same rights as everyone else to live in their own homes with freedom of choice.”

James Van Winkle of Houston sports a long, gray beard. He is a wheelchair rider who has been disabled twenty years. “People with disabilities deserve the same rights that everyone else has. We deserve a safe place to live the life we choose in our own homes.” He spoke of what community integration means to him as he showed pictures of whimsical artwork and useful products he makes.

Nicky Boyte is the mother of a twelve year old and wheelchair rider. She is an ADAPT leader who is committed to the Community Integration Act. “In two words, it says it all. Those words speak to the services and supports that would mean civil rights for people with disabilities.”

Having more youth in ADAPT means a way better social media presence. Look at all those tweets!

While we waited for a White House response to our demands, there was another trip down an old road. We were served Micky D’s burgers and fries with salad for the vegetarians.

After this quintessential ADAPT dining experience, we learned the President and his staff ignored our demands. That was when over 1/3 of us rushed the White House fence and were later arrested. Once all of us were reunited, we lined up single file and headed back to our home away from home.

It had been 80 degrees and many of us had sunburns. As we left a light rain cooled us. (In my state, they call that kind of rain an Oregon facial). Then later that evening a huge lightening and thunder storm let loose on Washington, DC. It was the universe honoring the strength and awesomeness of ADAPT.

How do you spell power?

http://www.adapt.org/freeourpeople/2015dc/report03.php

for ADAPT website: http://www.adapt.org/main

Rating System Helps Patients Compare & Choose Hospitals for 2015

from a PRESS RELEASE | April 16, 2015
Centers for Medicare & Medicaid Services (CMS) 


CMS Releases First Ever Hospital Compare Star Ratings

Comparison Ratings that Help Consumers Compare and Choose Among Hospitals

Today, the Centers for Medicare & Medicaid Services (CMS) for the first time introduced star ratings on Hospital Compare, the agency’s public information website, to make it easier for consumers to choose a hospital and understand the quality of care they deliver. Today’s announcement builds on a larger effort across HHS to build a health care system that delivers better care, spends health care dollars more wisely, and results in healthier people. 

The Hospital Compare star ratings relate to patients’ experience of care at almost 3,500 Medicare-certified acute care hospitals. The ratings are based on data from the Hospital Consumer Assessment of Healthcare Providers and Systems Survey (HCAHPS) measures that are included in Hospital Compare. HCAHPS has been in use since 2006 to measure patients’ perspectives of hospital care, and includes topics like:
•           How well nurses and doctors communicated with patients
•           How responsive hospital staff were to patient needs
•           How clean and quiet hospital environments were
•           How well patients were prepared for post-hospital settings

“The patient experience Star Ratings will make it easier for consumers to use the information on the Hospital Compare website and spotlight excellence in health care quality,” said Dr. Patrick Conway, Acting Principal Deputy Administrator for CMS and Deputy Administrator for Innovation and Quality. “These star ratings also encourage hospitals and clinicians to strive to continuously improve the patient experience and quality of care delivered to all patients.”

The Hospital Compare ratings are just one example of how CMS is committed to helping consumers make informed health care decisions. The Nursing Home Compare site already uses star ratings to help consumers compare nursing homes and choose one based on quality. Physician Compare has started to include star ratings in certain situations for physician group practices, and CMS recently added star ratings to the Dialysis Facility Compare site to help to make data on dialysis centers easier to understand and use. Star ratings are planned for Home Health Compare later this year.

These ratings continue to move the health care system toward the Affordable Care Act call for transparent, easily understood and widely available public reporting. They also are a part of the Obama Administration’s Digital Government Strategy by providing content in customer-centric ways.

Consumers will now see 12 HCAHPS Star Ratings on Hospital Compare, one for each of the 11 publicly reported HCAHPS measures, plus a summary star rating that combines or rolls up all the HCAHPS Star Ratings. These star ratings will be updated each quarter.

For more information on today’s announcement, please visit here: http://www.cms.gov/Newsroom/MediaReleaseDatabase/Fact-sheets/2015-Fact-sheets-items/2015-04-16.html
For more information about the HCAHPS Survey please visit the official HCAHPS On-Line Web site, here: www.HCAHPSonline.org.

http://www.cms.gov/Newsroom/MediaReleaseDatabase/Press-releases/2015-Press-releases-items/2015-04-16.html

RELATED POST:
U.S. Nursing Home Rating System Strengthened