31 August 2012

What's New in August

August 2012 news, events, and updates.


SIS [Supports Intensity Scale] Community Forums

FYI...

Important information about Supports Intensity Scale (SIS) evaluation will be shared in these Community Forums.... this information is for those affected by IDDwho currently receive and those who do not currently receive CAP services.... you have to register to attend! Please be sure to click on link in the email forwarded below!!

Note that all areas of NC will be under Innovations Waiver in January according to current set timelines. Innovations Waiver is replacing the CAP Waiver. The SIS evaluation will go into effect as one of the tools of choice for determining need for services for those affected by IDD. These evaluations will be done by trained teams in each area. For most up-to-date info, please attend one of these sessions in your area!

Anna

p.s. The closest one to those in Durham / Raleigh is on Monday, Sept 24th from 5-8pm at Alliance Office located at 4600 Emperor Blvd, Durham (near RTP in the 540/40 area). Register early to secure your seat!

----- Forwarded Message -----
From: "Titus, Trina" <trina.titus@dhhs.nc.gov>
To:
Sent: Friday, August 31, 2012 1:47 PM
Subject: SIS [Supports Intensity Scale] Community Forums

Please see the information below regarding the Supports Intensity Scale.
http://ddti.unc.edu/CommForSIS.asp

Thank you.

Trina Titus
Administrative Assistant
DHHS/Division of Mental Health
Advocacy and Customer Service Section
P: 919.715.3197

30 August 2012

DOJ Settlement Good for People with Mental Illness, but May Leave People with I/DD Out

From The Arc of North Carolina

DOJ Settlement Good for People with Mental Illness, but May Leave People with I/DD Out

[ view at ArcNC.org ]

While it is too soon to know what the U.S. Department of Justice (DOJ) Settlement will mean for people with mental illness, now is the time to begin thinking about the effects it will have on our Mental Health/Developmental Disability/Substance Abuse (MH/DD/SA) system.

We appreciate the N.C. Department of Health and Human Services (DHHS) and DOJ finding a way to avoid costly litigation by reaching a settlement. While people can argue about the settlement’s details, there is really no question that NC’s placement of people with mental illness [and people with I/DD] in adult care homes is not appropriate. These settings were designed for people who are elderly, and are not settings where individuals who are young and have a disability will thrive. Spending large amounts of money defending a federal lawsuit would have been a true waste of taxpayer money.

The settlement does several things. The core of it requires the state to create new housing options [defined as slots]. These housing slots will include rental assistance and support services for 3,000 people, 2,000 that currently live in adult care homes, and 1,000 that are in jeopardy of being placed in adult care homes (or rest homes, as they are sometimes called) by 2020. It also requires the state to create, or increase, the availability of community services for people with mental illness including supported employment and additional Assertive Community Treatment Team services. The effort will have an independent monitor who will hold the state accountable. If the state fails to meet timelines, the DOJ can take the State to court.

One of the most disappointing parts of the Settlement is its lack of inclusion of people with developmental disabilities. Though the original complaint was about people with mental illness, there is no doubt that NC continues to rely upon similar institutional settings for people with I/DD. That people with I/DD were leftout of this settlement is concerning. Not only is the state allowed to continue its bias towards institutional settings in placements, community options made available to people with mental illness could come a the cost of community options for those with I/DD, given the State's limited resources.

Creating “scattered-site housing” is a great idea for all people with disabilities. The Arc continues to develop housing options that meet this criteria, but it is a slow process. We are also concerned that policy-makers in Washington and NC are adhering to conflicting policy in terms of housing and people with disabilities. One example is the HUD (US Dept. of Housing and Urban Development) funded properties The Arc manages for people with mental illness. Many of the properties are apartments that will not meet the scattered-site definition, yet have rental assistance vouchers as part of the project. Under the settlement agreement, very few of these properties will be available for people coming out of adult care homes. The changes that would be needed to make them available for these people currently run afoul of federal HUD regulations. We hope the DOJ and HUD will work together so future efforts will not exclude housing options promoted by federal agencies.

While the state has agreed to this promising settlement, we have significant related problems in our service system that must be addressed. One such problem is the crisis that will be created if we do not find a solution to the personal care issue. While the state will be creating community housing options for one group of individuals, others will be losing services and potentially their housing. This is not the way a system should work. While it is impressive that the General Assembly found funds to support the settlement, it should be noted that critical services are being sliced because of budget cuts at the same time.

While this settlement agreement is a step in the right direction, it is far from perfect. It does much for people with mental illness who have faced institutional bias, but at the same time it does nothing for people with I/DD facing a nearly identical problem. This is an opportunity for the leadership of the General Assembly and Administration to proactively take the spirit of this settlement and apply it to other populations. The best possible outcome is a more responsive system for all.

On Wednesday of next week the legislative Blue Ribbon Commission on Transitions to Community Living will hold its first meeting. Hopefully this committee will be the catalyst to create such change.

Crisis for those Receiving Personal Care Services


Crisis for those Receiving Personal Care Services


On August 14th during the Health and Human Services Oversight Committee meeting, members of the General Assembly and others got a first look at the impact of their special provision changing the requirements for Personal Care Services for people with mental illness and developmental disabilities. What they saw was not good.

Within this year’s budget, the legislature set new guidelines on who qualifies for Personal Care Services. The changes were in response to legal action by the Center for Medicaid Services (CMS) that required the state to address comparability between in home care services and those services provided in licensed group and adult care homes. In other words, the State had to make it just as easy for someone to receive Personal Care Services in a community setting as it was to receive them in an institutional setting, as long as it costs the same or less to do so.

To meet new eligibility standards, recipients must have a medical condition, disability, or cognitive impairment. They also must require limited hand-on assistance with three activities of daily living (ADLs), or hands-on assistance with two ADLs including one at the extensive assistance or full dependence level (clinical terms). The ADLs that qualify are bathing, dressing, mobility, toileting and eating.

Tara Larsen, Chief Clinical Operations Officer of DHHSs Division of Medical Assistance, opened the presentation by reviewing the legal situation surrounding the change in PCS eligibility. She reviewed the process that the state is undertaking to evaluate all current recipients of PCS to see if they will continue to receive this Medicaid service under the new requirements. Ms. Larsen informed the members that the target date for completion of these assessments is November 30, 2012.

