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Since our founding in 1998, we have provided over 225 million meals in 73 countries. This year, we will package 45 million meals, and ship over $9 million in donated aid, mainly vitamins and medical supplies. Based in Raleigh, N.C., we operate meal-packaging programs at 20 cities in the U.S. and in South Africa, Malaysia, India, Italy, Peru and the Philippines. We have engaged over 500,000 corporate, student, civic and faith-based volunteers in meal-packaging. In just under two hours, a group of 40 to 50 volunteers can package 10,152 nutrient-rich meals for the undernourished globally. We also educate volunteers about hunger and inspire them to help end it.
San Diego Hospice and The Institute for Palliative Medicine is a San Diego, CA-based company in the Non-profit sector.
Connecticut Naral Foundation is a Hartford, CT-based company in the Non-Profit sector.
Mensa International Limited is a Arlington, TX-based company in the Non-profit sector.
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.