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.
The National Kidney Foundation of Arizona is the major voluntary health agency in Arizona seeking solutions for kidney and urinary tract diseases through education, prevention and treatment.
Committed to improve the quality of life for Arizonans with kidney failure, the Foundations many programs bring help and hope to thousands of dialysis patients and transplant recipients. NKF AZ kidney health initiatives provide community education about kidney health and the prevention of chronic kidney disease, and advocates for organ donation.
These efforts are made possible solely and in partnership with federal, state and local governments, public and private institutions, foundations and individuals.
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.
The Arthritis Foundation is the Champion of Yes. Leading the fight for the arthritis community, the Arthritis Foundation helps conquer everyday battles through life-changing information and resources, access to optimal care, advancements in science and community connections. Our goal is to chart a winning course, guiding families in developing personalized plans for living a full life and making each day another stride towards a cure. We also publish Arthritis Today, the award-winning magazine that reaches 4.2 million readers.
The mission of the Cystic Fibrosis Foundation is to cure cystic fibrosis and to provide all people with the disease the opportunity to lead full, productive lives by funding research and drug development, promoting individualized treatment, and ensuring access to high-quality, specialized care.
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.
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.