During the presentation, one slide stood out. That slide detailed the significant effect that this change will have on people with mental illness and developmental disabilities living in group homes and receiving PCS. According to DMA (Division of Medical Assistance), 86% of residents with I/DD in group homes will not qualify for PCS under the new rules and 100% of residents with mental illness will not qualify.

In total 12,000 North Carolinians will see their Personal Care Services eliminated under the new rules.

DHHS, DMA and the legislature has yet to articulate a response to this looming crisis. The current budget did allocate $39 million dollars to be used to assist adult care homes in transitioning their residents who do not qualify under the new rules, but that is just a fraction of the affected residential settings. For the people in mental health group homes and DDA group homes, their wait for help continues.

The Arc continues to work with DHHS, DMA, and the legislature on this imminent crisis. We will keep you informed as the situation progresses, and let you know when we fill grassroots action is needed.

NCGA JLOC-HHS Meeting Notice 9/11

NORTH CAROLINA GENERAL ASSEMBLY
Raleigh, North Carolina 27601

August 27, 2012

MEMORANDUM

TO: Members, Joint Legislative Oversight Committee-Health and Human Services

FROM: Senator Louis Pate, Co-Chair
Representative Justin Burr, Co-Chair
Representative Nelson Dollar, Co-Chair

SUBJECT: Meeting Notice

DAY: Tuesday
DATE: September 11, 2012
TIME: 10:00 am - 3:00 pm
ROOM: 643

NOTE: For scheduling purposes future meetings dates are as follows:

October 9, 2012
November 13, 2012
December 11, 2012
January 8, 2013

If you are unable to attend or have any questions concerning this meeting, please contact Rennie Hobby at 733-5639 or mentalhealthca@ncleg.net.

cc: Committee Record _X_
Interested Parties _X_

25 August 2012

Apples, Oranges & Supported Employment

With all the talk of community support, naturally the issue of supported employment for persons with intellectual / developmental disabilities comes up... After all, doesn't everyone need to be needed and have a sense of accomplishment? Does not every life have a purpose?

A while back, I met with NC Representative Bill Current to discuss my concerns surrounding the statewide Medicaid overhaul and the recipients and families who will be affected. Dr. Current, a retired dentist, is a kindly conservative southern gentleman rooted firmly in his strong beliefs of integrity and hard work among other things - and does not hesitate to share his views regardless of yours (much like my late grandfather, a WWII veteran and former magistrate). I liked him immediately.

We chatted briefly about UNC (his alma mater), UNC basketball, and changing times in the field of dentistry before settling down for business. Before I could get started, Dr. Current was quick to share with me his position regarding government handouts and free for alls. I listened quietly as he spoke and then I told him,

"I agree completely."

I highlighted for him my 7 years as a struggling single parent raising a young child with disabilities without child support or much of any other... of undergoing a major back surgery when my child did not walk, going back to school, working and eventually buying my first home on my own - never once receiving government assistance, because I made too much money to qualify and some months, not even enough to live on.

I told him I knew exactly what he was talking about, that I could fill up a page on his legal pad with names of people I knew on welfare or capable persons receiving disability who have made a career mooching off the system, residing in supplemented housing and living and eating far better than my own family and driving brand new SUVs - and my husband and I work our butts off.

"But let's separate the apples from the oranges. I'm talking about a population of people who would do absolutely anything to be able to work, give back, and have a sense of independence, pride and accomplishment. People who desperately want to have just a taste of what the rest us us take for granted every day..."

So, today when I saw this image from The Arc of San Francisco, promoting supported employment through their We Can Do It program, I could not help but smile all the way through! It is absolutely, positively AWESOME and I LOVE IT!


Saturday Humor for Special Parents

Hard to imagine a world without Facebook isn't it? A life our children will never know. I mean, where ever would we get our latest news and entertainment without it? 

We've all seen these smart aleck little ecards swimming around our inboxes, Facebook and Pinterst and while they often make me chuckle, I just had to share this one for the parents out there who, like me, have received loads of unsolicited and painfully unhelpful parenting advice from usually well-meaning strangers and even experts over the years... This one I can truly appreciate. =)


24 August 2012

Re Appeals & Due Process from DRNC

Because I do make every effort to assure the information I disseminate for families and other interested parties / agencies is factually acurate, I followed up with the good folks over at DRNC regarding the preceding post, Appeals & Due Process (or Lack There Of), so see if there had been any changes since my last missive was sent and posted which included due process concerns...

Below is the response I received:

-----------

From: Jennifer Bills
Sent: Friday, August 24, 2012 11:37 AM

The post is not inaccurate, especially if you read to the end about the status of Final Agency decision-making; however, Elizabeth and I consulted and feel that the tone is far too pessimistic.

Our response post would be:

Document, Document, Document

Medicaid recipients have a decent track record, both when they are represented by counsel but also pro se, of prevailing in Medicaid appeals. The key is to obtain and provide adequate documentation of the medical necessity of the service, and specific details regarding the amount of hours the individual needs. Understanding the criteria used to evaluate requests for services is particularly important. Decisions can only be based on sufficient evidence of the precise amount and type of Medicaid service that is medically necessary for the individual. Appeals should focus on the individual’s medical and social needs, as opposed to the family’s needs, even when families are providing the care. Although hardships to a recipient’s natural supports may provide context for an appeal, that alone may not meet the criteria in the service definition. Letters from clinicians, social workers, direct care staff, case managers or community guides, and families are essential to justify services. Additionally, documentation from medical providers, or a log of behaviors created by the family or direct care staff, may be more persuasive than testimony based on recollection or memory.

Even at the Reconsideration stage, if you provide additional information supporting the request, there is a chance of getting a different decision. Although OAH is not yet making the final decisions, the State legislature directed DHHS to submit a request to CMS to grant OAH this authority, and that process is ongoing. Many cases settle during the appeals process, and cases rarely go all the way to Superior Court. OAH rules allow mediators and judges to assist pro se clients with navigating the appeals process. Although they are neutral and not advocates, they help ensure the process is fair. Our message would be: don’t give up on due process. Rather, utilize it and win!

And it would be great if she could add a link to our MCO Medicaid Appeals fact sheet, attached here.

