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HEALTH EQUITY, CARE, DELIVERY, & ACCESS TO CARE
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HEALTH EQUITY, CARE, DELIVERY, & ACCESS TO CARE
HEALTH EQUITY, CARE, DELIVERY, & ACCESS TO CARE
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(350) Examining Representation, Education and Resources as Barriers to Engagement in CF Communities of Color
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(351) Rounding out the pediatric CF care team: Including the profession of occupational therapy
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(352) Evaluation of Outcomes in Black People with Cystic Fibrosis using the CF Foundation Patient Registry
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(353) Risk Factors Associated with Meeting the Standard of Care and Use of Telehealth in 2020 among Persons with Cystic Fibrosis in the United States
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(354) Racial disparities in cystic fibrosis-related diabetes outcomes
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(355) Investigating Disparities in Cystic Fibrosis Clinical Trial Participation: One Cystic Fibrosis Center’s Self-Study
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(356) The Battle Over State Lines: Leveraging an Interstate Compact to Ensure Continuity of Care
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(357) Implementing a Social Determinants of Health (SDoH) screener in a large pediatric Cystic Fibrosis Center
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(358) Patient and family perceptions and opportunities for improvement for transition from pediatric to adult cystic fibrosis clinic
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(359) Access to Endoscopic Retrograde Cholangiopancreatography in Children and Adolescents with Cystic Fibrosis
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(360) Inter-clinician diagnostic concordance assessing adults presenting with possible cystic fibrosis
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(361) Distribution and cost of common CF prescription drugs using claims data
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(362) CF community experiences with self-funded employer insurance
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(363) Preventive Service Utilization among Cystic Fibrosis Adults with Private Insurance is Comparable to the General Population
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(364) Detection of Disease-Causing
CFTR
Variants In State Newborn Screening Programs
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(365) Flow diagram template to recognize roles of race and ethnicity in health inequity among patients with cystic fibrosis
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(366) Attitudes amidst the pandemic: virtual delivery of care in an adult cystic fibrosis population
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(367) Measuring Burden of Disease for Canadians, both Adult and Pediatric, with Cystic Fibrosis (CF) and their Caregivers - A Systematic Literature Review
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(368) Benefits of Medically Tailored Meal Interventions for People with CF
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(369) CF Global Work in Egypt: Progress of Collaboration Between University of Michigan and Four Universities Across the Country>
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(370) Current prices versus minimum costs of production for CFTR modulators
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(371) Hospitalization data in the era of highly-effective cystic fibrosis transmembrane conductance regulator (CFTR) modulator therapy
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(372) Increasing interest in post-secondary education in the CF population
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(373) Is there a Disparity in Access for Elexacaftor/Tezacaftor/Ivacaftor in Hispanic Versus Non-Hispanic Patients with Cystic Fibrosis?
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(374) Optimizing screening for food insecurity in a pediatric CF Center
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(375) SNAP & WIC: CF program knowledge and utilization
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(376) The Implementation of the CF R.I.S.E. Program in CF Pediatric Clinics
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(377) The Utility of Telemedicine in Cystic Fibrosis Clinic Visits
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(378) Underutilization of Allergist Care In The Management of CF
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(379) When Insurance Doesn’t Cover It: Advocating to Protect State CF Programs
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