PUBLIC AND PATIENT INVOLVEMENT
IN RESEARCH (PPI)
Patient and Public Involvement in Research (PPI) is all about involving someone affected by a condition in all aspects of research. This can be a person with the condition, their family members or their carers.
At Myelopathy.org we believe that every voice is important. Involving people with lived-experience of Degenerative Cervical Myelopathy (DCM) will enhance both the quality and the impact of research.
At Myelopathy.org we have an extensive network of people with DCM and their carers and families who are willing to become involved in all aspects of DCM research.
If you would like to know more about how we can help you involve people with DCM in your research please contact us at firstname.lastname@example.org.