This Study is to Evaluate Whether Receiving Education and Glucose Monitoring With the CGM Device Will Improve Patient-reported Outcomes by Improving Patient's Satisfaction and Quality of Life (QOL) With Glucose Monitoring Device

Inclusion Criteria:

• aged 18 or older

• diagnosed with Type 1 or Type 2 Diabetes who are on insulin

• able to speak and understand English language

• scheduled to receive a standard inpatient diabetes education consultation

• must not have used CGM in the six months prior to admission

• owns a smartphone

• demonstrates the ability to follow instructions and be capable of providing informedconsent to participate in the program

Exclusion Criteria:

• those who are known to be pregnant. This is due to complexity of pregnancy-relatedchanges in glucose metabolism and increased skin sensitivity, or changes in skincondition to adhesives and materials used in CGM devices.

• non-English speakers. As this is small study to evaluate which method is favorableusing a survey only validated in English, enrolling non-English speakers wouldrequire additional resources/translations/personnel for evaluation and the educationintervention that are not logistically possible right now.