PATIENT-CAREGIVER ADVOCACY NETWORK
The National LeioMyoSarcoma Foundation announces a signature program launching in 2020.
NLMSF Patient-Caregiver Advocacy Network (PCAN)
By coming together, we can achieve anything!
individual voices unite to serve as a core transformative component for the care paradigm with an emphasis on patient experience. This network can generate recommendations for changes to the standard of care—from initial diagnosis to end of treatment—that will create a legacy for those patients and caregivers who come after us.
Join us for our next call on Wednesday, February 19
at 7 pm EST, 4 pm PST
This is not a support group. Rather an effort to impact care by sharing your actionable suggestions with the oncology care and research communities. A “think-tank” if you will, in which your voice will be important and will be heard.
The January meeting was well attended and the February meeting is forming now. For more information or to register your participation, please contact Annie Achee at 303-808-3437 or [email protected]
SIGN IN TO JOIN THE PATIENT-CAREGIVER ADVOCACY NETWORK