Jennifer Bills, Senior Attorney
Disability Rights North Carolina
Champions for Equality and Justice

Disability Rights NC is the state's protection and advocacy system. DRNC is a 501 (c)(3) organization. If you are a state government employee, you can support Disability Rights North Carolina through the State Employees Combined Campaign (SECC). Please use code # 1544. Donations support our efforts to promote a clear and independent voice for North Carolinians with disabilities.

Appeals & Due Process (or Lack There Of)

I try very hard not to post a great deal of personal commentary. Though today I just couldn't help myself...

The North Carolina Department of Health and Human Services reached a settlement agreement with the US Department of Justice yesterday (8/23) regarding the State's ADA and Olmstead violations surrounding the improper placement and warehousing of mentally ill and developmentally disabled adults in adult care / nursing homes across the state. [ read more... ]

It is a victory. --However big or small it may seem is moot; it is nonetheless a victory in the recognition of a tremendous need and an acknowledgement of individuals deserving of a quality life and community interaction. Definitely a step in the right direction and I commend everyone involved for their diligence and efforts toward a just resolution.

Not to rain on the parade, but...

What continues to be of concern however, is that while we scurry to "deinstitutionalize" one vulnerable population and invest in services and programs to assure these individuals are properly supported in community environments as they are entitled, we are failing to bolster all the many thousands of other special populations who are already living in integrated settings, be it at home with their families or in supported living, etc. -- the ones who are not institutionalized and don't want to be -- whose loved ones desperately want to keep them in their homes... And yet, it seems that the very supports that allow that to happen, that they also are entitled to, continue to be trimmed away.

It's the human shell game: while we move one population toward community stability, we are pushing much of the rest, slowly but surely, straight into crisis. 

Without proper supports and proper funding for those supports, the reality is that many families will be forced to make the hardest decision of our lives - surrendering our loved ones to the state either because we will have to quit our jobs to provide full time care or we just cannot physically nor mentally do it anymore because we're already hanging on by a bare thread or both (which puts us right back where we started from and begs to question: where will they go? Can't put 'em in nursing homes, that's how we got into this mess to begin with.)

I had an exchange today with a weary and frustrated fellow mom in the eastern part of NC who is about to embark upon the grueling appeals process fighting for proper services and supports for her adult DD children that her family depends upon for their very existence. 

Yes, I said existence - not just the quality of life, certainly not for convenience and most definitely NOT for financial gain; EXISTENCE.

Like filing an appeal because services for your DD child(ren) are being drastically decreased and you simply cannot make do with less because you already are.

Through this dialogue I realized that the critical issues surrounding Medicaid appeals for DD recipients and Due Process, or lack of, are still not understood even on a basic level and misinformation continues to circulate.

Unless something has changed since June 2012 when I sent out and posted my Open Letter and Outline of Critical Medicaid Waiver Issues (with supporting documents), there remains NO FAILSAFE CONSTITUTIONALLY PROTECTED DUE PROCESS APPEALS PROCEDURE for Medicaid Waiver recipients and families

If something has changed, someone please let me know; I will be thrilled to update.

Otherwise, currently this is the way it works - or doesn't, as the case may be (from the outline):

What do we know about the Due Process / appeal procedures under the new 1915(b)(c) Medicaid Innovations managed care plan?
  • The current appeals process reflects a consumer appeals process to a unilateral hierarchy with no third-party authority to fairly referee.
  • As outlined in the PBH brochure and 2012 Provider Manual (pgs. 62-67) is as follows:
    • If consumer caregiver has recipient service hours and / or benefits reduced, suspended or terminated,
    • consumer caregiver will receive a letter 10 days prior to changes via US Certified Mail a letter, outlining instructions to request a ‘Reconsideration Review’ through PBH (or respective LME/MCO)’s ‘Reconsideration Review Process’ within 30 days of notification.
    • If Reconsideration Review, does not yield a response in favor of consumer, consumer caregiver can appeal to both DHHS and the Office of Administrative Hearings (OAH) by filing a request for a State fair hearing within 30 days.
    • Once appeal is processed, consumer caregiver may participate in an informal attempt to resolve the conflict through the Mediation Network of North Carolina;
    • if the conflict cannot be resolved in mediation or if consumer declines mediation, the matter will be set for hearing before an Administrative Law Judge (ALJ) at the OAH.
    • The ALJ will hear the matter and evidence and make a recommendation regarding the consumer’s matter and forward the decision to DMA,
    • where DMA will review and make a final decision.
  • What’s the point? More time and State financial resources wasted.
  • The only recourse following a final decision by DMA is for the consumer to retain counsel and file suit in Superior Court - an extraordinary expense of tens of thousands of dollars that the vast majority of consumer families, including mine, could not afford.
  • It should be noted that under the new PBH model, service eligibility for DD Medicaid Waiver recipients is determined by the Supports Intensity Scale (SIS) which arguably provides a more detailed client pictorial, however, the formula specifics which equates a recipient’s level of need by the State’s representative LME is deemed “proprietary information’:
    • LME representatives are required to sign and enter into a “Non-Disclosure Agreement” with PBH to protect the SIS methodology.
    • This non-disclosure further prevents a fair an adequate appeals process for consumers as how can one effectively challenge information which is withheld from them?
    • Proprietary information as such held by an agent of the State providing public services to citizens on behalf of the State - services which are funded by Federal and State monies is, in fact, a conflict of interest.
    • This is NOT transparency and only perpetuates mistrust.
  • Also noteworthy: PBH recently had a federal lawsuit against acting NC DHHS Secretary Delia and Mann [5:12-CV-46] suing to not only remove final decision-making authority from the State government entity who is to oversee and govern the managed care operation and all LME’s, but to seemingly assure totalitarian authority.
    • It is my understanding that this case has since been withdrawn.
OAH, ALJs and the Regulator Reform Act of 2011.
  • NC SL 2011-398, commonly referred to as the Regulatory Reform Act, became State Law July 25, 2011, granting final authoritative ruling to OAH / ALJs over Medicaid cases, effective January 1, 2012 and applies to cases contested after that date.
    • SECTION 32. G.S. 108A-70.9A(f) reads as rewritten: "(f) Final Decision. – After a hearing before an administrative law judge, the judge shall return the decision to the Department in accordance with G.S. 150B-37. The Department shall promptly notify the recipient of the final decision and of the right to judicial review of the decision pursuant to Article 4 of Chapter 150B of the General Statutes."
    • SECTION 33. G.S. 108A-70.9B(g) reads as rewritten: "(g) Decision. – The administrative law judge assigned to a contested Medicaid case shall hear and decide the case without unnecessary delay. The judge shall prepare a written decision and send it to the parties in accordance with G.S. 150B-37."
  • Despite the January 1, 2012 effective date for OAH final authority over recipient disputes in Medicaid matters, federally-funded Medicaid Waiver programs by design have a “single agency rule” which dictates that a single state agency makes final decisions in Medicaid issues which is somewhat conflicting given the design of the new statewide managed care waiver, therefore Centers for Medicare and Medicaid Services (CMS) must grant an exception waiver to the State of NC to permit alternate authority. Currently, NC governing officials and other interested stakeholders are working toward mutually agreeable waiver submission terms, though to date, an agreement has not be solidified.
  • Thus there remains NO appropriate fail-safe due process for recipients and families save the unrealistic and unfeasible hardship of unnecessary legal expenses and lengthy court battles.

