http://www.metroland.net/back_issues/vol29_no01/features.html
Breaking theTrust
By
Miriam Axel-Lute
Some have
traumatic brain injuries from accidents. Some have multiple sclerosis. Others have
had strokes. Across
But late in
2005, many of them found themselves distracted from the everyday challenge of
living with their disabilities. They, or their caretakers, had gotten notices
in the mail from the county announcing a major change in a financial tool many
of them they rely on to make ends meet.
Thanks to a new
way of interpreting the law, the amount of their Social Security Disability
checks that they had been setting aside each month in a trust to be used only
for their care was now going to be owed to the county before they could
continue to qualify for Medicaid. This would mean the effective loss of several
hundred dollars a month in income, and would leave them with standard Medicaid
eligibility income levels—barely more than half the earnings of a full-time
minimum-wage job, about $100 per month below the official poverty level for a
single person—to cover all their living and health-care expenses not paid for
by Medicaid.
Those who could
afford to appeal the change are doing so. So are some who can’t quite afford
to. “It’s just a great time of the year for this to be happening,” says Rob Korotitsch sarcastically, a few days before Christmas. Korotitsch is a service coordinator for people with
traumatic brain injuries at the nonprofit Living Resources, and several of his
clients are affected. “I’ve got one man who can’t afford Christmas because of
this; he had to give all his money to his lawyer.”
But the ones
who can’t afford to appeal are in an even worse limbo. “I’ve got people who are
having breakdowns over this because they simply cannot deal with the stress of
this happening to them,” says Korotitsch. “I have
some people so cognitively overwhelmed that I worry about them hurting
themselves.”
From the date
of the notice, trust beneficiaries have to file an appeal within 10 days if
they want their benefits to stay active during the appeals process. For many
affected people, that may just not be happening, says Ed Wilcenski,
a lawyer who works with the special needs community and is vice chair of the
state bar association’s Medicaid committee. “What happens often, something
comes in the mail, they read and set it aside because it scares the bejesus out of them, and they don’t get these timelines.”
It’s true a few
trusts may have large balances in them, but the majority of the people who have
them are “living on fumes,” says Wilcenski.
No one’s
benefits have yet been affected. In fact, the county may be backing down
on the change, despite its formal change notices. But even if so, it has left
many in the disabled community and those who serve them feeling under attack.
“I have people
who have been teachers, doctors, paid into the system, they’ve always done the
right things,” says Korotitsch. “They paid their
taxes, shared all of their information with the county up front. . . . They’re
not hiding anything. They need Medicaid to live. . . . Now they feel that they
are being attacked by
The change that
the law department of Albany DSS is trying to implement is arcane and
technical. It involves new interpretations of a small part of a regulation
applying to a special kind of trust that most of us wouldn’t have even known
existed, let alone how it worked. But there are two reasons to pay attention
anyway: First, these kinds of rule changes could have real and devastating
effects on vulnerable citizens. Second, it’s characteristic of local, state,
and federal trends to try to deal with the burgeoning cost of Medicaid through
punitive short-term measures that merely set up the country, and its poor and
disabled, for further, costlier, crises down the road.
Here’s the
crash course in
Medicaid is
generally intended for the completely destitute: To qualify in 2006 in
However, since
1993, federal and state laws have recognized that the disabled are a special
case: They generally can’t work, at least not full time; they often need
extensive medical care and specialized therapies, some of which might not even
be covered by Medicaid; and they are likely to be institutionalized if they
don’t receive financial support and targeted services to help them stay living
in the community. In addition, younger disabled people who are
institutionalized may have more health and social needs than a typical nursing
home can accommodate.
As Korotitsch puts it, federal law wanted to make it so that
“people who had a working history, who through no fault of their own became
disabled, wouldn’t have to become poverty-stricken to get their medical needs
taken care of.”
And so
lawmakers created a special legal provision called a supplemental-needs trust.
Resources put into such a trust are exempt when determining Medicaid
eligibility. In 1997,
First-person
supplemental-needs trusts (hereafter SNTs) often are
initially funded with a lawsuit settlement, inheritance, or a small amount of
savings, and contributed to with pensions or Social Security checks.
Some SNTs are administered by family members, others by
nonprofits like NYSARC, Inc. The funds in the trust can be spent by the trustee
only for the disabled person’s needs, support, and comfort, according to
a careful set of guidelines. The trustee pays service providers directly—the
disabled beneficiary cannot get cash directly.
Trusts are
often used for supplemental therapies not covered by Medicaid, a chance for
younger institutionalized disabled people to attend programs outside their
nursing home, or for basic needs like rent and groceries.
