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Society Joins Patient Advocacy Organizations to Express Support for Keeping the No Surprises Act Intact

February 9, 2022

The No Surprises Act, which went into effect on January 1, 2022, made it illegal for insured patients to be billed for more than their in-network rate for costs resulting from emergency-related care and treatments from out-of-network providers at in-network facilities. The National Multiple Sclerosis Society persistently advocated for this bill to be enacted into law.

Although the No Surprises Act is already in effect, the Texas Medical Association and the American Medical Association (Plaintiffs) both brought separate legal challenges against the U.S. Department of Health and Human Services (HHS) to strip the No Surprises Act of its key protections for patients against surprise billing arguing against the rules that were developed to implement the law. In response, The National Multiple Sclerosis Society and 11 other patient advocacy groups, led by the Leukemia & Lymphoma Society, respectfully submitted an amicus brief in each case to further advocate in support of the implementing regulations for the No Surprises Act.

The Society strongly supports the dismissal of these lawsuits because the implementing regulations align with the Congressional intent, to protect patients from surprise bills and lower health care costs. Many people living with MS are among the one in six Americans who have received a surprise medical bill in the past. Given the devastating financial impact that these bills can have, the Society has proudly joined the amici to protect patients and the enactment of the No Surprises Act.

About Multiple Sclerosis

Multiple sclerosis is an unpredictable disease of the central nervous system. Currently there is no cure. Symptoms vary from person to person and may include disabling fatigue, mobility challenges, cognitive changes, and vision issues. An estimated 1 million people live with MS in the United States. Early diagnosis and treatment are critical to minimize disability. Significant progress is being made to achieve a world free of MS.

About the National Multiple Sclerosis Society

The National MS Society, founded in 1946, is the global leader of a growing movement dedicated to creating a world free of MS. The Society funds cutting-edge research for a cure, drives change through advocacy and provides programs and services to help people affected by MS live their best lives. Connect to learn more and get involved: nationalMSsociety.org, Facebook, X, formerly known as Twitter, Instagram, YouTube or 1-800-344-4867.

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© 2024 The National Multiple Sclerosis Society is a tax exempt 501(c)3 nonprofit organization. Its Identification Number (EIN) is 13-5661935.