Defining My Rights

A few weeks ago Dave (my podcast partner and friend) and I were approached with an interesting challenge: to develop an Amputee Bill of Rights. At first the task felt overwhelming, but we decided that the process would be fascinating. Without conferring with each other, we each developed ten core principles that we believed every amputee deserved to expect. Only after we each completed our list did we share our ideas and thoughts.

This exercise forced me to reflect upon what I really valued and believed. What do I want for the limb loss community? What do I expect as a right versus something that might be negotiable? In the end I carefully chose those principles for which I would fight and advocate.

This exercise was cathartic as I was forced to become retrospective. While I was evaluating every aspect of my life, questioning what was a true entitlement, I uncovered clarity. I now have a concrete list that will become my springboard for future work.

As expected, Dave and I had several core principles that were nearly identical. About half of our principles were vastly different and unique to our life experiences and perspective. Dave focused more on insurance and access to devices whereas I tended towards addressing issues that were more personal in nature.

After much back and forth, we managed to merge both lists into one document. Our Bill of Rights is still in its infancy and we are seeking input from the community. What would you add to the list, or what would you take away? I would love and appreciate feedback.