So essentially, if you disagree with an LME's decision regarding Medicaid services / supports, you pretty much are appealing to the person who instructed the decision to be made in the first place. If that doesn't work out, you can opt to undergo mediation and have a hearing before an ALJ who will then advise DMA of their opinion, but ultimately DMA still has final say.

The confusion seems to come from in between the State Law and the federal hang-up with CMS. 

Yes, NC State Law 2011-398 does in fact grant OAH final decision making authority BUT because of the federal "single agency rule," CMS must have a specific waiver from the State of NC in order for the federal government to allow another governing entity (e.g. OAH) to make decisions which affect federal monies. 

If North Carolina officials cannot agree on the waiver language for exception and this exception waiver is not submitted and approved by CMS before the final implementation of the statewide 1915(b)(c) managed care waiver, the period for appeals will have been exhausted and we may all be stuck with whatever decisions are made for us.

If you are in an appeals process, keep your representatives and advocacy groups informed - and as always, feel free to forward to me anything you wish to share.

*Update : More on Appeals and Due Process (feedback on this post) from Disability Rights NC.

23 August 2012

FW: National Core Indicators Adult Consumer Survey

Below is an email I received regarding the National Core Indicators (NCI) surveys and reports conducted as a collaborative effort between the National Association of State Directors of Developmental Disabilities Services (NASDDDS) and the Human Services Research Institute (HSRI) as pertaining to the Durham Center LME (now Alliance Behvioral Health Care).

From the NCI website
The purpose of the program, which began in 1997, is to support NASDDDS member agencies to gather a standard set of performance and outcome measures that can be used to track their own performance over time, to compare results across states, and to establish national benchmarks.
Currently, my daughter is 14 years old and personally I have never received a survey of any kind from any state nor federal agency regarding services she has received over the years that I can recall, nor have I ever been asked for my opinion nor feedback, though I'm certain it's no surprise to anyone who knows me that I happily provide it anyway. 

But apparently some folks are asked for input on their experiences. 

-----------

Subject: FW: National Core Indicators Adult Consumer Survey

DMHDDSAS conducts National Core Indicators surveys of people with intellectual / developmental disabilities (IDD) through the Division's Core Indicators Projects annually. The surveys consist of (1) family surveys that are mailed to the family members or guardians of random samples of people with IDD who received a service other than case management or care coordination in the past fiscal year and (2) the adult consumer survey. The latter consists of two parts: (a) the background information section that is completed by a service provider, and (b) the adult consumer section that is completed through a direct interview of the person with IDD for the first part of the section and a direct interview either with the person with IDD or with others (e.g. a family member or an advocate, or a service provider).


HSRI analyzes NCI data and publishes reports that show how each state performs against other participating states. The final report for 2009-2010 for the state of North Carolina may be accessed at the following HSRI website: http://www.hsri.org/files/uploads/publications/NCI_CS_09-10_FINAL_Report.pdf. DMHDDSAS will be publishing LME-specific reports on its own website on or before the end of this month.

We believe that the findings generated from the NCI surveys are extremely valuable for improving the system at the state and local levels and we hope that you will share them with your stakeholders, including members of your Community and Family Advisory Committee (CFAC).

If you have questions about the report or the project, please do not hesitate to get in touch with Maria Fernandez (919-733-0696; maria.fernandez@dhhs.nc.gov).

NC-DHHS Settlement Agreement Dox w/ US DOJ

Settlement Documents (123KB pdf)

The above link will prompt a pdf download of the full settlement documents between the North Carolina Department of Health and Human Services and the United States Department of Justice, Civil Rights Division;

Documents to include:
  • Complaint for Declaratory and Injunctive Relief 
  • Joint Motion to Dismiss Without Prejudice and Retain Jurisdiction
  • Proposed Order
  • Settlement Agreement (Exhibit A)
  • Memorandum in Support of the Joint Motion


Hubert H. Humphrey said, "The moral test of government is how it treats those who are in the dawn of life . . . the children; those who are in the twilight of life . . . the elderly; and those who are in the shadow of life . . . the sick . . . the needy . . . and the disabled."

On behalf of so many, THANK YOU North Carolina!! 

Disability Rights NC Applauds North Carolina’s Settlement with U.S. DOJ


FOR IMMEDIATE RELEASE
Thursday, August 23, 2012


Disability Rights NC Applauds North Carolina’s Settlement with U.S. DOJ

Raleigh – Governor Beverly Perdue took a major step today toward resolving one of the greatest challenges facing our State’s mental health system by signing a settlement agreement with the U.S. DOJ. The agreement addresses findings made July 28, 2011, that the State violates the ADA by segregating North Carolinians with mental illness in Adult Care Homes rather than allowing people the choice to live and be supported in the community.

“Disability Rights NC applauds the Governor and the Secretary Delia for their leadership. This agreement will protect the rights of people with disabilities and help the State avoid costly litigation,” said Vicki Smith, Executive Director.