That’s how it
has worked in
Then this
summer,
The Tenth
Circuit court case is being appealed to the Supreme Court as being opposed to
the decisions of several other courts, and as being contrary to the intention
of federal law. Those appealing the case also say there’s nothing involuntary
about individuals receiving Social Security checks and then depositing them
into a trust for their own benefit.
Nonetheless,
this fall, the legal department of
The memo is
unambiguous and makes no indication that it is presenting a change in policy.
Under the heading “Funding,” it reads, “Social Security Disability (‘SSD’) benefits
can not be used to fund a SNT. . . . (meaning all SSD income . . . should be spent down in order
to receive means tested benefits.)” It says the same about Supplemental
Security Income (usually received by a dependent disabled person who was never
able to work, or sometimes by those who don’t qualify for enough SSD to live
on).
The memo
concludes with a bolded paragraph titled “Warning,” which says that failure to
follow the above guidelines will result in the discontinuance of benefits and
may also lead to legal action against the trustee in the state’s Supreme Court
and a referral to the attorney general’s office for “possible prosecution of
breach of fiduciary responsibility.”
Beginning after
this memo, and continuing through the end of 2005, individuals with SNTs who were receiving Medicaid (DSS says there are about
90 in the county), began receiving “Notice of Intent to Discontinue/Change
Medical Assistance” forms. The handwritten explanation on one such form, sent
on Dec. 29, reads, “Your entire Social Security Disability Benefits must be
considered available money for purposes of determining Medicaid Eligibility. So
you cannot meet your medicaid excess income Spendown by depositing your Social Security Disability
income into your NYSARC or (SNT) Special Needs Trust.”
For those
disabled individuals whose only source of income is their SSD checks, this
change would mean they would have to “spend down” on medical expenses all but $692
per month ($900 for a family of two) in order to continue to qualify for
Medicaid.
For those whose
trust balances were high enough to afford a lawyer, many trust beneficiaries,
or their trustees, are ap
pealing the change notice. Wilcenski says he’s filed
at least five already. But, he notes, quite a few more are not going to have
the resources to appeal—especially within the 10 days required to keep the
benefits in place while the appeal goes forward.
Reached on
Tuesday, Albany DSS Commissioner Elizabeth Berlin insisted that the matter was
actually still under review. “It’s a matter we will continue to be looking at
over the next several months,” she said. “We will continue to be working with
other legal counsel in other districts, to understand their interpretation [of
the Tenth Circuit case] . . . as well as seek clarity from the governance
bodies over us, the state health department, the federal government.”
Berlin said the
policy in the October memo was still the interpretation that her legal department
stood by, but that despite the formal change notices, they “are not going to be
taking any action at this point in time. . . . The matter is still under
review.”
Asked if the
department usually sends formal notices about questions still under review, she
said, “Certainly it’s our desire to have the review completed before we issue
anything that would come out of the department. In this situation the matter
was still under review and the notices got out. I think that did cause some
confusion as to the direction the department was taking.”
Responding to
this assertion on Wednesday, Korotitsch said that the
county certainly seems to be acting on the notices, given that his
organization has already been called to represent clients in “fair hearings”
(i.e., appeals). Wilcenski concurred, saying the
county had made no move to settle or withdraw the notices in response to his
filing for appeals.
Even aside from
the effect on those in these trusts,
First, both
Albany County Comptroller Mike Connors and Greg Olson, a staffer for Steve Englebright (
Preventing
people from setting aside SSD income is also not likely to save the county
much, if any, money. The average amount of Social Security income being
deposited into these trusts per person is a couple hundred dollars per month,
say various advocates. Making those individuals turn that over to the county
before they become eligible for Medicaid will amount to a small short-term
savings.
But, say those
working with these clients, for many of the people affected, that couple
hundred could mean the difference between being able to maintain a home and
live in the community and going into an institution, which is much more
expensive. The room rate at the public Albany County Nursing Home, for example,
is $230 per day. Even those who manage to stay in the community will do
so only by drawing on other types of county assistance, such as food stamps or
rental subsidies.
“The endgame
for this, which nobody wants to acknowledge, [is] then there’ll be a new crisis
because the hospitals are flooded with people with no payment source and
everyone will start pointing fingers, saying ‘How did this all happen?’ ” says Louis Pierro of Pierro and Associates LLC. “They’re hoisting themselves on
their own petard, because the people they are chasing out of the community, who
they’re paying a couple hundred dollars a month for now in foregone income,
they’re chasing them into a setting that’s going to cost them 50 times as much.
