Synchronizing Your Journey to Wellness
At Cue Telehealth, we believe that healthcare should never feel like a series of disconnected events.
At Cue Telehealth, we believe that healthcare should never feel like a series of disconnected events.
Our Care Coordination team serves as the "connective tissue".
Care Coordination is the deliberate organization of patient care activities. In a hybrid healthcare world, this means bridging the gap between your virtual consultations, in-person specialist visits, and home monitoring data.
We act as your central hub, ensuring everyone on your care team reads from the same playbook.
Getting started
True healing happens when every provider, specialist, and data point is in perfect alignment.
Whether you are moving from a virtual primary care visit to an in-person visit, we manage the hand-off.
We ensure your electronic health records (EHR) are updated and shared securely in real-time.
Our coordinators schedule your tests and specialist appointments so you don't have to.
Proactive Advocacy
You aren't just a patient; you’re the center of the process. Our coordinators act as your advocates within the healthcare system.
Research shows that coordinated care leads to fewer hospital readmissions, reduced medical errors, and a significantly better patient experience.
By removing the administrative burden from your shoulders, we allow you to focus on what matters most: getting well.
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The Cue COVID-19 Test for Home and Over The Counter (OTC) Use, the Cue COVID-19 Test for CLIA Certified Healthcare Providers and Laboratories, and the Cue Mpox (Monkeypox) Molecular Test have not been FDA cleared or approved, but they have been authorized for emergency use by the FDA under Emergency Use Authorizations (EUAs). These products have been authorized only for the detection of nucleic acid from SARS-CoV-2 or monkeypox virus, respectively, not for any other viruses or pathogens. The emergency use of these products is only authorized for the duration of the declarations that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of infection with COVID-19 or the monkeypox virus, including in vitro diagnostics that detect and/or diagnose infection with non-variola Orthopoxvirus, under Section 564(b)(1) of the Federal Food, Drug, and Cosmetic Act, 21 U.S.C. § 360bbb3(b)(1), unless the relevant declaration is terminated or authorization is revoked sooner.
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