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Approximately 200,000 children with serious medical conditions receive health coverage through the California Children’s Services (CCS) program, whose responsibilities include ensuring that these children are provided with the medically necessary durable medical equipment (DME) and supplies that they require. 

Although data are scant, three recent surveys and dozens of interviews point to frequent long delays in obtaining equipment and supplies.  Children suffer when deliveries are delayed, and parents report that these delays distract them from caring for their children, cause unnecessary developmental lags, and increase physical pain and suffering. 

This report examines the administrative barriers that are behind these chronic delays, and offers recommendations for what can be done to address them.  


Also See: A related fact sheet that highlights the recommendations.

Related Grants

This policy brief by the National Alliance to Advance Adolescent Health looks at what happens when low-income youth and young adults with chronic conditions and disabilities age out of the Title V Program for Children and Youth with Special Health Care Needs and provides policy recommendations.

This fact sheet from the National Health Law Program is designed to inform families about the steps they can take to appeal decisions about their child’s CCS benefits and highlight key resources available to support the process.