William Nored v. Tenn. Dep't of Intellectual & Dev. Disabilities

Court of Appeals for the Sixth Circuit·Decided September 9, 2022·No. 21-5826·Unpublished

Opinion

NOT RECOMMENDED FOR PUBLICATION File Name: 22a0369n.06

No. 21-5826

UNITED STATES COURT OF APPEALS FOR THE SIXTH CIRCUIT

WILLIAM F. NORED and LAWANDA JEAN ) FILED NORED, as conservators, parents, and next friends ) Sep 09, 2022 of WILLIAM F. NORED, JR. (BILL), individually ) DEBORAH S. HUNT, Clerk )

Plaintiffs-Appellants, )

) ON APPEAL FROM THE v.

) UNITED STATES DISTRICT OF ) COURT FOR THE EASTERN TENNESSEE DEPARTMENT DEVELOPMENTAL ) DISTRICT OF TENNESSEE INTELLECTUAL & DISABILITIES; COMMISSIONER BRAD ) TURNER, in his official capacity as the ) OPINION Commissioner of the Tennessee Department of )

)

Intellectual & Developmental Disabilities, )

Defendants-Appellees. )

)

Before: CLAY, GRIFFIN, and WHITE, Circuit Judges.

HELENE N. WHITE, Circuit Judge. Plaintiffs-Appellants William F. Nored (“Mr. Nored”) and LaWanda Jean Nored (“Mrs. Nored”), collectively “the Noreds,” are the parents, conservators, and next friends of their son, William F. Nored, Jr. (“Bill”). They appeal the district court’s determination that Defendants-Appellees Tennessee Department of Intellectual and Developmental Disabilities, and its Commissioner, Brad Turner—collectively “DIDD”—did not violate the Americans with Disabilities Act, Rehabilitation Act, Medicaid Act, or 42 U.S.C. § 1983 by failing to find a willing home-care provider for Bill, who is entitled to that service under the Medicaid waiver program. We affirm.

I.

A.

The Noreds adopted Bill in 1970 when he was an infant. Bill is now in his fifties.

When Bill was still an infant, the Noreds began to notice that he suffered from chronic seizures. After Bill’s first grand mal seizure at approximately eighteen months old, doctors performed a myelogram and determined that Bill had an extensive brain injury that likely resulted from a stroke or other traumatic incident at birth. This brain injury caused a severe seizure disorder that could not be controlled with medications and resulted in significant weight loss, vomiting, and diarrhea. At fourteen years old, Bill underwent a partial hemispherectomy, which removed the entire right side of his brain. This surgery completely resolved Bill’s severe seizure disorder but left him with other medical issues; he has partial paralysis on the left side of his body; a blind spot in his left eye; cannot do math; cannot understand the denominations of money or manage his finances; cannot enter into a contract; cannot drive; and cannot be relied on to understand the severity of emergencies or react appropriately to them. Bill also occasionally struggles with impulse control; telling the difference between reality and fiction; and has been diagnosed with intermittent explosive disorder, which may result in aggressive or violent behavior if he feels stressed or “backed into a corner.” R. 134, PID 969–70. However, Bill is a functional reader, communicates clearly, dresses himself, and largely manages his own personal hygiene.

Bill lived with his parents until he was about twenty, when his younger brother went to college and Bill told his parents that he, too, wanted to be more independent. Bill’s parents found a house in downtown Sevierville, Tennessee, which is a town Bill knew well and liked because of the numerous attractions. Bill lived in the Sevierville house without assistance for about three years, but then began confusing reality with an American Western soap opera and believed that he

was part of the show. The Noreds brought Bill back to their home in Knoxville and had him evaluated by medical professionals, who diagnosed him with intermittent explosive disorder and committed him to the Clover Bottom Middle Tennessee Mental Health Institute in Nashville, Tennessee, where he remained for twelve years. Clover Bottom employees determined that Bill could not have a roommate because he touched his roommate’s things, became agitated when other people touched his things, and “just could not function in a room with another person.” Id. at 972.

Bill moved into home and community-based care in approximately 2013, after Clover Bottom was ordered to close. He enrolled in the 1915(c) Medicaid Home and Community-Based Services (“HCBS”) Waiver program, a federally funded program that pays for medical services for individuals who prefer to remain in their homes and communities, rather than in institutionalized care. DIDD administers the 1915(c) waiver program in Tennessee, and Bill’s particular waiver—the “comprehensive aggregated cap waiver”—has no limit on the amount of care or services he is entitled to receive. Id. As part of the 1915(c) program, DIDD contracted Engstrom Services, Inc. (“Engstrom”) to be Bill’s Independent Support Coordinator, or “ISC.”1

1 As the Tennessee agency that oversees the provision of care for disabled Tennesseans, DIDD provides two types of services: direct care through state-run intermediate care facilities (“ICFs”), and indirect care by funding providers who support individuals in their homes through the Medicaid waiver program.

To provide indirect care to patients such as Bill, DIDD “contract[s] with providers that will actually perform [] the direct care or provide services in the person’s home or in the community” across the state. R. 135, PID 1101. DIDD also contracts with ISCs that help patients identify DIDD-authorized provider agencies by providing them with a list of potential providers. After the patient selects from this preauthorized list of qualified and willing providers, DIDD contracts with and pays the provider, and then provides oversight of the quality of care. If the patient requires a new provider or additional staff, the ISC will search for DIDD-approved providers and will pass along a list of interested providers to the patient. The patient and/or conservators have the final say over which authorized provider is selected for services.

ISCs also create annual Individual Support Plans (“ISPs”) for the patient, which “provide a comprehensive description of the person supported and the services required to meet his or her needs.” ECF No. 21, PID 37. As a representative from Bill’s ISC testified, the ISP is designed to “capture what’s important to Bill, what’s important for Bill, what kind of help, supports he needs, risks and things of that

After Bill was released from Clover Bottom, Engstrom helped Bill locate an apartment in Nashville, where he was able to live alone and receive assisted-living services paid for by DIDD and provided by a DIDD-approved agency called Benchmark. Bill received “Level 6” services at this time, which meant that he was provided two staff for twenty-four hours a day, seven days a week.

After about eighteen months in Nashville, Bill became unhappy so far away from his parents. The Noreds moved Bill back to his previous home in Sevierville but had to switch providers because Benchmark did not service East Tennessee. Engstrom helped the Noreds find New Haven, LLC (“New Haven”), which became Bill’s new, DIDD-approved provider in Sevierville.

Bill was happy in his Sevierville home. He enjoyed interacting with the community and spent the majority of his days wandering around town, seeing the Sevierville attractions, eating at favorite restaurants, and making purchases with an allowance provided by his parents. He also greatly enjoyed his independence.

While Bill lived in Sevierville, New Haven provided a variety of services: attendants fixed his meals, ensured that he took his medications, helped him with cleaning the home and remembering certain hygienic tasks, drove him and escorted him wherever he wanted to go around town, and were generally available in case of an emergency.2 Additionally, the Noreds maintained

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