The agreement provides for the creation of appropriate community mental health care, employment services and housing options for people with mental illness in our State. “This agreement will improve the lives of N.C. families – our brothers and sisters, mothers and fathers. Disability Rights NC pledges to remain vigilant, ensuring the agreement’s promise is permanent,” said Smith. “North Carolina has seized an opportunity to cultivate a robust system of care for people with mental illness which all of us can be proud of.”

Background on North Carolinians with Mental Illness Housed in Adult Care Homes

In July 2010, Disability Rights NC filed a complaint with the US DOJ alleging that the State of North Carolina is in violation of the Americans with Disabilities Act (ADA) because the State has a bias towards placing people with mental illness in Adult Care Homes (ACHs) rather than supporting them in more integrated settings in their home communities. ACHs are institutional settings that do not provide appropriate services to support recovery and meaningful community integration. Disability Rights NC alleged that the State, in relying on placements in these types of Adult Care Homes, is violating the ADA. Please see the Report: Trapped in a Fractured System - People with Mental Illness in Adult Care Homes on the website (www.disabilityrightsnc.org). Under the ADA the unjustified segregation of persons with disabilities is an illegal form of discrimination. The integration mandate allows individuals to interact with non-disabled persons to the fullest extent possible so people with disabilities are not isolated from their communities.

The US DOJ, Civil Rights Division, issued a letter of findings on July 28, 2011, concluding that North Carolina "fails to provide services to individuals with mental illness in the most integrated setting appropriate to their needs in violation of the ADA," and that "[r]eliance on unnecessary institutional settings violates the civil rights of people with disabilities." The central finding of the US DOJ is that North Carolina lacks an adequate community support system for people with mental illness. As a result, individuals are institutionalized in more expensive and more restrictive settings in Adult Care Homes. "Most people with mental illness receiving services in adult care homes could be served in more integrated settings, but are relegated indefinitely and unnecessarily to adult care homes because of systemic State actions and policies," wrote U.S. Assistant Attorney General Thomas Perez. "Reliance on unnecessary institutional settings violates the civil rights of people with disabilities.”
###

NC DHHS, US DOJ Reach Agreement on Community Based Care for Only Citizens with Serious Mental Illness

From The Arc of North Carolina

Breaking: NC DHHS, US DOJ Reach Agreement on Community Based Care for Only Citizens with Serious Mental Illness

[ view release at arcnc.org ]

Press Release from NC Dept. of Health & Human Services:

Raleigh — The North Carolina Department of Health and Human Services and the United States Department of Justice today reached an agreement on the state’s plan to offer more choices of where and how citizens with serious mental illness receive care and supportive services.

The plan, which was announced last month, will create housing slots in the community to offer the choice of community-based care for many adults with serious mental illness. It will also invest in job training and employment assistance for those citizens and will set up a comprehensive, 24/7 crisis care program for people with a serious mental illness.

This agreement will modernize our mental health system and ensure that North Carolina is providing the best possible treatment for adults diagnosed with severe mental illness. It will also provide the opportunity for many of these individuals to live in community settings if they choose to do so, and ensure that North Carolina is fully complying with the Americans with Disabilities Act and other federal laws.

This agreement is similar to ones signed by governors of a number of other states including, among others, the governors of Virginia and Georgia.

DHHS Secretary Al Delia agrees that more should be done to ensure access to community-based treatment for those with mental illness. “North Carolinians who have a serious mental illness have a right to choose the very best care environment to meet their personal needs,” he said. “That choice – whether they live in the community or in an adult care home – will be supported with access to mental health and other support services that will be available in part due to this agreement. Moving forward with a solution to help them identify and access those choices is the right thing to do,” he said.

“Disability Rights NC applauds the Governor and Secretary Delia for their leadership on this matter. They have not only done the right thing to protect the rights of people with disabilities, they have helped the state avoid costly litigation and destabilizing uncertainty,” said Vicki Smith, executive director of Disability Rights NC.

The agreement outlines DHHS’s plan of action to provide community-based services to people with mental illness. The budget the General Assembly passed in July expressly contemplated a settlement and appropriated funding to make this agreement possible. The timeline for completing the plan is eight years; this transition period will enable people who want to move to community-based settings to do so on a workable timetable and will allow sufficient time for North Carolina’s mental health infrastructure to implement this agreement.

# # #

20 August 2012

NC Division of Vocational Rehab Input & Public Forum 9/20


The NC Division of Vocational Rehabilitation Services in partnership with the NC State Rehabilitation Council invites you to join us for an Input Session and Public Forum in Morganton on Thursday, September 20, 2012 from 4:30-6:30 pm. at our WorkSource West location.  Please see the attached flyer for further details.

We hope to see you there!

Sincerely,

Kim Schmidt
SRC Liaison
Interim Client Appeals Coordinator
NC Division of Vocational Rehabilitation Services
Program Policy Planning & Evaluation Section
2801 Mail Service Center
Raleigh, NC  27699-2801
Ph:  919-855-3533
Fax: 919-715-1050
Kim.Schmidt@dhhs.nc.gov

Panel Discussion on Housing 8/27

Panel Discussion about impact of PCS & IMD laws on Housing for People with Mental Illness: 8/27 @ 7pm

There is an impending crisis for people with mental illness who need assistance and/or supervision to live successfully in the community. There are two serious issues:
  1. The state has changed the requirements for residents in Group Homes, Adult Care Homes, and Family Care Homes to qualify for Personal Care Services (PCS). The new rules will make it virtually impossible for people with mental illness to qualify.

    All of this adds up to lots of problems for people with mental illness living in group homes and family care homes. In fact, the Chief Clinical Operating Officer of the State Division of Medical Assistance told the Legislative Oversight Committee for the NC DHHS on Tuesday, August 14 that the projected impact on supervised living group homes for people with mental illness is that nearly “0%” of residents will qualify based on the new guidelines and assessments. People with mental illness in other congregate living settings (Adult Care Homes and Family Care Homes) will be equally affected. The state projects that 12,000 people total will no longer qualify.

