Home > Uncategorized > DDS hearing officer’s denials of appeals for placements at Wrentham Center appear to show bias against families and guardians

DDS hearing officer’s denials of appeals for placements at Wrentham Center appear to show bias against families and guardians

It’s becoming clear that the legal division and even the internal appeals division of the Department of Developmental Services (DDS) have a bias against families and guardians seeking residential placements for their loved ones at state-run congregate care centers in Massachusetts.

A decision by a DDS hearing officer last summer marks at least the second time in the course of a year that the Department shot down appeals by families to transfer intellectually disabled persons from corporate, provider-run group homes to the Wrentham Developmental Center.

Concerns downplayed

In both cases, the same DDS hearing officer, William O’Connell, denied the appeals in rulings that used the same language in many instances. And O’Connell appeared to downplay or even ignore concerns raised by the families about a lack of adequate care and meaningful activities in the “community-based” group homes and day programs.

In his decisions, O’Connell stated either that he did not give “substantial weight” to testimony of the families, or that they had not provided “substantial and probative evidence” that their adult children were receiving inadequate services or that Wrentham had more services and less turnover among staff.  At the same time, he found to be “credible” every argument raised against the families by DDS in its closing briefs.

In particular, O’Connell didn’t explain why he didn’t give substantial weight to what is arguably easily verifiable and true assessments about the Wrentham Center regarding services and staff turnover. This is clearly due to the fact that O’Connell fully subscribes to the administration’s ideology that all congregate residential care is institutional and therefore bad.

Also, as explained below, O’Connell’s decisions appear to be internally contradictory with regard to whether clients in the DDS system have a right to placements at the Wrentham Center and the Hogan Regional Center in Danvers, which are known as Intermediate Care Facilities for individuals with intellectual disabilities (ICFs).

As we previously reported, O’Connell denied an appeal in July 2023 filed by a father and mother who had been trying to get their son into the Wrentham Center. Last summer, O’Connell denied a second appeal by another mother to gain admission to Wrentham for her son. Then DDS Commissioner Jane Ryder upheld both of O’Connell’s decisions.

We have frequently noted that both ICFs are critical backstops for care in the DDS system. Yet these facilities are being targeted for eventual closure by the administration. Families and guardians of persons needing residential placements are not informed that the two ICFs exist; and, if they do ask for placements there, are almost always denied.

Conclusion stated at outset of decisions

The DDS bias was evident at the start of each of O’Connell’s decisions in which he stated that care in the community in each case had been “successful.”

In both cases, O’Connell stated that one of the “issues presented” was, “Does (the) appeal … entitle (the individual) to a change in residential placement, specifically admission to a specific ICF, after…years of successfully being supported in a less-restrictive community-based residence.” (my emphasis)

It appears from this language in both appeal decisions that O’Connell had already made up his mind before even hearing testimony. He listed, as an “issue presented” (meaning the case had yet to be heard), that the individual’s supports in the community had been successful.

However, in each case, the family had appealed based on an argument that the community-based supports had not been successful.

Also, a guardian in at least one of the cases claimed that her son was leading a highly restricted life in his community-based group home. And both families noted that they found that the Wrentham Center is highly interactive with its surrounding community, and offers many services and activities that are normally not available in their sons’ group homes.

So, the hearing officer’s presumption from the start in these cases that ICFs are automatically more restrictive than are community-based group homes indicates an unwillingness to consider evidence in individual cases that the opposite may be true.

Also, his presumption that care in the community-based system is uniformly successful ignores years of evidence that the community-based system has become highly dysfunctional and is rife with abuse and neglect.

 Claims of inadequate services not given weight

As noted, O’Connell actually acknowledged that he didn’t give “substantial weight” to allegations by each family about a lack of specific activities or supports in the community-based system. Instead, he accepted DDS’s assertions that the individuals in each case were “well supported” or “successfully supported” in that system.

