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The Michael J. Fox Foundation for Parkinson is a New York, NY-based company in the Non-Profit sector.
National Kidney Foundation of Georgia is a Atlanta, GA-based company in the Non-Profit sector.
The International Association of Foundation Drilling is a Dallas, TX-based company in the Non-profit sector.
Today, autism affects one out of 50 children throughout the nation. It is the fastest growing developmental disability at an astounding 1,148% growth rate.Individuals at Little City Thankfully, for more than 50 years, Little City Foundation has successfully created hope, changed lives and challenged the limits placed on children and adults with autism and other intellectual and developmental disabilities. Our comprehensive services and programs make us the preeminent organization of our kind in Illinois and we invite you to learn more and join us in our advocacy! Become a champion for individuals with disabilities.
The National Organization for Rare Disorders, a 501(c)(3) organization, is an independent patient advocacy organization dedicated to helping individuals with rare diseases and the organizations that serve them. NORD, along with its 280 patient organization members, is committed to the identification, treatment, and cure of rare disorders through programs of education, advocacy, research, and patient support services. NORD serves all stakeholders in the rare disease community, including patients and their families, patient organizations, researchers, medical professionals, medical students, and companies developing orphan products. NORD also works closely with many government agencies, most notably the National Institutes of Health (NIH) and the Food and Drug Administration (FDA). All NORD programs are focused on one ultimate goal -- to improve the lives of individuals and families affected by rare diseases. NORD is the official sponsor of Rare Disease Day in the U.S., an observance day held on the last day of February each year worldwide. Its goals are to raise awareness for rare diseases and improve access to treatment and medical representation for individuals with rare diseases and their families.