    We estimate that, on average group homes are billing about $6,000 per year for each resident for PCS. Loss of this amount of revenue will undoubtedly force some homes to close and those that stay open will need another source of revenue to be able to provide the quality care that is needed. The revenue from SSI and SA funds alone is not enough.
  2. The Department of Justice has ruled that the state is in violation of the Americans with Disabilities Act by housing people with disabilities in congregate settings. One outcome is that the federal Center for Medicaid and Medicare Services is requiring NC to enforce a 1965 Law. It is called the Institutions for Mental Disease (IMD) provision. It does not allow Medicaid payments for resident’s doctor’s visits or medication if a single provider has more than 16 individuals taking medications for mental illness even if they are in separate, small homes in different locations.

    One of the first things we have planned is a Panel Discussion on August 27, 7-8:30 pm at Highland United Methodist Church, 1901 Ridge Rd., Raleigh, NC in the Church Conference Rm (adjacent to the church office). You will have an opportunity to hear from the individuals who are involved in making and implementing these new policies as well as hearing from a group home manager and consumer who are impacted (See below). We hope to see you there and to hear your thoughts about this issue.
  • Selden Holt from UNC Center for Excellence in Community Mental Health, Moderator
  • Vicki Smith, DRNC – Background on PCS changes
  • Leza Wainwright, Chief Clinical Operations Branch, NC Division of Medical Assistance
  • Jenny Gadd, Group Home Director ‐ Likely Financial Impact of PCS Changes 
  • Robert Bullock, Group Home Resident, Why Group Homes are Needed 
  • Jim Jarrard, Div MH/DD/SAS, Viability of 5600A Group Homes in the Housing Continuum
  • Ann Akland, Advocacy Chair, NAMI Wake

Eric S. Fox, M.A.
Mental Health Program Coordinator
NC DHHS MH/DD/SAS
Advocacy & Customer Service Section
Consumer Empowerment Team
3009 Mail Service Center
Raleigh, NC 27699-3009
(919) 715-3197 ext 235
email: eric.fox@dhhs.nc.gov
website: http://www.dhhs.state.nc.us

14 August 2012

FAN Stewards of Children Workshop 9/8

Stewards of Children Workshop

Where: Freedom House, 102 New Stateside Dr., Chapel Hill, NC 27514

When: Saturday September 8, 2012 from 9:00 AM to 12:00 PM EDT


Dear Friend of FAN:

Recent headline news about the trial of Penn State coach Jerry Sandusky who sexually victimized children entrusted to his care has caused parents across the country to question the safety of their kids when in the care of others. And they should be concerned. Statistics reveal that 1 in 4 girls and 1 in 6 boys are sexually abused before their 18th birthday.

Children with special needs have a higher rate of victimization than non-disordered children.

In an effort to help parents and other interested members of the community learn more about child sexual abuse, the Family Advocacy Network (FAN), a program of Mental Health America of the Triangle, proudly presents a training from Darkness to Light, "Stewards of Children: Confronting Child-Sexual Abuse With Courage." The training will be facilitated by Amy Martin-Jewett, RN, Saturday, September 8th, 9:00am to 12:00-noon at Freedom House Recovery Center, 102 New Stateside Dr., Chapel Hill.

Child safety is every adult's responsibility. In this workshop, participants will learn:

  • how to prevent abuse
  • how to recognize warning signs
  • how to react responsibly when it occurs

This workshop is offered free of charge. Donations are gratefully accepted. Training materials and refreshments will be provided. Stewards of Children is an initiative of the Chapel Hill-Carrboro YMCA, partnering with FAN and other area organizations in an effort to maximize opportunities for trainings throughout the community.

Registration is limited to 25 participants. Registration will discontinue when maximum registration is reached or on Thursday, September 6th, whichever comes first.



Please let me know if you have any questions about the workshop. I look forward to seeing you on September 8th.

Sincerely,

Georgia Gamcsik, Family Advocate
Family Advocacy Network (FAN)
a program of Mental Health America of the Triangle
georgia@mhatriangle.org
919-942-8083

10 August 2012

NCGA Draft Agenda for 8/14

JOINT LEGISLATIVE OVERSIGHT COMMITTEE ON
HEALTH AND HUMAN SERVICES
(DRAFT) AGENDA

August 14, 2012
10:00 A.M. ; Room 643, Legislative Office Building
Representative Justin Burr, Co-Chair, Presiding

Introductions and Comments 10:00 – 10:15

2012 Session Overview (Budget and Substantive Laws) 10:15 - 11:00
Update on BC Waiver Implementation 11:00 – 12:30
Lunch 12:30

Institutes of Mental Disease, US DOJ Complaint and PCS: Status Update 1:30 - 2:10
  • USDOJ – Emery Milliken, General Counsel, DHHS
  • IMD – Tara Larson, Chief Clinical Operating Officer, DMA
  • PCS – Tara Larson, Chief Clinical Operating Officer, DMA
Evaluation of Medicaid 2:10 – 2:40
  • Division of Medical Assistance – RFP for Medicaid Evaluation
  • Michael Watson, Director DMA
  • State Auditor’s Office Audit of Medicaid – To Be Determined
Update on Consolidation of Leased Space for DHHS Administrative Offices 2:40 – 3:00
  • Terry Hatcher, Director, Division of Property and Construction
Adjourn.

09 August 2012

From Arc NC: Unintended Budget Cuts Must Be Fixed!


Unintended Budget Cuts Must Be Fixed!

[ view original posting ]

It’s time for the Governor and members of the General Assembly to fix the “unintended” reductions of the Social Services Block Grant (SSBG) for people with disabilities. Both legislators and the Governor’s administration seem to agree that an additional cut of $4.3 million to the community system was unintended. Unintended or not, this cut, on top of the $20 million intended reduction by the General Assembly, is causing serious harm to people with disabilities and their families.

It is hard do imagine that while the state is attempting to negotiate a settlement with the U.S. Department of Justice on ADA issues, we would allow further reductions to the fragile infrastructure of the community system. Services that allow people to live at home or in community residential settings are affected by this cut the most. Letting this “accidental” cut stand will hurt people.

The Arc, in a letter to the Governor, has asked that she take the lead on eliminating this cut. We are sending a similar letter to the House and Senate leadership asking them to join with the Governor to fix this unfortunate mistake. Hopefully, all parties will work together to do so.

Members can help by letting the Governor and General Assembly know that this cut must be restored. Let them know that our fragile community system cannot stand more reductions and that people with disabilities deserve better!

