

NHF’s Community Voices in Research (formerly MyBDC) connects the experiences of people with bleeding disorders and their family members to researchers investigating improving treatments and care.
How does it work?
As a participant in NHF’s Community Voices in Research (CVR), you complete surveys about your experiences living with a bleeding disorder. Researchers seeking to better understand specific aspects of living with a bleeding disorder may submit targeted surveys that you can choose to complete. Surveys through research studies offer compensation for completion. All information will be reported in a de-identified, aggregate manner to protect your privacy. Your personal identified information will never be sold or shared. For more information, please read the CVR privacy policy.