Find answers to common questions about Limb Outcomes Voice (LOV), participation, privacy, and how your experiences help improve care.
What is Limb Outcomes Voice (LOV)?
LOV is a patient-centered initiative designed to amplify the voices and experiences of individuals living with limb loss, limb difference, and limb-threatening conditions.
What is the mission of LOV?
To empower individuals with trusted resources and gather real-world evidence that improves care.
How is LOV connected to LLPR?
LOV is part of the Limb Loss and Preservation Registry (LLPR).
What can I find on the LOV Resource Portal?
Educational articles, community resources, research updates, outcomes reports, and sponsor resources.
How long does the LOV survey take?
Approximately five minutes or less.
What topics are included?
Mobility, pain, sleep, falls, quality of life, satisfaction with care, and daily activities.
Is my personal information private?
Yes. Only you can see your individual responses.
What does de-identified mean?
Personal identifiers are removed before information is analyzed.
Does LOV sell my information?
No. Personal information and individual survey responses are never sold.
How does my participation help?
It improves patient care, research, innovation, healthcare decisions, and amplifies the patient voice.