Contact:

From The Arc NC: Lessons from the Western Highlands Network overruns

From The Arc of North Carolina

Lessons from the Western Highlands Network overruns

[ view original posting ]

The cost overruns at Western Highlands Network (WHN), the first LME to become an MCO under a new law, are a serious issue. The solution to these overruns that the state and WHN has come up with is clear: further service cuts. Hopefully, these overruns are just a bump in the road and not the light of an oncoming train, indicative of a system-wide underestimation of managed care cost. Most likely it will be somewhere in the middle.

We can only hope that people with disabilities will not be harmed further by these overruns than they already have been by the shift to managed care. The Arc hopes WHN survives these problems and succeeds for the sake of the individuals they are in the business of supporting.

Regardless of the reasons for the problem, the State, meaning both the Administration and the Legislature, should be paying close attention. Though we do not yet know the specifics that led to these overruns, several things should be perfectly clear:
  1. We need a real examination of the process. Regardless of why, no MCO should have such significant funding issues six months into operation. Some are understandably questioning the leadership of former CEO Arthor Carder, but it’s hard to believe anyone would question his commitment to the people WHN served, or the commitment of WHN’s staff. The fact that this MCO was allowed to go live without the tools to succeed is not only a mark on WHN, but more importantly a significant mark on the DHHS processes that deemed them ready.
  2. We should not only examine the process that led to these overruns, but the 1915(b)(c) waiver model as a whole. It is no secret that The Arc does not believe this model is appropriate for people with IDD. The issues with WHN should cause public officials to question the model as well. As WHN looks for places to cut Medicaid rates, it becomes clear that the system prevents them from even considering state operated facilities [state institutions] for reductions comparable to community services. Managed Care was sold to legislators, and the public, on the assumption of MCOs’ ability to effectively manage all public resources. Clearly, that was not true then, nor is it now. This disconnect makes the state’s difficult transition to a new model of care even more difficult. If the 1915(b)(c) managed care model works for community-based services it should also work for state-managed facilities. This issue is just one of many model design questions that must be questioned.
  3. State officials told the WHN Board that they should expect no additional state funds to make up for overruns. This begs the question: is the stated goal of “better access to services” just spin? When rate reductions, utilization reductions, and Medicaid paybacks are the primary tools used to eliminate deficits, it is difficult to take seriously that better access is a real goal. Better service access would more likely be achieved if the state were willing to adjust the capitation rate or infuse some money while WHN becomes better prepared to “manage.”

Though not enough details have been released yet to determine the specifics of the WHN overruns, we do know:
  1. The only way “savings” will be achieved through this managed care model is through cuts. That should be clear as we review the differences in what WHN was paid and what they have said they needed to provide services. We know that Medicaid cost must be controlled but an honest discussion of how managed care achieves this is critical if people will have faith in this system.
  2. The way “at risk” is used in this model is insulting to families, consumers and the people who provide the supports for them. Public MCO’s are not really “at risk” entities. They have raised no capital to fund their organizations; they receive generous administrative allocations separate from services funds, and have the ability to cut rates and services to consumers if they exceed budgets. Providers of services are the ones really at risk. With subjective decision making, constant rate reductions, no guaranteed “administrative” funds or excise payments to fund a MCO’s “risk” reserves, many providers will likely go out of business. Most importantly, people with disabilities and their families are the most at risk…at risk for another failed effort at reform jeopardizing their ability to live successful lives in the community.

06 August 2012

WRAL re NC MH Reform & Parent Info.

WRAL report re Managed Care and IDD, etc.
1 message


MaryKShort@aol.com <MaryKShort@aol.com>Sun, Aug 5, 2012 at 11:15 AM
To: MaryKShort@aol.com

FYI ... very well written and researched article by Mark Binker at WRAL.com.  I can see that there are a lot of good talking points to use when you contact your elected representatives to express your concerns or your experiences. 


In the article, a Ms. Laurie Haley is quoted:  Laurie Haley has seen ups and downs as North Carolina has slogged through mental health reform efforts over the past decade. For a three-year period from 2005 through 2008, she said, reform seemed to have worked for her daughter, Alissa. Other times, dealing with local and state mental health bureaucrats was more fraught.

That period of time covers the pre-Home Supports service definitions.  I happen to agree totally with her EXCEPT for the fact that it was at the end of 2007 and into early 2008 when the state first tried to implement the 40-hour limit!  I don't know if she was impacted by that at the time or if she even knows it is part of the Innovations waiver.  I have written the reporter to ask.

Mary K. Short
828-632-5888 or 704-451-4144 (cell)


Posted: 7:09 p.m. Friday (August 3, 2012) Updated: 12:11 a.m. yesterday

Patients, advocates wary as NC again reforms mental health system

By MARK BINKER, WRAL.com Multimedia Reporter


Raleigh, N.C. — North Carolina is in the midst of an effort to remake the state's public safety net for those with mental health, substance abuse and developmental disabilities.

Lawmakers, administrators and taxpayers want to see if the change to a "managed care" model can really save millions of dollars and avoid the over-spending debacles that marked the first system remake a decade ago.

At stake is how the North Carolina manages more than $2.4 billion in state and federal mental health dollars that flow through local mental health agencies, and how individuals with mental illness will live their lives every day.

"All I want to do is keep my daughter at home," said Laurie Haley.

For her, reforms success or failure will be measured by how it affects her daughter, Alissa. The 27-year-old woman has severe developmental disabilities and also suffers from seizures. Alissa needs help dressing, eating and taking care of other needs. Those who help her need to be able to administer medicine and prepared to act in case a seizure makes her fall in the shower or comes on her in public.

Haley says that she has, for now, ensured that the transition to managed care won't mean fewer services for her daughter. But she said other families making the switch are still encountering problems.

"What I'm hearing is that they're still trying to reduce services for people," Haley said.

That small-scale skepticism of the new system was amplified this summer when a blistering report said that one of the first local mental health authorities given permission to make the transition was not ready for the switch to managed care.

State and local mental health administrators say that one experience should not color the entire transition effort and that the system is on the road to improvement. Advocates, some who work providing services to clients and even some lawmakers say the process may be moving too fast. They worry that counties such as Wake and Durham, which have just begun the move toward managed care, could encounter the same mistakes and problems seen elsewhere.

...

