Skip to navigation Skip to content



35 Patient Organizations Celebrate Rule to Protect Patients from Short-Term Health Plans

March 28, 2024

On behalf of patients with serious and chronic health concerns, our 35 groups welcome and celebrate the Biden Administration’s new rule that will better protect patients from short-term, limited-duration health plans, a risky form of low-quality health coverage.

In 2018, a federal rule change— strongly opposed by our organizations—allowed for the proliferation of short-term health plans. Since that time, our organizations have repeatedly warned lawmakers about the risks these plans bring both to individual patients and the larger health coverage market.

The new rule will ensure that short-term health plans are used as they were originally intended: as short-term, stop-gap coverage while consumers are between other plans.

Marketed as an alternative to traditional health insurance, short-term plans are exempt from many important consumer protections. They often do not cover essential care, like prescription drugs or mental health services, and allow insurers to penalize consumers with pre-existing conditions and charge women more for their coverage. Further, these plans can utilize annual and lifetime coverage limits—leaving patients responsible for extraordinary costs. Due to deceptive marketing practices, consumers often do not even know they’ve purchased a short-term plan until they attempt to use their coverage – only to discover its limitations. By then, it’s too late; they already face insurmountable medical bills.

As we celebrate 14 years of Affordable Care Act protections, it’s clear that patients now have access to far better and more affordable coverage and premiums. We expect the new rule to improve clarity for consumers and provide greater assurance about the quality of the health coverage they purchase.

We applaud the Biden Administration’s efforts and look forward to seeing the rule’s positive impact on patients.

ALS Association
American Cancer Society Cancer Action Network
American Diabetes Association
American Heart Association
American Kidney Fund
American Lung Association
Arthritis Foundation
Asthma and Allergy Foundation of America
Cancer Support Community
Child Neurology Foundation
Chronic Disease Coalition
Crohn's & Colitis Foundation
Cystic Fibrosis Foundation
Epilepsy Foundation
Foundation for Sarcoidosis Research
Hemophilia Federation of America
Immune Deficiency Foundation
Lupus Foundation of America
March of Dimes
Muscular Dystrophy Association
National Bleeding Disorders Foundation
National Coalition for Cancer Survivorship
National Eczema Association
National Health Council
National Kidney Foundation
National Multiple Sclerosis Society
National Organization for Rare Disorders
National Patient Advocate Foundation
National Psoriasis Foundation
NMDP (formerly National Marrow Donor Program)
Pulmonary Hypertension Association
Susan G. Komen
The AIDS Institute
The Leukemia & Lymphoma Society

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:, Facebook, X, formerly known as Twitter, Instagram, YouTube or 1-800-344-4867.


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