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Our mission is to mobilize a community for patient support and advocacy, as well as drive and support impactful research that translates into advances for patients with migraine and other disabling diseases that cause severe head pain. Our core beliefs guide everything we do, from the research we promote to our efforts to build a supportive, welcoming community for all people living with migraine. Advocacy and education is the only way we will increase awareness and recognition of migraine for the disabling disease it truly is.

Despite significant reductions across the nation, tobacco use is still the number one cause of preventable death in the United States, killing more than 400,000 people every year. Since being established in 1999, the American Legacy Foundation (Legacy) has developed a comprehensive understanding of the tobacco crisis and the many issues that surround it. Legacy is the nation's largest and most effective independent public health charity dedicated to tobacco use prevention and smoking cessation. Our mission is to build a world where young people reject tobacco and anyone can quit. By giving young people the facts and information they need to reject tobacco and adult smokers the tools they need to quit and stay quit, Legacy is helping people live longer, healthier lives. Legacy employs community intervention and population-based public education strategies to reach current and potential tobacco users, customizing our approach to recognize, respect and address cultural differences.

To engage, educate and empower people to prevent bone loss, osteoporosis, and fractures and to keep strong bones for long and independent lives.

The Kidney Cancer Association's mission is to be a global community dedicated to serving and empowering patients and caregivers, and leading change through advocacy, research, and education. Our vision is to be the universal leader in finding the cure for kidney cancer.

Families are at the heart of MDA's mission. We wake up every morning to create more hope and answers for families living with muscular dystrophy and related diseases that take away physical strength and mobility. We do this by finding research breakthroughs across diseases, caring for kids and adults from day one and empowering families with services and support in hometowns across America.

To discover treatments and a cure for ALS (Amyotrophic Lateral Sclerosis), and to serve, advocate for, and empower people affected by ALS to live their lives to the fullest.

To be a leader in the quest to cure ankylosing spondylitis and related diseases, and to empower those affected to live their lives to the fullest.

New Horizons empowers individuals with special needs to fulfill their dreams. Through partnerships, community outreach, and advocacy, we create a brighter future in which the people we serve are accepted by, participate in, and add value to the community.

Our mission at the Dion Children Foundation for Rare Disease is to increase awareness of rare and ultra-rare genetic diseases such as Limb-Girdle Muscular Dystrophy, that affect children with the intention of allocating funds for research and development of potential treatments and cures of these devastating diseases. Our belief at Dion Children Fund is that no child should be left behind. Our children matter, and so do the lives of so many other children affected by rare genetic neuromuscular diseases.

The Global Foundation for Children with Hearing Loss is committed to helping young children who are deaf or hard of hearing living in developing countries access the early identification, hearing technology, and locally-based professional expertise they need to learn to listen and talk and reach their full potential.