8 min read
21 July 2026

What Tennessee’s Immigration Law Could Mean for Medically Fragile Children

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Table of contents

What Is Children’s Special Services?

For more than 50 years, Tennessee’s Children’s Special Services (CSS) program has served as a safety net for children with serious illnesses and disabilities whose healthcare needs are not fully covered by private insurance or Medicaid. The program supports children with conditions such as cancer, cerebral palsy, spina bifida, seizure disorders, congenital heart disease, traumatic brain injuries, and other medically complex conditions requiring ongoing treatment, specialized equipment, medications, or coordinated care. The program is administered by the Tennessee Department of Health and supported through a combination of state funding and federal Title V Maternal and Child Health funds.

For many families, CSS is not simply another public benefit. It helps pay for services and equipment that allow children to remain safely at home, attend school, and receive treatment that might otherwise be financially out of reach. Depending on a child’s condition, that support may include feeding tubes, wheelchairs, oxygen, seizure medications, specialty clinics, home medical equipment, and care coordination.

Because CSS often serves families who have exhausted other options, any disruption in services can have immediate consequences for children with significant medical needs.

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What Changed Under Tennessee’s New Immigration Law?

In May 2026, Tennessee enacted Public Chapter 1106 (SB 1915/HB 1710), expanding immigration verification requirements for applicants seeking certain public benefits. The law requires state agencies, local governments, and local health departments to verify that applicants age 18 or older are either U.S. citizens or lawfully present in the United States, unless federal law prohibits that verification. It also establishes reporting requirements when individuals are determined not to be lawfully present while receiving covered public benefits.

The law itself does not specifically mention Children’s Special Services.

The controversy began when the Tennessee Department of Health informed local health departments that the law would be applied to families participating in CSS. Letters sent to parents explained that continuing to receive services after June 30 could result in identifying information being shared with the state’s Centralized Immigration Enforcement Division. Similar guidance was provided to healthcare providers working with affected families.

This raised an important legal question.

Although the statute specifically refers to applicants who are 18 years of age or older, state officials interpreted portions of the law as requiring reporting connected to children enrolled in CSS. That interpretation is now at the center of ongoing litigation.

Why Did Healthcare Providers Challenge the Policy?

The lawsuit challenging the Tennessee Department of Health’s implementation of the law was not initially brought by parents. Instead, it was filed by three Nashville physicians – Dr. Brent Snader, Dr. Jule West, and Dr. Kristin Martel, who argue that the reporting requirement could discourage families from seeking or continuing medically necessary care for children enrolled in Children’s Special Services. The complaint also contends that the Department exceeded its authority in applying the law to the program and failed to follow required administrative procedures.

According to the complaint, physicians began hearing from families who feared remaining enrolled in CSS because they believed doing so could expose them or members of their household to immigration enforcement. Some reportedly considered withdrawing from the program despite their children’s ongoing medical needs.

The physicians argue that this creates an ethical conflict that extends beyond immigration policy.

Healthcare depends on trust. When families become concerned that seeking medical assistance could trigger government reporting unrelated to treatment, providers worry that patients may delay appointments, discontinue therapies, or avoid necessary care altogether.

The lawsuit also argues that the Department of Health exceeded its legal authority in applying the statute to CSS and failed to follow required administrative procedures before changing how the program operates. Additional claims involve questions surrounding federal funding requirements, statutory interpretation, and whether the state’s implementation conflicts with federal law governing portions of the program. Those issues have not yet been resolved by the courts.

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What Has the Court Decided So Far?

At this stage, the court has not ruled on whether Tennessee’s law is legal or unconstitutional. Instead, a judge issued a temporary restraining order preventing the Tennessee Department of Health from sharing identifying information related to affected children while the litigation moves forward. Temporary restraining orders are designed to preserve the status quo while courts consider the legal arguments presented by both sides. They are not final decisions on the merits of a case.

Several important legal questions remain unresolved. The court will need to determine whether the Tennessee Department of Health correctly interpreted Public Chapter 1106, whether federal law limits how Title V-funded programs verify or disclose immigration information, and whether the Department followed Tennessee’s required administrative procedures before implementing the policy. The answers will likely shape not only this case but also how similar healthcare policies are interpreted and implemented in the future.

Why This Case Matters Beyond Tennessee

Although the litigation centers on one state program, the broader issues extend well beyond Tennessee.

Across the country, healthcare organizations increasingly find themselves navigating situations where public policy intersects with patient care. Questions about eligibility, documentation, reporting obligations, privacy, and access to services have become more common as states adopt differing approaches to immigration enforcement.

For healthcare professionals, the central issue is understanding how legal requirements affect clinical practice.

When providers believe a policy could discourage patients from seeking medically necessary care, they face difficult questions about continuity of care, patient communication, informed decision-making, and professional ethics. Attorneys representing hospitals, physicians, health systems, and government agencies must also consider how statutory language, administrative rulemaking, and federal funding requirements interact.

Regardless of where someone stands politically, most healthcare professionals share the same goal: ensuring patients receive appropriate medical care while complying with the law.

Cases like this highlight how difficult that balance can become when healthcare administration and public policy overlap.

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What Healthcare Professionals Should Watch Next

The legal questions surrounding Tennessee’s Children’s Special Services program are far from settled.

As the case moves through the courts, providers, attorneys, healthcare administrators, and policy professionals should pay close attention to several developments:

How the court interprets Public Chapter 1106

The court’s reading of the statute may clarify whether the Department of Health’s application of the law was consistent with legislative intent or extended beyond what lawmakers authorized.

Future guidance from the Tennessee Department of Health

Additional agency guidance could affect how Children’s Special Services and other public health programs administer eligibility verification and reporting requirements.

The role of federal funding

Because CSS receives support through federal maternal and child health funding, the relationship between state implementation and federal program requirements may become an important part of the litigation.

The practical impact on patient care

Beyond the legal arguments, healthcare organizations will be watching whether reporting requirements influence enrollment, continuity of care, emergency department utilization, or treatment adherence among medically vulnerable populations.

The outcome of this case may ultimately provide guidance not only for Tennessee but for other states considering similar approaches at the intersection of healthcare policy and immigration enforcement.

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