Home > Uncategorized > When Big Brother (thinks he) knows best about the developmentally disabled

When Big Brother (thinks he) knows best about the developmentally disabled

It can be frustrating when government administrators take it upon themselves to tell citizens what is in their best interest, and that includes telling them what is in the best interest of their family members with developmental disabilities.

It’s particularly frustrating when the state and federal governments tell people that they know best where their family members should or should not live.

For instance, the folks at the federal Centers for Medicare and Medicaid Services (CMS) have determined that farm-based residential programs are not good for developmentally disabled people. Also bad are residential schools for the developmentally disabled, group homes on the grounds of a private developmental or Intermediate Care Facility (ICF), and group homes located in “close proximity” to each other.

Both CMS and the Massachusetts Department of Developmental Services have decided that all of those types of residential settings “isolate” the participants from the “broader community.”  But while the feds are not banning those particular settings outright, the state DDS, in a new policy, appears to be proposing to do just that. According to the DDS policy, residents of “noncompliant programs” will be given “the opportunity to move to a compliant setting” or else face possible dis-enrollment from the HCBS program.

It doesn’t appear to matter that the participants may greatly enjoy living on a farm, for instance, or that they may derive many important skills from farm programs that improve their self-care, receptive and expressive language, learning, mobility, self-direction, and capacity for independent living.  It doesn’t matter either that their families and guardians may value those skills highly and consequently value those programs themselves.

It also doesn’t appear to matter that thousands of people in Massachusetts are waiting for residential and other care options, and that eliminating potential options, as CMS and DDS are doing, is only going to make that situation worse.

CMS issued a new regulation earlier this year that states that the residential settings they have identified as isolating may not qualify for Medicaid funding that is specifically earmarked for “home and community-based services.”  In “guidance” provided on the regulation, CMS criticized residential farm programs, in particular, because “an individual generally does not leave the farm to access HCBS (Home and Community Based Services) or participate in community activities.” CMS said similar things in the guidance document about residential schools for people with developmental disabilities, and about other programs that “provide  multiple types of services and activities on-site.”

In its new policy based on the CMS regulation, DDS states that it will not fund or support new residential settings such as farmsteads, “gated or secured communities,” residential schools, settings that “congregate a large number of people with disabilities for significant shared programming and staff,” or even new group homes with more than five residents.

DDS has scheduled public forums on its policy and a “transition plan” to comply with the CMS regulation on November 6 at 6 p.m. at Massachusetts Bay Community College in Wellesley, and November 12 at 10:30 a.m. at Westfield State University in Westfield.

It is not clear what evidence CMS has to make the claims that people in farm-based and other congregate care programs are not provided with access to community activities.  The federal agency’s guidance offers no citations or backup information or studies to support its claims.

Moreover, even if it were true that on most residential farms and in other programs providing “multiple services” that  the residents are not regularly taken into the community, wouldn’t it make more sense to require that those programs periodically take participants into the community than to effectively ban the programs altogether?  Isn’t that throwing the baby out with the bath water?  CMS acknowledged that it received many comments about how valuable and therapeutic those farm programs, in particular, are.

By the same token, CMS appears to be ignoring evidence that there is often little or no community integration by residents of small group homes.  Yet, even CMS isn’t willing to prohibit Medicaid funding for farm programs, residential schools, or multiple group home settings outright.   In contrast to the Massachusetts DDS, CMS has stated that it will subject so-called isolating programs to “heightened scrutiny,” which may result in continuing to fund them if a state makes the case that the settings do not have institutional qualities.

CMS, in fact, specifically rejected the idea of banning group homes with more than a set number of residents.  In responses posted on the Federal Register to public comments on the proposed regulation, CMS stated that it had previously proposed defining institutional care based on the number of residents living in a facility, but that:

…we were persuaded by public comments that this was not a useful or appropriate way to differentiate between institutional and home and community-based care. As a result, we have now determined not to include or exclude specific kinds of facilities from qualifying as HCBS (home and community based services) settings based on the number of residents in that facility (my emphasis).

