AzMN was founded in June 2004 by Barbara B. Kavanagh. Our mission is to promote awareness, education and advocacy for improved treatment and quality of life, for multiple myeloma patients, their families and caregivers. Our members are patients, families, health care professionals, volunteers and others concerned about myeloma. AzMN is a nonprofit charity (501)(c)(3) organization that conducts outreach Events and Educational programs for Arizona Myeloma cancer patients, their families and caregivers, with special consideration for the under served: African American, Asian /Pacific, Hispanic American and Native American.
Our Vision:
Our Mission:
Our mission is to promote collaboration, awareness, education and advocacy for improved treatment and quality of life, for multiple myeloma patients, their families and ALL cancer caregivers with special consideration to the underserved.
Education
Awareness
Alerting patients to Arizona support group locations, specialist doctors and medical facilities with Myeloma experience
Advocacy
Why Focus on Cancer Caregivers?
“Family caregivers have been ‘silent partners’ in health care delivery, functioning as de facto care coordinators. During care handoffs, family caregivers make important contributions to ensuring quality, safety, and adherence to patient preferences; their role needs to be formally recognized and supported.” (Source: Coleman & Williams, Journal of Hospital Medicine, Sept/Oct 2007)