PX Policy Forum - Resources

Best Practices for Collecting Self-Reported Patient Demographic Data: “Collecting data for us and not about us.”

PXPF'S Measurement and Reporting Workgroup calls for healthcare to mandate the collection of self-reported patient data specific to race, ethnicity or primary language (REaL) and sexual orientation and gender identity (SOGI). 

Read the Paper

Telehealth Toolkit

Telehealth makes it easier for more people to get quality healthcare with less cost and hassle. Help up make telehealth permanent.

Learn More

Virtual and Telehealth Recommendations

Whether for telehealth appointments or for virtual connection during hospitalizations and long-term care, access to technology has the potential to greatly increase family and care partner engagement with the healthcare team.

Read the Blog

Addressing Visitation and Access for Guests and Care Partners

It is essential to acknowledge and act on the need for policies and practices that ensure this basic need for care partners is met and the associated evidence-based outcomes that result from effective patient and family engagement are realized.

Watch the Video

A Commitment to Patient & Family Advisors (PFAs) In Improving the Human Experience in Healthcare

The Beryl Institute community calls on health system leaders and organizations to commit to the industry standard of ensuring formal, intentional, and continuous partnerships with patients, families, and care partners.

Read the Statement