Rare Patient Voice, LLC provides patients and caregivers with rare and non-rare diseases an opportunity to voice their opinions through surveys and interviews to improve medical products and services.
Wes Michael, President and Founder of Rare Patient Voice, has been involved in rare and orphan diseases since 1998, interviewing and surveying patients, caregivers, physicians, nurses and advocacy leaders. Wes has more than 40 years experience in marketing research, and more than 20 years in healthcare marketing research.
While we started by focusing on rare diseases, we now welcome patients and caregivers with all medical conditions.
Rare Patient Voice takes an active approach to meet patients at conferences and events. Our phone is always open to members. The more we can engage with patients, the more we can advocate for them and help their voices be heard.
Since launching in the United States in 2013, RPV has expanded across the globe! We now recruit patients and caregivers for research studies in the US, Canada, Germany, Italy, France, Spain, Australia, and New Zealand. Visit our global site for more information.