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Children’s Health Foundation of Vancouver Island is a registered charity whose purpose is to raise funds to support the health and well being of children and youth in need on Vancouver Island and the Gulf Islands. Our roots go back to 1922, and we were previously known as the Queen Alexandra Foundation for Children. Governed by a volunteer Board of Directors and audited annually, funds are carefully allocated to facilities, services, programs, special projects and urgently needed medical equipment that help ensure children and youth develop to their full potential. Children mean the world to us.

We seek to better understand the roots of disease and narrow the gap between new biological insights and impact for patients. The Broad Institute of MIT and Harvard is a research organization that convenes a community of researchers from across many disciplines and partner institutions—MIT, Harvard, and Harvard-affiliated hospitals. Based in Cambridge, Massachusetts, the Broad Institute was founded in 2004 to fulfill the promise of genomic medicine—three years after completion of the Human Genome Project, which Broad scientists helped create and lead. Our origins are rooted in genomics, and as biomedical research and knowledge have expanded since 2004, so have we. Our researchers are deeply collaborative, nimbly launching innovative, high-risk projects at every scale, inventing new technologies, building and implementing computational tools, developing new therapeutics to advance into the clinic, mentoring and training the next generation of scientists, and sharing our data and tools openly to enable breakthroughs anywhere. Accelerating biomedical research and improving human health require diversity of all kinds in our community—in education, training, background, perspectives, interests, and identity—because it expands our creativity in how we approach problems and find solutions. Broad aims to ensure that the benefits of genomic medicine are shared by all.

Hands of Hope Foundation is designed to operate and develop faith based communities that will function on a local, national, and international level to provide financial and/or direct assistance to individuals, families, and other organizations in meeting a wide variety of needs to include: short term housing, medical care, education assistance, drinkable water, food and clothing; as well as a place of respite for Ministers and their families. Offering Hope in Christ in the spirit of 1 Peter 3:15. Our current projects include: educational services in Liberia, Bulgaria, and Thailand. Medical clinic in Weala, Liberia. 5 new churches in Pattaya, Thailand.

Ekam USA Inc Mission Statement To develop a high quality, comprehensive, continuous healthcare model that will ensure the care of every neonate, infant, child, adolescent and mother in a respectful, caring and family-centered environment, regardless of their financial situations by supporting and improving the public health care system. To support and improve health care for children in financial need. To remove financial constraints on parents of needy children. To develop a healthy world population by improving awareness through education and preventive program, as well as providing support for children’s health care. To develop a sense of service in the community by local service projects.

Parkinson Society Canada is a not for profit, national charitable organization. The Society raises money through corporate sponsorships,public donations, and planned gifts. Finding the cause and cure for Parkinson's disease remains our chief mission. However, while we wait for answers, we must not forget the patients and caregivers. New publications, increased patient conferences, clinical assistance programs, as well as other projects also require your support and funding. While we have come a long way towards raising Parkinson's disease in the consciousness of Canadians, we have more to do.

MMI's vision is to care annually for 100 million of the world's needy by the year 2050. MMI is committed to meet the need for medical care among the world's poor with lasting solutions through excellence in medicine, patient care, and health education. We do this by mobilizing volunteers on short-term medical projects and establishing and equipping permanent medical centers. We work alongside national doctors and helpers from the countries we go to, joining the efforts of the local church where possible. This healing ministry strengthens village churches and enhances missions outreach in our participants' home churches.

The mission of the Southern Arizona AIDS Foundation (SAAF) is to cultivate a healthy & stigma-free society through transformative action. In 1997, three AIDS service organizations in Tucson (Tucson AIDS Project, PACT for Life, and Shanti Foundation) merged to form SAAF. In 2014, SAAF took over several initiatives from Wingspan, formerly Southern Arizona's LGBTQ community center. In 2015, SAAF celebrated 30 years of providing services and continues to be the only community-based organization in southern Arizona providing case management and ancillary support services for people living with HIV/AIDS and their families; culturally appropriate prevention and education programs to reduce the rate of infection; & LGBTQ community outreach & engagement.