. . . The people making these decisions have no clue what’s going to happen on
the back end of this. Nor do they want to. They don’t want to know.”
Not only that,
but the balance of these trusts goes back to the county when the beneficiary
dies, to recoup some of what was spent for that person’s medical care. Since
anyone with a trust who can afford a lawyer is appealing this change, often
spending most of the balance of the trust on legal fees, the action is directly
cutting away at balances that eventually could have returned to the Medicaid
program.
Besides, in
2005, the state finally capped the amount counties have to pay for Medicaid,
reducing their unpredictable double-digit growth in costs to a small, fixed
percentage, which would seem to reduce the immediate pressure for the county to
scramble to cut its Medicaid costs by any means necessary.
Commissioner
Berlin even says that this decision didn’t have to do with trying to cut costs;
in fact, she claims she hasn’t even done a cost analysis of what the
change would mean for the county. Rather, she says, “This has really been about
ensuring integrity of the program, fairness of the program, and the
appropriateness of adhering to the parameters that exist,” as well as “making
sure we are abiding by the direction given at the federal and state level.”
What does this
mean? Berlin, who is careful to note that the Medicaid program is “wonderful”
and that the county has been doing added outreach over the past year in senior
centers and hospitals to make sure everyone who qualifies applies, has two
specific concerns regarding the trusts: “Dollars that are used in a manner outside
of the fundamental purpose of putting in place a supplemental-needs trust,”
and, “Is there a population that is not having to meet certain eligibility
criteria because they have a special-needs trust, but that is inconsistent with
those individuals who are in similar situations but just do not have a
special-needs trust?”
“Those trusts
have sometimes millions of dollars in them,” she notes, though she admits she
does not know the average balance of the trusts in the county.
A DSS employee
told a trust beneficiary who called in late December that an example of the
sorts of problems they were concerned about was a trust paying for a
beneficiary to bring his whole family, rather than just one traveling companion
(allowed under trust rules), with him on a trip to Florida.
Although this
decision would go against established state practice, it seems that
“It’s not cost
cutting” is not everyone’s story, however. DSS lawyer Marshall Day, reached
last week, said he couldn’t comment on the specifics of the interpretation and
policy change as it was still under review, but responded to the observation
that there were many people who had received these notices who were panicking
about the possible effects by saying, “I’m sure there are, and some should be,
but we’re trying to control spending on Medicaid, that’s why we’re looking at
these issues.”
That rings more
true for those who have been following Medicaid trends over the years. “My
sense is they’re trying to recoup any finances they can,” says Korotitsch.
Disallowing
Social Security income in the trusts “is very much a result of a much broader
effort by states and localities to cut Medicaid expenditures,” says Wilcenski.
“They’re saying
it’s about program integrity, but it’s about money,” says Olson. “I’d really
love to see their fiscals on this.”
Even fairness
and program integrity would seem to be questionably served by preventing Social
Security income from going into these trusts. One of the reasons the Tenth
Circuit case is being appealed is that it’s discriminatory against people who
rely on public disability, still letting disabled people who have lawsuit
settlements, inheritances or private pensions shield that income from Medicaid
means testing, while singling out those relying on SSD and SSI.
As for problems
with misuse of funds already in the trusts, they may well be happening. Wilcenski notes that sometimes individual trustees are not
well-equipped to understand and follow the details of the legal requirements.
But how is that related to what sort of income is funding the trust? It could
be addressed separately, whether through better education or the October memo’s
threatened legal actions. (
Will the county
end up backing away from this rule change? Will the state weigh in and either
tell them to knock it off or change their own rules to support the county? “I
think until they’re sued, nobody will react,” says Pierro.
“The unfortunate part of this is they’re playing a game of chicken. If people
don’t do anything, if they simply take the rules and try to live by them, the
rules will fly.”
Either way,
says Pierro, this one case is merely a representative
example of a larger disturbing trend. “It’s really just one little pinprick,
but when you look at the other things that are happening at the federal level
and state level. . .” He mentions the federal government’s recent budget, which
cuts $10 billion from Medicaid, tightens eligibility, and increases Medicaid
co-payments and deductibles, and also several rule changes that he expects Gov.
George Pataki to propose again this year including one that would no longer
allow people to keep their own income when their spouse becomes disabled and
needs Medicaid.
And yet, he
says, “On the other side, you have local government telling people that they
can’t utilize this tool [SNTs] that the federal
government created to help keep people at home. Where do people go?”
maxel-lute@metroland.net
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