In fact, O’Connell used the exact same language in stating in each decision that:

I find credible (DDS’s) testimony that admission to (Wrentham) is not appropriate for (the individual) because there was no immediate risk to (the individual’s) health or safety and no indication that (the individual’s) needs cannot continue to be met in the community.”

O’Connell just updated the name from the first to the second decision.

In both decisions, O’Connell also stated that DDS was “continuing to work” or “willing to accommodate” some of the specific services and supports requested by the parentsBut those promises, in the parents’ view, are vague and ultimately empty. If DDS were really committed to doing these things, they would have been done years ago, and the parents would not be appealing for placements at Wrentham. 

Hearing officer’s decisions and DDS policy are internally contradictory regarding ICF admissions 

In each decision, O’Connell accepted the DDS argument that the federal Medicaid law “does not entitle (the individual) admission to an Intermediate Care Facility at the Wrentham Center… “

O’Connell, as noted, also accepted DDS’s uniform position that each individual “is not entitled to admission because (Wrentham) is not the least restrictive environment available to serve (the individual.” And in each decision, O’Connell added that, “the Medicaid Act choice provision does not entitle (the individual) to choose between ICF or in a community home on an annual basis.”

But DDS, in fact, does offer such a “choice.” It’s just that DDS, not the Medicaid Act, insists the “choice” must always be a community-based home.

DDS requires families and guardians to sign a waiver of ICF care in order to receive DDS services. In what is referred to as a “Choice Statement” on the form, the applicant for DDS services is required to sign the following:

CHOICE STATEMENT:

I ____________________________________(Applicant or guardian) choose to apply for the Home and Community-Based Services Adult Waiver Programs and live and receive my services in the community rather than in an ICF/ID. (my emphasis)

DDS essentially admits here that a choice of ICF care exists in that the Department requires families and guardians to waive that choice in order to receive DDS services.

In fact, O’Connell explicitly stated in each appeal decision that the family applied for enrollment of their child “in the HCBS (Home and Community Based Services) Waiver …, exercising their choice for community rather than ICF services in so doing.” (my emphasis)

Despite that apparent choice, O’Connell stated in both decisions, as noted, that the individuals in question did not have a right under federal law to placement in an ICF. DDS, in fact, asserted in each case that:

DDS avoids institutionalization at the ICFs except in cases where there is a health or safety risk to the individual or others, and generally, when all other community-based options have been exhausted.

This, in our view, appears to violate federal law, which does confer a right to institutional care for those who desire it. The U.S. Supreme Court, in Olmstead v. L.C., also held that a right to institutional care exists.

Not only does federal law specify that there people who are found to eligible for ICF-level care are entitled to choose it, but DDS and O’Connell both acknowledge that such a choice exists. It is not a real choice, though, if DDS requires families and guardians to waive their right to one of the available options.

It is moreover, disingenuous of DDS and the hearing officer to tie families and guardians forever to community-based care by falsely claiming that those persons had freely chosen it years before in many cases.

What is ultimately so frustrating about this situation is that DDS and the administration as a whole continue to cling to an ideological position against congregate care that ignores reality. They continue to maintain that ICF care is more restrictive than care in the community, no matter what evidence may be presented to the contrary.

And DDS and the administration continue to ignore evidence that community-based care is beset by serious problems. As a result, when families and guardians appeal the inevitable denials by DDS of a full continuum of choice in residential care, the official adjudication process they encounter is anything but fair and impartial.

  1. November 21, 2024 at 10:56 am

    DDS, and it’s many entities, including the system of hearings allowed for those who disagree with placements, providers, state operated homes, and ICF’s have all become cogs in the wheels of the state system, with little thought given to individual needs and desires of people with intellectual disabilities and their families. There is no meaningful investigation of different opportunities for people, and families are supposed to be satisfied and feel lucky and grateful for what they have. The system of hearings has unfortunately become a sham, when it was something that used to be meaningful. Families statements and positions are not given the same weight as those of DDS officials.

