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The Tennessee Department of Health sent letters to parents of undocumented children with critical illnesses or physical disabilities stating the agency would share information on the child’s immigration status with the state’s immigration enforcement office if they continued receiving care through the Children’s Special Services program after June 30.
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Brenda, a mother from Honduras, has a 12-year-old daughter named Sofia who lives with cerebral palsy and epilepsy.
Brenda
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"I read the letter. I read it many times to make sure I understood it properly," said Brenda.
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The Children’s Special Services program is a publicly funded program that helps low-income families afford costly treatments such as surgeries, medications, and rehabilitation services.
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Confidence90%
An estimated 400 immigrant children are at risk of losing access to Children’s Special Services services at the end of June 2026.
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Tennessee lawmakers approved a law in May 2026 that requires local health departments to report individuals and all identifying information about such individuals who are not lawfully present in the United States.
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State Rep. Dennis Powers is the lead sponsor of the bill requiring health departments to report undocumented individuals.
Dennis Powers, state representative
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"No child receiving lifesaving medical treatment is denied care because of this new law. Federal protections for emergency and lifesaving medical services remain fully in place regardless of immigration status, criminal status or insurance. It simply ensures taxpayer-funded public benefits are reserved for those who are legally eligible to receive them," said Dennis Powers.
Brenda
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"But if we stay, they’ll come knocking on our door asking about our children as if they were criminals," said Brenda.
Brenda
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"We are waiting for a miracle to stop the new state law from going into effect next month," said Brenda.
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Brenda left Honduras for the U.S. ten years ago.
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Sofia was diagnosed with cerebral palsy, epilepsy, and a congenital heart disease after arriving in the U.S.
Relevance: supporting · Type: background
Confidence100%
Sofia’s heart surgery, which occurred when she was younger, was covered by the Children’s Special Services program.
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The Children’s Special Services program helps Brenda afford her daughter’s anti-seizure medications and visits to medical specialists such as cardiologists and neurologists.
Brenda
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"She knows that she depends heavily on her medications. Without it, I fear, she will have a seizure," said Brenda.
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Sofia requires a wheelchair, physical therapy for mobility issues, and occupational therapy for speech development.
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One therapy session can cost over $1,000 without the Children’s Special Services program, according to Brenda.
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In 2024, the Children’s Special Services program spent $2.19 million in claims to support 4,640 children in Tennessee who received medical payment assistance and essential care coordination services.
Relevance: supporting · Type: background
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The Children’s Special Services program receives a mix of state funding and a federal block grant.
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Dr. Jill Obremskey is a pediatrician and former Tennessee Department of Health official.
Jill Obremskey, pediatrician
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"Those interruptions will lead to worsening health, more emergency room visits, more hospitalizations, more suffering, and for some children, death," said Dr. Jill Obremskey.
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Families, physicians, and immigrant rights advocates held a news conference calling on Republican Gov. Bill Lee to take steps to protect undocumented children receiving care through the program.
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Gov. Bill Lee signed the bill into law last month.
Lisa Sherman Luna, executive director of the Tennessee Immigrant and Refugee Rights Coalition
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"We won’t know if they didn’t understand the bill or didn’t care that this would be the effect, but here we are with children, really vulnerable sick children, paying the price for politics," said Lisa Sherman Luna.
Relevance: primary · Type: action
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The Tennessee Justice Center filed a lawsuit on behalf of three Nashville physicians seeking a temporary restraining order to block the new law from going into effect in July.
Michele Johnson, executive director of the Tennessee Justice Center
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"When doctors are warning that even brief interruptions in treatment could be harmful or even deadly, we believe the state has a responsibility to protect these children rather than place them at greater risk," said Michele Johnson.
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