NAMI Arizona is a statewide grassroots organization dedicated to serving individuals and families affected by mental illness to improve their quality of life and achieve recovery.NAMI Arizona promotes activities, in partnership with local NAMI affiliates, through education, advocacy, research, and support.
The Arizona Spinal Cord Injury Association is a non-profit organization dedicated to enhancing the lives of individuals with spinal cord injuries. Our goal is to promote physical, intellectual, spiritual, emotional and social recovery. The Association focuses on peer and family support, education of consumers, families, caregivers, and professionals, and linking people to vocational, social, and recreational resources.
DES provides supports and services to more than 35,000 people with developmental disabilities and their families throughout Arizona. The Department strives to provide support by promoting and providing flexible, quality, member-driven services and supports within communities. We value our community connections and emphasis on looking at a persons strengths and gifts.
The National Multiple Sclerosis Society exists because there are people with MS. Our vision is a world free of MS. Everything we do is focused so that people affected by MS can live their best lives as we stop MS in its tracks, restore what has been lost and end MS forever.
We are more than an organization. We are a movement. United in our collective power to do something about MS now and end this disease forever. The gathering place for people with MS, their family and loved ones, healthcare providers, volunteers, donors, fundraisers, advocates, community leaders and all those that seek a world free of MS. A place to connect and take action. In order to change the world, we mobilize all possible human and financial resources to achieve results.
Founded by Jane Kallal, a parent and leading advocate for parents and caregivers raising children and young adults with emotional, physical, and behavioral health challenges, her vision was to foster a system of care in which parents and families were valued and respected for their knowledge and expertise. Moreover, parents and families would be primary stakeholders and valuable partners at all levels including childrens service planning and delivery and program and policy development impacting childrens services. Jane believed then, as she does today, that parents know their children best.
The Leukemia & Lymphoma Society (LLS) is the largest voluntary health organization dedicated to funding research, finding cures and ensuring access to treatments for blood cancer patients.
Since 1949 LLS has been on the forefront of blood cancer advances such as chemotherapies and stem cell transplantation leading the way to the targeted therapies and immunotherapies that are saving thousands of lives today.
LLS is changing the landscape of cancer with more than 300 active research projects that explore different avenues of new and adventurous research; ones with promise and ones that will save lives not someday, but today.
Whenever we talk about cancer, we always use the same word. Someday. Someday there will be a cure. Someday we wont lose the people we love. But when is someday? With LLSs research partnerships and collaborations with pharmaceutical and biotechnology companies, patients support services and advocates working for blood cancer patients everywhere, someday is today.
What started in 1920 as an Americanization Agency, a local initiative providing educational resources to refugees, has evolved into a multi-service organization with wide-ranging programs aimed at addressing the pressing needs of our diverse community. Over the years our efforts have resulted in building resilient communities that are helping to spur economic development, stabilize neighborhoods and revitalize our city.
Our programs focus on four major pillars of service- Education, Workforce Development, Family Services and Immigration- each comprising of resources to support individual and community growth.