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North Carolina is denying care to disabled children and calling it “policy.”
Under the North Carolina Medicaid CAP/C waiver, families are being capped at 20–40 hours, pushed out of paid caregiving, and told to accept less care.
Some are even being told:
“You should be doing this for free anyway.”
This violates federal standards under 42 CFR §441.301, EPSDT, and the Olmstead v. L.C. requirement for care in the least restrictive setting.
This isn’t policy. It’s rationing at the expense of medically complex children. Stop the rhetoric that that devalues medically necessary care as “just parenting”.
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