By Fran Gonzalez
Belfast — Maine
Department of Health and Human Services is proposing an amendment to
the Section 21 waiver program that aids people with intellectual and
developmental disabilities or autism spectrum disorders.
The federally funded Home and Community-Based Services waiver program
gives people with IDD the option of receiving long-term care services
and supports in their home or community, rather than in an institutional
setting.
With the proposed changes, only biological family members would be
allowed as "legal guardians," and be paid for their services. The
measure must be approved by the Centers for Medicare and Medicaid
Services.
The amendment reads, "...services provided directly or indirectly by
the legal guardian will not be reimbursed unless the legal guardian is
the participant's parent, sibling or other biological family member, and
that this provision will not be avoided by adult adoption."
The Maine DHHS website says the reason for the amendment is to make
the application consistent with MaineCare policy 21.06-8, which reads
the same as the department's amendment.
One local service provider who spoke with The Journal said DHHS is
"trying to prevent people from exploiting people who have disabilities
by guardians adopting them to enable themselves to continue to be paid
to care for the person."
Debbie Ogle is the legal guardian of David, a 62-year-old man with
IDD. We are not using his last name to protect his privacy. Ogle feels
the amendment will have the opposite effect of the one intended, because
it will push people with guardians who are not biological family
members into institutions. This, she said, would also ultimately cost
taxpayers much more.
Ogle has battled DHHS in the past and come out on top. She said that
after having David living in her house for a year, DHHS told her it
wanted to pull him out, saying she was not biologically connected.
After three years of appeals, in a desperate effort, she camped out
at the Statehouse, where she was surprised with an invitation to meet
with Gov. Paul LePage.
"Miraculously, David had shared living in about three weeks," she
said. David's mental retardation diagnosis was accepted by the state and
he received a shared living situation on Verona Island.
Ogle feels she is being singled out for her persistent efforts to get
services and because she has spoken up. After fighting the policy for
years, she said, DHHS still has not answered her questions.
DHHS discriminates in its policy, she said, by allowing some to be
paid as Section 21 Shared Living providers and others not. It also
discriminates against those in the class who have a guardian who is not a
blood relative, who are denied Medicaid Home and Community Based
Services waiver benefits and services.
"DHHS workers will pick and choose which non-biological guardians
they will allow to be Shared Living Providers," she said. "They allow
some adoptive parents, and some foster parents. It depends on what the
DHHS caseworker subjectively decides."
According to Ogle, DHHS receives two thirds of the cost of caring for
people with IDD from the federal government. In exchange for federal
assistance, Maine must abide by federal laws, which, she said, it is not
doing.
Jackie Farwell, communications director at DHHS, said, "The
department proposed a waiver amendment at the request of the U.S.
Centers for Medicare and Medicaid Services, to make the waiver
consistent with the MaineCare (Medicaid) rule regarding payments to
legal guardians for providing Shared Living Services.
"Our policy is intended to support families in caring for their
relatives while protecting individuals from situations in which an
unrelated guardian is a paid provider who has authority to keep that
individual in the person’s home. This policy is additionally in line
with the Maine Probate Code, which prohibits unrelated guardians from
being paid providers of services."
Full Article & Source:
Proposed changes to guardianship rules could backfire, caregiver says
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