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Villa Fiore Lifestyle - Taking Care of Elderly man - We are a residential care home dedicated to providing compassionate care, service and advocacy on behalf of our residents. Our mission is to enrich the lives of those who live with us by responding to their unique needs and universal desire for dignity and respect. We actively advocate for their needs by working on their behalf with physicians, hospitals, state and federal agencies, insurance companies, Medicare and Medicaid, pension programs and more. We pride ourselves on having a comfortable, clean and quiet home. We work to foster a peaceful, safe environment. With two decades of experience, we offer unparalleled care, service and advocacy in a family environment. We proudly provide professional, patient-centric supervisory, assisted and directed care, short-term respite stays, and memory-care support for Alzheimer’s and dementia patients. We also have knowledgeable and fully engaged staff on site 24/7, as well as an on-call Nurse Practitioner (NP). Under a single home care umbrella, Desert Haven Home Care, Apollo Residential Assisted Living, Oasis of Prescott, and Villa Fiore Assisted Living feature unparalleled care, service and advocacy in the compassionate treatment of senior citizens in need of medical attention. Offered in a familial setting, the facilities are teamed by professionals passionate about their work and fully engaged in the welfare of residents. Each facility proudly provides patient-centric supervisory, assisted and directed care, short-term respite stays and memory care support for Alzheimer’s and dementia patients.

Two decades of 

HOME CARE

experience.

Our residential care homes are dedicated to
enriching the lives of our seniors. 

We’re pleased to offer the widely used
BinaxNOW™ COVID-19 rapid test onsite for our residents and staff.

The BinaxNOW™ COVID-19 Ag Card Home Test is a lateral flow immunoassay intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2. The BinaxNOW™ COVID-19 Ag Card Home Test has not been FDA cleared or approved. It has been authorized by the FDA under an emergency use authorization. The test has been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens, and is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostic tests for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. § 360bbb-3(b)(1), unless the declaration is terminated or authorization is revoked sooner.

Contact

Contact us or request a tour!

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