[ There's much more... Read the Full Story on WRAL.com ]

And while statewide success will be measured in millions of dollars, Haley and others like her will measure it in terms of what it means for their loved ones.

"My daughter is not a disability, she's a human being with a disability," Haley said. "If I have the right to live at home and you have the right to live at home, she should too."

----------- more from Mary Short...

EXTRA:  Mercer Report link
2ND EXTRA:  Federal Report link and quote from that report

C. Health, Safety and Quality

Abuse, neglect, exploitation, the use of mechanical and chemical restraints, unexplained injuries and denial of services are far too prevalent in our current long-term system of services. CMS has made significant strides in holding states accountable for addressing health and safety issues in the 1915(c) Medicaid Home and Community Based Waiver program; but requirements governing program design, state monitoring and reporting to CMS have not been mandated for managed care programs approved under Section 1115 demonstration waivers or under the dual eligible pilot demonstrations.
3rd EXTRA:  Other news reports from Raleigh sources regarding other budget cuts and budget overruns

http://projects.newsobserver.com/under_the_dome/mental_health_office_needs_lots_of_work_consultant_says#storylink=cpy
Submitted  by lbonner on 2012-07-26 14:37
Under the Dome | mental health | N.C.  Department of Health and
Human Services | Western Highlands  Network

Last week, we wrote about a local mental health office that  covers
western North Carolina counties losing $3 million since switching  to
managed care in January.

A consultant's report issued this week  describes problems at Western
Highlands Network, one of the first local  mental heath offices to
convert to a managed care system.

Among other  things, the report says that the information Western
Highlands leaders  receive about services, use and costs is inadequate,
and that it is not  keeping good track of Medicaid claims.

The report goes on for nine pages.  In short, it says Western Highlands
needs lots of improvements, and the  consultant recommends close
monitoring by the state Department of Health and  Human Services.

Under managed care, the local mental health office gets a  set amount
of money to treat mentally ill patients who rely on Medicaid or  state
funds.

Western Highlands Network became a managed care  organization in
January. By next January, managed care organizations  for
government-paid mental health services will cover the entire  state.
And ... news article re WHN & Mercer Report is in it and easy to read!

Program Coordinator Needed for Lifetime Connections

FIF Lifetime Connections Program Seeks Program Coordinator

Program Coordinator for Lifetime Connections program; full-time, possible part-time options; generous benefits. Position is located in Durham at headquarters of statewide non-profit providing innovative supports and services to people with disabilities and their families. The Coordinator: recruits and maintains relationships with members, community connector staff and volunteers, ensures quality of services and support for member families, coordinates workshops, and manages budget. Seeking person interested in and experienced with disability issues and family support concepts, Community Development expertise, membership and volunteer recruitment, and budgeting. Applicant should have strong communication, organizational skills, be flexible to travel for some night and weekend meetings, and have use of car. 

First In Families of NC is an Equal Opportunity Employer. Review our website before applying: www.fifnc.org. Apply in writing to Human Resources; First In Families of NC; 3109 University Dr Suite 100, Durham NC 27707 or email betsym@fifnc.org. No calls or unscheduled visits please.

Betsy MacMichael
State Director
First In Families of North Carolina
3109 University Drive; suite 100
Durham, NC 27707
(919) 251-8368 X100
Fax: (919) 400-4846


Believe, Achieve, Give Back




03 August 2012

Volunteers Needed: NCDVRS Community Rehabilitation Program (CRP) Steering Committee

From the NC Department of Health and Human Services: NCDVRS Community Rehabilitation Program (CRP) Steering Committee


Title of committee: NCDVRS Community Rehabilitation Program (CRP) Steering Committee

General overview of committee’s purpose: Employment Service Providers, known as Community Rehabilitation Programs (CRPs), are integral partners in the network of services designed to provide people with disabilities with equal opportunities in achieving their highest level of economic and social independence. With representatives from DVR, DMH/DD/SAS and CRP providers, the NCDVRS CRP Steering Committee focuses on budgetary and program issues and makes recommendations to the NCDVRS Division Director. The committee’s goal is to help ensure the delivery of quality services with informed choice by our consumers. More information on the workgroup can be found at the bottom of this webpage.

Specific Criteria being sought for consumer/family member representation: MH or MH/SA co-occurring or DD Consumers

Number of individuals need for the group: 2

Additional skills or knowledge required of individuals participating in the group: We are seeking consumers who have experienced VR services and/or have tried to access VR services and may have ideas to share on improving the quality of services.

When and where does the committee meet and how frequently? This committee meets quarterly at the NCDVRS offices on the Dix Campus, Raleigh, NC.

Date and time of the first meeting: Next meeting is tentatively scheduled for October 3rd, 2012

Does the opportunity for teleconference or webinar exist? (Briefly explain) Yes, a call-in number is available but attendance in person is preferred.

Is there any remuneration for participants? If yes, please describe in detail. No

Deadline by which recommendations need to be received: Friday, August 10, 2012

What is the selection process? Participants will be selected based on the criteria above (background with VR service/access) and a random sample will be chosen.

01 August 2012

DRNC PAIMI Advisory Council members needed

Disability Rights NC's PAIMI Advisory Council is in need of members from Region 2 (counties listed below). Applications are available on the Council's web page along with further information about the Council.

At least 60% percent of the Council is to be comprised of individuals who have received or are receiving mental health services or family members of such individuals with the Council striving to maintain a balance between consumers and family members.

In addition to geographic representation, the Council is mandated to include at least: one family member who is the primary caregiver for a minor child who is receiving or has received mental health services, one attorney, one mental health professional, one provider of mental health services and one member of the public who has demonstrated a substantial commitment to improving mental health services.

Right now, however, the Council's greatest need is for members from Region 2, regardless of whether they fit a specific slot, although fitting one or more of the mandated slots is certainly a plus. Those interested and living in other regions are certainly encouraged to apply as well with their applications considered as the need arises.

My thanks in advance,

David

Region 2 counties:

  • Anson
  • Cabarrus
  • Davidson
  • Davie
  • Forsyth
  • Guilford
  • Iredell
  • Montgomery
  • Randolph
  • Richmond
  • Rockingham
  • Rowan
  • Stanly
  • Stokes
  • Surry
  • Union
  • Yadkin