{"id":2,"date":"2017-04-20T13:14:07","date_gmt":"2017-04-20T13:14:07","guid":{"rendered":"https:\/\/cancercarealliance.org\/?page_id=2"},"modified":"2020-07-29T10:29:17","modified_gmt":"2020-07-29T14:29:17","slug":"about","status":"publish","type":"page","link":"https:\/\/cancercarealliance.org\/about\/","title":{"rendered":"About the Alliance"},"content":{"rendered":"
Despite advances in cancer diagnosis and treatment, access to high-quality cancer care continues to be challenging for some patients in the United States, especially those in vulnerable and underserved communities. The burden of cancer falls disproportionately on some segments of the U.S. population, including racial and ethnic minorities; low-income, uninsured and underinsured populations; and rural populations.<\/p>\n
For people newly diagnosed with cancer, the health care system can be challenging and overwhelming. The delivery of cancer care is often fragmented and poorly coordinated, and patients often face barriers to receiving timely and patient-centered care. \u00b2,\u00b3<\/p>\n
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In a landmark 2013 publication, Delivering High-Quality Cancer Care: Charting a New Course for a System in Crisis<\/a>, the Institute of Medicine (IOM) issued recommendations to improve the delivery of cancer care in the United States. The IOM called for strengthening patient-centered care and reducing disparities in care for vulnerable and underserved populations.<\/p>\n