National Organization for Rare Disorders (NORD) Releases Annual State Report Card, Revealing Trends in Rare Disease Health Care Coverage

NORD’s State Report Card reveals grades on state policies that could jeopardize health care coverage, access and affordability for rare disease patients

QUINCY, Mass., March 6, 2024 /PRNewswire/ — The National Organization for Rare Disorders (NORD) released its annual State Report Card, which grades each U.S. state on critical issues impacting access to care for the 1 in 10 Americans living with a rare disease. This year’s State Report Card highlights state policies that can jeopardize health care coverage, access, and affordability for rare disease patients, including limitations on Medicaid enrollment, inadequate state-regulated insurance, and failure to protect against high out-of-pocket prescription drug costs.

Major findings include:

Availability of junk insurance plans: Half of U.S. states received failing grades on state-regulated insurance due to permitting broad access to inadequate short-term, limited-duration health plans to patients. These types of plans offer inadequate insurance coverage, typically failing to provide essential health benefits required by the Affordable Care Act and are allowed to deny coverage based on pre-existing conditions. The availability of these plans, which are unable to meet the complex needs of most rare disease patients, results in higher costs for health insurance plans that do offer comprehensive coverage.

Patchwork reductions in out-of-pocket prescription drug costs: 22 states received C grades indicating they only have one patient out-of-pocket prescription drug cost protection policy in place while Idaho, Nevada, and Pennsylvania have zero patient out of pocket cost protections and received F grades. For people living with rare diseases, protections against high out-of-pocket costs mean easier access to innovative new treatments and scientific advancements.

Expanded access to Medicaid for many, but not everyone: 10 states have still not expanded Medicaid eligibility for adults leaving millions of Americans without access to vital health care services. However, two states, Georgia and North Carolina, expanded patient access to their state Medicaid programs last year, enabling more adults living with rare diseases to access necessary doctors and treatments. Gaining access to health care coverage through Medicaid expansion is particularly critical for rare disease patients who have complex and costly care needs and who may also struggle to work due to their medical condition.

NORD and its network of rare disease advocates in every state remain committed to moving the needle on each of these issues in 2024 and beyond.

One means of advancing favorable rare disease policies at the state level is through each state establishing their own Rare Disease Advisory Council (RDAC). RDACs, in partnership with NORD, patient advocacy organizations and stakeholders in the rare disease community, serve as forums for experts in rare disease, including patients, caregivers, and health care providers to strategically identify and address barriers that prevent individuals living with rare diseases from obtaining proper treatment and care for their condition. In 2023, three more states signed RDAC legislation into law: Delaware, Indiana, and Maryland – bringing the total number of states with an RDAC to 27. In 2024 and beyond, NORD sees tremendous potential for creating RDACs in Western states, as the majority of existing RDACs are concentrated in the East.

NORD encourages any individuals looking to get involved in rare disease advocacy to join the NORD Rare Action Network today. 

For more information about NORD’s State Report Card, or to speak with patients and caregivers currently impacted by these issues, please contact media@rarediseases.org.

Read the full NORD State Report Card here for the complete list of grades received by each state in each category, along with explanations from NORD policy experts. 

About the National Organization for Rare Disorders (NORD)
With a more than 40-year history of advancing care, treatments and policy, the National Organization for Rare Disorders (NORD) is the leading and longest-standing patient advocacy group for the 30 million Americans living with a rare disease. An independent 501(c)(3) nonprofit, NORD is dedicated to individuals with rare diseases and the organizations that serve them. NORD, along with its more than 340 patient organization members, is committed to improving the health and well-being of people with rare diseases by driving advances in care, research and policy. For more information, visit rarediseases.org. 

About NORD’s State Report Card
Since its inception in 1983, the National Organization for Rare Disorders (NORD) has worked to ensure that the voice of the rare disease patients is front and center when important policy and regulatory decisions are made by federal and state governments. 

In 2015, NORD launched its State Report Card with the goal of evaluating how effectively states serve people with rare diseases and giving the rare disease community a useful tool to help advocate for necessary changes. It is important to note that the nine issues evaluated within this report card, while critical, are not exhaustive and there are many others that impact the lives of rare disease patients. 

The latest edition of the State Report Card was compiled using data current as of November 2023. 

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SOURCE National Organization for Rare Disorders (NORD)