The Lived Experience Advisory Panel (LEAP), composed of cancer patient advocates, provides strategic and operational guidance for the Pediatric Cancer Data Commons. 

Purpose:

  • To offer insights on initiatives of the Pediatric Cancer Data Commons from the perspective of those with lived experiences with pediatric and AYA cancers.
  • To represent patient populations whose data are or may be included in the PCDC and to safeguard patient agency.
  • To amplify the voices of patients and patient advocates within the work of the Pediatric Cancer Data Commons.

LEAP Members

NamePCDC InvolvementCountry
Sarah BartoszParent and patient advocateUnited States
Kim BuffParent advocateUnited States
Evan ConnellyPatient advocateUnited States
Parag DasPatient advocate, pediatric oncologistIndia
Sloane DyerPatient advocateUnited States
Mindy DykesParent advocateUnited States
Mariah Forster OlsonPatient advocateUnited States
Parker MossParent advocate, EAB memberUnited States
Max PenzerPatient advocate, ARC memberUnited States
Carlos SandiParent advocate, EAB memberUnited States
Johnny SchroepferParent advocateUnited States
Greg SimonParent and patient advocate, EAB memberUnited States
Eshan VishwakarmaPatient advocateUnited States
Michaela WilliPatient advocate, SAC memberAustria