The overall mission of Blue Hope is to raise funds, resources, social awareness, and provide other support for a variety of self-sustaining social development projects and programs, both domestically and abroad, in order to effectively fight social injustice at a grass roots level. As of its founding, Blue Hope is primarily focusing on working with education, poverty, and children’s issues in Tanzania, East Africa and has done so by constructing and supporting a residential and educational facility and its outreach program. House of Blue Hope pulls kids off the streets and puts them into a safe living and learning environment. With such access to one of the top schools in the country, the current and future residents of the House of Blue Hope will be provided with top-notch educational opportunities in a country in which only about 12% of the population receives a secondary education. Furthermore, the facility has become a large part of the local high school’s community service program, as well as a catalyst to keep alumni involved and connected after graduation.

Founded in 1996, this community based organization provides health care services through its legacy namesake, The James A. Watson Wellness Center. The non-profit charity foundation, Preventive Care Pathways, also provides educational outreach to underserved and/or marginalized communities throughout the Bay Area. Our goal is to decrease the disparities in health care services, education and mortality outcomes among those most marginalized or underserved through culturally sensitive care and education. We seek to start at the beginning, with the Youth of our community and "Keep Youth Alive" and firmly believe that "Art Saves Lives". The primary function of Preventive Care Pathways in serving the community is to bring together the resources that are most beneficial to our youth followed by incorporating Youth and their needs within the community of Adults in business and medicine, and especially in science, technology, reading, engineering, arts and mathematics or, in short, "S.T.R.E.A.M." "Remember, your health is your wealth and if you knew better you would do better! (c)". So we move to bring all of the educational instruments to our Youth and those who are there to support them, starting with our Youth in Arts Project. Please give generously and give frequently. Every amount helps. Thank you.

1) To provide the LATEST MEDICAL / RESEARCH information and EDUCATION so that they may make wise medical decisions and continue their independence despite their vision. Provide information and research data to the medical and research community so that they may join in our fight against blindness. The AFI International Aniridia Medical Registry and Gene Bank is the main project of our research. 2) To SUPPORT the low vision / blind people born with aniridia and their families who struggle emotionally and financially due to having aniridia. To assist them in accomplishing their dreams and remain independent, self sufficient and a productive member of society. 3) To help fund RESEARCH especially the AFI created program which collects DNA samples, comphrehensive medical questionaires, and clinical photographs to add knowledge to physicians and advance research. Our international faculty of AFI Medical Advisory and Scientific Boards assist us with this program. We also help fund research and patient care services as funds allow and look forward to raising funds to expand our efforts to stop this genetic condition from continuing into future generations.. 4) To further PUBLIC AWARENESS about all the conditions that make up aniridia, and the misconceptions of people who are blind or low vision,

The Ehlers-Danlos Society is a global community of patients, caregivers, health care professionals, and supporters, dedicated to saving and improving the lives of those affected by the Ehlers-Danlos syndromes and related disorders. We are a nonprofit organization, established in 1985 as the Ehlers-Danlos National Foundation by Nancy Hanna Rogowski (1957–1995) Our Vision We support collaborative research and education initiatives, awareness campaigns, advocacy, community-building, and care for the EDS and HSD (Hypermobile Spectrum Disorders) population. Our goals are world-wide awareness—and a better quality of life for all who suffer from these conditions. Research is at the center of what we do, so that one day we will have a cure. Our strength begins with hope. Our Mission Collaborative research bringing together medical professionals from all over the world to work on groundbreaking management and care. Organizing medical and scientific symposiums to examine the latest research and update the diagnostic criteria and guidelines for management and care. Bringing together and uniting our community, providing annual conferences globally to distribute information and create opportunities to interact. Producing reliable up-to-date medical literature though our esteemed medical and scientific board and International Consortium on EDS and Related Disorders. Guiding both patients and medical professionals to the most up to date information, resources, support, and education. Uniting support groups and charities from around the world, providing resources and information where needed. Working with our Affiliates on local issues and projects that affect our communities around the globe. One person fighting is a start, but many together build an army. Giving HOPE to all those whose lives are affected by Ehlers-Danlos syndromes.

Mountain States Children’s Home extends Christian services to wounded children in an effort to meet theirphysical needs, heal their emotional hurts, challenge their minds and teach them moral principles in order to reachthe goals of reuniting them with their families or preparing them for independence. This is accomplished using afamily model of care, strengthened by professional counselors and teachers.