CMS also noted on the same Federal Register site that the goal of its new Medicaid regulation:

… is not to take services from individuals, or make individuals move from a location where they have always lived… The goal of this regulation is to widen the door of opportunity for individuals receiving Medicaid HCBS… to have a choice in how, when, and where they receive services; and to remove unnecessary barriers and controls. (My emphasis).

So CMS states that its goal is to give people choices and NOT to make people move from a location where they have always lived; but the Massachusetts DDS has made it their goal since the Patrick administration came into office to move people away from where they’ve always lived. It’s evident from the language of the DDS policy and from DDS’s own actions over the past several years that the choices of individuals and their families and guardians do not signify here. For instance, only corporate provider-run settings are routinely offered by DDS as options for people seeking residential care.

Yet while the Massachusetts DDS is going beyond what CMS apparently intended in moving to eliminate available options for residential care, CMS has given the states the latitude to do so. As Tamie Hopp of the VOR, a national advocacy organization for the developmentally disabled, noted, states have “incredible discretion in terms of how they operate their Medicaid programs.”

In a publication, VOR contends that the new CMS regulation “continues to demonstrate an ideological bias against disabled people who find friendships and benefits from living together and accessing services and amenities ‘under one roof.'”   VOR further suggests that:

…if CMS determines some settings to be too ‘institutional’… it is likely that states will realize higher costs to accommodate transitions to likely smaller, scattered settings where economies of scale will not be realized. Quality of care and access to specialized services may also be affected, exacting an untold cost on affected individuals.

For some, this is really all about cutting Medicaid programs and diverting Medicaid funding to corporate providers, who are being encouraged to operate more and more widely dispersed, and smaller, group homes.  The corporate providers in Massachusetts are apparently fine with all of this. In fact, DDS notes in its transition plan that it consulted with “a small stakeholder group (including providers, advocates and participants/family members).”   The usual advisors to DDS are listed in the transition plan, including the Arc of Massachusetts and The Association of Developmental Disability Providers (ADDP).

It may just be that the people who are truly isolated in institutions are the folks working at CMS and the Massachusetts DDS, who appear to have little idea of how things work in the real world. Someone needs free them from their ivory towers!

You can help by sending your comments on DDS’s policy to their email address at HCBSWaivers@MassMail.State.MA.US.  You can also write to: HCBS Waiver Unit, 1 Ashburton Place, 11th Floor, Boston, MA 02108.  Comments must be submitted by November 15.

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  1. Barb Bussard
    October 30, 2014 at 3:03 pm

    This is exactly what is happening in Ohio as well. The county in which I live and my son receives services from without prior discussions tried to close one of our county workshops which caused quite concern. Our families spoke out and have been able to at least slow a proposed 8 week closure back to a projected 9month closing date with hopes to stop that as well. But this is a BIG e

  2. Anonymous
    October 31, 2014 at 2:46 pm

    The entire nation is demanding more close knit communities, a more densely populated stock of housing and state provided healthcare. Only governments and corporations (nonprofit and for profit alike) want the intellectually disabled scatted and isolated because its more lucrative for them. Tens of millions of dollars are spent every year on bloated corporate administrative costs that serve no other purpose of than patronage and future employment for senior DDS employees. Why does this continue?

  3. October 31, 2014 at 2:56 pm

    As noted by Barb B in Ohio, PUBLIC COMMENT is key and can make a difference. The Federal Rule REQUIRES that states provide opportunities for public comment AND include this public comment in its proposal to CMS. If Massachusetts’ proposal is counter to the weigh of the public opinion, it will have to sell why to CMS. By Nov. 1, PLEASE submit your comments to HCBSWaivers@MassMail.State.MA.US, or by mailing to the address provided at the end of the blog. It’s up to us. If not us, then who?

  4. October 31, 2014 at 5:21 pm

    How does one “widen the door of opportunity” – by LIMITING choices? And, “Anonymous”, please don’t blame the nonprofits, many of which would love to offer more true choices. Tell your Congressman, your Senator what CMS is doing. These regulations are not in the law; they are merely a bureaucratic interpretation of the law. Defining “choice” and “options” by removing true alternatives is a perversion of the concept of “choice”.

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