    The supposed choice of an ICF is now stated as “Well, that’s not really true”, when it is in fact, true, and the law has not changed. Least restrictive setting, while well meaning, has become a meaningless term when residents at Wrentham and Hogan have far more opportunities for work, recreation, leisure activities, and yes, community inclusion, than the residents who sit trapped in group homes, some with no day programs at all, others with boring day hab programs that are no longer allowed to provide any “work” for the participants following the closure of “sheltered workshops”.

    A lot of rubber stamping going on during hearings. It is just wrong.

    Liked by 3 people

  2. Mina Murray's avatar
    Mina Murray
    November 21, 2024 at 10:57 am

    some individuals are higher need than others.

    Liked by 1 person

  3. Unknown's avatar
    Anonymous
    November 22, 2024 at 8:56 am

    I am not looking at an ICF for my loved one. My concern from what I read is if we ever felt we needed that type of home the answer is always no!

    We simply need independent hearing officers not bias DDS ones. It is well known DDS is against admissions to ICFs so these hearing officers are following the direction as they have to answer to their management.

    Parents pay thousands for attorneys to represent them, plus their taxes pay for the DDS attorneys. To make things equitable parents attorneys should be paid by the state as well.

    I get DDS wants individuals in group homes in the community and that works great for many but not for all.

    Liked by 1 person

  4. Unknown's avatar
    Anonymous
    November 30, 2024 at 3:09 pm

    When the DDS does not comply with the law and parents need to involve attorneys, then attorney fees should be paid by the state, no further action allowed.. Period.

    And where are all these clients that the DDS wanted in the “community?” I have not seen one in the “community” in years!

    Like

  5. Unknown's avatar
    Anonymous
    December 7, 2024 at 9:11 pm

    Hello everyone!

    I’ve been reading with alarm about how the state seems to be arranging plans to close Wrentham Development Center (WDC). I have written a little bit below about how my dear sister Maria has benefiter over the years from being at WDC, and what a tragedy it would be if this great resource were made unavailable.

    My sister Maria has benefited greatly from being at WDC. Most importantly, she would have died at a young age if not for the care she received at a developmental center, but more on that later in the text.

    Maria loves the gym and the workshops at WDC. She has been totally visually impaired and severely brain damaged since birth, but only when she moved to the WDC did the staff and we ourselves fully realize that she understands a little bit of language, but simply cannot express any words at all. It is like being a stroke victim trapped inside her own body.

    In spite of her severe disabilities, she has one strong ability. The staff noticed that she orients extremely well with her cane, both around her residence building and around her activity building. She recently won a statewide prize for cane orientation, and three staff people, including her Certified Mobility Specialist took her to the awards ceremony at the Hall of Flags in the State House. We could see so much joy in Maria’s face at the event and hear so much joy in her vocalizations!

    This is such a contrast to an earlier placement, where my mother was horrified to see her little child strapped into a chair and unable to move!

    Even now, Maria is quite helpless. She cannot protect herself from almost anything. She can only do extremely simple sensorimotor tasks, which she has insisted on doing over and over for many years. Even smallest change in routine is extremely upsetting to her.

    Another important thing is Maria’s medical care. She has very dry eyes, serious skin sensitivities and dental issues (as do I on all three counts!). The caretakers and nurses have always arranged prompt treatment and immediately called me when needed. I know that staff would not have that kind of expertise in a group home.

    If not for the Developmental Centers, my sister would most likely have died at a young age. The staff and medical people at her previous Developmental Center, which later closed due to state funding issues, noticed that Maria had a very serious cancer and promptly arranged for her to be treated. She has been cancer free now for many many years.

    Maria and those like her have so few things in their lives. Still Maria is so grateful for everything she gets. Please do not deprive Maria and others like her of what little joy their lives can give them! Their joy also spreads to their families and everyone who interacts with them.

    Ona Girnius Brown, sister and co-guardian of Maria

    Like

  1. No trackbacks yet.

Leave a comment